{"month": "2026-04", "count": 673, "recalls": [{"id": "fda-device-z-0145-2027", "source": "FDA", "category": "device", "recall_number": "Z-0145-2027", "title": "Power F2 Powered Fastening System recall (Ferno-Washington Inc)", "product": "Power F2 Powered Fastening System, Power F2, Item No. 0567093 used with Power X2 Stretchers, Power X2, Item No. 0015816 and PowerX2 Premium, Item No. 0015821", "reason": "Firmware issue may result in intermittent loss or degradation of powered functionality when paired with compatible stretcher. The issue may lead to the system not operating in powered mode, or exhibiting reduced powered performance. Issue may result in interruption or delay in patient transport.", "hazard_level": "Class II", "company": "Ferno-Washington Inc", "company_location": "Wilmington, OH, United States", "date": "2026-04-28", "report_date": "2026-10-21", "status": "Ongoing", "distribution": "Worldwide - US Nationwide distribution in the states of AL, AR, AZ, CA, CO, FL, ID, IL, KY, LA, ME, MN, MO, MT, NC, NE, NJ, NM, NY, OH, OK, PA, SC, TN, TX, UT, VA, WA, WI, WV and the countries of Netherlands and Poland.", "states": ["AL", "AR", "AZ", "CA", "CO", "FL", "ID", "IL", "KY", "LA", "ME", "MN", "MO", "MT", "NC", "NE", "NJ", "NM", "NY", "OH", "OK", "PA", "SC", "TN", "TX", "UT", "VA", "WA", "WI", "WV"], "nationwide": true, "quantity": "319", "codes": "Power F2 UDI-DI 00190790006570 Firmware versions: PF2 Carriage V0.51/V1.42, PF2 Rail V0.41, PF2 Connect V108 Serial Numbers 25C227687 25C228205 25C228204 25C227690 25C227691 25C227692 25C227688 25C227689 25C227695 25C227700 25C227698 25C227699 25C227702 25C227703 25C227704 25C227696 25C227701 25C227710 25C227708 25C227711 26C231799 26C231800 26C231801 25C227709 25C227707 26C231797 26C232002 26C232004 26C232007 26C232005 26C232008 26C232009 26C231798 26C232010 26C232006 26C232011 26C232374 26C232377 26C232375 26C232379 26C232378 26C232382 26C232717 26C232715 26C232380 26C232384 26C232710 26C232713 26C233032 26C232381 26C232712 26C232718 26C232716 26C233035 26C232714 26C233033 26C233038 26C233041 26C233090 26C233040 26C233039 26C233037 26C233092 26C233036 26C233091 26C233094 26C233111 26C232711 26C233098 26C233097 26C233095 26C233096 26C233115 26C233114 26C233099 26C233113 26C233112 26C233117 26C233443 26C233119 26C233120 26C233118 26C233444 26C233451 26C233450 26C233449 26C233452 26C233692 26C233694 26C233693 26C233697 26C233699 26C233696 26C233701 26C233700 26C234074 26C234078 26C234072 26C234073 26C234076 26C233698 26C234077 26C234079 26C234080 26C234081 26C234082 26C234083 26C234071 26C234084 26C234085 26C234087 26C234086 26C234088 26C234356 26C234346 26C234353 26C234566 26C234352 26C234357 26C234361 26C234359 26C234355 26C234350 26C234362 26C234630 26C234363 26C234364 26C234649 26C234639 26C234632 26C234634 26C234631 26C234635 26C234648 26C234641 26C234640 26C234644 26C234646 26C234642 26C234647 26C234799 26C234797 26C234800 26C234805 26C234812 26C234567 26C234807 26C234801 26C234806 26C234810 26C234804 26C234808 26C234811 26C234814 26C234636 26C234809 26C235037 26C234813 26C234815 26C234816 26C235036 26C235045 26C235047 26C235048 26C235044 26C235046 26C235041 26C235049 26C235050 26C235052 26C235053 26C235054 26C235139 26C235135 26C235137 26C235055 26C235136 26C235138 26C235143 26C235134 26C235141 26C235142 26C235140 26C235144 26C235147 26C235151 26C235149 26C235150 26C235146 26C235148 26C235145 26C235152 26C235431 26C235429 26C235433 26C235432 26C235434 26C235438 26C235437 26C235436 26C235443 26C235446 26C235444 26C235445 26C235686 26C235447 26C235687 26C235700 26C235693 26C235696 26C235688 26C235692 26C235695 26C235697 26C235698 26C235699 26C235702 26C235694 26C235705 26C235701 26C236027 26C235703 26C236029 26C236030 26C236032 26C236035 26C235704 26C236028 26C236038 26C236039 26C236037 26C236042 26C236036 26C236034 26C236033 26C236040 26C236041 26C236026 26C236107 26C236109 26C236110 26C236043 26C236044 26C236045 26C236105 26C236108 26C236106 26C236116 26C236119 26C236113 26C236112 26C236244 26C236121 26C236245 26C236122 26C236123 26C236246 26C236250 26C236255 26C236118 26C236247 26C236729 26C236124 26C236254 26C236257 26C236258 26C236249 26C236260 26C236262 26C236734 26C236256 26C236728 26C236735 26C236731 26C236736 26C236732 26C236733 26C236737 26C236741 26C236746 Power X2 UDI-DI 00190790003210 (Power X2) and 00190790006600 (PowerX2 Premium) Firmware versions PX2 V1.11/V1.18 Serial Numbers 25G036128 25G036612 25G036614 25G036801 25G036802 25G036803 25G036804 25G036827 25G036830 25G036833 25G036834 25G036835 25G036837 25G036836 25G036953 25G036954 25G036958 25G036959 25G036960 25G036961 25G036962 25G036963 25G036964 25G037067 25G037068 25G037071 25G037094 25G037072 25G037095 25G037098 25G037100 25G037161 25G037163 25G037217 25G037225 25G037226 25G037227 25G037228 25G037229 25G037285 25G037289 25G037288 25G037298 25G037299 25G037305 25G037338 25G037342 25G037337 25G037466 25G037467 25G037468 25G037470 25G037471 25G037472 25G037473 25G037474 25G037526 25G037596 25G037595 25G037623 25G037665 25G037691 25G037692 25G037705 25G037707 25G037703 25G037704 25G037706 25G037713 25G037770 25G037772 25G037774 25G037780 25G037781 25G037782 25G038074 25G038075 25G038076 25G038080 25G038081 25G038082 25G038079 25G038083 25G038084 25G038536 25G038088 25G038539 25G038540 25G038615 25G038616 25G038617 25G038618 25G038625 25G038627 25G038578 25G038626 25G038619 25G038765 25G038767 25G038766 25G038768 25G038769 25G038948 25G038991 25G039003 25G039001 25G039002 25G039004 25G039005 25G039068 25G039069 25G039070 25G039065 25G039066 25G039067 25G039072 25G039071 25G039073 25G039189 25G039188 25G039191 25G039192 25G039193 25G039210 25G039248 25G039249 25G039190 25G039350 25G039653 25G039720 25G039728 25G039724 25G039725 25G039726 25G039727 25G039728 25G039737 25G039730 25G039732 25G039738 25G039729 25G039754 25G039736 25G040014 25G040015 25G040016 25C227713 25C227714 25G039773 25G040077 25G040078 25G040079 25G039774 25G039776 25G040073 25G040074 25G039775 25G040075 25G040076 25G039878 25G039879 26G046003 26G046004 26G046005 26G046006 25G039777 25G039872 25G040062 26G046007 26G046008 26G046009 26G046010 26G046011 26G046012 26G046013 26G046014 26G046015 26G046049 26G046051 26G046052 25G039881 26G046048 26G046111 26G046050 25G039779 25G039882 25G040061 26G046045 26G046046 26G046110 26G046112 26G046113 25G039880 26G046047 26G046105 25G040070 26G046016 26G046103 26G046106 26G046109 25G040067 25G040069 25G040071 25G040072 26G046236 26G046237 26G046239 25G040068 26G046238 26G046240 26G046265 26G046266 26G046267 26G046268 26G046269 26G046313 26G046318 26G046319 26G046320 26G046321 26G046310 26G046311 26G046312 26G046314 26G046315 26G046316 26G046317 26G046336 26G046322 26G046334 26G046335 26G046324 26G046401 26G046389 26G046388 26G046390 26G046393 26G046396 26G046397 26G046398 26G046399 26G046400 26G046455 26G046458 26G046459 26G046391 26G046394 26G046454 26G046456 26G046457 26G046460 26G046461 26G046387 26G046392 26G046395 26G046629 26G046630 26G046631 26G046632 26G046633 26G046634 26G046635 26G046636 26G046637 26G046638 26G046721 26G046722 26G046583 26G046855 26G046580 26G046581 26G046646 26G046774 26G046802 26G046805 26G046806 26G046803 26C234762 26C234763 26C234764 26C234765 26C234766 26C234767 26G046808 26C234770 26C234771 26G046582 26G046647 26G046723 26G046801 26G046804 26G046807 26G046818 26C234768 26G046775 26G046819 26G046820 26G046821 26G046822 26G046856 26G046857 26G046859 26G046884 26G046882 26G046883 26G046885 26G046858 26G046887 26G046888 26G046907 26G046908 26G046909 26G046910 26G046911 26G046927 26G046928 26G046923 26G046924 26G046925 26G046987 26G046988 26G046989 26G046886 26G046926 26G046929 26G046984 26G046985 26G046982 26G046983 26G046986 26G047001 26G046996 26G046997 26G046998 26G046999 26G047002 26G047003 26G047004 26G047066 26C236801 26G047008 26G047009 26G047012 26G047013 26C236726 26C236727 26G047000 26G047010 26G047014 26G047011 26G047059 26G047060 26G047061 26G047062 26G047099 26C236723 26C236725 26G047063 26G047064 26G047097 26C236803 26C236804 26C236722 26C236802 26C236805 26C236806 26C236807 26C236840 26C236841 26C236724 26C236842 26C236843 26C236844 26C236854 26C236932 26C236935 26C236857", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0145-2027%22", "url": "https://recallledger.net/recalls/device-z-0145-2027-power-f2-powered-fastening-system-power-f2-item-no-0567093-used-wit/"}, {"id": "fda-food-h-1263-2026", "source": "FDA", "category": "food", "recall_number": "H-1263-2026", "title": "Addall XR Shot 1 single bottle recall (ZMB Enterprises)", "product": "Addall XR Shot 1 single bottle, 2 fl. oz., liquid dietary supplement", "reason": "The product contains 1,4-DMAA, Phenylethylamine and Phenibut.", "hazard_level": "Class I", "company": "ZMB Enterprises", "company_location": "Carlsbad, CA, United States", "date": "2026-04-03", "report_date": "2026-09-02", "status": "Ongoing", "distribution": "The firm markets their products online via their website addallxr.com", "states": [], "nationwide": false, "quantity": "unknown", "codes": "Sold between July - December 2025", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-1263-2026%22", "url": "https://recallledger.net/recalls/food-h-1263-2026-addall-xr-shot-1-single-bottle-2-fl-oz-liquid-dietary-supplement/"}, {"id": "fda-device-z-2913-2026", "source": "FDA", "category": "device", "recall_number": "Z-2913-2026", "title": "navify Digital Pathology recall (Ventana Medical Systems, Inc.)", "product": "navify Digital Pathology (on-prem) v2.5, Material Number 10092343001 navify Digital Pathology (Cloud) v2.5. Material Number 09453733001 UDI-DI Code: 761333602095AQ In the United States, navify Digital Pathology software (previously known as uPath Enterprise Software) is a component of the Roche Digital Pathology Dx device cleared by the US FDA for Whole Slide Imaging purposes. Roche Digital Pathology Dx is an automated digital slide creation, viewing, and management system.", "reason": "Due to complaints received for the Image Management System regarding image/metadata discrepancy with the Viewer window", "hazard_level": "Class II", "company": "Ventana Medical Systems, Inc.", "company_location": "Tucson, AZ, United States", "date": "2026-04-20", "report_date": "2026-08-19", "status": "Ongoing", "distribution": "Worldwide - U.S. Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT, FL, GA, IA, ID IL, IN, KS, KY, MA, MD, MI, MN, MO, MS, NC, NJ, NY, OH, OK, PA, PR, SC, SD, TN, TX, UT, WI, and WV. The countries of Austria, Belgium, Czech Republic, France, Germany, Ireland, Italy, Netherlands, Romania, Spain, and Switzerland, Argentina, Bosnia & Herzegovina, Brazil, Chile, Colombia, Dominican Republic, Ecuador, Jordan, Mexico, Myanmar, Peru, Turkey, United Kingdom, Australia, Bahrain, Colombia, Hong Kong, Portugal and India.", "states": ["AL", "AR", "AZ", "CA", "CO", "CT", "FL", "GA", "IA", "ID", "IL", "IN", "KS", "KY", "MA", "MD", "MI", "MN", "MO", "MS", "NC", "NJ", "NY", "OH", "OK", "PA", "PR", "SC", "SD", "TN", "TX", "UT", "WI", "WV"], "nationwide": true, "quantity": "190", "codes": "navify Digital Pathology (on-prem) v2.5, Material Number 10092343001 navify Digital Pathology (Cloud) v2.5. Material Number 09453733001 UDI-DI Code: 761333602095AQ Software version Numbers: 2.5.0, 2.5.0.1, 2.5.0.2, and 2.5.1", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2913-2026%22", "url": "https://recallledger.net/recalls/device-z-2913-2026-navify-digital-pathology-on-prem-v2-5-material-number-10092343001/"}, {"id": "fda-device-z-2912-2026", "source": "FDA", "category": "device", "recall_number": "Z-2912-2026", "title": "BOBBY Balloon Guide Catheter REF: BOB-895-CN BOB-895-EMEA BOB-895-EMEA-AL ... recall (MICROVENTION INC.)", "product": "BOBBY Balloon Guide Catheter REF: BOB-895-CN BOB-895-EMEA BOB-895-EMEA-AL BOB-895-US MV-BGA01095 For use in facilitating the insertion and guidance of an intravascular catheter into a selected blood vessel in the peripheral and neurovascular systems.", "reason": "Due to an increase rate of balloon pinhole defects.", "hazard_level": "Class II", "company": "MICROVENTION INC.", "company_location": "Aliso Viejo, CA, United States", "date": "2026-04-30", "report_date": "2026-08-19", "status": "Ongoing", "distribution": "Worldwide - U.S. Nationwide distribution in the states of AL, AR, AZ, CA, FL, GA, IA, IL, KS, KY, LA, MI, MN, MO, MT, NC, NH, NM, NY, OH, PA, SD, TN, TX, WA, and WI. The countries of Europe - Austria, Belgium, Denmark, Finland, France, Germany, Greece, Iceland, Ireland, Italy, Lithuania, Netherlands, Norway, Poland, Romania, Slovenia, South Africa, Spain, Sweden, Switzerland, Ukraine, and United Kingdom. Asia - China, Japan, Jordan, New Zealand, South Korea, and United Arab Emirates.", "states": ["AL", "AR", "AZ", "CA", "FL", "GA", "IA", "IL", "KS", "KY", "LA", "MI", "MN", "MO", "MT", "NC", "NH", "NM", "NY", "OH", "PA", "SD", "TN", "TX", "WA", "WI"], "nationwide": true, "quantity": "5500 devices", "codes": "Catalog Number: BOB-895-CN UDI codes: (01)00842429111062(11)250819(17)280731(10)0001218734 (01)00842429111062(11)250822(17)280731(10)0001222844 (01)00842429111062(11)250825(17)280731(10)0001224137 (01)00842429111062(11)250828(17)280731(10)0001226522 (01)00842429111062(11)250910(17)280831(10)0001264372 (01)00842429111062(11)250911(17)280831(10)0001281308 (01)00842429111062(11)250917(17)280831(10)0001283704 Lot Numbers: 0001218734 0001222844 0001224137 0001226522 0001264372 0001281308 0001283704 Catalog Number: BOB-895-EMEA UDI code: (01)00842429108550(11)241108(17)271031(10)0000756596 (01)00842429108550(11)241109(17)271031(10)0000757384 (01)00842429108550(11)241118(17)271031(10)0000758945 (01)00842429108550(11)241120(17)271031(10)0000765270 (01)00842429108550(11)241121(17)271031(10)0000767660 (01)00842429108550(11)241126(17)271031(10)0000772588 (01)00842429108550(11)241202(17)271130(10)0000774885 (01)00842429108550(11)241128(17)271031(10)0000778089 (01)00842429108550(11)241204(17)271130(10)0000779647 (01)00842429108550(11)241207(17)271130(10)0000781240 (01)00842429108550(11)241210(17)271130(10)0000784041 (01)00842429108550(11)241210(17)271130(10)0000799436 (01)00842429108550(11)241213(17)271130(10)0000802183 (01)00842429108550(11)241210(17)271130(10)0000802619 (01)00842429108550(11)241214(17)271130(10)0000809792 (01)00842429108550(11)241217(17)271130(10)0000812812 (01)00842429108550(11)241217(17)271130(10)0000814498 (01)00842429108550(11)241220(17)271130(10)0000816560 (01)00842429108550(11)250108(17)271231(10)0000818876 (01)00842429108550(11)250110(17)271231(10)0000823404 (01)00842429108550(11)241217(17)271130(10)0000823532 (01)00842429108550(11)250113(17)271231(10)0000828250 (01)00842429108550(11)250115(17)271231(10)0000830529 (01)00842429108550(11)250118(17)271231(10)0000836906 (01)00842429108550(11)250118(17)271231(10)0000837785 (01)00842429108550(11)250118(17)271231(10)0000863256 (01)00842429108550(11)250123(17)271231(10)0000866698 (01)00842429108550(11)250124(17)271231(10)0000874138 (01)00842429108550(11)250125(17)271231(10)0000875976 (01)00842429108550(11)250129(17)271231(10)0000906381 (01)00842429108550(11)250131(17)271231(10)0000912667 (01)00842429108550(11)250204(17)280131(10)0000915955 (01)00842429108550(11)250203(17)280131(10)0000919813 (01)00842429108550(11)250205(17)280131(10)0000922930 (01)00842429108550(11)250206(17)280131(10)0000927345 (01)00842429108550(11)250207(17)280131(10)0000930383 (01)00842429108550(11)250212(17)280131(10)0000937458 (01)00842429108550(11)250210(17)280131(10)0000945855 (01)00842429108550(11)250220(17)280131(10)0000976589 Lot Numbers: 0000756596 0000784041 0000823532 0000912667 0000757384 0000799436 0000828250 0000915955 0000758945 0000802183 0000830529 0000919813 0000765270 0000802619 0000836906 0000922930 0000767660 0000809792 0000837785 0000927345 0000772588 0000812812 0000863256 0000930383 0000774885 0000814498 0000866698 0000937458 0000778089 0000816560 0000874138 0000945855 0000779647 0000818876 0000875976 0000976589 0000781240 0000823404 0000906381 Catalog Number: BOB-895-EMEA-AL UDI codes: (01)00842429118511(11)250213(17)280131(10)0000985070 (01)00842429118511(11)250217(17)280131(10)0000991168 (01)00842429118511(11)250219(17)280131(10)0000992810 (01)00842429118511(11)250222(17)280131(10)0000993790 (01)00842429118511(11)250225(17)280131(10)0000994829 (01)00842429118511(11)250228(17)280131(10)0000995565 (01)00842429118511(11)250303(17)280229(10)0000996450 (01)00842429118511(11)250305(17)280229(10)0001015817 (01)00842429118511(11)250307(17)280229(10)0001016002 (01)00842429118511(11)250310(17)280229(10)0001018992 (01)00842429118511(11)250321(17)280229(10)0001021878 (01)00842429118511(11)250311(17)280229(10)0001023107 (01)00842429118511(11)250313(17)280229(10)0001025449 (01)00842429118511(11)250319(17)280229(10)0001028255 (01)00842429118511(11)250324(17)280229(10)0001029974 (01)00842429118511(11)250327(17)280229(10)0001031633 (01)00842429118511(11)250415(17)280331(10)0001053417 (01)00842429118511(11)250416(17)280331(10)0001055173 (01)00842429118511(11)250514(17)280430(10)0001056470 (01)00842429118511(11)250423(17)280331(10)0001060464 (01)00842429118511(11)250425(17)280331(10)0001061678 (01)00842429118511(11)250426(17)280331(10)0001062354 (01)00842429118511(11)250502(17)280430(10)0001069356 (01)00842429118511(11)250505(17)280430(10)0001071207 (01)00842429118511(11)250506(17)280430(10)0001072898 (01)00842429118511(11)250508(17)280430(10)0001074123 (01)00842429118511(11)250521(17)280430(10)0001083156 (01)00842429118511(11)250612(17)280531(10)0001085850 (01)00842429118511(11)250522(17)280430(10)0001093696 (01)00842429118511(11)250527(17)280430(10)0001101233 (01)00842429118511(11)250528(17)280430(10)0001103095 (01)00842429118511(11)250529(17)280430(10)0001104602 (01)00842429118511(11)250604(17)280531(10)0001108650 (01)00842429118511(11)250605(17)280531(10)0001110938 (01)00842429118511(11)250609(17)280531(10)0001112366 (01)00842429118511(11)250610(17)280531(10)0001113474 (01)00842429118511(11)250612(17)280531(10)0001115761 (01)00842429118511(11)250613(17)280531(10)0001117185 (01)00842429118511(11)250616(17)280531(10)0001118973 (01)00842429118511(11)250617(17)280531(10)0001120771 (01)00842429118511(11)250619(17)280531(10)0001121934 (01)00842429118511(11)250620(17)280531(10)0001123077 (01)00842429118511(11)250623(17)280531(10)0001125524 (01)00842429118511(11)250625(17)280531(10)0001128348 (01)00842429118511(11)250626(17)280531(10)0001136555 (01)00842429118511(11)250703(17)280630(10)0001144745 (01)00842429118511(11)250702(17)280630(10)0001146471 (01)00842429118511(11)250707(17)280630(10)0001147975 (01)00842429118511(11)250716(17)280630(10)0001158399 (01)00842429118511(11)250718(17)280630(10)0001171840 (01)00842429118511(11)250721(17)280630(10)0001173474 (01)00842429118511(11)250729(17)280630(10)0001174976 (01)00842429118511(11)250730(17)280630(10)0001178541 (01)00842429118511(11)250731(17)280630(10)0001197582 (01)00842429118511(11)250730(17)280630(10)0001202766 (01)00842429118511(11)250730(17)280630(10)0001210548 Lor Numbers: 0000985070 0001031633 0001101233 0001136555 0000991168 0001053417 0001103095 0001144745 0000992810 0001055173 0001104602 0001146471 0000993790 0001056470 0001108650 0001147975 0000994829 0001060464 0001110938 0001158399 0000995565 0001061678 0001112366 0001171840 0000996450 0001062354 0001113474 0001173474 0001015817 0001068354 0001115761 0001174976 0001016002 0001069356 0001117185 0001176501 0001018992 0001071207 0001118973 0001178541 0001021878 0001072898 0001120771 0001197582 0001023107 0001074123 0001121934 0001202766 0001025449 0001083156 0001123077 0001210548 0001028255 0001085850 0001125524 0001029974 0001093696 0001128348 Catalog Number: BOB-895-US UDI codes: (01)00842429108543(11)250513(17)280430(10)0001079888 (01)00842429108543(11)250520(17)280430(10)0001081226 (01)00842429108543(11)250628(17)280531(10)0001141186 (01)00842429108543(11)250630(17)280531(10)0001173179 (01)00842429108543(11)250909(17)280831(10)0001262241 (01)00842429108543(11)251110(17)281031(10)0001437101 (01)00842429108543(11)251112(17)281031(10)0001438674 (01)00842429108543(11)251113(17)281031(10)0001441913 (01)00842429108543(11)251114(17)281031(10)0001443802 (01)00842429108543(11)251117(17)281031(10)0001446069 (01)00842429108543(11)251120(17)281031(10)0001453708 Lot Numbers: 0001079888 0001081226 0001141186 0001173179 0001262241 0001437101 0001438674 0001441913 0001443802 0001446069 0001453708 Catalog Number: MV-BGA01095 UDI codes: (01)04987892126550(11)250328(17)280229(10)0001040227 (01)04987892126550(11)250401(17)280331(10)0001042037 (01)04987892126550(11)250402(17)280331(10)0001044937 (01)04987892126550(11)250404(17)280331(10)0001046984 (01)04987892126550(11)250405(17)280331(10)0001047845 (01)04987892126550(11)250404(17)280331(10)0001049680 (01)04987892126550(11)250410(17)280331(10)0001051771 (01)04987892126550(11)250428(17)280331(10)0001065613 (01)04987892126550(11)250509(17)280430(10)0001076001 (01)04987892126550(11)250512(17)280430(10)0001078798 (01)04987892126550(11)250523(17)280430(10)0001097321 (01)04987892126550(11)250602(17)280531(10)0001105939 (01)04987892126550(11)250603(17)280531(10)0001107168 (01)04987892126550(11)250630(17)280531(10)0001141182 (01)04987892126550(11)250708(17)280630(10)0001152231 (01)04987892126550(11)250729(17)280630(10)0001185056 (01)04987892126550(11)250827(17)280731(10)0001225126 (01)04987892126550(11)250829(17)280731(10)0001246712 (01)04987892126550(11)250903(17)280831(10)0001252741 (01)04987892126550(11)251022(17)280930(10)0001266651 (01)04987892126550(11)250912(17)280831(10)0001269171 (01)04987892126550(11)250918(17)280831(10)0001287190 (01)04987892126550(11)250925(17)280831(10)0001289538 (01)04987892126550(11)250925(17)280831(10)0001292699 (01)04987892126550(11)250926(17)280831(10)0001294020 (01)04987892126550(11)251018(17)280930(10)0001313654 (01)04987892126550(11)251018(17)280930(10)0001324855 (01)04987892126550(11)251006(17)280930(10)0001327705 (01)04987892126550(11)251010(17)280930(10)0001338930 (01)04987892126550(11)251013(17)280930(10)0001340374 (01)04987892126550(11)251018(17)280930(10)0001354479 (01)04987892126550(11)251023(17)280930(10)0001355468 (01)04987892126550(11)251027(17)280930(10)0001358653 (01)04987892126550(11)251028(17)280930(10)0001368184 (01)04987892126550(11)251028(17)280930(10)0001372365 (01)04987892126550(11)251030(17)280930(10)0001384037 (01)04987892126550(11)251118(17)281031(10)0001447547 (01)04987892126550(11)251126(17)281031(10)0001456760 (01)04987892126550(11)251126(17)281031(10)0001458008 (01)04987892126550(11)251127(17)281031(10)0001461756 (01)04987892126550(11)251202(17)281130(10)0001464579 (01)04987892126550(11)251203(17)281130(10)0001466946 (01)04987892126550(11)251205(17)281130(10)0001467787 (01)04987892126550(11)251208(17)281130(10)0001467789 (01)04987892126550(11)251209(17)281130(10)0001470337 (01)04987892126550(11)251216(17)281130(10)0001485515 Lot Numbers: 0001040227 0001107168 0001292699 0001384037 0001042037 0001141182 0001294020 0001447547 0001044937 0001152231 0001313654 0001456760 0001046984 0001154356 0001324855 0001458008 0001047845 0001185056 0001327705 0001461756 0001049680 0001225126 0001338930 0001464579 0001051771 0001246712 0001340374 0001466946 0001065613 0001252741 0001354479 0001467787 0001076001 0001266651 0001355468 0001467789 0001078798 0001269171 0001358653 0001470337 0001097321 0001287190 0001368184 0001485515 0001105939 0001289538 0001372365", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2912-2026%22", "url": "https://recallledger.net/recalls/device-z-2912-2026-bobby-balloon-guide-catheter-ref-bob-895-cn-bob-895-emea-bob-895/"}, {"id": "fda-device-z-2834-2026", "source": "FDA", "category": "device", "recall_number": "Z-2834-2026", "title": "REMISOL Advance with Software Version 2.5 UDI-DI code: 15099590802073 The Normand... recall (Beckman Coulter Biomedical GmbH)", "product": "REMISOL Advance with Software Version 2.5 UDI-DI code: 15099590802073 The Normand Info REMISOL Advance Data Manager collects and manages data and workflow for 128 connections", "reason": "Due to software issues where does not handle combo assay results. The software may replace the final combo test result with one of the sub-results resulting in incorrect reporting of test outcomes.", "hazard_level": "Class II", "company": "Beckman Coulter Biomedical GmbH", "company_location": "Munchen, Germany", "date": "2026-04-29", "report_date": "2026-08-12", "status": "Ongoing", "distribution": "U.S.: FL, GA, IL, MI, and PA O.U.S.: Belgium, France, Hungary, Poland, Taiwan (Province of China), Tunisia, United Arab Emirates, and United Kingdom of Great Britain and Northern Ireland.", "states": ["FL", "GA", "IL", "MI", "PA"], "nationwide": false, "quantity": "20 systems", "codes": "Software Version 2.5 UDI-DI code: 15099590802073", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2834-2026%22", "url": "https://recallledger.net/recalls/device-z-2834-2026-remisol-advance-with-software-version-2-5-udi-di-code-15099590802073/"}, {"id": "fda-device-z-2798-2026", "source": "FDA", "category": "device", "recall_number": "Z-2798-2026", "title": "Halyard convenience kits containing recalled Medline Namic Angiographic Star Off... recall (AVID Medical, Inc.)", "product": "Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Manifolds. HEART CATH, SELF REGIONAL SELF131-05", "reason": "Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds, which were recalled by the manufacturer due to presence of particulates within fluid path of the Manifolds. Particulate within the fluid path has the potential to be introduced into blood circulation and become lodged within blood vessels.", "hazard_level": "Class I", "company": "AVID Medical, Inc.", "company_location": "Toano, VA, United States", "date": "2026-04-30", "report_date": "2026-08-12", "status": "Ongoing", "distribution": "US Nationwide distribution in the states of NC and TX.", "states": ["NC", "TX"], "nationwide": true, "quantity": "5168 kits", "codes": "UDI-DI 10809160408650 Lots 1618351 1621441 1627930 1635908 1644501 1646021 1651957 1654887 1656581 1656582 1659713 1670884 1670885 1671950", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2798-2026%22", "url": "https://recallledger.net/recalls/device-z-2798-2026-halyard-convenience-kits-containing-recalled-medline-namic-angiographi/"}, {"id": "fda-device-z-2797-2026", "source": "FDA", "category": "device", "recall_number": "Z-2797-2026", "title": "Halyard convenience kits containing recalled Medline Namic Angiographic Star Off... recall (AVID Medical, Inc.)", "product": "Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Manifolds. SAMMC ANGIOGRAPHY SAMM066-15", "reason": "Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds, which were recalled by the manufacturer due to presence of particulates within fluid path of the Manifolds. Particulate within the fluid path has the potential to be introduced into blood circulation and become lodged within blood vessels.", "hazard_level": "Class I", "company": "AVID Medical, Inc.", "company_location": "Toano, VA, United States", "date": "2026-04-30", "report_date": "2026-08-12", "status": "Ongoing", "distribution": "US Nationwide distribution in the states of NC and TX.", "states": ["NC", "TX"], "nationwide": true, "quantity": "5168 kits", "codes": "UDI-DI 10809160388495 Lots 1561685 1575926 1583048 1584017 1589652 1595715 1599634 1605749 1611810 1621476 1637222 1637224 1637225 1643118 1645143 1645637 1663929 1663930 1663931 1663932", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2797-2026%22", "url": "https://recallledger.net/recalls/device-z-2797-2026-halyard-convenience-kits-containing-recalled-medline-namic-angiographi/"}, {"id": "fda-device-z-2796-2026", "source": "FDA", "category": "device", "recall_number": "Z-2796-2026", "title": "Halyard convenience kits containing recalled Medline Namic Angiographic Star Off... recall (AVID Medical, Inc.)", "product": "Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Manifolds. CARDIAC CATH PACK EAMC1000-05", "reason": "Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds, which were recalled by the manufacturer due to presence of particulates within fluid path of the Manifolds. Particulate within the fluid path has the potential to be introduced into blood circulation and become lodged within blood vessels.", "hazard_level": "Class I", "company": "AVID Medical, Inc.", "company_location": "Toano, VA, United States", "date": "2026-04-30", "report_date": "2026-08-12", "status": "Ongoing", "distribution": "US Nationwide distribution in the states of NC and TX.", "states": ["NC", "TX"], "nationwide": true, "quantity": "5168 kits", "codes": "UDI-DI 10809160377314 Lots 1573593 1583827 1609541 1612134 1612516 1619132 1623384 1627013 1635459 1672306 1675159", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2796-2026%22", "url": "https://recallledger.net/recalls/device-z-2796-2026-halyard-convenience-kits-containing-recalled-medline-namic-angiographi/"}, {"id": "fda-device-z-2769-2026", "source": "FDA", "category": "device", "recall_number": "Z-2769-2026", "title": "Brand Name: Silent Nite Product Name: Silent Nite Sleep Appliance Model/Catalog... recall (Prismatik Dentalcraft, Inc.)", "product": "Brand Name: Silent Nite Product Name: Silent Nite Sleep Appliance Model/Catalog Number: SILNT Product Description: Silent Nite Sleep Appliance is a mandibular advancement device (MAD) intended to treat snoring and mild to moderate obstructive sleep apnea (OSA).", "reason": "Due to device not having FDA Clearance", "hazard_level": "Class II", "company": "Prismatik Dentalcraft, Inc.", "company_location": "Irvine, CA, United States", "date": "2026-04-27", "report_date": "2026-07-29", "status": "Ongoing", "distribution": "U.S. Nationwide distribution in the states of AZ, CA, FL, GA, IL, IN, MD, MO, NY, TX, and VA.", "states": ["AZ", "CA", "FL", "GA", "IL", "IN", "MD", "MO", "NY", "TX", "VA"], "nationwide": true, "quantity": "20", "codes": "Item Number: NITESL UDI-DI code: D745SILNT0 Lot/Serial Numbers: 1020214577 1020784354 1030007997 1030439672 1030523763 1030722759 1106770735 1107310424 1107642834 1108530251 1110784932 1117400787 1118814629 1121913952 1122251905 1122958036 1124408531 1125495087 1127571733 1131149684", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2769-2026%22", "url": "https://recallledger.net/recalls/device-z-2769-2026-brand-name-silent-nite-product-name-silent-nite-sleep-appliance/"}, {"id": "fda-device-z-2675-2026", "source": "FDA", "category": "device", "recall_number": "Z-2675-2026", "title": "The intended use is to be paired with a weapon for aiming purposes. recall (Wilcox Industries Corp.)", "product": "The intended use is to be paired with a weapon for aiming purposes.", "reason": "Wilcox is notifying all customers who have purchased a product from the BOSS Xe family that a software enhancement to increase safety has been released and all units should be returned to implement this change.", "hazard_level": "Class II", "company": "Wilcox Industries Corp.", "company_location": "Newington, NH, United States", "date": "2026-04-06", "report_date": "2026-07-29", "status": "Ongoing", "distribution": "US Nationwide distribution in the state of NH.", "states": ["NH"], "nationwide": true, "quantity": "N/A", "codes": "None provided.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2675-2026%22", "url": "https://recallledger.net/recalls/device-z-2675-2026-the-intended-use-is-to-be-paired-with-a-weapon-for-aiming-purposes/"}, {"id": "fda-food-h-1156-2026", "source": "FDA", "category": "food", "recall_number": "H-1156-2026", "title": "Winfield's CWB Chocolate Bar recall (Chocolate Bar Holdings LLC)", "product": "Winfield's CWB Chocolate Bar, packed in clear cello bag with fabric bow on top. Manufactured by CBSL Commissary (DBA Winfield's Chocolate Bar) 9127 Stella Link Rd Houston Texas. Multiple product shapes/sizes: 1) Cat, Net wt. 8oz (226.8g), UPC: 00810079833030, Unit size 5 x 3 1/2 x 2. 2) Teddy Bear, Net wt. 8oz (226.8g), UPC: 00810079833405, Unit size 5 1/2 x 2 1/2 x 2. 3) Easter Bunny, Net wt. 16oz (453.59g), UPC: 00810079837892, Unit size 4 x 1 x 8 1/2.", "reason": "Undeclared milk allergen.", "hazard_level": "Class II", "company": "Chocolate Bar Holdings LLC", "company_location": "Houston, TX, United States", "date": "2026-04-27", "report_date": "2026-07-22", "status": "Completed", "distribution": "Houston, TX", "states": ["TX"], "nationwide": false, "quantity": "24 total units (various shapes/sizes)", "codes": "No lot numbers are on these products, so the firm's recall scope is for the entire production line for the following product numbers: 00810079833030 00810079833405 00810079837892", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-1156-2026%22", "url": "https://recallledger.net/recalls/food-h-1156-2026-winfield-s-cwb-chocolate-bar-packed-in-clear-cello-bag-with-fabric-bo/"}, {"id": "fda-device-z-2712-2026", "source": "FDA", "category": "device", "recall_number": "Z-2712-2026", "title": "Brand Name: Geneva Product Name: Brachytherapy Applicator Product Description: The... recall (Elekta, Inc.)", "product": "Brand Name: Geneva Product Name: Brachytherapy Applicator Product Description: The device is intended for intracavitary brachytherapy for cancer treatment of the cervix and the endometrium. Optional needles can be placed for interstitial therapy.", "reason": "Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.", "hazard_level": "Class II", "company": "Elekta, Inc.", "company_location": "Atlanta, GA, United States", "date": "2026-04-03", "report_date": "2026-07-15", "status": "Ongoing", "distribution": "Worldwide - U.S. Nationwide distribution including in the states of AR, AZ, CA, CO, CT, DC, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MO, MS, NC, ND, NE, NJ, NV, NY, OH, OK, OR, PA, SC, SD, TX, UT, VA, WI, and WV. The countries of Argentina, Australia, Austria, Bahrain, Bangladesh, Belgium, Bolivia, Botswana, Brazil, Burkina Faso, Cambodia, Canada, Chile, China, Colombia, Croatia, Cyprus, Czech Republic, Denmark, Ecuador, Egypt, Finland, France, Georgia, Germany, Greece, Guatemala, Honduras, Hong Kong, Hungary, India, Indonesia, Iran (Islam Republic of), Iraq, Ireland, Italy, Japan, Kazakhstan, Kenya, Korea (Republic of), Kosovo, Malaysia, Mexico, Morocco, Netherlands, New Zealand, Norway, Pakistan, Panama, Peru, Philippines, Poland, Portugal, Romania, Russian Federation, Rwanda, Saudi Arabia, Singapore, Slovakia, South Africa, Spain, Swaziland, Sweden, Switzerland, Taiwan, Thailand, Togo, Turkey, Ukraine, United Arab Emirates, United Kingdom, Venezuela, Viet Nam, and Zambia.", "states": ["AR", "AZ", "CA", "CO", "CT", "DC", "FL", "GA", "IA", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "MI", "MO", "MS", "NC", "ND", "NE", "NJ", "NV", "NY", "OH", "OK", "OR", "PA", "SC", "SD", "TX", "UT", "VA", "WI", "WV"], "nationwide": true, "quantity": "1317", "codes": "Lot Code: 08717213056039, 08717213056053, 08717213056077, 08717213056091, 08717213056398, 08717213056411, 08717213056435, 08717213056459, 08717213056473, 08717213056497, 08717213056510,08717213056534, 08717213056558, 08717213056572, 08717213056596, 08717213056619, 08717213056633, 08717213056657", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2712-2026%22", "url": "https://recallledger.net/recalls/device-z-2712-2026-brand-name-geneva-product-name-brachytherapy-applicator-product-de/"}, {"id": "fda-device-z-2711-2026", "source": "FDA", "category": "device", "recall_number": "Z-2711-2026", "title": "Brand Name: Brachytherapy Applicator Product Name: Advanced Gynecological Applicator ... recall (Elekta, Inc.)", "product": "Brand Name: Brachytherapy Applicator Product Name: Advanced Gynecological Applicator Product Description: The intended use of the Advanced Gynecological Applicator is intracavitary brachytherapy for cancer treatment of the cervix and endometrium. Optional needles can be placed for interstitial brachytherapy.", "reason": "Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.", "hazard_level": "Class II", "company": "Elekta, Inc.", "company_location": "Atlanta, GA, United States", "date": "2026-04-03", "report_date": "2026-07-15", "status": "Ongoing", "distribution": "Worldwide - U.S. Nationwide distribution including in the states of AR, AZ, CA, CO, CT, DC, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MO, MS, NC, ND, NE, NJ, NV, NY, OH, OK, OR, PA, SC, SD, TX, UT, VA, WI, and WV. The countries of Argentina, Australia, Austria, Bahrain, Bangladesh, Belgium, Bolivia, Botswana, Brazil, Burkina Faso, Cambodia, Canada, Chile, China, Colombia, Croatia, Cyprus, Czech Republic, Denmark, Ecuador, Egypt, Finland, France, Georgia, Germany, Greece, Guatemala, Honduras, Hong Kong, Hungary, India, Indonesia, Iran (Islam Republic of), Iraq, Ireland, Italy, Japan, Kazakhstan, Kenya, Korea (Republic of), Kosovo, Malaysia, Mexico, Morocco, Netherlands, New Zealand, Norway, Pakistan, Panama, Peru, Philippines, Poland, Portugal, Romania, Russian Federation, Rwanda, Saudi Arabia, Singapore, Slovakia, South Africa, Spain, Swaziland, Sweden, Switzerland, Taiwan, Thailand, Togo, Turkey, Ukraine, United Arab Emirates, United Kingdom, Venezuela, Viet Nam, and Zambia.", "states": ["AR", "AZ", "CA", "CO", "CT", "DC", "FL", "GA", "IA", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "MI", "MO", "MS", "NC", "ND", "NE", "NJ", "NV", "NY", "OH", "OK", "OR", "PA", "SC", "SD", "TX", "UT", "VA", "WI", "WV"], "nationwide": true, "quantity": "586", "codes": "Lot Code: 08717213055001, 08717213055018, 08717213055025, 08717213055049, 08717213055056, 08717213055063, 08717213055087, 08717213055094, 08717213055100, 08717213055117, 08717213055131", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2711-2026%22", "url": "https://recallledger.net/recalls/device-z-2711-2026-brand-name-brachytherapy-applicator-product-name-advanced-gynecolog/"}, {"id": "fda-device-z-2710-2026", "source": "FDA", "category": "device", "recall_number": "Z-2710-2026", "title": "Brand Name: Fletcher CT/MR Shielded Applicator Set Product Name: Intracavitary Remote... recall (Elekta, Inc.)", "product": "Brand Name: Fletcher CT/MR Shielded Applicator Set Product Name: Intracavitary Remote Afterloading Applicator Product Description: The Fletcher CT/MR Shielded Applicator Set is intended for gynecological brachytherapy treatment of the cervix and endometrium.", "reason": "Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.", "hazard_level": "Class II", "company": "Elekta, Inc.", "company_location": "Atlanta, GA, United States", "date": "2026-04-03", "report_date": "2026-07-15", "status": "Ongoing", "distribution": "Worldwide - U.S. Nationwide distribution including in the states of AR, AZ, CA, CO, CT, DC, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MO, MS, NC, ND, NE, NJ, NV, NY, OH, OK, OR, PA, SC, SD, TX, UT, VA, WI, and WV. The countries of Argentina, Australia, Austria, Bahrain, Bangladesh, Belgium, Bolivia, Botswana, Brazil, Burkina Faso, Cambodia, Canada, Chile, China, Colombia, Croatia, Cyprus, Czech Republic, Denmark, Ecuador, Egypt, Finland, France, Georgia, Germany, Greece, Guatemala, Honduras, Hong Kong, Hungary, India, Indonesia, Iran (Islam Republic of), Iraq, Ireland, Italy, Japan, Kazakhstan, Kenya, Korea (Republic of), Kosovo, Malaysia, Mexico, Morocco, Netherlands, New Zealand, Norway, Pakistan, Panama, Peru, Philippines, Poland, Portugal, Romania, Russian Federation, Rwanda, Saudi Arabia, Singapore, Slovakia, South Africa, Spain, Swaziland, Sweden, Switzerland, Taiwan, Thailand, Togo, Turkey, Ukraine, United Arab Emirates, United Kingdom, Venezuela, Viet Nam, and Zambia.", "states": ["AR", "AZ", "CA", "CO", "CT", "DC", "FL", "GA", "IA", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "MI", "MO", "MS", "NC", "ND", "NE", "NJ", "NV", "NY", "OH", "OK", "OR", "PA", "SC", "SD", "TX", "UT", "VA", "WI", "WV"], "nationwide": true, "quantity": "1", "codes": "Lot Code: 08717213024205", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2710-2026%22", "url": "https://recallledger.net/recalls/device-z-2710-2026-brand-name-fletcher-ct-mr-shielded-applicator-set-product-name-intr/"}, {"id": "fda-device-z-2694-2026", "source": "FDA", "category": "device", "recall_number": "Z-2694-2026", "title": "Intracept Access Instruments recall (Boston Scientific Neuromodulation Corporation)", "product": "Intracept Access Instruments, Description/REF: INTRACEPT ACCESS INSTRUMENTS- DRILL/RLV0035, INTRACEPT ACCESS INSTRUMENTS- DRILL EU/RLV0035-EU, INTRACEPT ACCESS INSTRUMENTS- 2VB/RLV0045, INTRACEPT ACCESS INSTRUMENTS- 2VB EU/RLV0045-EU, INTRACEPT ACCESS INSTRUMENTS- 3VB/RLV0055, INTRACEPT ACCESS INSTRUMENTS- 3VB EU/RLV0055-EU, INTRACEPT ACCESS INSTRUMENTS 2 VB/RLV0065, INTRACEPT ACCESS INSTRMNTS ADDITIONAL VB/RLV0075, INTRACEPT ACCESS INSTRMNTS ADDTL VB EU/RLV0075-EU", "reason": "Intraosseous nerve ablation system instruments may have sterile barrier breach of the outer tray seal, which may introduce a risk of sterility breach, and if breached could lead to severe infection.", "hazard_level": "Class II", "company": "Boston Scientific Neuromodulation Corporation", "company_location": "Valencia, CA, United States", "date": "2026-04-22", "report_date": "2026-07-15", "status": "Ongoing", "distribution": "Worldwide - US Nationwide distribution including in the states of NJ, WI, MI, MN, AR, UT, OH, FL, CA, TX, PA, AZ, IN, LA, NE, OK, NY, MD, WY, CO, NC, IL, GA, WA, KS, AL, MO, VA, TN, KY, MS, MA, SC, OR, WV, MT, ID, SD, CT, NV, ND, NH, DE, NM, AK, IA, DC, HI, ME, VT, RI and the countries of Great Britain, Germany, United Arab Emirates.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "37,764", "codes": "REF/UDI-DI/Lot/Expiration Date Range: RLV0035/852454006240/36231634, 36266333, 36266334, 36266335, 36442451, 36556998, 36577474, 36577475, 37355534, 37374614, 37642257, 37642258, 37667047, 37667049, 38711750, 38711751/04-Mar-2027 to 21-Jul-2027; RLV0035-EU/852454006448/36267790, 36909569, 38889437/04-Mar-2027 to 26-Jun-2027; RLV0045/852454006301/35218150, 35218151, 35218152, 35218153, 35219469, 35219470, 35229010, 35229011, 35229012, 35256597, 35318740, 35318741, 35318742, 35329853, 35329854, 35338734, 35360990, 35360991, 35360992, 35406849, 35406850, 35406851, 35406852, 35406853, 35406854, 35498172, 35508065, 35508066, 35523483, 35523484, 35525666, 35535444, 35535445, 35535446, 35535664, 35535665, 35536282, 35538112, 35538113, 35538114, 35538115, 35717797, 35717798, 35717861, 35729587, 35729588, 35729589, 35738091, 35738092, 35738093, 35755411, 35755412, 35755413, 35788378, 35788379, 35788400, 35789578, 35789579, 35789840, 35822293, 35822294, 35822295, 35831721, 35831722, 35831723, 35884013, 35884014, 35884015, 35884018, 35884019, 35884200, 35929731, 35929732, 35929733, 35939403, 35939404, 35939405, 36007510, 36051631, 36051632, 36051633, 36061072, 36061073, 36063527, 36115270, 36115271, 36162140, 36201849, 36211661, 36211662, 36247081, 36247082, 36247083, 36299784, 36299785, 36306155, 36306908, 36312074, 36312075, 36312076, 36327640, 36327641, 36334682, 36334683, 36334684, 36337568, 36337569, 36356333, 36368650, 36368651, 36390837, 36390839, 36390960, 36390962, 36390963, 36411346, 36440610, 36440611, 36451984, 36455377, 36455378, 36528101, 36538547, 36538548, 36554903, 36576169, 36576170, 36576171, 36578105, 36578106, 36578107, 36578108, 36709018, 36714451, 36719971, 36731035, 36731036, 36731037, 36733644, 36733645, 36743247, 36743248, 36765841, 36765842, 36765843, 36778439, 36779700, 36779701, 36789363, 36789364, 36793775, 36793776, 36802652, 36802653, 36802654, 36814178, 36819483, 36819484, 36825817, 36835476, 36839951, 36839952, 36892404, 36892405, 36907158, 36920578, 36931525, 36938443, 36938444, 36938445, 36948565, 36965128, 36977051, 36984738, 37006934, 37006935, 37021399, 37038790, 37060446, 37072745, 37072746, 37115658, 37126596, 37126597, 37143684, 37143685, 37182176, 37182177, 37191624, 37203924, 37210305, 37222391, 37222392, 37248543, 37248544, 37257912, 37278064, 37278065, 37291738, 37422836, 37422837, 37422838, 37434285, 37434286, 37443230,37467700, 37467701, 37467702, 37499290, 37499291, 37513740, 37513741, 37527332, 37558530, 37558531, 37586529, 37604798, 37604928, 37752893, 37752894, 37808050, 37808051, 37818544, 37818545, 37818546, 37864351, 37864352, 37876714, 37876715, 37876716, 37876717, 37909770, 37909771, 37923968, 37941727, 37941728, 38243913, 38243914, 38243915, 38253672, 38253673, 38253674, 38253675, 38257979, 38258120, 38258121, 38393517, 38393518, 38461277, 38461278, 38462080, 38462081, 38462082, 38462587, 38472779, 38473000, 38473001, 38473954, 38484605, 38484606, 38496711, 38517754, 38531680, 38600809, 38600810, 38600811, 38600812, 38632672, 38632673, 38632674, 38711753, 38712187, 38917000, 38917002, 39009366/03-Oct-2026 to 03-Mar-2028; RLV0045-EU/852454006431/36190488, 36254922, 36411351, 36909570, 37575379, 38654200/11-Feb-2027 to 04-Nov-2027; RLV0055/852454006226/35235794, 35235795, 35235796, 35235797, 35235798, 35235799, 35235940, 35244678, 35244679, 35245420, 35265922, 35309126, 35309128, 35309130, 35316016, 35328273, 35328274, 35367311, 35367312, 35367313, 35453674, 35461292, 35461293, 35461294, 35461295, 35461296, 35469325, 35469326, 35469327, 35498173, 35498174, 35508414, 35508415, 35516633, 35518863, 35518864, 35520116, 35522815, 35522816, 35522817, 35522818, 35530433, 35530434, 35582150, 35582151, 35582152, 35585353, 35585354, 35590649, 35590650, 35738094, 35738095, 35738096, 35738097, 35738098, 35738099, 35780448, 35780449, 35780450, 35789910, 35789911, 35789912, 35796422, 35796423, 35796424, 35831784, 35831785, 35831786, 35841864, 35841865, 35841866, 35849369, 35849370, 35849371, 35871196, 35871197, 35871198, 35890764, 35890765, 35890766, 35989202, 35989203, 35989204, 36042033, 36042034, 36042035, 36051634, 36051635, 36051636, 36103927, 36103928, 36103930, 36168356, 36201850, 36254923, 36254924, 36258582, 36299786, 36299787, 36306157, 36306158, 36306159, 36315014, 36315015, 36327258, 36327259, 36334687, 36334688, 36334689, 36346737, 36346738, 36346739, 36346800, 36356510, 36356511, 36368652, 36368653, 36377745, 36421406, 36421407, 36421408, 36442449, 36442450, 36455379, 36466553, 36466554, 36474482, 36509579, 36509640, 36511507, 36518452, 36518454, 36519641, 36519642, 36538550, 36588268, 36588269, 36588270, 36588271, 36588273, 36627806, 36779702, 36779703, 36779704, 36789365, 36796277, 36796278, 36801923, 36879218, 36879219, 36879300, 36885626, 36885627, 36948834, 37018069, 37018070, 37021397, 37021398, 37030573, 37038794, 37060447, 37072747, 37072748, 37072749, 37085884, 37085885, 37097347, 37097348, 37097349, 37097352, 37105997, 37105998, 37114545, 37143682, 37143683, 37234124, 37234125, 37248545, 37266940, 37266941, 37278066, 37291818, 37291819, 37422839, 37423650, 37423651, 37434287, 37434288, 37476160, 37476161, 37486544, 37513375, 37513376, 37517300, 37527333, 37527334, 37527335, 37528240, 37528241, 37548528, 37548529, 37548530, 37548532, 37576081, 37586522, 37586530, 37597563, 37597564, 37606989, 37606990, 37606992, 37723478, 37752895, 37752896, 37752897, 37771990, 37771991, 37771993, 37772123, 37772124, 37772125, 37864353, 37864354, 37864355, 37885352, 37885353, 37930763, 37930764, 37930765, 37954165, 37954166, 37954167, 37954168, 38048470, 38196327, 38196328, 38243169, 38243170, 38252987, 38252988, 38252989, 38287216, 38287217, 38287218, 38404416, 38462594, 38474849, 38474880, 38474881, 38481950, 38481954, 38483325, 38496708, 38496709, 38529820, 38531658, 38531659, 38537775, 38540454, 38540782, 38540792, 38614681, 38711754, 38712189/10-Oct-2026 to 29-Oct-2027; RLV0055-EU/852454006318/36190489/30-Jan-2027 to 30-Jan-2027; RLV0065/852454006424/37166269, 37166270, 37205965, 37422790, 37422791, 37434847, 37434848, 37822997, 37822998, 37822999, 37837635, 37837636, 37837637, 37859920, 37903427, 37903428, 37909761, 37930774, 37930775, 37980230, 37980231, 37980232, 37980233, 38079204, 38079205, 38079206, 38079207, 38107765, 38107766, 38107767, 38107768, 38135922, 38135923, 38135924, 38154984, 38154985, 38159015, 38166823, 38166824, 38166825, 38166826, 38166827, 38166828, 38169819, 38170180, 38170693, 38170694, 38205657, 38205658, 38205659, 38222326, 38222327, 38222328, 38222329, 38222330, 38243916, 38339417, 38339418, 38339419, 38339880, 38339881, 38347588, 38355042, 38358582, 38358583, 38358584, 38360834, 38360835, 38366171, 38384137, 38384138, 38384139, 38392693, 38404412, 38404413, 38412000, 38412001, 38412003, 38412005, 38412006, 38412007, 38415242, 38415246, 38529822, 38531280, 38531281, 38559204, 38559205, 38559206, 38559207, 38568272, 38580272, 38580273, 38580274, 38580275, 38589983, 38589984, 38589985, 38590380, 38590381, 38590382, 38590383, 38590384, 38590385, 38590386, 38590387, 38590388, 38597090, 38623873, 38623874, 38623875, 38623876, 38632676, 38632678, 38643661, 38645060, 38645061, 38645062, 38645063, 38692073, 38692074, 38692075, 38692076, 38703597, 38708720, 38708721, 38708722, 38708723, 38712509, 38712511, 38712512, 38739451, 38739453, 38739454, 38739455, 38750004, 38750005, 38750007, 38774400, 38774401, 38802555, 38802556, 38802557, 38802558, 38809866, 38812686, 38812687, 38812688, 38821188, 38821189, 38821191, 38823209, 38823210, 38858563, 38858564, 38858565, 38858566, 38858570, 38869945, 38870375, 38870378, 38870783, 38870784, 38878535, 38878536, 38878538, 38878539, 38879225, 38879226, 38949331, 38949332, 38949333, 38949334, 39032543/30-Jul-2027 to 15-Mar-2028; RLV0075/852454006257/35490122, 35490123, 35490124, 35490125, 35490126, 35604788, 35615708, 35615709, 35705365, 35705366, 35901453, 35901454, 35901455, 35936488, 35936489, 35998826, 35998827, 35998828, 36159579, 36254921, 36349203, 36349204, 36404502, 36404503, 36421409, 36835470, 36870653, 36870654, 36874432, 36874433, 36929050, 36929051, 36929052, 36929053, 36929054, 36983480, 36983481, 37060448, 37107838, 37107839, 37191554, 37191555, 37191556, 37204731, 37210306, 37335984, 37355535, 37364022, 37535449, 37535450, 37752898, 37943227, 37976478, 37976479, 37977720, 37977721, 38048471, 38179848, 38249218, 38249700, 38249991, 38253644, 38253645, 38253670, 38253671, 38347590, 38384136, 38426598, 38451722, 38451723, 38508092, 38529821, 38531016, 38539792, 38540765, 38540766, 38655662, 38730788, 38763797, 38763799/29-Oct-2026 to 21-Nov-2027; RLV0075-EU/852454006455/36267789, 36932250, 37575378/23-Jan-2027 to 14-Aug-2027", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2694-2026%22", "url": "https://recallledger.net/recalls/device-z-2694-2026-intracept-access-instruments-description-ref-intracept-access-instr/"}, {"id": "fda-drug-d-0699-2026", "source": "FDA", "category": "drug", "recall_number": "D-0699-2026", "title": "Revitaderm Wound Care recall (Blaine Labs Inc)", "product": "Revitaderm Wound Care, First Aid Antiseptic Gel, Benzalkonium Chloride 0.1%) packaged as (a) 1.0 Fl OZ (16 mL) bottle, long pointy cap, NDC 63347-120-02; (b) 3.0 Fl OZ (85 g) tube, with short twist cap, NDC 63347-120-01; Manufactured By: Blaine Labs, Inc. 11037 Lockport Place, Santa Fe Springs, CA 90670,", "reason": "CGMP Deviations; product manufactured in the same facility under the same conditions as the product found to be contaminated", "hazard_level": "Class II", "company": "Blaine Labs Inc", "company_location": "Santa Fe Springs, CA, United States", "date": "2026-04-08", "report_date": "2026-07-08", "status": "Ongoing", "distribution": "Nationwide in the USA", "states": [], "nationwide": true, "quantity": "5,555 bottles and tubes", "codes": "Lots: (a) 1 oz - BL3435, Exp 11/06/26; BL3525, Exp 08/07/27. (b) 3 oz- Lots # BL3435, 11/06/26 & BL3525, 08/07/27", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0699-2026%22", "url": "https://recallledger.net/recalls/drug-d-0699-2026-revitaderm-wound-care-first-aid-antiseptic-gel-benzalkonium-chloride/"}, {"id": "fda-drug-d-0698-2026", "source": "FDA", "category": "drug", "recall_number": "D-0698-2026", "title": "Fungal Fusion ERADICATION Solution recall (Blaine Labs Inc)", "product": "Fungal Fusion ERADICATION Solution, Antifungal & Antimicrobial Kit. Contains, 1x2 oz bottle Fungal Fusion Antifungal (Miconazole Nitrate) Cream, 1x2oz bottle Fungal Fusion Antifungal Solution (25% Undecylenic Acid) and 1x1oz bottle of Fungal Fusion Eradication Antimicrobial Show Spray (isopropyl Alcohol, D-Limonene, Undecylenic Acid). Manufactured By: Blaine Labs, Inc., 11037 Lockport Place, Santa Fe Springs, CA 90670, Manufactured for Doctor's Inc", "reason": "CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry", "hazard_level": "Class II", "company": "Blaine Labs Inc", "company_location": "Santa Fe Springs, CA, United States", "date": "2026-04-08", "report_date": "2026-07-08", "status": "Ongoing", "distribution": "Nationwide in the USA", "states": [], "nationwide": true, "quantity": "1,500 bottles", "codes": "Lot BL3572, Exp 04/16/2028", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0698-2026%22", "url": "https://recallledger.net/recalls/drug-d-0698-2026-fungal-fusion-eradication-solution-antifungal-antimicrobial-kit-co/"}, {"id": "fda-drug-d-0697-2026", "source": "FDA", "category": "drug", "recall_number": "D-0697-2026", "title": "TERPENICOL Antifungal Solution recall (Blaine Labs Inc)", "product": "TERPENICOL Antifungal Solution, (Undecylenic (10-Undecenoic) acid 25%), 1.0 Fl Oz (29.6 mL), Manufactured By: Blaine Labs, Inc., 11037 Lockport Place, Santa Fe Springs, CA 90670. NDC 63347-600-01", "reason": "CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry", "hazard_level": "Class II", "company": "Blaine Labs Inc", "company_location": "Santa Fe Springs, CA, United States", "date": "2026-04-08", "report_date": "2026-07-08", "status": "Ongoing", "distribution": "Nationwide in the USA", "states": [], "nationwide": true, "quantity": "5,801 bottles", "codes": "Lots BL3411R, Exp Date 06/08/2027, BL3468, Exp Date 03/07/2027, & BL3535, Exp Date 09/25/2027.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0697-2026%22", "url": "https://recallledger.net/recalls/drug-d-0697-2026-terpenicol-antifungal-solution-undecylenic-10-undecenoic-acid-25/"}, {"id": "fda-drug-d-0696-2026", "source": "FDA", "category": "drug", "recall_number": "D-0696-2026", "title": "vite20 Antifungal Cream recall (Blaine Labs Inc)", "product": "vite20 Antifungal Cream, (10% Undecylenic Acid), 0.54 OZ (15 g) bottle, Manufactured By: Blaine Labs, Inc., 11037 Lockport Place, Sante Fe Springs, CA 90670, UPC 6 16728 00039 2.", "reason": "CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry", "hazard_level": "Class II", "company": "Blaine Labs Inc", "company_location": "Santa Fe Springs, CA, United States", "date": "2026-04-08", "report_date": "2026-07-08", "status": "Ongoing", "distribution": "Nationwide in the USA", "states": [], "nationwide": true, "quantity": "26,475 bottles", "codes": "Lot BL3462, Exp. 2/7/2027", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0696-2026%22", "url": "https://recallledger.net/recalls/drug-d-0696-2026-vite20-antifungal-cream-10-undecylenic-acid-0-54-oz-15-g-bottle/"}, {"id": "fda-drug-d-0695-2026", "source": "FDA", "category": "drug", "recall_number": "D-0695-2026", "title": "TERPENICOL Antifungal Cream recall (Blaine Labs Inc)", "product": "TERPENICOL Antifungal Cream (Undecylenic Acid 13%), 1.0 oz (28 g) bottles, Manufactured By: Blaine Labs, Inc., 11037 Lockport Place, Sante Fe Springs, CA 90670, NDC 63347-601-01.", "reason": "CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry", "hazard_level": "Class II", "company": "Blaine Labs Inc", "company_location": "Santa Fe Springs, CA, United States", "date": "2026-04-08", "report_date": "2026-07-08", "status": "Ongoing", "distribution": "Nationwide in the USA", "states": [], "nationwide": true, "quantity": "22,143 bottles", "codes": "Lots BL3431R, Exp Date 10/13/26 & BL3528, Exp Date 08/30/2027.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0695-2026%22", "url": "https://recallledger.net/recalls/drug-d-0695-2026-terpenicol-antifungal-cream-undecylenic-acid-13-1-0-oz-28-g-bott/"}, {"id": "fda-drug-d-0694-2026", "source": "FDA", "category": "drug", "recall_number": "D-0694-2026", "title": "TRIPENICOL S Antifungal Solution recall (Blaine Labs Inc)", "product": "TRIPENICOL S Antifungal Solution (Undecylenic Acid 25%), 1.25 FL OZ (37.5 mL) bottle, Manufactured For: Trifluent Pharma, LLC, San Antonio, TX 78213, NDC 73352-550-01.", "reason": "CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry", "hazard_level": "Class II", "company": "Blaine Labs Inc", "company_location": "Santa Fe Springs, CA, United States", "date": "2026-04-08", "report_date": "2026-07-08", "status": "Ongoing", "distribution": "Nationwide in the USA", "states": [], "nationwide": true, "quantity": "144 bottles", "codes": "Lot #BL3411R, Exp 6/8/2027", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0694-2026%22", "url": "https://recallledger.net/recalls/drug-d-0694-2026-tripenicol-s-antifungal-solution-undecylenic-acid-25-1-25-fl-oz-3/"}, {"id": "fda-drug-d-0693-2026", "source": "FDA", "category": "drug", "recall_number": "D-0693-2026", "title": "TRIFLUENT PHARMA TRIDERGEL Wound Care Gel recall (Blaine Labs Inc)", "product": "TRIFLUENT PHARMA TRIDERGEL Wound Care Gel, (Benzalkonium Chloride 0.1%), 1.0 fl oz, (29.6 mL) bottle with long pointy cap, Manufactured for: Trifluent Pharma, LLC. San Antonio, TX 78213. NDC 73352-520-01.", "reason": "CGMP Deviations: product manufactured in the same facility under the same conditions as the product found to be contaminated", "hazard_level": "Class II", "company": "Blaine Labs Inc", "company_location": "Santa Fe Springs, CA, United States", "date": "2026-04-08", "report_date": "2026-07-08", "status": "Ongoing", "distribution": "Nationwide in the USA", "states": [], "nationwide": true, "quantity": "519 - 1 oz bottles", "codes": "Lot #: BL3435, Exp. 11/06/26", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0693-2026%22", "url": "https://recallledger.net/recalls/drug-d-0693-2026-trifluent-pharma-tridergel-wound-care-gel-benzalkonium-chloride-0-1/"}, {"id": "fda-drug-d-0692-2026", "source": "FDA", "category": "drug", "recall_number": "D-0692-2026", "title": "Revitaderm Wound Care Gel recall (Blaine Labs Inc)", "product": "Revitaderm Wound Care Gel, Benzalkonium Chloride 0.1%, packaged in 1.0 FL OZ (37 mL) bottle, shorter twist cap, Manufactured By: Blaine Labs, Inc. 11037 Lockport Place Santa Fe Springs, CA 90670, NDC 63347-120-02.", "reason": "Microbial contamination of Non-Sterile Product: samples identified the presence of Lysinibacillus fusiformis and other Bacillus spp", "hazard_level": "Class I", "company": "Blaine Labs Inc", "company_location": "Santa Fe Springs, CA, United States", "date": "2026-04-08", "report_date": "2026-07-08", "status": "Ongoing", "distribution": "Nationwide in the USA", "states": [], "nationwide": true, "quantity": "1,171 - 1 oz bottles", "codes": "Lot#: BL3608, Exp. 07/01/28.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0692-2026%22", "url": "https://recallledger.net/recalls/drug-d-0692-2026-revitaderm-wound-care-gel-benzalkonium-chloride-0-1-packaged-in-1-0/"}, {"id": "fda-device-z-2653-2026", "source": "FDA", "category": "device", "recall_number": "Z-2653-2026", "title": "Covidien Shiley Disposable Decannulation Plug REF DDCP UDI-DI code: 10884522004060 ... recall (Covidien LLC)", "product": "Covidien Shiley Disposable Decannulation Plug REF DDCP UDI-DI code: 10884522004060 Product Codes that include the Covidien Shiley Disposable Decannulation Plug are: Product Number / UDI-DI code 4DCFN 10884522006576 4DCFS 10884522006583 4DFEN 10884522006606 6DCFN 10884522006613 6DCFS 10884522006620 6DFEN 10884522006644 8DCFN 10884522006651 8DCFS 40884522006690 8DFEN 10884522006675 10DCFN 20884522006535 10DCFS 10884522006545 10DFEN 10884522006569 The Shiley Disposable Decannulation Plug (DDCP) is a universal size and fits any size DCFS, DCFN, DFEN tracheostomy tube. The red DDCP snaplock connector is used to occlude the proximal end of the outer cannula on the Shiley Tracheostomy Tubes. Refer to Table 1 for model types. The DDCP blocks airflow through the tube and directs breathing through the mouth and nose. The Shiley Tracheostomy Tube and the accessory products are intended for use in providing tracheal access for airway management.", "reason": "Due to product labeling incorrectly including the symbol indicating non-DEHP (Bis(2-ethylhexyl) phthalate as the product includes 30 to 35% DEHP.", "hazard_level": "Class II", "company": "Covidien LLC", "company_location": "Boulder, CO, United States", "date": "2026-04-23", "report_date": "2026-07-08", "status": "Ongoing", "distribution": "U.S. Nationwide distribution including in the states and territories of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, and Virgin Islands. The countries of Albania, Andorra, Argentina, Australia, Austria, Belgium, Bhutan, Canada, Canary Islands, Chile, Colombia, Costa Rica, Croatia, Cyprus, Czech Republic, Denmark, Dominican Republic, Finland, France, Georgia, Germany, Greece, Guadeloupe, Guyana, Hungary, Ireland, Israel, Italy, Japan, Kazakhstan, Kuwait, Latvia, Lithuania, Luxembourg, Martinique, Mexico, Netherlands, New Caledonia, New Zealand, North Macedonia, Norway, Oman, Paraguay, Peru, Poland, Portugal, Qatar, Reunion, Romania, Saudi Arabia, Slovakia, South Africa, Spain, Sweden, Switzerland, Togo, Trinidad And Tobago, Turkey, Uganda, United Arab Emirates, Uruguay.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV"], "nationwide": true, "quantity": "293,659 devices", "codes": "Product Number: DDCP UDI-DI code: 10884522004060 The below product numbers and UDI-DI codes that DDCP are: 4DCFN / 10884522006576 4DCFS / 10884522006583 4DFEN / 10884522006606 6DCFN / 10884522006613 6DCFS / 10884522006620 6DFEN / 10884522006644 8DCFN / 10884522006651 8DCFS / 40884522006690 8DFEN / 10884522006675 10DCFN / 20884522006535 10DCFS / 10884522006545 10DFEN / 10884522006569", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2653-2026%22", "url": "https://recallledger.net/recalls/device-z-2653-2026-covidien-shiley-disposable-decannulation-plug-ref-ddcp-udi-di-code/"}, {"id": "fda-device-z-2638-2026", "source": "FDA", "category": "device", "recall_number": "Z-2638-2026", "title": "Adapter for Head Positioning recall (Baxter Healthcare Corporation)", "product": "Adapter for Head Positioning, Model/Catalog Number: 1739994, when used in conjunction with the side rails of the Upper Back Section H V U component (product code 1909813) on Baxter operating tables", "reason": "The Adapter for Head Positioning accessory may become loose during patient positioning and unintentionally move when used in conjunction with the side rails of the Upper Back Section H V U component on Baxter operating tables.", "hazard_level": "Class II", "company": "Baxter Healthcare Corporation", "company_location": "Deerfield, IL, United States", "date": "2026-04-21", "report_date": "2026-07-08", "status": "Ongoing", "distribution": "Worldwide - US Nationwide distribution in the states of Minnesota, Maryland, and Pennsylvania and the countries of Canada, Hong Kong, India, Japan, Korea, Philippines, Taiwan, Thailand, Vietnam, Austria, Belgium, Croatia, Czech Republic, Denmark, Finland, France, Germany, Greece, Hungary, Iraq, Israel, Italy, Jordan, Kenya, Lebanon, Libya, Malta, Morocco, Netherlands, Norway, Oman, Pakistan, Poland, Portugal, Qatar, Romania, Saudi Arabia, Senegal, Serbia, Slovakia, Spain, Sweden, Switzerland, Tunisia, Turkey, United Arabia Emrites, Ukraine, Argentina, Brazil, Chile, Colombia, Costa Rica, Mexico, and Peru.", "states": ["MD", "MN", "PA"], "nationwide": true, "quantity": "13 units", "codes": "Lot Code: Product Code: 1739994 UDI-DI: 00887761972780 Serial Numbers: 109931797, 109931798, 109931799, 109943588, 109943590, 109948550, 109964963, 109964964, 109964969, 109964970, 109964971, 109980700, and 110006694", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2638-2026%22", "url": "https://recallledger.net/recalls/device-z-2638-2026-adapter-for-head-positioning-model-catalog-number-1739994-when-used/"}, {"id": "fda-device-z-2618-2026", "source": "FDA", "category": "device", "recall_number": "Z-2618-2026", "title": "Short Monobloc Stem Broaches recall (Medacta Usa Inc)", "product": "Short Monobloc Stem Broaches, Size/REF: 7/04.01.10.0970, 8/04.01.10.0971, 9/04.01.10.0972, 10/04.01.10.0973, 11/04.01.10.0974, 12/04.01.10.0975, 13/04.01.10.0976, 14/04.01.10.0977, 15/04.01.10.0978, 16/04.01.10.0979 Part of Medacta Shoulder System", "reason": "Surgical instruments used during shoulder arthroplasty procedures does not progressively translate to replicate implant geometry, so the reaming guide and the stem reamer are positioned approximately 0.2 mm per size more laterally than intended, which may increase the risk of fracture in the medial region of the proximal humerus.", "hazard_level": "Class II", "company": "Medacta Usa Inc", "company_location": "Memphis, TN, United States", "date": "2026-04-30", "report_date": "2026-07-08", "status": "Ongoing", "distribution": "US Nationwide distribution in the states of CO, AR, IN, PA, UT, FL.", "states": ["AR", "CO", "FL", "IN", "PA", "UT"], "nationwide": true, "quantity": "50", "codes": "REF/UDI/Lot: 04.01.10.0970/07630542768910/2585086, 04.01.10.0971/07630542768927/2585087, 04.01.10.0972/07630542768934/2585088, 04.01.10.0973/07630542768941/2585089, 04.01.10.0974/07630542768958/2585090, 04.01.10.0975/07630542768965/2585091, 04.01.10.0976/07630542768972/2585092, 04.01.10.0977/07630542768989/2585093, 04.01.10.0978/07630542768996/2585094, 04.01.10.0979/07630542769009/2585095", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2618-2026%22", "url": "https://recallledger.net/recalls/device-z-2618-2026-short-monobloc-stem-broaches-size-ref-7-04-01-10-0970-8-04-01-10/"}, {"id": "fda-device-z-2614-2026", "source": "FDA", "category": "device", "recall_number": "Z-2614-2026", "title": "SYRINGE LUER LOK 10CC-200/BOX BD Product Code: 302995 Mentor Product Code: B9604 ... recall (Mentor Texas LP)", "product": "SYRINGE LUER LOK 10CC-200/BOX BD Product Code: 302995 Mentor Product Code: B9604 Syringe, Piston", "reason": "A single lot of expired syringes were distributed due to a distribution system control failure.", "hazard_level": "Class II", "company": "Mentor Texas LP", "company_location": "Coppell, TX, United States", "date": "2026-04-28", "report_date": "2026-07-08", "status": "Ongoing", "distribution": "U.S.: CA, FL, and PA", "states": ["CA", "FL", "PA"], "nationwide": false, "quantity": "1401 syringes", "codes": "BD Product Code: 302995 Mentor Product Code: B9604 Sales Unit Box UDI-DI/GTIN code: 30382903029952 Individual Unit UDI-DI/GTIN code: 00382903029952 Lot Number: 8298877", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2614-2026%22", "url": "https://recallledger.net/recalls/device-z-2614-2026-syringe-luer-lok-10cc-200-box-bd-product-code-302995-mentor-product/"}, {"id": "fda-food-h-1123-2026", "source": "FDA", "category": "food", "recall_number": "H-1123-2026", "title": "25# Sunflower Seeds C/S recall (George J Howe Company, Inc.)", "product": "25# Sunflower Seeds C/S", "reason": "The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.", "hazard_level": "Class I", "company": "George J Howe Company, Inc.", "company_location": "Grove City, PA, United States", "date": "2026-04-29", "report_date": "2026-07-01", "status": "Terminated", "distribution": "The recalled product was distributed to the following States: AL, AR, FL, GA, IA, IL, IN, KS, KY, MD, MI, MN, MO, MS, NC, NJ, NY, OH, OK, PA, SC, TN, VA,WI,WV,", "states": ["AL", "AR", "FL", "GA", "IA", "IL", "IN", "KS", "KY", "MD", "MI", "MN", "MO", "MS", "NC", "NJ", "NY", "OH", "OK", "PA", "SC", "TN", "VA", "WI", "WV"], "nationwide": false, "quantity": "2.00 Cases", "codes": "00601138", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-1123-2026%22", "url": "https://recallledger.net/recalls/food-h-1123-2026-25-sunflower-seeds-c-s/"}, {"id": "fda-food-h-1122-2026", "source": "FDA", "category": "food", "recall_number": "H-1122-2026", "title": "5# Sunflower Seeds C/NS recall (George J Howe Company, Inc.)", "product": "5# Sunflower Seeds C/NS", "reason": "The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.", "hazard_level": "Class I", "company": "George J Howe Company, Inc.", "company_location": "Grove City, PA, United States", "date": "2026-04-29", "report_date": "2026-07-01", "status": "Terminated", "distribution": "The recalled product was distributed to the following States: AL, AR, FL, GA, IA, IL, IN, KS, KY, MD, MI, MN, MO, MS, NC, NJ, NY, OH, OK, PA, SC, TN, VA,WI,WV,", "states": ["AL", "AR", "FL", "GA", "IA", "IL", "IN", "KS", "KY", "MD", "MI", "MN", "MO", "MS", "NC", "NJ", "NY", "OH", "OK", "PA", "SC", "TN", "VA", "WI", "WV"], "nationwide": false, "quantity": "7.00 Cases", "codes": "00501139", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-1122-2026%22", "url": "https://recallledger.net/recalls/food-h-1122-2026-5-sunflower-seeds-c-ns/"}, {"id": "fda-food-h-1121-2026", "source": "FDA", "category": "food", "recall_number": "H-1121-2026", "title": "5# Sunflower Seeds C/S recall (George J Howe Company, Inc.)", "product": "5# Sunflower Seeds C/S", "reason": "The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.", "hazard_level": "Class I", "company": "George J Howe Company, Inc.", "company_location": "Grove City, PA, United States", "date": "2026-04-29", "report_date": "2026-07-01", "status": "Terminated", "distribution": "The recalled product was distributed to the following States: AL, AR, FL, GA, IA, IL, IN, KS, KY, MD, MI, MN, MO, MS, NC, NJ, NY, OH, OK, PA, SC, TN, VA,WI,WV,", "states": ["AL", "AR", "FL", "GA", "IA", "IL", "IN", "KS", "KY", "MD", "MI", "MN", "MO", "MS", "NC", "NJ", "NY", "OH", "OK", "PA", "SC", "TN", "VA", "WI", "WV"], "nationwide": false, "quantity": "19.00 Cases", "codes": "00501138", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-1121-2026%22", "url": "https://recallledger.net/recalls/food-h-1121-2026-5-sunflower-seeds-c-s/"}, {"id": "fda-food-h-1120-2026", "source": "FDA", "category": "food", "recall_number": "H-1120-2026", "title": "8/9.5oz Tub Nut - Sunflower Seed recall (George J Howe Company, Inc.)", "product": "8/9.5oz Tub Nut - Sunflower Seed", "reason": "The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.", "hazard_level": "Class I", "company": "George J Howe Company, Inc.", "company_location": "Grove City, PA, United States", "date": "2026-04-29", "report_date": "2026-07-01", "status": "Terminated", "distribution": "The recalled product was distributed to the following States: AL, AR, FL, GA, IA, IL, IN, KS, KY, MD, MI, MN, MO, MS, NC, NJ, NY, OH, OK, PA, SC, TN, VA,WI,WV,", "states": ["AL", "AR", "FL", "GA", "IA", "IL", "IN", "KS", "KY", "MD", "MI", "MN", "MO", "MS", "NC", "NJ", "NY", "OH", "OK", "PA", "SC", "TN", "VA", "WI", "WV"], "nationwide": false, "quantity": "8.00 Cases", "codes": "07317102701", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-1120-2026%22", "url": "https://recallledger.net/recalls/food-h-1120-2026-8-9-5oz-tub-nut-sunflower-seed/"}, {"id": "fda-food-h-1119-2026", "source": "FDA", "category": "food", "recall_number": "H-1119-2026", "title": "6/11oz No Salt Sunflower Seeds recall (George J Howe Company, Inc.)", "product": "6/11oz No Salt Sunflower Seeds", "reason": "The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.", "hazard_level": "Class I", "company": "George J Howe Company, Inc.", "company_location": "Grove City, PA, 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All lots until the IFU update has been implemented", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2560-2026%22", "url": "https://recallledger.net/recalls/device-z-2560-2026-surgify-halo-4-0-mm-short-model-catalog-number-40-070-nvg-h1-dril/"}, {"id": "fda-device-z-2559-2026", "source": "FDA", "category": "device", "recall_number": "Z-2559-2026", "title": "Surgify Halo recall (SURGIFY MEDICAL OY)", "product": "Surgify Halo, 4.0 mm, Extendable, Model/Catalog Number: 40.000.SEE.U1; drills, burrs, trephines & accessories (simple, powered)", "reason": "Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).", "hazard_level": "Class II", "company": "SURGIFY MEDICAL OY", "company_location": "Espoo, N/A, Finland", "date": "2026-04-30", "report_date": "2026-07-01", "status": "Ongoing", "distribution": "US Nationwide distribution in the states of MN, MA, IN, LA, CA, NY, FL.", "states": ["CA", "FL", "IN", "LA", "MA", "MN", "NY"], "nationwide": true, "quantity": "N/A", "codes": "UDI: 06429811532281; All lots until the IFU update has been implemented", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2559-2026%22", "url": "https://recallledger.net/recalls/device-z-2559-2026-surgify-halo-4-0-mm-extendable-model-catalog-number-40-000-see-u1/"}, {"id": "fda-device-z-2558-2026", "source": "FDA", "category": "device", "recall_number": "Z-2558-2026", "title": "Surgify Halo recall (SURGIFY MEDICAL OY)", "product": "Surgify Halo, 4.0 mm, Extendable, Model/Catalog Number: 40.000.SEE.H1; drills, burrs, trephines & accessories (simple, powered)", "reason": "Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).", "hazard_level": "Class II", "company": "SURGIFY MEDICAL OY", "company_location": "Espoo, N/A, Finland", "date": "2026-04-30", "report_date": "2026-07-01", "status": "Ongoing", "distribution": "US Nationwide distribution in the states of MN, MA, IN, LA, CA, NY, FL.", "states": ["CA", "FL", "IN", "LA", "MA", "MN", "NY"], "nationwide": true, "quantity": "112 units", "codes": "UDI: 06429811532076; All lots until the IFU update has been implemented", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2558-2026%22", "url": "https://recallledger.net/recalls/device-z-2558-2026-surgify-halo-4-0-mm-extendable-model-catalog-number-40-000-see-h1/"}, {"id": "fda-device-z-2557-2026", "source": "FDA", "category": "device", "recall_number": "Z-2557-2026", "title": "Surgify Halo recall (SURGIFY MEDICAL OY)", "product": "Surgify Halo, 3.0 mm, Long, Model/Catalog Number: 30.125.NVG.U2; drills, burrs, trephines & accessories (simple, powered)", "reason": "Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).", "hazard_level": "Class II", "company": "SURGIFY MEDICAL OY", "company_location": "Espoo, N/A, Finland", "date": "2026-04-30", "report_date": "2026-07-01", "status": "Ongoing", "distribution": "US Nationwide distribution in the states of MN, MA, IN, LA, CA, NY, FL.", "states": ["CA", "FL", "IN", "LA", "MA", "MN", "NY"], "nationwide": true, "quantity": "N/A", "codes": "UDI: 06429811532212; All lots until the IFU update has been implemented", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2557-2026%22", "url": "https://recallledger.net/recalls/device-z-2557-2026-surgify-halo-3-0-mm-long-model-catalog-number-30-125-nvg-u2-drill/"}, {"id": "fda-device-z-2556-2026", "source": "FDA", "category": "device", "recall_number": "Z-2556-2026", "title": "Surgify Halo recall (SURGIFY MEDICAL OY)", "product": "Surgify Halo, 3.0 mm, Short, Model/Catalog Number: 30.070.NVG.U2; drills, burrs, trephines & accessories (simple, powered)", "reason": "Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).", "hazard_level": "Class II", "company": "SURGIFY MEDICAL OY", "company_location": "Espoo, N/A, Finland", "date": "2026-04-30", "report_date": "2026-07-01", "status": "Ongoing", "distribution": "US Nationwide distribution in the states of MN, MA, IN, LA, CA, NY, FL.", "states": ["CA", "FL", "IN", "LA", "MA", "MN", "NY"], "nationwide": true, "quantity": "N/A", "codes": "UDI: 06429811532205; All lots until the IFU update has been implemented", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2556-2026%22", "url": "https://recallledger.net/recalls/device-z-2556-2026-surgify-halo-3-0-mm-short-model-catalog-number-30-070-nvg-u2-dril/"}, {"id": "fda-device-z-2555-2026", "source": "FDA", "category": "device", "recall_number": "Z-2555-2026", "title": "Surgify Halo recall (SURGIFY MEDICAL OY)", "product": "Surgify Halo, 3.0 mm, Extendable, Model/Catalog Number: 30.000.SEE.U2; drills, burrs, trephines & accessories (simple, powered)", "reason": "Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).", "hazard_level": "Class II", "company": "SURGIFY MEDICAL OY", "company_location": "Espoo, N/A, Finland", "date": "2026-04-30", "report_date": "2026-07-01", "status": "Ongoing", "distribution": "US Nationwide distribution in the states of MN, MA, IN, LA, CA, NY, FL.", "states": ["CA", "FL", "IN", "LA", "MA", "MN", "NY"], "nationwide": true, "quantity": "15 units", "codes": "UDI: 06429811532229; All lots until the IFU update has been implemented", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2555-2026%22", "url": "https://recallledger.net/recalls/device-z-2555-2026-surgify-halo-3-0-mm-extendable-model-catalog-number-30-000-see-u2/"}, {"id": "fda-device-z-2552-2026", "source": "FDA", "category": "device", "recall_number": "Z-2552-2026", "title": "INZONE DETACHMENT SYSTEM recall (Stryker Neurovascular)", "product": "INZONE DETACHMENT SYSTEM, REF: M00345100950", "reason": "Embolization coil detachment system devices may experience premature battery drain causing devices to: 1) Not power on; 2) Power on with faint audible and visual indicators; 3) Be unable to detach a coil as intended, which may necessitate medical intervention if the procedure must be completed with an alternative technique.", "hazard_level": "Class II", "company": "Stryker Neurovascular", "company_location": "Fremont, CA, United States", "date": "2026-04-06", "report_date": "2026-07-01", "status": "Ongoing", "distribution": "Worldwide - US Nationwide distribution including in the states of PA, AZ, FL, CA, IL, AK, NY, MI, NJ, WI, SD, KY, AR, TX, AL, TN, MO, MA, IN, NE, WV, MT, CT, NC, VA, NV, CO, DC, DE, OH, ME, GA, WA, SC, GU, MN, OK, NH, MD, ND, UT, HI, OR, LA, MS, KS, NM, ID, IA, VT and the countries of ARGENTINA, AUSTRIA, BELGIUM, BRASIL, BULGARIA, CANADA, CANARY ISLANDS, CHILE, COLOMBIA, CROATIA, CZECH REPUBLIC, DENMARK, ESTONIA, FINLAND, FRANCE, GERMANY, GREECE, HONG KONG, HUNGARY, ICELAND, IRAN, IRELAND, ISRAEL, ITALIA, JAPAN, KOREA, LATVIA, LUXEMBOURG, MALAYSIA, MEXICO, NETHERLANDS, NORTHERN IRELAND, NORWAY, PHILIPPINES, POLAND, PORTUGAL, QATAR, ROMANIA, RUSSIA, SAUDI ARABIA, SINGAPORE, SLOVAKIA, SLOVENIA, SOUTH AFRICA, SOUTH PACIFIC, SPAIN, SWEDEN, SWITZERLAND, TAIWAN, THAILAND, TURKEY, UNITED ARAB EMIRATES, UNITED KINGDOM.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV"], "nationwide": true, "quantity": "44,937", "codes": "UDI-DI: 04546540697950. Lots: WMP133638, WMP133871, WMP133872, WMP133988, WMP133989, WMP134016, WMP134132, WMP134133, WMP134234, WMP134235, WMP134255, WMP134256, WMP134380, WMP134381, WMP134432, WMP134433, WMP134518, WMP134519, WMP134609, WMP134610, WMP134794, WMP134795, WMP134939, WMP134940, WMP135187, WMP135243, WMP135302, WMP135314, WMP135354, WMP135355, WMP135387, WMP135417, WMP135473, WMP135475, WMP135491, WMP135492, WMP135623, WMP135720, WMP135727, WMP135807, WMP135865, WMP135897, WMP136084, WMP136107, WMP136190, WMP136200, WMP136611, WMP136642, WMP136736, WMP136748, WMP136852, WMP136894, WMP136985", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2552-2026%22", "url": "https://recallledger.net/recalls/device-z-2552-2026-inzone-detachment-system-ref-m00345100950/"}, {"id": "fda-device-z-2526-2026", "source": "FDA", "category": "device", "recall_number": "Z-2526-2026", "title": "Multi-Snare Set: 5 mm x 125 cm recall (PFM MEDICAL INC.)", "product": "Multi-Snare Set: 5 mm x 125 cm, REF: 147305; 10 mm x 125 cm, REF: 147310", "reason": "A snare catheter including luer lock, indicated for removal or manipulation of a foreign body in the vascular system, failed to meet the biocompatibility requirements for in-vitro-cytotoxicity, which if in contact with a patient's vasculature could result in localized inflammation and tissue irritation.", "hazard_level": "Class II", "company": "PFM MEDICAL INC.", "company_location": "Carlsbad, CA, United States", "date": "2026-04-21", "report_date": "2026-07-01", "status": "Ongoing", "distribution": "US Nationwide distribution in the states of NY, MD.", "states": ["MD", "NY"], "nationwide": true, "quantity": "32", "codes": "REF/UDI-DI/Lot(Expiration): 147305/04042301061829/1049868(10/14/2028); 147310/04042301033567/1049960(10/20/28)", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2526-2026%22", "url": "https://recallledger.net/recalls/device-z-2526-2026-multi-snare-set-5-mm-x-125-cm-ref-147305-10-mm-x-125-cm-ref-1473/"}, {"id": "fda-device-z-2521-2026", "source": "FDA", "category": "device", "recall_number": "Z-2521-2026", "title": "Da Vinci ASSY recall (Intuitive Surgical, Inc.)", "product": "Da Vinci ASSY, PSS, SP1098, Part Number: 380601", "reason": "Operative components of surgical systems potentially distributed with E-brake retainer pin, so in event of a structural column failure, the E-brake pin would prevent E-brake engagement and may result in uncontrolled motion. In addition, if it moves/backs out it may cause restricted column range of motion and/or uncontrolled motion, which may cause patient tissue injury/crushing injury/bleeding.", "hazard_level": "Class II", "company": "Intuitive Surgical, Inc.", "company_location": "Sunnyvale, CA, United States", "date": "2026-04-22", "report_date": "2026-07-01", "status": "Ongoing", "distribution": "Worldwide - US Nationwide distribution including in the states of CA, GA, OH, PA, NY, MN, TN, OR, IL, MD, NJ, AL, NV, TX, FL, LA, CT, NC, AZ, IA, MO, WA, MI, WV, WI, KY, KS, VA, OK, MA, IN, CO, SC, SD, MS, NH, UT, ME and the countries of Belgium, Denmark, Sweden, France, Japan, Germany, Israel, Switzerland, South Korea, Czech Republic, Austria, United Kingdom, Italy, Spain, Ireland, Saudi Arabia, Greece, Taiwan, Australia, China, Turkey, Poland, United Arab Emirates, Hong Kong, Romania.", "states": ["AL", "AZ", "CA", "CO", "CT", "FL", "GA", "IA", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "NC", "NH", "NJ", "NV", "NY", "OH", "OK", "OR", "PA", "SC", "SD", "TN", "TX", "UT", "VA", "WA", "WI", "WV"], "nationwide": true, "quantity": "454", "codes": "UDI: 00886874114605. Serial Numbers: 605408, 606848, 612328, 628399, 609353, 614073, 617794, 616769, 10008062, 635659, 631694, 638771, 641430, 694998, 645433, 643209, 954097, 656203, 764644, 656319, 946098, 667190, 666480, 655562, 664662, 680530, 679266, 683974, 674171, 676962, 682694, 686777, 701248, 696877, 688725, 688225, 697922, 700316, 698277, 702699, 709536, 701751, 717804, 705366, 704731, 724178, 703152, 722803, 693262, 736468, 736338, 740359, 742366, 732233, 696089, 724835, 716520, 709987, 728391, 751529, 731765, 672743, 766366, 711517, 735003, 735252, 746457, 746623, 718940, 721722, 691190, 744094, 750174, 738718, 10211920, 759253, 761448, 752536, 812651, 754935, 790597, 811147, 793019, 761000, 812650, 919988, 919987, 913011, 913012, 926423, 759791, 926422, 938794, 771653, 938795, 766365, 963841, 797872, 769736, 794437, 970568, 970562, 977045, 10003059, 957781, 973824, 804588, 10009706, 936269, 10003509, 930240, 936268, 800142, 10003510, 982782, 967667, 10009707, 973355, 944585, 10065786, 935214, 10020729, 10012963, 10020705, 10031145, 10031144, 973825, 10012962, 10036960, 963856, 10711066, 10035476, 795038, 10043635, 944583, 10072852, 10072853, 966079, 10069899, 10076490, 10087446, 10054478, 10080929, 954096, 10130089, 10165287, 942811, 10180162, 10172589, 10103483, 10103484, 10056518, 10092007, 10246370, 10209961, 10183740, 10232634, 504007, 10231116, 10211880, 10194911, 10245457, 10112470, 10189443, 977044, 10238314, 10644376, 10036961, 10274101, 10112471, 10238315, 10172574, 10281524, 10278366, 10252751, 10289629, 10293276, 10261900, 10274102, 10285085, 10281525, 10243796, 10267796, 10278365, 10285084, 10308532, 10318311, 10293274, 10323177, 10322512, 10289630, 10326939, 10293275, 10333333, 10326938, 10492299, 10302474, 10302473, 10368392, 10332310, 10346946, 10354749, 10346943, 10333332, 10346942, 10267795, 10323178, 10295600, 10223509, 10252780, 10396330, 10263730, 10354748, 10337879, 10265272, 10354750, 10384455, 10359960, 10368393, 10366206, 10375031, 10363897, 10396329, 10363898, 10375032, 10375033, 10409934, 10401560, 10409933, 10408268, 10294693, 10408269, 10396331, 10480883, 10499186, 10499185, 10384456, 10502598, 10495654, 10502599, 10505838, 10512168, 10512167, 10512166, 10508290, 10368391, 10556776, 10417803, 10526733, 10417164, 10508289, 10384454, 10492298, 10480878, 10526735, 10526736, 10537191, 10495655, 10526734, 10526732, 530114, 10537202, 10568118, 10308533, 10547839, 10564979, 10550219, 10564978, 10550220, 10550221, 10561240, 10594744, 10575228, 10571615, 10575229, 10583123, 10571614, 10556769, 10583124, 10594746, 10556777, 10564977, 10594743, 10579531, 10613173, 10568117, 10571616, 10615325, 10583126, 10619701, 10594742, 10541679, 10579530, 10561239, 10594745, 10615326, 10590323, 10590322, 10583125, 10615941, 10608089, 10644375, 10604955, 10561241, 10624252, 10647203, 10670710, 10672825, 10624990, 10295599, 10633489, 10622883, 10647201, 10624251, 10686903, 10612973, 10619702, 10672839, 10696000, 10615940, 10659191, 10651445, 10651443, 10682596, 10702363, 10644374, 10653815, 10651444, 10627633, 10686902, 10672840, 10627632, 10695999, 10665125, 10604956, 10480877, 10682597, 10694981, 10633487, 10716881, 10659189, 10728578, 10627631, 10702364, 10734551, 10659190, 10633488, 10734552, 10706206, 650202, 10744259, 10706207, 10766233, 10766236, 10793380, 10759158, 10759159, 10759161, 10763608, 10763609, 10808841, 10766234, 10763611, 10741377, 10759160, 10763610, 10826493, 10776325, 10766235, 10741378, 10744258, 10734553, 10808839, 10808840, 10771126, 10803470, 10793379, 10817400, 10798922, 10803484, 10766232, 10887260, 10830719, 10771125, 10776323, 10815457, 10744257, 10823000, 10776324, 10782092, 10873054, 10879012, 10897582, 10856718, 10889592, 10864698, 10922820, 10912617, 10647204, 10869722, 10889594, 10871773, 10845441, 10859690, 10826495, 10579532, 10782090, 10826494, 10792831, 10883203, 10871774, 10856716, 10856732, 10859689, 10947466, 10798915, 10968849, 10952495, 10957321, 10875232, 10903586, 10927370, 10947464, 10951328, 10981839, 10787962, 10908841, 10908842, 10817401, 10938311, 10933815, 10938312, 10955031, 10927371, 10933816, 10998396, 10927372, 10240354, 10998395, 11004904, 10979952, 10875231, 10912618, 10897581, 10938310, 10991256, 10991257, 10991259, 10895278, 10883202, 10889593, 10912619, 11016764, 11013103", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2521-2026%22", "url": "https://recallledger.net/recalls/device-z-2521-2026-da-vinci-assy-pss-sp1098-part-number-380601/"}, {"id": "fda-device-z-2509-2026", "source": "FDA", "category": "device", "recall_number": "Z-2509-2026", "title": "Product Name: STAAR ICL Calculation Software Software Version: Version 8.00 Product... recall (Staar Surgical AG)", "product": "Product Name: STAAR ICL Calculation Software Software Version: Version 8.00 Product Description: The STAAR ICL Calculation Software is designed as an aide in the calculation of the size and diopter power (with residual refraction) for physician selection of the lens. For toric ICLs, an Implantation Orientation Diagram (IOD) is also produced to provide the physician with pictorial representation of the axis of rotation and alignment. Note: The STAAR ICL Calculation Software resides on STAAR Surgical's e-commerce website in STAAR ICL planning support (Stella), as referenced in the attached recall communication. Component: No", "reason": "Due to a software coding issues for calculating the implant orientation diagram printout for the implantation for toric implantable collamer lenses.", "hazard_level": "Class II", "company": "Staar Surgical AG", "company_location": "Nidau, Switzerland", "date": "2026-04-20", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "Worldwide - US Nationwide distribution including in the states and territory of AK, AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV and the countries of Austria, Australia, Belgium, Canada, Switzerland, Czech Republic, Germany Spain, Finland, France, Great Britain, Hong Kong, Ireland, Israel, India, Iran, Italy, Jordan, Korea, Kuwait, Kazakhstan, Morocco, Malaysia, Netherlands, Oman, Philippines, Poland, Saudi Arabia, Sweden, Singapore, Thailand, Turkey, Taiwan, Ukraine, USA, Vietnam.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "WA", "WI", "WV"], "nationwide": true, "quantity": "543", "codes": "Lot Code: UDI (01)00840311346288(0812)8.00 Software Version 8.00 The software error occurs if a customer generated an IOD for a toric implantation from April 13, 2026 to April 16, 2026 for multiple toric lens reservations for the same eye using the STAAR ICL Calculation Software.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2509-2026%22", "url": "https://recallledger.net/recalls/device-z-2509-2026-product-name-staar-icl-calculation-software-software-version-versio/"}, {"id": "fda-device-z-2460-2026", "source": "FDA", "category": "device", "recall_number": "Z-2460-2026", "title": "directCHECK ACT-LR whole blood quality control recall (Accriva Diagnostics, Inc.)", "product": "directCHECK ACT-LR whole blood quality control, level 2 Model/Catalog Number: DCGLR-2", "reason": "Assayed Whole blood control contains labeling with incorrect performance range.", "hazard_level": "Class II", "company": "Accriva Diagnostics, Inc.", "company_location": "San Diego, CA, United States", "date": "2026-04-30", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "Worldwide - US Nationwide distribution including in the states of AL, AR, AZ, CA, FL, GA, \tID, IL, IN, KY, MA, MD, MI, MN, MO, MT, NC, NJ, NM, NY, OH, OK, PA, SC, TN, TX, VA, VT, WA, \tWI, WV and the countries of Canada, Hong Kong, Spain.", "states": ["AL", "AR", "AZ", "CA", "FL", "GA", "ID", "IL", "IN", "KY", "MA", "MD", "MI", "MN", "MO", "MT", "NC", "NJ", "NM", "NY", "OH", "OK", "PA", "SC", "TN", "TX", "VA", "VT", "WA", "WI", "WV"], "nationwide": true, "quantity": "6060", "codes": "Lot #: A6DLA001 Unique Device Identifier: 10711234170373", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2460-2026%22", "url": "https://recallledger.net/recalls/device-z-2460-2026-directcheck-act-lr-whole-blood-quality-control-level-2-model-catalog/"}, {"id": "fda-device-z-2447-2026", "source": "FDA", "category": "device", "recall_number": "Z-2447-2026", "title": "Medline convenience kits: HYSTERECTOMY PACK-LF DYNJ20485L recall (Medline Industries, LP)", "product": "Medline convenience kits: HYSTERECTOMY PACK-LF DYNJ20485L", "reason": "Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.", "hazard_level": "Class II", "company": "Medline Industries, LP", "company_location": "Northfield, IL, United States", "date": "2026-04-27", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution. OUS distribution pending.", "states": [], "nationwide": true, "quantity": "49,654 kits total", "codes": "UDI-DI 10195327024369 Lot 25LMJ031", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2447-2026%22", "url": "https://recallledger.net/recalls/device-z-2447-2026-medline-convenience-kits-hysterectomy-pack-lf-dynj20485l/"}, {"id": "fda-device-z-2446-2026", "source": "FDA", "category": "device", "recall_number": "Z-2446-2026", "title": "Medline convenience kits: C SECTION CDS985505G C SECTION PACK DYNJ68260D ... recall (Medline Industries, LP)", "product": "Medline convenience kits: C SECTION CDS985505G C SECTION PACK DYNJ68260D C-SECTION DYNJ905094B C-SECTION RECOVERY #2 CDS820091P", "reason": "Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.", "hazard_level": "Class II", "company": "Medline Industries, LP", "company_location": "Northfield, IL, United States", "date": "2026-04-27", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution. OUS distribution pending.", "states": [], "nationwide": true, "quantity": "49,654 kits total", "codes": "CDS985505G UDI-DI 10195327412555 Lot 26AMC363 DYNJ68260D UDI-DI 10195327506513 Lot 25KBE168 DYNJ905094B UDI-DI 10193489858174 Lot 25KMB136 CDS820091P UDI-DI 10195327403539 Lots 26BBO404 26CBN891", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2446-2026%22", "url": "https://recallledger.net/recalls/device-z-2446-2026-medline-convenience-kits-c-section-cds985505g-c-section-pack/"}, {"id": "fda-device-z-2445-2026", "source": "FDA", "category": "device", "recall_number": "Z-2445-2026", "title": "Medline convenience kits: ADD-A-CATH ARTERIAL INSERTION ARTNC185 PED SCHOOL AGE... recall (Medline Industries, LP)", "product": "Medline convenience kits: ADD-A-CATH ARTERIAL INSERTION ARTNC185 PED SCHOOL AGE PICC DRSG TRAY DYNDC3291", "reason": "Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.", "hazard_level": "Class II", "company": "Medline Industries, LP", "company_location": "Northfield, IL, United States", "date": "2026-04-27", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution. OUS distribution pending.", "states": [], "nationwide": true, "quantity": "49,654 kits total", "codes": "ARTNC185 UDI-DI 10195327640729 Lot 25JBU463 DYNDC3291 UDI-DI 10195327334741 Lot 25KBH082", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2445-2026%22", "url": "https://recallledger.net/recalls/device-z-2445-2026-medline-convenience-kits-add-a-cath-arterial-insertion-artnc185/"}, {"id": "fda-device-z-2444-2026", "source": "FDA", "category": "device", "recall_number": "Z-2444-2026", "title": "Medline convenience kits: BIB AV FISTULA PACK DYNJ58304B CARDIAC MINOR... recall (Medline Industries, LP)", "product": "Medline convenience kits: BIB AV FISTULA PACK DYNJ58304B CARDIAC MINOR SURGICOUNT PACK DYNJ56573B ENDOVASCULAR PACK DYNJ29135N EP DEVICE DYNJ65916B FULL LINE ANEURYSM CDS CDS983672P GEN FEM POP #14-RF DYNJ21877W IMPLANT PACK DYNJ39316D OPEN HEART MRNGSD DYNJ58354F PACEMAKER PACK-LF DYNJ0618174N PACEMAKER SETUP PACK DYNJ35761D PACER / CATH LAB PACK-LF DYNJ0972604A PACER CDS CDS983686I PACER PACK DYNJ52059D PK, EP LAB PACEMAKER DYNJ43663A VENOUS ACCESS PACK DYNJ45640B", "reason": "Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.", "hazard_level": "Class II", "company": "Medline Industries, LP", "company_location": "Northfield, IL, United States", "date": "2026-04-27", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution. OUS distribution pending.", "states": [], "nationwide": true, "quantity": "49,654 kits total", "codes": "DYNJ58304B UDI-DI 10195327512699 Lot 25LBP470 DYNJ56573B UDI-DI 10193489903669 Lot 25KBK220 DYNJ29135N UDI-DI 10195327674755 Lot 25LMG563 DYNJ65916B UDI-DI 10193489902044 Lots 25KBG852 25LBB895 CDS983672P UDI-DI 10198459149139 Lots 25LBO027 26BBB852 DYNJ21877W UDI-DI 10195327104542 Lot 25JBW040 DYNJ39316D UDI-DI 10198459224447 Lot 25KBH774 DYNJ58354F UDI-DI 10195327515232 Lot 25KBI240 DYNJ0618174N UDI-DI 10195327227340 Lot 25KBC715 DYNJ35761D UDI-DI 10195327565374 Lot 26CBC772 DYNJ0972604A UDI-DI 10889942403905 Lot 25LMF965 CDS983686I UDI-DI 10193489852981 Lot 26ABE755 DYNJ52059D UDI-DI 10195327361785 Lots 25LBQ917 26CBE736 DYNJ43663A UDI-DI 10193489793680 Lot 26CBB662 DYNJ45640B UDI-DI 10193489494983 Lot 25LMJ305", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2444-2026%22", "url": "https://recallledger.net/recalls/device-z-2444-2026-medline-convenience-kits-bib-av-fistula-pack-dynj58304b-cardia/"}, {"id": "fda-device-z-2443-2026", "source": "FDA", "category": "device", "recall_number": "Z-2443-2026", "title": "Medline convenience kits: PORT A CATH DYNJ906818A recall (Medline Industries, LP)", "product": "Medline convenience kits: PORT A CATH DYNJ906818A", "reason": "Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.", "hazard_level": "Class II", "company": "Medline Industries, LP", "company_location": "Northfield, IL, United States", "date": "2026-04-27", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution. OUS distribution pending.", "states": [], "nationwide": true, "quantity": "49,654 kits total", "codes": "DYNJ906818A 10195327027261 25LBC291", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2443-2026%22", "url": "https://recallledger.net/recalls/device-z-2443-2026-medline-convenience-kits-port-a-cath-dynj906818a/"}, {"id": "fda-device-z-2442-2026", "source": "FDA", "category": "device", "recall_number": "Z-2442-2026", "title": "Medline convenience kits: FEMORAL BLOCK TRAY DYNJRA1739B recall (Medline Industries, LP)", "product": "Medline convenience kits: FEMORAL BLOCK TRAY DYNJRA1739B", "reason": "Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.", "hazard_level": "Class II", "company": "Medline Industries, LP", "company_location": "Northfield, IL, United States", "date": "2026-04-27", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution. OUS distribution pending.", "states": [], "nationwide": true, "quantity": "49,654 kits total", "codes": "DYNJRA1739B UDI-DI 10195327411237 Lot 25LBB731", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2442-2026%22", "url": "https://recallledger.net/recalls/device-z-2442-2026-medline-convenience-kits-femoral-block-tray-dynjra1739b/"}, {"id": "fda-device-z-2441-2026", "source": "FDA", "category": "device", "recall_number": "Z-2441-2026", "title": "Medline convenience kits: ACL PACK DYNJ64161C ARTHROSCOPY PACK DYNJ47103D ... recall (Medline Industries, LP)", "product": "Medline convenience kits: ACL PACK DYNJ64161C ARTHROSCOPY PACK DYNJ47103D DYNJ67197G DYNJ85197A DYNJT4007 BASIC ACCESS PACK-LF DYNJ36698B BASIC BACK TRAY DYNJ89037 BASIC PEDI PACK-LF DYNJ0171446I DYNJ0171446J BASIC SPINE DYNJ910915A BREAST PACK DYNJ87587A BREAST PLASTIC PACK DYNJ84482C C SECTION DYNJ49172I CAROTID ENDARTERECTOMY PACK DYNJ48013L CENTRAL LINE PACK-LF DYNJ0220136S CERVICAL FUSION DYNJ908135B CERVICAL SPINE PACK DYNJ53044G C-SECTION DYNJ909099F DAVINCI PROSTATE PACK DYNJ61711C DEPAUL FOOT & ANKLE-LF DYNJ20010L DIEP PACK DYNJ64964J DYNJ43210K DYNJ61787F DYNJ87065 EAR CUSTOM PACK DYNJ82564A ENT FREE FLAP PACK SAFETY DYNJ54720D EP PACEMAKER SAFETY #1 DYNJ54722F EPCH EXTREMITY PACK DYNJ83095B EXTREMITY PACK DYNJ32934F EXTREMITY PACK-LF DYNJ68935B FISTULA PACK DYNJ66502B GENDER AFFIRMING SURGERY DYNJ66252F GYN LAPAROSCOPY PACK AHSC DYNJT8381 HAND PACK WATCHMAKER-LF DYNJ34580D HEAD & NECK PACK-LF DYNJ0282388T DYNJ88308 HIP SCOPE DYNJ907120D KNEE ARTHRO PACK DYNJ58404F KNEE ARTHROSCOPY PACK DYNJ84740A LAMI OVERHEAD PACK DYNJ46531Q LAMINECTOMY NEURO MPH DYNJT5271 LAMINECTOMY PACK DYNJ68785D LAP APPY PACK DYNJT6005 LAP CHOLE PACK DYNJ82087A LEVY PACK DYNJ83939C MAJOR LAP VCH DYNJ39217P MAJOR NEURO PACK-LF DYNJ0578916AA MAJOR PACK DYNJ58528J MINOR GEN PACK DYNJ61661B MINOR LAPAROTOMY PACK-LF DYNJ0753436P MINOR PACK DYNJ54968B NEURO PACK DYNJ67628D NEURO SHUNT PACK-LF DYNJ0578815W OMFS PACK DYNJ54400C OPEN HEART PACK DYNJT5008 OPEN HEART-LF DYNJ48260F OPEN LAPAROTOMY PACK DYNJ39247I DYNJ39247J PACEMAKER PACK DYNJ31461I DYNJ61411C PACK,ORTHO FLIP DYNJ65471B PED OPEN HEART PACK DYNJ45373G PLASTIC PACK DYNJ82495D PLASTICS PK - NO SYR DYNJ62433F PODIATRY PACK OP7809M PPE BUNDLE KIT DT13351A PROSTATE ROBOTIC PACK DYNJ84120C RADIAL ART LINE INSERTION ARTNC234 ROBOTIC GENERAL WHH DYNJT5376 ROBOTIC PACK DYNJ47978G RR-SPINE PACK DYNJ62643B SHOULDER ARTH PACK DYNJ58410D SHOULDER ARTHROSCOPY PACK DYNJ54477C DYNJT8391 SHOULDER PACK DYNJ61052B DYNJT3266 SHOULDER PACK-LF DYNJ0122428K PHS656414I SPINE PACK DYNJ64949C DYNJ83649B SPINE SHOULDER PACK DYNJ47104D STERILE ACCESS KIT DYNDA2664 TOTAL KNEE PACK DYNJ84741B TUBAL PACK DYNJ68253F UNIVERSAL PACK DYNJ83246B VA TAMPA GENERAL ROBOTIC PACK DYNJT6993 W.C. MINOR LAPAROTOMY PK-LF DYNJ0509186J ZALE OTOLOGY CDS CDS983181G", "reason": "Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.", "hazard_level": "Class II", "company": "Medline Industries, LP", "company_location": "Northfield, IL, United States", "date": "2026-04-27", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution. OUS distribution pending.", "states": [], "nationwide": true, "quantity": "49,654 kits total", "codes": "DYNJ64161C UDI-DI 10198459146961 Lot 25KBH332 DYNJ47103D UDI-DI 10198459625008 Lot 25LMF684 DYNJ67197G UDI-DI 10198459481994 Lot 25JBA258 DYNJ85197A UDI-DI 10198459217395 Lot 25LMF727 DYNJT4007 UDI-DI 10198459381867 Lot 26BBC180 DYNJ36698B UDI-DI 10198459081811 Lots 25KBM204 26CBD413 DYNJ89037 UDI-DI 10198459229855 Lots 25KBI083 25KBM202 DYNJ0171446I UDI-DI 10195327589516 Lot 25JBT239 DYNJ0171446J UDI-DI 10198459591754 Lot 26CBB295 DYNJ910915A UDI-DI 10198459424960 Lot 25LBD596 DYNJ87587A UDI-DI 10198459114199 Lot 25JBR735 DYNJ84482C UDI-DI 10198459362491 Lot 26BBU043 DYNJ49172I UDI-DI 10198459042003 Lot 26AMA388 DYNJ48013L UDI-DI 10198459560941 Lot 25LBP624 DYNJ0220136S UDI-DI 10198459566073 Lot 25LMF648 DYNJ908135B UDI-DI 10198459586552 Lots 25LBC200 25LBR878 DYNJ53044G UDI-DI 10198459448768 Lot 25LMG369 DYNJ909099F UDI-DI 10198459375996 Lot 25JMF136 DYNJ61711C UDI-DI 10198459096754 Lot 25JBT124 DYNJ20010L UDI-DI 10198459229053 Lot 25JMD853 DYNJ64964J UDI-DI 10198459254109 Lot 25LMI867 DYNJ43210K UDI-DI 10198459546792 Lot 25LMI070 DYNJ61787F UDI-DI 10198459169694 Lot 25JBU635 DYNJ87065 UDI-DI 10198459007439 Lots 25KBD819 25LBP631 DYNJ82564A UDI-DI 10198459497551 Lot 25LBD560 DYNJ54720D UDI-DI 10195327549510 Lot 26CBC228 DYNJ54722F UDI-DI 10195327549633 Lots 25KBB967 25LBQ696 26CBE680 DYNJ83095B UDI-DI 10198459562068 Lot 25JMD325 DYNJ32934F UDI-DI 10195327697181 Lot 26CBC762 DYNJ68935B UDI-DI 10198459440373 Lot 25LBN254 DYNJ66502B UDI-DI 10198459395321 Lot 25KBC481 DYNJ66252F UDI-DI 10198459185397 Lot 25LBP873 DYNJT8381 UDI-DI 10198459702358 Lot 26CBD354 DYNJ34580D UDI-DI 10195327579661 Lot 25LMF989 DYNJ0282388T UDI-DI 10198459591990 Lot 25LBP896 DYNJ88308 UDI-DI 10198459143328 Lot 25KBJ822 DYNJ907120D UDI-DI 10198459427985 Lots 25KBK051 25KBT376 26DBF975 DYNJ58404F UDI-DI 10198459366413 Lots 25KBI176 26CBE677 DYNJ84740A UDI-DI 10198459421556 Lot 25KBB657 DYNJ46531Q UDI-DI 10198459526107 Lot 25LMJ845 DYNJT5271 UDI-DI 10198459471452 Lot 25LBC165 DYNJ68785D UDI-DI 10198459546952 Lot 25JBU924 DYNJT6005 UDI-DI 10198459531187 Lot 25JBU086 DYNJ82087A UDI-DI 10198459078019 Lot 25LMH034 DYNJ83939C UDI-DI 10198459342523 Lot 25JBY263 DYNJ39217P UDI-DI 10198459102356 Lot 25JME213 DYNJ0578916AA UDI-DI 10198459117565 Lot 25JME873 DYNJ58528J UDI-DI 10198459322815 Lot 26CBE343 DYNJ61661B UDI-DI 10198459096785 Lot 25KBA722 DYNJ0753436P UDI-DI 10198459466854 Lot 25LMJ282 DYNJ54968B UDI-DI 10198459428753 Lot 25KBD827 DYNJ67628D UDI-DI 10198459383373 Lot 25LMG428 DYNJ0578815W UDI-DI 10198459466892 Lot 25LMI628 DYNJ54400C UDI-DI 10195327646905 Lot 25KBI070 DYNJT5008 UDI-DI 10198459463525 Lot 26BBC492 DYNJ48260F UDI-DI 10198459220241 Lot 25KBL822 DYNJ39247I UDI-DI 10195327633509 Lot 25JBR808 DYNJ39247J UDI-DI 10198459640698 Lot 26BBD397 DYNJ31461I UDI-DI 10198459519734 Lot 25JBV372 DYNJ61411C UDI-DI 10198459493591 Lot 25KBA043 DYNJ65471B UDI-DI 10198459168574 Lot 25JMF211 DYNJ45373G UDI-DI 10198459254635 Lot 25LMI203 DYNJ82495D UDI-DI 10198459439834 Lots 25KBI927 25LBR381 DYNJ62433F UDI-DI 10198459627514 Lot 25LBO801 OP7809M UDI-DI 10198459368493 Lot 26CBB615 DT13351A UDI-DI 10653160325581 Lots 25JBA293 25KBB632 DYNJ84120C UDI-DI 10198459574177 Lot 26AMA032 ARTNC234 UDI-DI 10198459566974 Lot 25KBJ985 DYNJT5376 UDI-DI 10198459470783 Lot 25LBP929 DYNJ47978G UDI-DI 10198459416606 Lot 26AMA586 DYNJ62643B UDI-DI 10198459164446 Lot 25LMG407 DYNJ58410D UDI-DI 10198459366468 Lot 25LBI975 DYNJ54477C UDI-DI 10198459004155 Lot 25LMI210 DYNJT8391 UDI-DI 10198459703140 Lot 26CBJ555 DYNJ61052B UDI-DI 10198459421587 Lot 26BBC156 DYNJT3266 UDI-DI 10198459320965 Lot 25LMH283 DYNJ0122428K UDI-DI 10198459533297 Lot 25EBP843A PHS656414I UDI-DI 10198459006258 Lot 25LMG515 DYNJ64949C UDI-DI 10198459190216 Lot 25LMH829 DYNJ83649B UDI-DI 10198459110177 Lot 25KBC046 DYNJ47104D UDI-DI 10198459624964 Lot 25LMJ846 DYNDA2664 UDI-DI 10193489342635 Lots 25JBT011 26CBD503 DYNJ84741B UDI-DI 10198459421563 Lot 25KBC487 DYNJ68253F UDI-DI 10198459185366 Lot 25KBA720 DYNJ83246B UDI-DI 10195327665463 Lots 25KBN031 25LBQ952 DYNJT6993 UDI-DI 10198459588211 Lot 25KBI629 DYNJ0509186J UDI-DI 10198459117626 Lot 25LMI076 CDS983181G UDI-DI 10198459038174 Lot 25LBA047", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2441-2026%22", "url": "https://recallledger.net/recalls/device-z-2441-2026-medline-convenience-kits-acl-pack-dynj64161c-arthroscopy-pack/"}, {"id": "fda-device-z-2440-2026", "source": "FDA", "category": "device", "recall_number": "Z-2440-2026", "title": "Medline convenience kits: DRIVELINE MANAGEMENT KIT EBSI1688 PORT DRESSING... recall (Medline Industries, LP)", "product": "Medline convenience kits: DRIVELINE MANAGEMENT KIT EBSI1688 PORT DRESSING CHANGE KIT EBSI1328A", "reason": "Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.", "hazard_level": "Class II", "company": "Medline Industries, LP", "company_location": "Northfield, IL, United States", "date": "2026-04-27", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution. OUS distribution pending.", "states": [], "nationwide": true, "quantity": "49,654 kits total", "codes": "EBSI1688 UDI-DI 10653160370130 Lot 2025102890 EBSI1328A UDI-DI 10653160382980 Lot 2025103090", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2440-2026%22", "url": "https://recallledger.net/recalls/device-z-2440-2026-medline-convenience-kits-driveline-management-kit-ebsi1688-por/"}, {"id": "fda-device-z-2439-2026", "source": "FDA", "category": "device", "recall_number": "Z-2439-2026", "title": "Medline convenience kits: 20CM CVC INSERTION KIT ECVC6805B 2L 8.5FR 16CM CVC... recall (Medline Industries, LP)", "product": "Medline convenience kits: 20CM CVC INSERTION KIT ECVC6805B 2L 8.5FR 16CM CVC INSERTION KIT ECVC8055A VANTEX PI CVC 7F, 3L, 20CM BUNDLE ECVC6915A ECVC6985B", "reason": "Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. 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"https://recallledger.net/recalls/device-z-2436-2026-medline-convenience-kits-acd-dynj904999j-acdf-dynj907336b-dy/"}, {"id": "fda-device-z-2435-2026", "source": "FDA", "category": "device", "recall_number": "Z-2435-2026", "title": "Medline convenience kits: BASIC EYE DYNJ905154I TUBAL LIGATION CDS CDS760053K recall (Medline Industries, LP)", "product": "Medline convenience kits: BASIC EYE DYNJ905154I TUBAL LIGATION CDS CDS760053K", "reason": "Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. 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OUS distribution pending.", "states": [], "nationwide": true, "quantity": "49,654 kits total", "codes": "UDI-DI 10198459028274 Lot 25LMI820", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2430-2026%22", "url": "https://recallledger.net/recalls/device-z-2430-2026-medline-convenience-kit-smsc-pelviscopy-pack-lf-dynj0161619m/"}, {"id": "fda-device-z-2429-2026", "source": "FDA", "category": "device", "recall_number": "Z-2429-2026", "title": "Medline convenience kit: recall (Medline Industries, LP)", "product": "Medline convenience kit: (82)LABOR & DELIVERY C-SECTION DYNJ907895F", "reason": "Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. 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OUS distribution pending.", "states": [], "nationwide": true, "quantity": "49,654 kits total", "codes": "UDI-DI 10198459366390 Lot 25KBL873", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2429-2026%22", "url": "https://recallledger.net/recalls/device-z-2429-2026-medline-convenience-kit-82-labor-delivery-c-section-dynj907895f/"}, {"id": "fda-device-z-2428-2026", "source": "FDA", "category": "device", "recall_number": "Z-2428-2026", "title": "Medline convenience kit: BHS NEURO DYNJ904900N MEDTRX NEURO PACK DYNJ67267B ... recall (Medline Industries, LP)", "product": "Medline convenience kit: BHS NEURO DYNJ904900N MEDTRX NEURO PACK DYNJ67267B MRI DBS PACK DYNJ9814630O NEURO CDS-LF CDS983383L NEURO PACK DYNJ59397Q DYNJT7315 NEURO PACK-LF DYNJ25097I NEURO VP SHUNT/VAGAL NERVE-RF DYNJ21925S PK NEURO SHUNT BUMC DYNJT6428 RR-NEURO DBS HEAD PACK-LF DYNJ0785736M VP SHUNT SYNJ10307B", "reason": "Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. 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OUS distribution pending.", "states": [], "nationwide": true, "quantity": "49,654 kits total", "codes": "DYNJ904900N UDI-DI 10198459504273 Lot 25LBB457 DYNJ67267B UDI-DI 10198459084331 Lot 25LBQ732 DYNJ9814630O UDI-DI 10195327587291 Lot 25LBD665 CDS983383L UDI-DI 10198459224577 Lot 25LBC092 DYNJ59397Q UDI-DI 10198459495427 Lot 25LMG049 DYNJT7315 UDI-DI 10198459620225 Lot 25LBO095 DYNJ25097I UDI-DI 10198459449550 Lot 25KBC747 DYNJ21925S UDI-DI 10195327105020 Lots 25KBD835 25LBR371 DYNJT6428 UDI-DI 10198459553660 Lot 26AMA602 DYNJ0785736M UDI-DI 10198459487149 Lot 25LMI831 SYNJ10307B UDI-DI 10195327007249 Lot 25LBE309", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2428-2026%22", "url": "https://recallledger.net/recalls/device-z-2428-2026-medline-convenience-kit-bhs-neuro-dynj904900n-medtrx-neuro-pac/"}, {"id": "fda-device-z-2427-2026", "source": "FDA", "category": "device", "recall_number": "Z-2427-2026", "title": "Medline convenience kit: HERNIA REPAIR TOTE DYNJ908337D recall (Medline Industries, LP)", "product": "Medline convenience kit: HERNIA REPAIR TOTE DYNJ908337D", "reason": "Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. 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OUS distribution pending.", "states": [], "nationwide": true, "quantity": "49,654 kits total", "codes": "UDI-DI 10198459409431 Lot 25KBB755", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2427-2026%22", "url": "https://recallledger.net/recalls/device-z-2427-2026-medline-convenience-kit-hernia-repair-tote-dynj908337d/"}, {"id": "fda-device-z-2426-2026", "source": "FDA", "category": "device", "recall_number": "Z-2426-2026", "title": "Medline convenience kit: KIT: DRESSING CHANGE PED DYNDC3359 recall (Medline Industries, LP)", "product": "Medline convenience kit: KIT: DRESSING CHANGE PED DYNDC3359", "reason": "Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.", "hazard_level": "Class II", "company": "Medline Industries, LP", "company_location": "Northfield, IL, United States", "date": "2026-04-27", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution. OUS distribution pending.", "states": [], "nationwide": true, "quantity": "49,654 kits total", "codes": "UDI-DI 10195327495589 Lots 25KBK310 25LBN341", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2426-2026%22", "url": "https://recallledger.net/recalls/device-z-2426-2026-medline-convenience-kit-kit-dressing-change-ped-dyndc3359/"}, {"id": "fda-device-z-2425-2026", "source": "FDA", "category": "device", "recall_number": "Z-2425-2026", "title": "Medline convenience kit: IV START KIT W/HUBGUARD DYNDV2662 recall (Medline Industries, LP)", "product": "Medline convenience kit: IV START KIT W/HUBGUARD DYNDV2662", "reason": "Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.", "hazard_level": "Class II", "company": "Medline Industries, LP", "company_location": "Northfield, IL, United States", "date": "2026-04-27", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution. OUS distribution pending.", "states": [], "nationwide": true, "quantity": "49,654 kits total", "codes": "UDI-DI 10653160378518 Lot 26CBC731", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2425-2026%22", "url": "https://recallledger.net/recalls/device-z-2425-2026-medline-convenience-kit-iv-start-kit-w-hubguard-dyndv2662/"}, {"id": "fda-device-z-2424-2026", "source": "FDA", "category": "device", "recall_number": "Z-2424-2026", "title": "Medline convenience kits: BASIC DYNJ905869G BASIC PACK DYNJ68484B BIB... recall (Medline Industries, LP)", "product": "Medline convenience kits: BASIC DYNJ905869G BASIC PACK DYNJ68484B BIB GENERAL LAPAROSCOPY PA DYNJ58305 CHRISTUS CH PEDIATRIC BASIC DYNJ61167G CVC INSERTION BUNDLE CVI3940A DAVINCI PACK SURGICOUNT DYNJ45544F EPCH BASIC PACK DYNJ83094C GENERAL PACK DYNJ39682B DYNJ84882 GENERAL RFD DYNJ906336F GENERAL SURGERY PACK DYNJT6003 GV MACD PACK DYNJ46952M IMPLANT PACK - BBI AR DYNJ63508A KIT THORACOSCOPY DYNJ908872F LVAD TRAY DM1120A MAJOR UROLOGY PACK-LF DYNJ0368525M MICRODISECT DECOMPRESS-LF DYNJ911467 MINOR PACK DYNJ86972 MULTI PURPOSE PACK DYNJ58406B OPEN HEART DYNJ903245C P&K PACK DYNJT5838 PACK,PEDIATRIC MAJOR DYNJ906888F PCNL DYNJ904468C PEDIATRIC MINOR RFD DYNJ906296I PEDIATRIC PACK DYNJ54239K PEDIATRIC SURGERY DYNJ81474B PERLMUTTER PACK DYNJT7387 RFT ISC NOBLES MINOR PACK DYNJ43954B ROBOTICS FMOL LADY OF THE LAKE DYNJ89584 ROBOTICS PACK DYNJ83622B SCOLI PACK NTX DYNJ68415C SMALL ABDOMINAL PACK-LF PHS41749G STIM IMPLANT TRIALS DYNJ87790A SUPPLEMENTAL PACK DYNJ65244 TENEX PACK DYNDH2190 THORACIC PACK DYNJ56616G THORACIC PACK SHD DYNJ68416C THORACOSCOPY DYNJ9425843R THORACOTOMY PM DYNJ906815A THORACOTOMY THORACOSCOPY DYNJ902882D TRAY,NEONATAL PICC DRSG CHANGE DYNDC1533B UNIVERSAL-ASC DYNJ900071C", "reason": "Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. 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Butyrate tubing may crack during actuation and render product unusable for application.", "hazard_level": "Class II", "company": "Medline Industries, LP", "company_location": "Northfield, IL, United States", "date": "2026-04-27", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution. OUS distribution pending.", "states": [], "nationwide": true, "quantity": "49,654 kits total", "codes": "DYNJT5893 UDI-DI 10198459517839 Lot 25KBA123 SYNJ10306A UDI-DI 10193489296891 Lots 25LBO305 26CBD081 DYNJ68023 UDI-DI 10193489468083 Lot 25KBI169 DYNJ909926C UDI-DI 10198459423109 Lots 25LBC067 25LBR659 DYNJ84081B UDI-DI 10198459462474 Lot 25LMI881 DYNJ905362C UDI-DI 10198459346842 Lots 25KBN239 25LBF694 DYNJ0660040R UDI-DI 10889942220083 Lots 25JME572 26AMA936 DYNJ89023A UDI-DI 10198459388316 Lot 25KBC500 DYNJ902510M UDI-DI 10198459683374 Lots 26CBM279 26CBO942 DYNJ84766 UDI-DI 10195327414108 Lot 26BBC049 DYNJ0578842M UDI-DI 10193489288292 Lot 25LMG027 DYNJ63803C UDI-DI 10198459149825 Lots 25LBN476 26CBC156 DYNJ62433D UDI-DI 10198459498176 Lots 25KBC752 25KBM917 DYNJ81772C UDI-DI 10198459349362 Lots 25LMH594 25LMI396 DYNJT7588 UDI-DI 10198459635182 Lot 26AMA250 DYNJ89048A UDI-DI 10198459388477 Lot 26BBD124", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2423-2026%22", "url": "https://recallledger.net/recalls/device-z-2423-2026-medline-convenience-kits-breast-imaging-dynjt5893-chog-plastic/"}, {"id": "fda-device-z-2422-2026", "source": "FDA", "category": "device", "recall_number": "Z-2422-2026", "title": "Medline convenience kits: ABD PACK DYNJ81673B BARIATRIC DYNJ902515K ... recall (Medline Industries, LP)", "product": "Medline convenience kits: ABD PACK DYNJ81673B BARIATRIC DYNJ902515K BARIATRIC + DYNJ904119O BARIATRIC CDS CDS983883J BWNBORO LAP CHOLE PACK-LF DYNJ32836B CCSB KARIN JWIRE LUMPECTOMY DYNJ910459B CHRISTUS CHILDRENS LAP CHOLE DYNJ61165G CUH MINOR PACK-LF DYNJ60095B FREE FLAP CUSTOM PACK B DYNJ82736B FREE NIPPLE GRAFT DYNJ911160B GEN MINOR DYNJ900906L GEN SURG LAPAROSCOPY PACK DYNJ55248F GEN SURG MINOR PACK DYNJ69142F GENERAL LAP DYNJ61475A DYNJT3759 GENERAL LAP PACK DYNJ61515I DYNJT4452 GENERAL LAP PACK-LF DYNJ37208D GENERAL LAPAROSCOPY DYNJ905870G GENERAL LAPAROSCOPY PACK DYNJ17443T DYNJ45263B DYNJT4504 LAP CHOLE DYNJ45664D DYNJ912005 LAP CHOLE PACK DYNJ81695B LAP CHOLE PACK-LF DYNJ0614113C DYNJ0618369V LAP CHOLE PROCEDURE-LF CDS981184D LAP CHOLE RFD DYNJ906302F LAP CHOLE SURGICOUNT DYNJ45531G LAP CHOLE TOTE DYNJ908339F LAP GASTRIC BYPASS CDS CDS860146M LAP GASTRIC PACK DYNJ62065A LAP HERNIA RFD DYNJ906301F LAP PACK DYNJ38871J DYNJ51389A LAPAROSCOPIC CDS920082AC LAPAROSCOPIC PACK DYNJ52605K LAPAROSCOPIC PACK-LF PHS41736G LAPAROSCOPY PACK DYNJT8313 LAPAROSCOPY PACK-LF DYNJ02309D DYNJ0551175T LAPAROSCOPY UM RF DYNJ902324D LAPAROSCOPY-LF DYNJ903241B LAPAROTOMY PACK-LF DYNJ21091O LARGE ABDOMINAL PACK-LF PHS41737D LEX GENERAL LAPAROSCOPY DYNJ900969K MINOR GENERAL PACK DYNJT3884 MINOR PACK-LF DYNJ0105608I MINOR PK DYNJ61335D MINOR PROCEDURE CDS CDS981793G PEDIATRIC MOSES DYNJ58864B PK, GEN-LAPAROSCOPY DYNJ53837B RMC GENERAL LAPAROSCOPIC DYNJ907087C ROBOTIC GENERAL DYNJ906861D SM-GENERAL LAP PACK-LF DYNJ0780078W SMJ GENERAL ABDOMINAL PACK-LF DYNJ25765Q UOFL HOSP GENERAL LAPAROSCOPY DYNJ909321A", "reason": "Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.", "hazard_level": "Class II", "company": "Medline Industries, LP", "company_location": "Northfield, IL, United States", "date": "2026-04-27", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution. OUS distribution pending.", "states": [], "nationwide": true, "quantity": "49,654 kits total", "codes": "DYNJ81673B UDI-DI 10195327494728 Lot 26AMA776 DYNJ902515K UDI-DI 10195327662608 Lot 25KBO749 DYNJ904119O UDI-DI 10198459073151 Lots 26ABB899 26ABI225 26ABJ235 CDS983883J UDI-DI 10198459429798 Lot 25KBK403 DYNJ32836B UDI-DI 10195327037369 Lot 25LMF151 DYNJ910459B UDI-DI 10198459477409 Lot 26AML096 DYNJ61165G UDI-DI 10198459386701 Lots 25LBO683 26ABE316 DYNJ60095B UDI-DI 10198459413377 Lots 25KBB960 25LBO686 DYNJ82736B UDI-DI 10198459038907 Lot 25LMG794 DYNJ911160B UDI-DI 10198459398001 Lot 26AMB749 DYNJ900906L UDI-DI 10198459408526 Lot 26AMG179 DYNJ55248F UDI-DI 10195327633486 Lot 25KBA350 DYNJ69142F UDI-DI 10198459478499 Lot 25LMF407 DYNJ61475A UDI-DI 10195327605797 Lot 25JBT649 DYNJT3759 UDI-DI 10198459351037 Lot 25KBJ720 DYNJ61515I UDI-DI 10198459542992 Lot 25KBI633 DYNJT4452 UDI-DI 10198459460678 Lot 25JBR785 DYNJ37208D UDI-DI 10195327434182 Lot 25LBJ032 DYNJ905870G UDI-DI 10198459394591 Lots 25JBP623 25LBR135 DYNJ17443T UDI-DI 10195327692971 Lot 25KBJ329 DYNJ45263B UDI-DI 10193489852394 Lot 25KBH088 DYNJT4504 UDI-DI 10198459456701 Lot 25LMI354 DYNJ45664D UDI-DI 10193489898514 Lot 25KBB002 DYNJ912005 UDI-DI 10198459597121 Lot 25KBT433 DYNJ81695B UDI-DI 10198459023453 Lot 25LMJ938 DYNJ0614113C UDI-DI 10198459352539 Lot 25KBC852 DYNJ0618369V UDI-DI 10889942826599 Lot 26BBC627 CDS981184D UDI-DI 10193489324815 Lot 26AMG257 DYNJ906302F UDI-DI 10198459419850 Lot 25KBG656 DYNJ45531G UDI-DI 10195327006037 Lots 25JBR413 25LBN719 26BBD403 DYNJ908339F UDI-DI 10198459409554 Lot 25KBM957 CDS860146M UDI-DI 10195327224547 Lots 25KBK359 26ABG747 26ABQ780 DYNJ62065A UDI-DI 10193489273472 Lot 25LMH990 DYNJ906301F UDI-DI 10198459419843 Lot 25LBA148 DYNJ38871J UDI-DI 10198459240218 Lot 25LMJ264 DYNJ51389A UDI-DI 10889942881222 Lot 25LBR750 CDS920082AC UDI-DI 10198459237324 Lot 25KBR576 DYNJ52605K UDI-DI 10198459254789 Lot 25LMG367 PHS41736G UDI-DI 10198459438745 Lot 25LMG005 DYNJT8313 UDI-DI 10198459697159 Lot 26CBD042 DYNJ02309D UDI-DI 10198459134432 Lot 25LBP128 DYNJ0551175T UDI-DI 10198459533419 Lot 25KBE001 DYNJ902324D UDI-DI 10198459125683 Lot 25KBQ907 DYNJ903241B UDI-DI 10193489818987 Lot 26ABF331 DYNJ21091O UDI-DI 10198459485183 Lots 25KBA313 26CBD177 PHS41737D UDI-DI 10198459438752 Lot 25LMG512 DYNJ900969K UDI-DI 10198459452314 Lot 26ABG612 DYNJT3884 UDI-DI 10198459366840 Lot 25JBX326 DYNJ0105608I UDI-DI 10198459533259 Lots 25KBA344 25KBM306 25LBE190 DYNJ61335D UDI-DI 10195327128586 Lot 25KBA763 CDS981793G UDI-DI 10198459493683 Lot 25KBT360 DYNJ58864B UDI-DI 10198459346965 Lot 25LBP018 DYNJ53837B UDI-DI 10193489209730 Lot 25LBP490 DYNJ907087C UDI-DI 10198459201301 Lot 26AMA102 DYNJ906861D UDI-DI 10198459293702 Lot 26AMC100 DYNJ0780078W UDI-DI 10195327633929 Lots 25JME845 25LMK134 DYNJ25765Q UDI-DI 10198459603679 Lot 25LMG846 DYNJ909321A UDI-DI 10195327545628 Lot 25KBT731", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2422-2026%22", "url": "https://recallledger.net/recalls/device-z-2422-2026-medline-convenience-kits-abd-pack-dynj81673b-bariatric-dynj90/"}, {"id": "fda-device-z-2421-2026", "source": "FDA", "category": "device", "recall_number": "Z-2421-2026", "title": "Medline convenience kits: DISCECTOMY PACK DYNJ86476B EAR DYNJ81460C ... recall (Medline Industries, LP)", "product": "Medline convenience kits: DISCECTOMY PACK DYNJ86476B EAR DYNJ81460C DYNJ900004J DYNJ901779J DYNJ902900F EAR PACK DYNJ81419D ENT PACK DYNJ40498B HEAD & NECK CDS DYNJ901246J JEWISH DR SEVERTSON EAR DYNJ909252C JEWISH HEAD&NECK DYNJ909255C KIT HEAD AND NECK MHS DYNJ905364B MAJOR EAR CDS983347S MAJOR EAR FMOL LADY OF THE LAK DYNJ89581 MAJOR EAR PACK DYNJT4872 MAJOR HEAD AND NECK PACK DYNJ38985G MAJOR HEAD NECK PACK DYNJ45706B MZ EAR CDS DYNJ905642F PARATHYROID PACK DYNJ81389F PK,ENT-EAR DYNJ43700B SM-HEAD AND NECK PACK-LF DYNJ0780036W THYROID CDS CDS983693I TYMPANOPLASTY CDS982720S TYMPANOPLASTY MASTOIDECTOM DYNJ66231B TYMPANOPLASTY PACK-LF DYNJ62820D WH FACIAL HEAD AND NECK PACK DYNJ89028A WMC COCHLEAR IMPLANT ADD ON DYNJ907206G", "reason": "Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.", "hazard_level": "Class II", "company": "Medline Industries, LP", "company_location": "Northfield, IL, United States", "date": "2026-04-27", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution. OUS distribution pending.", "states": [], "nationwide": true, "quantity": "49,654 kits total", "codes": "DYNJ86476B UDI-DI 10198459440366 Lot 25KBL478 DYNJ81460C UDI-DI 10198459434679 Lot 25KBE552 DYNJ900004J UDI-DI 10198459560354 Lot 26AMA112 DYNJ901779J UDI-DI 10193489979749 Lot 25LMI890 DYNJ902900F UDI-DI 10198459496936 Lot 25KBA607 DYNJ81419D UDI-DI 10198459113444 Lot 25KBM670 DYNJ40498B UDI-DI 10193489806779 Lots 25KBC776 25LBO494 DYNJ901246J UDI-DI 10198459447310 Lots 25KBQ989 26ABI798 26DBH373 DYNJ909252C UDI-DI 10198459318726 Lots 25JBS227 25KBC598 25LBR040 DYNJ909255C UDI-DI 10198459210167 Lot 25LBH411 DYNJ905364B UDI-DI 10198459346255 Lots 25LBM363 26BBO336 CDS983347S UDI-DI 10198459397370 Lots 26BBC029 26CBR342 DYNJ89581 UDI-DI 10198459278594 Lot 25LBP819 DYNJT4872 UDI-DI 10198459459672 Lot 25KBA908 DYNJ38985G UDI-DI 10195327385682 Lots 25JBA164 25KBG575 DYNJ45706B UDI-DI 10193489856293 Lot 25KBK200 DYNJ905642F UDI-DI 10195327587277 Lot 26AME607 DYNJ81389F UDI-DI 10198459394775 Lot 26BBC753 DYNJ43700B UDI-DI 10195327523039 Lot 25LBD750 DYNJ0780036W UDI-DI 10198459036972 Lot 25LMJ600 CDS983693I UDI-DI 10193489953848 Lot 25KBQ399 CDS982720S UDI-DI 10198459530258 Lots 25KBU081 25LBT481 26ABC446 DYNJ66231B UDI-DI 10195327341640 Lots 25JBY408 25KBK197 DYNJ62820D UDI-DI 10198459105463 Lot 25LMH554 DYNJ89028A UDI-DI 10198459472565 Lot 25KBI158 DYNJ907206G UDI-DI 10198459368028 Lot 25LBM564", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2421-2026%22", "url": "https://recallledger.net/recalls/device-z-2421-2026-medline-convenience-kits-discectomy-pack-dynj86476b-ear-dynj8/"}, {"id": "fda-device-z-2420-2026", "source": "FDA", "category": "device", "recall_number": "Z-2420-2026", "title": "Medline convenience kits: BREAST-HERNIA-PORT CDS-LF CDS984853L recall (Medline Industries, LP)", "product": "Medline convenience kits: BREAST-HERNIA-PORT CDS-LF CDS984853L", "reason": "Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.", "hazard_level": "Class II", "company": "Medline Industries, LP", "company_location": "Northfield, IL, United States", "date": "2026-04-27", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution. OUS distribution pending.", "states": [], "nationwide": true, "quantity": "49,654 kits total", "codes": "UDI-DI 10198459293535 Lots 26AME511 26AMG737", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2420-2026%22", "url": "https://recallledger.net/recalls/device-z-2420-2026-medline-convenience-kits-breast-hernia-port-cds-lf-cds984853l/"}, {"id": "fda-device-z-2419-2026", "source": "FDA", "category": "device", "recall_number": "Z-2419-2026", "title": "Medline convenience kits: INPATIENT CENTRAL LN DRSG KIT DYNDC3525 ... recall (Medline Industries, LP)", "product": "Medline convenience kits: INPATIENT CENTRAL LN DRSG KIT DYNDC3525 PICC/CVC/MIDLINE DRSG CHG KIT DT13191A PORT A CATH CDS982047S VEIN ABLATION PACK DYNJ62889C", "reason": "Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.", "hazard_level": "Class II", "company": "Medline Industries, LP", "company_location": "Northfield, IL, United States", "date": "2026-04-27", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution. OUS distribution pending.", "states": [], "nationwide": true, "quantity": "49,654 kits total", "codes": "DYNDC3525 UDI-DI 10198459576294 Lot 25KBM985 DT13191A UDI-DI 10653160998914 Lot 26AMA168 CDS982047S UDI-DI 10198459385735 Lot 26AMB202 DYNJ62889C UDI-DI 10198459416453 Lot 26AMA584", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2419-2026%22", "url": "https://recallledger.net/recalls/device-z-2419-2026-medline-convenience-kits-inpatient-central-ln-drsg-kit-dyndc3525/"}, {"id": "fda-device-z-2418-2026", "source": "FDA", "category": "device", "recall_number": "Z-2418-2026", "title": "Medline convenience kits: LOOP PACK DYNJ61460C OPEN HEART CDS840150Y ... recall (Medline Industries, LP)", "product": "Medline convenience kits: LOOP PACK DYNJ61460C OPEN HEART CDS840150Y PACEMAKER DYNJ56297C PACEMAKER PK DYNJT3454 PACEMAKER/ICD PACK DYNJ33822L PAD OPEN HEART DYNJ900962O PEDIATRIC OPEN HEART DYNJ54238L DYNJT6766 STAZ BASIC VASCULAR DYNJ909794C VASCULAR ACCESS KIT CVI5323A VASCULAR CDS CDS983040M", "reason": "Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.", "hazard_level": "Class II", "company": "Medline Industries, LP", "company_location": "Northfield, IL, United States", "date": "2026-04-27", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution. OUS distribution pending.", "states": [], "nationwide": true, "quantity": "49,654 kits total", "codes": "DYNJ61460C UDI-DI 10198459422133 lot 25KBA098 CDS840150Y UDI-DI 10198459303029 lots 25JBW220 26BBD028 DYNJ56297C UDI-DI 10198459513954 lot 25LMJ874 DYNJT3454 UDI-DI 10198459325663 lot 25KBG761 DYNJ33822L UDI-DI 10198459385582 lot 26AMA072 DYNJ900962O UDI-DI 10198459452581 lot 26CBC302 DYNJ54238L UDI-DI 10198459443114 lot 25LMH549 DYNJT6766 UDI-DI 10198459580888 lot 25KBM870 DYNJ909794C UDI-DI 10198459528002 lot 25LBF702 CVI5323A UDI-DI 10198459582035 lot 25KBM758 CDS983040M UDI-DI 10198459579813 lots 25KBO682 26BBB926", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2418-2026%22", "url": "https://recallledger.net/recalls/device-z-2418-2026-medline-convenience-kits-loop-pack-dynj61460c-open-heart-cds8/"}, {"id": "fda-device-z-2417-2026", "source": "FDA", "category": "device", "recall_number": "Z-2417-2026", "title": "MINOR CATH LAB PACK DYNJ84775A OR VASCULAR ANGIO PACK DYNJ47269D PORT-A-CATH ... recall (Medline Industries, LP)", "product": "MINOR CATH LAB PACK DYNJ84775A OR VASCULAR ANGIO PACK DYNJ47269D PORT-A-CATH DYNJ63276G", "reason": "Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.", "hazard_level": "Class II", "company": "Medline Industries, LP", "company_location": "Northfield, IL, United States", "date": "2026-04-27", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution. OUS distribution pending.", "states": [], "nationwide": true, "quantity": "49,654 kits total", "codes": "DYNJ84775A UDI-DI 10195327606527 lot 25LMH070 DYNJ47269D UDI-DI 10195327674786 lot 25LMJ234 DYNJ63276G UDI-DI 10198459458835 lot 26BBC598", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2417-2026%22", "url": "https://recallledger.net/recalls/device-z-2417-2026-minor-cath-lab-pack-dynj84775a-or-vascular-angio-pack-dynj47269d/"}, {"id": "fda-device-z-2416-2026", "source": "FDA", "category": "device", "recall_number": "Z-2416-2026", "title": "BLOCK TRAY DYNJRA2119A INDWELLING NERVE BLOCK DYNJRA1011A recall (Medline Industries, LP)", "product": "BLOCK TRAY DYNJRA2119A INDWELLING NERVE BLOCK DYNJRA1011A", "reason": "Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.", "hazard_level": "Class II", "company": "Medline Industries, LP", "company_location": "Northfield, IL, United States", "date": "2026-04-27", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution. OUS distribution pending.", "states": [], "nationwide": true, "quantity": "49,654 kits total", "codes": "DYNJRA2119A UDI-DI 10198459194702 lot 25LBB738 DYNJRA1011A UDI-DI 10888277783614 lots 25KBB849 25LBB734", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2416-2026%22", "url": "https://recallledger.net/recalls/device-z-2416-2026-block-tray-dynjra2119a-indwelling-nerve-block-dynjra1011a/"}, {"id": "fda-device-z-2415-2026", "source": "FDA", "category": "device", "recall_number": "Z-2415-2026", "title": "Medline CCI Nerve Block Tray DYNJRA2742 Medline CPNB DYNJRA2716 recall (Medline Industries, LP)", "product": "Medline CCI Nerve Block Tray DYNJRA2742 Medline CPNB DYNJRA2716", "reason": "Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.", "hazard_level": "Class II", "company": "Medline Industries, LP", "company_location": "Northfield, IL, United States", "date": "2026-04-27", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution. OUS distribution pending.", "states": [], "nationwide": true, "quantity": "49,654 kits total", "codes": "DYNJRA2742 UDI-DI 10198459627330 Lot 26AMA185 DYNJRA2716 UDI-DI 10198459567988 Lot 25KBA971", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2415-2026%22", "url": "https://recallledger.net/recalls/device-z-2415-2026-medline-cci-nerve-block-tray-dynjra2742-medline-cpnb-dynjra2716/"}, {"id": "fda-device-z-2414-2026", "source": "FDA", "category": "device", "recall_number": "Z-2414-2026", "title": "Medline EBSI Kit EBSI1534 recall (Medline Industries, LP)", "product": "Medline EBSI Kit EBSI1534", "reason": "Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.", "hazard_level": "Class II", "company": "Medline Industries, LP", "company_location": "Northfield, IL, United States", "date": "2026-04-27", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution. OUS distribution pending.", "states": [], "nationwide": true, "quantity": "49,654 kits total", "codes": "UDI-DI 10653160350507 Lot 2025110490", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2414-2026%22", "url": "https://recallledger.net/recalls/device-z-2414-2026-medline-ebsi-kit-ebsi1534/"}, {"id": "fda-device-z-2397-2026", "source": "FDA", "category": "device", "recall_number": "Z-2397-2026", "title": "Description/REF: RA CATH KIT: 20 GA X 1-1/2IN/NA-04220-1A recall (ARROW INTERNATIONAL, LLC)", "product": "Description/REF: RA CATH KIT: 20 GA X 1-1/2IN/NA-04220-1A; RA CATH KIT: 20 GA X 1-1/2IN/NA-04220-X1A; ARTERIAL CATHETER KIT: 18 GA X 16 CM/ASK-04018-HCA; ARTERIAL CATHETER KIT: 18 GA X 16 CM/ASK-04018-UPM; RA CATH KIT: 20 GA X 1-3/4IN/ASK-04020-HC; ARTERIAL LINE KIT: 20 GA X 5IN (12 CM)/ASK-04020-HMC; RADIAL ARTERY CATHETER KIT: 20 GA X 30MM/ASK-04020-MMC; RA CATH KIT: 20 GA X 1-1/2IN (3.81 CM)/ASK-04020-SV; ARTERIAL CATH KIT: 20 GA X 5 IN (12 CM)/ASK-04100-AMC-S1; ARTERIAL CATHETER KIT: 20 GA X 12 CM/ASK-04100-NS; RADIAL ARTERY KIT/ASK-04500-AH; RAD ART:20GAX3.81CM / ART LINE:20GAX12CM/ASK-04500-HF-S; ARTERIAL LINE KIT: 1L 20 GA X 12 CM/ASK-04510-HA; ARTERIAL LINE KIT: 20 GA. X 5 IN (12 CM)/ASK-04510-HF; ARTERIAL LINE KIT: 20 GA X 5 IN (12 CM)/ASK-04510-IHC1; ARTERIAL LINE KIT: 20 GA X 5 IN (12 CM)/ASK-04510-MSK2; ARTERIAL CATH KIT: 20GA X 5IN/ASK-04510-NS; ARTERIAL CATHETER KIT: 20 GA X 12 CM/FS-04510-S; ARTERIAL LINE KIT/HF-04510-1; RA CATH KIT: 20 GA X 1-3/4IN/ASK-04020-BSM; RA CATH KIT: 20 GA X 1 3/4 IN (4.45CM)/ASK-04020-HH1; RA CATH KIT: 20 GA X 1 3/4 IN (4.45 CM)/ASK-04020-JMH1; RA CATH KIT: 20 GA X 1-3/4 IN/ASK-04020-MAS; RA CATH KIT: 20 GA X 1 3/4 IN/ASK-04020-MCC; RA CATH KIT: 20 GA X 1-3/4IN (4.45 CM)/ASK-04020-MHT; RA CATH KIT: 20 GA X 1-3/4IN (4.45 CM)/ASK-04020-MI; RA CATH KIT: 20 GA X 1 3/4 IN (4.45 CM)/ASK-04020-MIHS; RA CATH KIT: 20 GA X 1-3/4IN (4.45 CM)/ASK-04020-MUSC; RA CATH KIT: 20 GA X 1-3/4IN (4.45 CM)/ASK-04020-NCB; RA CATH KIT: 20 GA X 1 3/4 IN/ASK-04020-PMC; RA CATH KIT: 20 GA X 1-3/4IN (4.45 CM)/ASK-04020-SPH; RA CATH SET: 20 GA X 1-3/4IN (4.45CM)/ASK-04020-UPM; RA CATH KIT: 20 GA X 1 3/4 IN (4.45 CM)/ASK-04020-UR1; RA CATH KIT: 20 GA X 4.45 CM/NA-04020-X1A; RA CATH KIT: 20 GA X 1-3/4IN/WBH-04020-1; CVC KIT: 20 GA X 12CM/ASK-04510-UCLA; ARTERIAL ACCESS TRAY WITH .025IN SWG/ASK-04001-BW1", "reason": "Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.", "hazard_level": "Class I", "company": "ARROW INTERNATIONAL, LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-21", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "310,606", "codes": "REF(Material)/UDI-DI/Lot(Batch): NA-04220-1A/10801902193275/33F26B0027; NA-04220-X1A/10801902193275/33F24G0553, 33F25E0272, 33F25E1053, 33F25H0760, 33F25J0636; ASK-04018-HCA/10801902119268/33F24A0078; ASK-04018-UPM/50801902117644, 10801902193275/33F23B0953, 33F24A0389, 33F24B0140, 33F24D0028, 33F24H0480, 33F24J0550, 33F24K0164, 33F25A0505, 33F25C0742, 33F25C0792, 33F25E0961, 33F25E1070, 33F25E1071, 33F25E1072, 33F25G0105, 33F25H0062, 33F25J0866, 33F25L0353, 33F26B0507; ASK-04020-HC/10801902121384, 10801902193275/33F24A0828, 33F24B0246, 33F24C0148, 33F24D0113, 33F24G0409, 33F24J0559, 33F24K0172, 33F24L0693, 33F25C0136, 33F25C0933, 33F25E0128, 33F25H0070, 33F25L0356; ASK-04020-HMC/10801902117691, 10801902193275/33F24A0324, 33F24A0743, 33F24B0248, 33F24C0150, 33F24D0115, 33F24H0475, 33F24K0174, 33F24L0802, 33F25H0072, 33F25J0872, 33F25L0395, 33F26B0650, 33S24A0743, 33S24C0150, 33F26B0673; ASK-04020-MMC/10801902117769, 10801902193275/33F24C0160, 33F24D0123, 33F24E0423, 33F24G0420, 33F24H0487, 33F24J0571, 33F24K0183, 33F24L0692, 33F25A0523, 33F25C0974, 33F25E0139, 33F25H0081, 33F25J0880, 33F25L0346, 33F25M0853; ASK-04020-SV/10801902117837, 10801902117837/33F24A0868, 33F24B0269, 33F24E0436, 33F24E0437, 33F24L0746, 33F25H0087, 33F25J0885, 33F26B0512; ASK-04100-AMC-S1/10801902124927, 10801902193275/33F24D0139, 33F24E0446, 33F24G0439, 33F24K0199, 33F25A0532, 33F25E0153, 33F25G0116, 33F25H0093, 33F25J0516, 33F26B0656; ASK-04100-NS/10801902193275, 10801902117929/33F24G0440, 33F24L0579, 33F24M0266, 33F25A0533, 33F25C0151, 33F25C0788, 33F25E0155, 33F25H0095, 33F25J0518, 33F25K0256, 33F25L0448, 33F25M0945, 33F26B0649, 33F26B0667; ASK-04500-AH/10801902114041, 10801902193275/33F24A0153, 33F24A0803, 33F24B0282, 33F24C0181, 33F24E0452, 33F24G0444, 33F24J0586, 33F25A0538, 33F25H0101, 33F25J0893; ASK-04500-HF-S/10801902118001, 10801902193275/33F24A0141, 33F24A0753, 33F24A1157, 33F24B0283, 33F24C0182, 33F24D0143, 33F24E0453, 33F24G0445, 33F24J0587, 33F24K0206, 33F24L0766, 33F25C0154, 33F25C0966, 33F25E0161, 33F25H0102, 33F25J0894, 33F25L0492, 33R25C0966; ASK-04510-HA/10801902193275/33F24J0591, 33F24K0210, 33F25B0685, 33F25C0911, 33F25E0166, 33F25E0993, 33F25J0524, 33F25L0449; ASK-04510-HF/10801902193275, 10801902118025/33F24G0450, 33F24J0305, 33F24K0211, 33F24L0543, 33F24L0558, 33F25A0540, 33F25C0896, 33F25E0167, 33F25G0119, 33F25H0104, 33F25J0525, 33F25K0412, 33F25L0339, 33F26B0648, 33F26B0666, 33F26C0588; ASK-04510-IHC1/10801902193275/33F24J0306, 33F24L0699, 33F25C0157, 33F25C0782, 33F25E0168, 33F25H0105, 33F25L0475; ASK-04510-MSK2/10801902118049, 10801902193275/33F24A0872, 33F24B0290, 33F24D0150, 33F24E0461, 33F24G0453, 33F24J0594, 33F25A0541, 33F25C0852, 33F25E0170, 33F25H0740; ASK-04510-NS/10801902193275, 10801902224177/33F25K0324, 33F26B0653; FS-04510-S/10801902193275, 10801902119824/33F24L0738, 33F25C0188, 33F25C0755, 33F25L0426, 33F26B0657; HF-04510-1/10801902119855, 10801902193275/33F24D0036, 33F24G0537, 33F24J0652, 33F24L0576, 33F25A0593, 33F25C0897, 33F25E0260, 33F25E1044, 33F25H0166, 33F25J0936, 33F26B0652, 33F26B0675; ASK-04020-BSM/10801902193275/33F24J0365, 33F24M0075, 33F25A0079, 33F25B0312, 33F25D0116, 33F25D0297, 33F25E0367, 33F25F0400, 33F25G0653, 33F25J0983, 33F25L0155; ASK-04020-HH1/10801902193275, 10801902128536/33F24K0173, 33F24L0729, 33F25C0137, 33F25C0914, 33F25E0129, 33F25H0071, 33F25J0871, 33F25L0420, 33F26B0563; ASK-04020-JMH1/10801902114089, 10801902193275/33F24A0792, 33F24C0152, 33F24D0117, 33F24E0416, 33F24H0481, 33F24J0562, 33F24L0775, 33F25A0515, 33F25C0139, 33F25C0970, 33F25E0975, 33F25H0074, 33F25J0875, 33F25L0330, 33F26A0969; ASK-04020-MAS/10801902193275/33F25K0032; ASK-04020-MCC/10801902193275/33F24K0063, 33F24M0043; ASK-04020-MHT/10801902117721, 10801902193275/33F24A0094, 33F24B0019, 33F24D0052, 33F24D0966, 33F24J0475, 33F24L0083, 33F25C0739, 33F25E0980, 33F25F0529, 33F25J0506, 33F25K0329, 33F26A0403, 33F26C0056, 33F26C0260; ASK-04020-MI/10801902193275/33F24K0549, 33F25A0521, 33F25E1149, 33F25F0453, 33F25G0679, 33F25H0079, 33F25H0734, 33F25J0794, 33F25K0327, 33F25L0207, 33F25M0689, 33F26A0398; ASK-04020-MIHS/10801902193275/33F25A0442, 33F25B0233, 33F25C0379, 33F25D0035, 33F25H0494, 33F25K0426; ASK-04020-MUSC/10801902117776, 10801902193275/33F24A0751, 33F24A1138, 33F24B0259, 33F24C0162, 33F24D0125, 33F24E0425, 33F24G0421, 33F24K0184, 33F24L0640, 33F25C0141, 33F25C0830, 33F25E0140, 33F25H0083, 33F25J0881, 33F26B0575; ASK-04020-NCB/10801902117783, 10801902193275/33F24A0864, 33F24B0260, 33F24C0163, 33F24E0426, 33F24G0422, 33F24J0572, 33F24K0185, 33F24L0711, 33F25C0921, 33F25E0141, 33F25H0084, 33F25J0508, 33F25M0857; ASK-04020-PMC/30801902158896, 10801902193275/33F24F0095, 33F24L0242; ASK-04020-SPH/10801902193275/33F25C0143, 33F25C0977, 33F25E0985, 33F25H0735, 33F26A1075; ASK-04020-UPM/10801902117851, 10801902193275/33F24A0255, 33F24A0385, 33F24A1037, 33F24B0141, 33F24C0033, 33F24E0095, 33F24G0434, 33F24J0299, 33F24K0195, 33F24L0578, 33F25A0529, 33F25C0147, 33F25C0898, 33F25E0149, 33F25H0090, 33F25J0886, 33F25L0405, 33F26B0553; ASK-04020-UR1/10801902193275/33F24K0196, 33F24L0748, 33F25C0148, 33F25C0850, 33F25E0150, 33F25G0114, 33F25L0460, 33F25M0953; NA-04020-X1A/10801902193275, 30801902119927/33F24J0683, 33F24K0295, 33F24L0575, 33F24L0784, 33F25A0601, 33F25A0622, 33F25C0951, 33F25E0271, 33F25E1051, 33F25G0153, 33F25H0178, 33F25J0634, 33F25J0941, 33F25K0322, 33F25K0323, 33F25L0327, 33F25M0837, 33F26B0491; WBH-04020-1/10801902162943, 10801902193275/33F24B0465, 33F24C0787, 33F24E0780, 33F24G0659, 33F24J0435, 33F25A0124, 33F25B0054, 33F25B0110, 33F25B0227, 33F25C0404, 33F25C0522, 33F25E1163, 33F25G0630, 33F25H0349, 33F25J0080, 33F25L0162, 33F26B0060, 33F26C0408; ASK-04510-UCLA/10801902118070, 10801902193275/33F24C0189, 33F24E0465, 33F24G0455, 33F24K0215, 33F25A0543, 33F25C0861, 33F25E0173, 33F25H0106, 33F25J0897, 33F25L0347; ASK-04001-BW1/10801902117585/33F24D0105, 33F24G0277, 33F24H0240, 33F24J0546, 33F24K0158;", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2397-2026%22", "url": "https://recallledger.net/recalls/device-z-2397-2026-description-ref-ra-cath-kit-20-ga-x-1-1-2in-na-04220-1a-ra-cath-kit/"}, {"id": "fda-device-z-2396-2026", "source": "FDA", "category": "device", "recall_number": "Z-2396-2026", "title": "Description/REF: CVC KIT: 16 GA X 8IN/AK-04210 recall (ARROW INTERNATIONAL, LLC)", "product": "Description/REF: CVC KIT: 16 GA X 8IN/AK-04210, CVC KIT: 1-L 16 GA X 8IN (20 CM)/AK-04300, CVC KIT: 14 GA X 6 IN/CK-04711", "reason": "Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.", "hazard_level": "Class I", "company": "ARROW INTERNATIONAL, LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-21", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "35,540", "codes": "REF(Material)/UDI-DI/Lot(Batch): AK-04210/10801902121582, 10801902193275/33F24A1009, 33F24B0106, 33F24C0009, 33F24D0014, 33F24G0324, 33F24J0490, 33F24K0089, 33F24L0671, 33F25A0456, 33F25C0899, 33F25E0037, 33F25H0011, 33F25J0461; AK-04300/10801902121636, 10801902193275/33F24A1257, 33F24B0435, 33F24C0734, 33F24E0704, 33F24F0011, 33F24G0224, 33F24G0684, 33F24H0373, 33F24M0148, 33F25A0364, 33F25B0084, 33F25D0193, 33F25D0693, 33F25E0479, 33F25H0686, 33F25J0587, 33F25J0651, 33F26C0397; CK-04711/20801902118787, 10801902193275/33F24A0137, 33F24A1212, 33F24B0382, 33F24C0255, 33F24E0572, 33F24G0531, 33F24J0648, 33F24L0731, 33F25A0590, 33F25C0979, 33F25E1039, 33F25J0622, 33F26B0640", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2396-2026%22", "url": "https://recallledger.net/recalls/device-z-2396-2026-description-ref-cvc-kit-16-ga-x-8in-ak-04210-cvc-kit-1-l-16-ga-x-8/"}, {"id": "fda-device-z-2395-2026", "source": "FDA", "category": "device", "recall_number": "Z-2395-2026", "title": "Description/REF: PICC ACCESS TRAY/ASK-04001-CG1 recall (ARROW INTERNATIONAL, LLC)", "product": "Description/REF: PICC ACCESS TRAY/ASK-04001-CG1", "reason": "Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.", "hazard_level": "Class I", "company": "ARROW INTERNATIONAL, LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-21", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "360", "codes": "REF(Material)/UDI-DI/Lot(Batch): ASK-04001-CG1/10801902193275/33F25C0224, 33F25D0647, 33F25G0390, 33F25J0348", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2395-2026%22", "url": "https://recallledger.net/recalls/device-z-2395-2026-description-ref-picc-access-tray-ask-04001-cg1/"}, {"id": "fda-device-z-2394-2026", "source": "FDA", "category": "device", "recall_number": "Z-2394-2026", "title": "Description/REF: MIDLINE CATHETER KIT: 3 FR X 20 CM/CDC-02031-MK1A recall (ARROW INTERNATIONAL, LLC)", "product": "Description/REF: MIDLINE CATHETER KIT: 3 FR X 20 CM/CDC-02031-MK1A; AM/AT PI MIDLINE 1L: 4.5FR X 15CM/CDC-41541-MPK1A; AM/AT PI MIDLINE 2L: 5.5FR X 15CM/CDC-41552-MPK1A; AGBA PI MIDLINE 1L: 4.5FR X 15CM/ASK-41541-VFHM; AGBA PI MIDLINE 1-L: 4.5FR X 15CM/CDC-41541-MPK; AGBA PI MIDLINE 1-L: 4.5FR X 15CM/CDC-41541-MPKB; AGBA PI MIDLINE 1-L: 4.5FR X 15CM/CDC-41541-MPKC; AGBA PI MIDLINE 2-L: 5.5FR X 15CM/CDC-41552-MPK; AGBA PI MIDLINE 2-L: 5.5FR X 15CM/CDC-41552-MPKB; AGBA PI MIDLINE 2-L: 5.5FR X 15CM/CDC-41552-MPKC; PI MIDLINE 1-L: 4FR X 20CM/CDC-32041-MPK; PI MIDLINE 1-L: 4FR X 20CM/CDC-32041-MPKB; PI MIDLINE 1L: 4FR X 20CM/CDC-32041-MPKC; PI MIDLINE 2-L: 5FR X 20CM/CDC-32052-MPKB; PI PICC NaviCurve: 1L 4FR x 55CM w BP/DLX-35541-CURVB; PI PICC: 1L 4FR x 55CM w Biopatch/DLX-35541-HPKB; PI PICC: 1L 4FR x 55CM w CHG/DLX-35541-HPKC; PI PICC: 2L 5FR x 55CM w Biopatch/DLX-35552-HPKB; PI PICC: 2L 5FR X 55CM w CHG/DLX-35552-HPKC; PI PICC: 3L 6FR x 55CM w Biopatch/DLX-35563-HPKB; AGBA PICC/DELTA KIT: 1L 4.5 FR X 40 CM/ASK-44041-NS; AGBA PICC/DELTA FG: 2L 5.5 FR X 40 CM/ASK-44052-NS; AGBA PICC/DELTA KIT: 1L 4.5 FR X 50 CM/ASK-45041-NS; PI PICC KIT: 2L 5.5 FR X 50 CM/ASK-45052-TG; PI AGBA PICC KIT: 3L 6 FR X 50 CM W/VPS/ASK-45063-NS; PICC KIT: 1L 4.5 FR X 55 CM CG+ VPS/ASK-45541-RH; AGBA PICC: 1L 4.5FR x 55CM w Teg CHG/DLX-45541-HPKC; AGBA PICC: 2L 5.5FR x 55CM w Teg CHG/DLX-45552-HPKC; AGBA PICC NaviCurve: 3L 6FR x 55CM TCG/DLX-45563-CURVC; AGBA PICC: 3L 6FR x 55CM w Biopatch/DLX-45563-HPKB; AGBA PICC: 3L 6FR x 55CM w Teg CHG/DLX-45563-HPKC; PI PICC KIT: 1-L 4 FR X 55 CM TIPTRACKER/CDC-35541-TTS; PI PICC NaviCurve: 1L 4FR x 55CM w CHG/DLX-35541-CURVC; PI PICC G4 Stylet: 1L 4FR x 55CM w BP/DLX-35541-VPSB; PI PICC NaviCurve: 2L 5FR x 55CM w CHG/DLX-35552-CURVC; PI PICC G4 Stylet: 2L 5FR x 55CM w BP/DLX-35552-VPSB; PI PICC G4 Stylet: 2L 5FR x 55CM w CHG/DLX-35552-VPSC; PI PICC NaviCurve: 3L 6FR x 55CM w CHG/DLX-35563-CURVC; PI PICC G4 Stylet: 3L 6FR x 55CM w CHG/DLX-35563-VPSC; AGBA PICC/DELTA KIT: 1-L 4.5 FR X 40 CM/CDC-44041-VPS2; PICC KIT: 1L 4.5 FR X 55 CM VPS/ASK-45541-UWH1; PI AGBA PICC KIT: 2L 5.5FR X 55CM W/ VPS/ASK-45552-UWH1; AGBA PICC G4 Stylet: 1L 4.5FR x 55CM BP/DLX-45541-VPSB; ACCESS TRAY/ASK-04001-NWM; ACCESS TRAY/ASK-04001-VCUH3; PI PICC:1L 4FR X 40CM PRELOAD VPS STYLET/CDC-34041-VPS; PI PICC:2L 5FR X 50CM PRELOAD VPS STYLET/CDC-35052-VPS; ACCESS KIT/ASK-04001-BWK2; ARROW(R) VPS(R) ACCESS KIT/ASK-04001-DU11; MULTI LUMEN PI CVC KIT: 3L 7 FR X 6 IN/ASK-42703-PVD; MULTI LUMEN PI CVC KIT: 3L 7 FR X 16CM/ASK-12703-LMDTG1; MULTI LUMEN PI CVC KIT: 3L 7 FR X 8IN/ASK-15703-ECMC4; MULTI LUMEN PI CVC KIT: 3L 7 FR X 20 CM/ASK-15703-PNM; CVC KIT: 3 LUMEN 12 FR X 6IN/ASK-22123-UAB; 2-L CVC KIT: 4 FR X13 CM/CDC-24402-X1A; LBCVC KIT: 3L 12 FR X 20 CM AGB/CDC-25123-X1A; CVC KIT: 3L 7 FR X 16 CM/ASK-42703-CPR; CVC KIT: 2L 8 FR X 6 IN (16 CM) AGB+/ASK-42802-DMC2; CVC KIT: 2 LUMEN 8 FR X 8 IN (20 CM)/ASK-45802-PCMH1; PI CVC KIT: 3L 7 FR X 6 IN (16 CM) AGB+/ASK-42703-MM1; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-PHUMC1; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-PMSG1; MULTILUMEN PI CVC KIT: 3L 7 FR X 6/ASK-42703-POSU3; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-PSAU1; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-RHR1; PI CATHETER 2L: 8 FR X 16 CM AGB+/ASK-42802-DU1; PI CVC KIT: 2L 8 FR X 6 IN/ASK-42802-PHF4; PI CVC KIT: 2L 8 FR X 16 CM AGB+/ASK-42802-PHHN1; MULTILUMEN CVC KIT: 2L 8 FR X 6 IN/ASK-42802-POSU3; PI CVC KIT: 2-L 8 FR X 16 CM AGB+/ASK-42802-PUCD1; MULTI-LUMEN CVC KIT:2-L 8FR X 6IN (16CM)/ASK-42802-PWHC1; PI CVC KIT: 2L 8 FR X 16 CM AGB+/ASK-42802-UHC; PI CVC KIT: 4L 8.5 FR X 16 CM AGB+/ASK-42854-MCY1; PI CVC KIT: 3L 7FR X 8IN (20 CM) AGB+/ASK-45703-BCH; PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-EMC; PI CVC KIT: 3 LUMEN 7 FR X 8 IN (20 CM)/ASK-45703-MHMC1; PI CVC KIT: 3-L 7 FR X 20 CM AGB+/ASK-45703-NWM; MULTILUMEN PI CVC KIT: 3L 7 FR X 20 CM/ASK-45703-PCOR; MULTILUMEN PI CVC KIT: 3L 7 FR X 20 CM/ASK-45703-PIMH; MULTI LUMEN CVC KIT: 3L", "reason": "Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.", "hazard_level": "Class I", "company": "ARROW INTERNATIONAL, LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-21", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "177,014", "codes": "REF(Material)/UDI-DI/Lot(Batch): CDC-02031-MK1A/10801902193275/33F25C0444; CDC-41541-MPK1A/10801902193275/33F24L1137; CDC-41552-MPK1A/10801902193275, 50801902130162/33F24L0382, 33F25A0315, 33F25B0630, 33F25K0421, 33S24B0571; ASK-41541-VFHM/10801902193275, 10801902218862/33F24L1080, 33F25B0475, 33F25C0351, 33F25D0404, 33F25E0556, 33F25E0784, 33F25F0186, 33F25J0218, 33F25K0077, 33F25K0100, 33F25M0182, 33F26A1549, 33F26B0823; CDC-41541-MPK/10801902193275, 10801902193275/33F25H0768, 33S23K0382; CDC-41541-MPKB/10801902193275, 10801902205411/33F24H0429, 33F24K0043, 33F24M0067, 33F24M0149, 33F25A0390, 33F25B0099, 33F25B0343, 33F25C0578, 33F25E0421, 33F25F0401, 33F25G0515, 33F25G0710, 33F25H0817, 33F25J1008, 33F25L0015, 33F25L0050, 33F25L0295, 33F25M0499, 33F26A0330, 33X25J0003; CDC-41541-MPKC/10801902205435, 10801902193275/33F24D0982, 33F24F0166, 33F24F0167, 33F24H0398, 33F24H0454, 33F24J0380, 33F24J0389, 33F24K0581, 33F24L0182, 33F24M0022, 33F24M0077, 33F25A0348, 33F25B0228, 33F25B0281, 33F25B0289, 33F25B0344, 33F25C0513, 33F25C0532, 33F25C0558, 33F25D0710, 33F25D0736, 33F25F0020, 33F25F0025, 33F25F0032, 33F25H0818, 33F25J0577, 33F25J0657, 33F25L0251, 33F25L0296, 33S25A0211, 33F26C0435; CDC-41552-MPK/10801902201505/33F24D0561, 33F26B0490, 33S24A0521; CDC-41552-MPKB/10801902193275, 10801902205428/33F24J0183, 33F24J0221, 33F24L0010, 33F24L0173, 33F24M0114, 33F25B0223, 33F25B0299, 33F25D0724, 33F25F0436, 33F25G0640, 33F25K0354, 33F25L0265, 33F26B1048; CDC-41552-MPKC/10801902205442, 10801902193275/33F24C0861, 33F24D0343, 33F24F0090, 33F24K0474, 33F25C0208, 33F25D0559, 33F25E0827, 33F25H0608, 33F25J0434, 33F25M0248, 33F26A1559, 33F26C0776; CDC-32041-MPK/10801902193275, 10801902201475/33F25C0701, 33F25H0613, 33F25J0433, 33F25L0115, 33F25M0250, 33F26B0436; CDC-32041-MPKB/10801902205398, 10801902193275/33F24D0854, 33F24F0897, 33F24L0952, 33F25B0502, 33F25D0512, 33F25E0825, 33F25G0327, 33F25J0327, 33F25M0210, 33F26B0434, 33S23E0870; CDC-32041-MPKC/10801902193275/33F25D0513, 33F25H0590, 33F26A1387; CDC-32052-MPKB/10801902205404, 10801902193275/33F24F0825, 33F24L0381, 33F25D0514, 33F25H0609; DLX-35541-CURVB/10801902193275, 10801902208757/33F25D0674, 33F25J0186, 33S23G0883, 33S23H0988; DLX-35541-HPKB/10801902193275/33F25D0129, 33F25E0708; DLX-35541-HPKC/10801902193275/33F25D0244, 33F25E0830; DLX-35552-HPKB/10801902193275/33F25D0246, 33F25D0518, 33F25F0149; DLX-35552-HPKC/10801902193275, 10801902216721/33F25D0247, 33F25D0519, 33F25H0460, 33S23K0380; DLX-35563-HPKB/10801902193275/33F25K0318; ASK-44041-NS/10801902193275, 10801902216462/33F24L0347, 33S23H0298; ASK-44052-NS/10801902193275, 10801902216455/33F25A0302, 33S23J0265; ASK-45041-NS/10801902216677/33S24A0529; ASK-45052-TG/10801902193275/33F24L0864, 33F25D0409, 33F25H0490, 33F26A1379; ASK-45063-NS/10801902193275/33F24L1002; ASK-45541-RH/10801902193275/33F25B0574, 33F25E0607, 33F25H0427, 33F25J0161, 33F26A1412; DLX-45541-HPKC/10801902208849, 10801902193275/33F24D0604, 33F25D0128, 33F25E0763, 33F25J0131, 33F25M0315, 33F26B0456; DLX-45552-HPKC/10801902208856, 10801902193275/33F24F0097, 33F25C0450, 33F25D0252, 33F25D0625, 33F25G0321, 33F25H0601, 33F26B0213; DLX-45563-CURVC/10801902193275, 10801902208740/33F25A0321, 33F25B0635, 33F25D0522, 33F25E0766, 33F25G0394, 33F26C0707; DLX-45563-HPKB/10801902193275/33F25D0384, 33F25F0226; DLX-45563-HPKC/10801902208863, 10801902193275/33F24D0184, 33F25B0698, 33F25E0661, 33F26A1545; CDC-35541-TTS/10801902193275/33F25B0468; DLX-35541-CURVC/10801902193275, 10801902216684/33F25D0574, 33F25E0759, 33F25G0216, 33F25H0591, 33F25M0200, 33F26B0192; DLX-35541-VPSB/10801902193275, 10801902208665/33F25C0212, 33F25D0378, 33F25E0831, 33F25F0101, 33F25G0364, 33F25J0128, 33F25J0256, 33F25K0193, 33F25M0164, 33F26A1131, 33F26B0180, 33F26C0699; DLX-35552-CURVC/10801902193275, 10801902216714/33F25C0373, 33F25D0619, 33F25F0222, 33S24C0282; DLX-35552-VPSB/10801902193275, 10801902208672/33F25B0536, 33F25D0248, 33F25D0379, 33F25D0575, 33F25H0471, 33F25H0603, 33F26C0042; DLX-35552-VPSC/10801902193275, 10801902216738/33F25B0389, 33F25D0249, 33F25J0122, 33F25J0335, 33F25M0445, 33F26A0470, 33S24B0733; DLX-35563-CURVC/10801902193275, 10801902216745/DLX-35563-CURVC, DLX-35563-CURVC, DLX-35563-CURVC; DLX-35563-VPSC/10801902193275, 10801902216769/33F25C0395, 33F26B0380; CDC-44041-VPS2/10801902193275, 50801902120699/33F24K0430, 33S23L0922; ASK-45541-UWH1/10801902193275, 10801902217216/33F24L0991, 33F25C0198, 33F25E0572, 33F25H0457, 33F25J0400, 33F25M0151, 33F26B0384; ASK-45552-UWH1/10801902193275/33F24L0431, 33F25B0576, 33F25G0212, 33F25H0589, 33F25J0225, 33F25M0229, 33F26A1554; DLX-45541-VPSB/10801902193275, 10801902208603/33F24L1122, 33F25B0679, 33F25D0064, 33F25D0521, 33F25H0403, 33F25H0605, 33F26C0119; ASK-04001-NWM/10801902193275, 10801902222715/33F25F0005, 33F25F0125, 33F26A1493, 33F26B0829; ASK-04001-VCUH3/10801902214895, 10801902193275/33F24D0895, 33F24F0785, 33F24L1087, 33F25B0172, 33F25F0161, 33F25G0221, 33F25H0522, 33F25J0198, 33F26B0228, 33F26B0831, 33F26C0534; CDC-34041-VPS/10801902193275/33F24L0236; CDC-35052-VPS/10801902193275/33F25E0425; ASK-04001-BWK2/10801902193275/33F25A0226, 33F25D0389, 33F25E0519, 33F25F0076, 33F25F0139, 33F25H0660, 33F25J0347, 33F26A1341; ASK-04001-DU11/10801902193275/33F25C0425, 33F25D0328, 33F25F0140, 33F25H0506; ASK-42703-PVD/10801902156966, 10801902193275/33F24F0977, 33F24L1004, 33F25C0302, 33F25K0144, 33F26B0157; ASK-12703-LMDTG1/10801902193275, 10801902205688/33F25D0262, 33F25G0280, 33F26B0212; ASK-15703-ECMC4/10801902159950, 10801902193275/33F24E0649, 33F24F1039, 33F25B0439; ASK-15703-PNM/10801902193275/33F25E0312; ASK-22123-UAB/10801902144956, 10801902193275/33F24F0854, 33F24L0318, 33F25C0281, 33F25D0267, 33F25D0593, 33F25J0380; CDC-24402-X1A/10801902193275, 10801902168099/33F24L1111, 33F25C0206, 33F25E0747, 33F25G0341, 33F25H0554, 33F25J0324, 33F26A1561, 33F26B0165, 33F26B0803; CDC-25123-X1A/10801902193275, 10801902168105/33F25B0675, 33F25D0501, 33F25E0887, 33F25G0379, 33F26A1562, 33F26B0892; ASK-42703-CPR/10801902193275, 10801902135220/33F25C0744, 33F25E0234, 33F25J0559, 33F25J0797, 33F25K0401, 33F26B0244; ASK-42802-DMC2/10801902193275/33F25E0005; ASK-45802-PCMH1/10801902193275/33F25D0034; ASK-42703-MM1/10801902193275, 10801902221916/33F25E0509, 33F25E0559, 33F25M0205, 33F25M0449, 33F26A1659, 33F26B0196; ASK-42703-PHUMC1/10801902193275/33F25E0009, 33F25G0174, 33F25G0682, 33F25L0138, 33F26A0234; ASK-42703-PMSG1/10801902193275/33F25F0363; ASK-42703-POSU3/10801902193275, 10801902222579/33F25D0758, 33F25E0563, 33F25L0109, 33F26A1436, 33F26B0782; ASK-42703-PSAU1/10801902193275, 10801902159486/33F25A0258, 33F25C0300, 33F25D0543, 33F25J0108, 33F25J0273, 33F25M0093, 33F26B0758; ASK-42703-RHR1/10801902193275, 10801902163643/33F25E0311, 33F25G0262, 33F25H0425, 33F25L0060, 33F26A0238, 33F26C0483; ASK-42802-DU1/10801902161007, 10801902193275/33F24C0924, 33F24F0870, 33F24L0870, 33F25D0356, 33F25E0566, 33F25F0191, 33F25J0285, 33F26B0423; ASK-42802-PHF4/10801902200485, 10801902193275/33F24F0759, 33F25B0357, 33F25B0478, 33F25E0568, 33F25F0079, 33F25G0176, 33F25J0392, 33F25M0059, 33F26A1528, 33F26B0190, 33F26B0793; ASK-42802-PHHN1/10801902193275/33F25E0004, 33F25G0265, 33F25K0045, 33F25M0065; ASK-42802-POSU3/10801902193275, 10801902222586/33F25D0759, 33F25E0569, 33F25F0193, 33F25G0186, 33F25J0393, 33F26A1548, 33F26B0859; ASK-42802-PUCD1/10801902193275/33F25E0313, 33F25E1206; ASK-42802-PWHC1/10801902193275, 10801902134858/33F25B0498, 33F25E0680, 33F25F0195, 33F25J0160, 33F26B0418, 33F26C0164; ASK-42802-UHC/10801902193275, 10801902159745/33F25C0306, 33F25E0605, 33F25J0289, 33F26B0200; ASK-42854-MCY1/10801902193275, 10801902220995/33F24H0126, 33F24J0099, 33F25B0479, 33F25E0570, 33F25F0196, 33F25J0396, 33F26B0779; ASK-45703-BCH/10801902193275, 10801902222784/33F25F0004, 33F25F0117, 33F25G0184, 33F25G0185, 33F25H0508, 33F26A1381, 33F26B0876; ASK-45703-EMC/10801902160468, 10801902193275/33F24D0579, 33F24L0911, 33F25D0411, 33F25G0406, 33F25M0181, 33F26C0225; ASK-45703-MHMC1/10801902193275, 10801902213850/33F25B0580, 33F25D0366, 33F25E0574, 33F25G0224, 33F25H0463, 33F25J0231, 33F26B0129; ASK-45703-NWM/10801902193275/33F25F0006, 33F25F0105, 33F25M0009, 33F26A1463; ASK-45703-PCOR/10801902193275/33F24L0088, 33F25C0736, 33F25H0755; ASK-45703-PIMH/10801902193275/33F25B0588; ASK-45703-PK/10801902193275/33F25A0271, 33F25E0623; ASK-45703-PLGH2/10801902144536, 10801902193275/33F24D0901, 33F24F0995, 33F24L0213, 33F24L0964, 33F25C0315; ASK-45703-PMM4/10801902193275/33F25A0272; ASK-45703-PMM5/10801902193275, 10801902221947/33F25E0505, 33F25E0624, 33F25G0192, 33F25L0105, 33F25L0269, 33F26A1368, 33F26B0207, 33F26C0153; ASK-45703-POSU3/10801902193275, 10801902222593/33F25D0760, 33F25E0576, 33F25E0686, 33F25M0097, 33F26A1346, 33F26B0148, ASK-45703-PPHP1/10801902193275/33F24K0067, 33F25C0584, 33F25G0555, 33F26A0240; ASK-45703-PSAM/10801902116373, 10801902193275/33F24E0560, 33F24G0518, 33F24J0638, 33F25C0818, 33F25G0144, 33F25J0931, 33F26B0509; ASK-45703-PUCD1/10801902193275, 10801902221640/33F25D0237, 33F25D0607, 33F25H0653, 33F25K0159, 33F25M0228, 33F26A1499, 33F26B0374; ASK-45703-PUNCC2/10801902164268, 10801902193275/33F24D0696, 33F24F0690, 33F24K0439, 33F25B0598,33F25D0373, 33F25E0690, 33F25F0147, 33F25H0204, 33F25H0631, 33F25J0233, 33F26B0415; ASK-45854-PAMC1/10801902193275/33F25C0363, 33F25H0519, 33F25K0162, 33F26A0524; ASK-45854-PLGH1/10801902193275/33F24L0191, 33F25B0361, 33F25E0309, 33F25H0775, 33F26A0247; CDC-45802-XPN1A/10801902193275/33F25A0290, 33F25B0632, 33F25E0757, 33F25J0255, 33F26A1565; CDC-42703-XPN1A/10801902193275, 10801902162066/33F25F0069, 33F25F0332, 33F25H0879, 33F25H0881, 33F25J0224, 33F25J0693, 33F25J0697, 33F25J0717, 33F25J0721, 33F25L0014, 33F25L0250, 33F25M0019, 33F25M0028,33F26A0312, 33F26A0338, 33F26B0624, 33F26C0066, 33F26C0074, 33F26C0087, 33F26C0101, 36F25A0010, 36F25B0035, 36F25B0038, 36F25B0069, 36F25E0017, 36F25G0013, 36F25H0001, 36F25H0002, 36F25H0026, 36F25J0003; CDC-45703-PB1A/10801902117202, 10801902193275/33F24C1072, 33F24E0626, 33F24F0945, 33F25E0754, 33F25G0581, 33F25H0435, 33F25J0118, 33F25J0328; CDC-45854-P1A/30801902117275/33F24D0700, 33F24F0086, 33F24F0794, 33F25C0210, 33F25D0571, 33F25E0705, 33F25G0276, 33F25H0444, 33F25J0121, 33F25J0184, 33F25K0191, 33F26A1558, 33F26B0886;", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2394-2026%22", "url": "https://recallledger.net/recalls/device-z-2394-2026-description-ref-midline-catheter-kit-3-fr-x-20-cm-cdc-02031-mk1a-am/"}, {"id": "fda-device-z-2393-2026", "source": "FDA", "category": "device", "recall_number": "Z-2393-2026", "title": "Description/REF: PSI KIT: 7 FR X 4 IN/ASK-09701-UP recall (ARROW INTERNATIONAL, LLC)", "product": "Description/REF: PSI KIT: 7 FR X 4 IN/ASK-09701-UP; PSI KIT: 8.5 FR X 4 1/8 IN (10 CM)/ASK-09803-OSU5; PSI KIT: 8.5 FR/ASK-09807-UC; PSI KIT: 9 FR X 4 1/8IN (10 CM)/ASK-09903-HH2; PSI KIT: 9 FR X 10 CM/ASK-09903-LMDTG; PSI KIT: 9 FR X 4 1/8 IN (10 CM)/ASK-09903-OSU5; PSI KIT: 9 FR X 10 CM/CDC-09903-1A; MAC KIT: 2L 9 FR DISTAL X 11.5 CM/ASK-11242-KSF2; MAC TWO LUMEN/PSI KIT: 9 FR X 11.5 CM/ASK-11242-KSF1 AGB MAC KIT: 2L 9 FR DISTAL/ASK-21242-MCY1; MULTI LUMEN PSI KIT: 9 FR DISTAL X 4 1/2/ASK-21242-OSU4; MAC KIT: 2-L 9 FR DISTAL X 11.5 CM/ASK-21242-UCD1; 2L MAC KIT: 9 FR DISTAL X 4 IN/ASK-21142-HHC MAC KIT: 2L 9 FR DISTAL X 11.5 CM AGB/ASK-21242-LMDT; PSI KIT: 8.5 FR X 4IN (10 CM)/ASK-09804-CCH; PSI KIT: 8.5 FR X 4 1/8 IN (10 CM)/ASK-29803-MM2; PSI KIT: 9 FR X 4 1/8 IN (10 CM)/ASK-29903-DU1; PSI KIT: 9 FR X 4 IN (10 CM)/ASK-29903-HHC; PSI KIT: 9 FR X 10 CM ANTIMICROBIAL/ASK-29903-LMDT; PSI KIT: 9 FR X 4 1/8 (10 CM)/ASK-29903-NWM; PSI KIT: 9 FR X 10 CM ANTIMICROBIAL/ASK-29903-SL1; PSI KIT: 8.5 FR X 10 CM ANTIMICROBIAL/CDC-29803-XCN1A; PSI KIT: 8.5 FR X 4 1/8 IN (10 CM)/ASK-29803-HF6; PSI KIT: 8.5 FR X 4 1/8 IN (10 CM)/ASK-29804-HHN1; MULTI LUMEN/MAC KIT: 9 FR X 4 IN (10 CM)/ASK-21142-YWH;", "reason": "Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.", "hazard_level": "Class I", "company": "ARROW INTERNATIONAL, LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-21", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "72,354", "codes": "REF(Material)/UDI-DI/Lot(Batch): ASK-09701-UP/10801902143874, 10801902193275/33F23K0811, 33F24B0340, 33F24E0524, 33F24G0489, 33F25C0874, 33F25E1018, 33F25H0747, 33F25J0795, 33F26A0402, 33F26B0243, 33F26B1031; ASK-09803-OSU5/10801902193275/33F25D0761, 33F25E0533, 33F25M0683; ASK-09807-UC/10801902145847, 10801902193275/33F24B0018, 33F24F0004, 33F24J0478, 33F25C0175, 33F25E0210, 33F25E1208, 33F25G0676, 33F25L0211; ASK-09903-HH2/10801902193275/33F25E0534, 33F25G0167, 33F25H0565, 33F25J0358, 33F25M0234, 33F26C0332; ASK-09903-LMDTG/10801902193275/33F25E1184, 33F25F0112, 33F25H0375; ASK-09903-OSU5/10801902193275/33F25D0762; CDC-09903-1A/60801902116729, 10801902193275/33F24D0504, 33F24F0227, 33F24H0267, 33F24H0434, 33F24J0219, 33F24K0023, 33F24M0015, 33F24M0109, 33F25B0006, 33F25B0067, 33F25C0417, 33F25D0696, 33F25D0718, 33F25E1148, 33F25F0023, 33F25G0445, 33F25G0513, 33F25G0605, 33F25G0668, 33F26A1644; ASK-11242-KSF2/10801902193275, 10801902222500/33F25D0231, 33F25D0468, 33F25E0592, 33F25K0131, 33F26A1360, 33F26B0425; ASK-11242-KSF1/10801902193275/33F24L0840, 33F25B0190; ASK-21142-NWM/10801902193275, 10801902222746/33F25F0007, 33F25F0173, 33F25J0207, 33F25M0008, 33F26A1438, 33F26B0197; ASK-21242-MCY1/10801902193275, 10801902221022/33F24H0123, 33F25C0342, 33F25E0671, 33F25K0138, 33F26B0441; ASK-21242-OSU4/10801902193275, 10801902222562/33F25D0757, 33F25E0672, 33F25H0445, 33F25H0651, 33F25L0230, 33F26B0795; ASK-21242-UCD1/10801902193275, 10801902221633/33F25E0314, 33F25M0681, 33F26B0138; ASK-21142-HHC/10801902193275, 10801902211450/33F24L0309, 33F25C0273, 33F25G0170, 33F25H0440, 33F25J0372, 33F26B0125; ASK-21242-LMDT/10801902193275, 10801902220698/33F25C0696, 33F25E0544, 33F26A1526, 33F26B0464; ASK-09804-CCH/10801902141023, 10801902193275/33F24D0899, 33F24F0836, 33F24L0295, 33F25B0184, 33F25C0261, 33F25E0777, 33F25G0410, 33F25J0356, 33F26A1369, 33F26C0041; ASK-29803-MM2/10801902193275, 10801902221930/33F25E0549, 33F26A1352, 33F26B0176, 33F26C0031; ASK-29903-DU1/10801902193275/33F24H0139, 33F25A0171, 33F25E0553, 33F25H0426, 33F25M0012; ASK-29903-HHC/10801902193275/33F25D0235, 33F25L0263, 33F26A1431; ASK-29903-LMDT/10801902193275/33F25D0480, 33F25K0208, 33F25K0420; ASK-29903-NWM/10801902193275/33F25F0008, 33F25F0098, 33F25L0264, 33F26A1396; ASK-29903-SL1/10801902193275/33F25C0289, 33F25G0296, 33F25J0104, 33F25J0266, 33F26A1391; CDC-29803-XCN1A/10801902193114, 10801902193275/33F24E0214, 33F24F0024, 33F24F0173, 33F24F0248, 33F24G0163,33F24H0396, 33F24H0431, 33F24L0539, 33F24M0036, 33F24M0113, 33F25A0368, 33F25B0047, 33F25B0118, 33F25B0342, 33F25C0531, 33F25D0708, 33F25D0735, 33F25E1103, 33F25E1154, 33F25F0417, 33F25G0053, 33F25G0514, 33F25H0287, 33F25H0816, 33F25K0293, 33F25L0079, 33F26A1628, 33F26B0565, 33F26C0064, 33F26C0454, 33F26C0099; ASK-29803-HF6/10801902200478,10801902193275/33F24D0625, 33F24F0889, 33F24L0246, 33F25B0441, 33F25D0268, 33F25F0180, 33F25J0151, 33F25M0832; ASK-29804-HHN1/10801902193275/33F25B0236, 33F25E0550, 33F25G0691, 33F25K0053; ASK-21142-YWH/10801902135473/33F25A0440, 33F25D0030;", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2393-2026%22", "url": "https://recallledger.net/recalls/device-z-2393-2026-description-ref-psi-kit-7-fr-x-4-in-ask-09701-up-psi-kit-8-5-fr-x/"}, {"id": "fda-device-z-2392-2026", "source": "FDA", "category": "device", "recall_number": "Z-2392-2026", "title": "Description/REF: ACCESS TRAY/ASK-04001-MC3 recall (ARROW INTERNATIONAL, LLC)", "product": "Description/REF: ACCESS TRAY/ASK-04001-MC3", "reason": "Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.", "hazard_level": "Class I", "company": "ARROW INTERNATIONAL, LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-21", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "8,265", "codes": "REF(Material)/UDI-DI/Lot(Batch): ASK-04001-MC3/", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2392-2026%22", "url": "https://recallledger.net/recalls/device-z-2392-2026-description-ref-access-tray-ask-04001-mc3/"}, {"id": "fda-device-z-2391-2026", "source": "FDA", "category": "device", "recall_number": "Z-2391-2026", "title": "Description/REF: RA CATH KIT: 20 GA X 1-3/4IN/AK-04020-SPC recall (ARROW INTERNATIONAL, LLC)", "product": "Description/REF: RA CATH KIT: 20 GA X 1-3/4IN/AK-04020-SPC; RA CATH KIT: 20 GA X 5 IN/ASK-04020-MW; ARTERIAL LINE KIT: SL 20 GA X 5 IN/ASK-04510-MM5; CATH SL 20 GA X 5 CM HYDROPHILIC/ASK-00520-JH; CATH S-L 20 GA X 5 CM HYDROPHILIC/ASK-00520-UHC; ARTERIAL LINE KIT: 20 GA x 5IN/ASK-00820-CL; RA CATH KIT: 20 GA X 8 CM X 12 CM/ASK-00820-WC; ARTERIAL CATHETERIZATION KIT/ASK-01218-HM; SAC KIT: 20 GA X 12CM/ASK-01220-HMH; ARTERIAL CATH KIT: 20GA X 12CM/ASK-01220-NWM; ARTERIAL CATH KIT: 20 GA X 12 CM/ASK-01220-UH; ARTERIAL CATH: 18 GA X 6 1/2IN/ASK-01618-AU; RA CATH KIT: 18 GA X 6 IN/ASK-01618-CL; ARTERIAL CATH KIT: 18 GA X 6 1/2 IN/ASK-01618-JH; ARTERIAL CATHETERIZATION KIT/ASK-01618-PH; ARTERIAL CATH KIT: 18 GA X 6 1/2IN/ASK-01618-RU; ARTERIAL CATH KIT: 18 GA X 6IN (16 CM)/ASK-04018-HF; ARTERIAL CATH KIT: 18 GA X 6 IN (16 CM)/ASK-04018-NS; ARTERIAL CATHETER KIT: 18 GA X 16 CM/ASK-04018-ST; RA CATH KIT: 20 GA X 1 1/2 IN (3.81 CM)/ASK-04120-BGH; ART/VESS CATH KIT:20GAX4.45CM/20GAX12CM/ASK-04500-SM; ARTERIAL LINE KIT/ASK-04500-UCH; ARTERIAL LINE KIT/ASK-04510-EUH2; ARTERIAL LINE KIT: 20GA X 5IN (12CM)/ASK-04510-MS4; ARTERIAL LINE KIT/ASK-04510-UPM; ARTERIAL CATH KIT: 20GA X 5CM/SAC-00520-1A; ARTERIAL CATH KIT: 20GA X 5CM/SAC-00520-X1A; ARTERIAL CATH KIT: 22GA X 5CM/SAC-00522-1A ARTERIAL CATH KIT: 22 GA X 5CM/SAC-00522-X1A; ARTERIAL CATH KIT: 20GA X 8CM/SAC-00820-1A; ARTERIAL CATH KIT: 20GA X 8CM/SAC-00820-X1A; SAC KIT: 18 GA X 12CM/SAC-01218-1A; SAC KIT: 18 GA X 12CM/SAC-01218-X1A; SAC KIT: 20 GA X 12CM/SAC-01220-1A; SAC KIT: 20 GA X 12CM/SAC-01220-X1A; SAC KIT: 18 GA X 16CM/SAC-01618-1A; SAC KIT: 18 GA X 16CM/SAC-01618-X1A; ACCESS TRAY/UM-04018; RA CATH KIT: 20 GA X 4.45 CM/ASK-04020-ABM; RA CATH KIT: 20 GA X 1 3/4 IN (4.45 CM)/ASK-04020-BGH; RA CATH KIT: 20 GA X 1 3/4 IN/ASK-04020-LOL; RA CATH KIT: 20 GA X 1 3/4 IN (4.45 CM)/ASK-04020-MHS; RA CATH KIT: 20 GA X 1 3/4IN (4.45 CM)/ASK-04020-MIB3; RA CATH KIT: 20 GA X 1 3/4 IN/ASK-04020-PMC1; RA CATH SET: 20 GA X 1 3/4 IN/ASK-04020-URMC; RA CATH KIT: 20 GA X 1 1/2 IN (3.81 CM)/ASK-04220-FMH1; RA CATH KIT: 20 GA X 4.45 CM/NA-04020-1A; RA CATH KIT: 20 GA X 4.45 CM W BIO/NA-04020-B; RA CATH KIT: 20 GA X 4.45 CM W CHG/NA-04020-C; VESSEL CATH KIT: 20 GA X 5IN (12 CM)/ASK-04550-NYP; CVC KIT: 16 GA X 8 IN (20 CM)/ASK-04300-PHP1; CVC KIT: 16 GA X 8 IN (20 CM)/ASK-04301-TJ; ARTERIAL ACCESS KIT/ASK-04001-VAMC1; RA CATH KIT: 20 GA X 1-3/4IN/ASK-04020-WBH", "reason": "Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.", "hazard_level": "Class I", "company": "ARROW INTERNATIONAL, LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-21", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "491,489", "codes": "REF(Material)/UDI-DI/Lot(Batch): AK-04020-SPC/10801902121551, 10801902193275/33F23M0171, 33F24C0729, 33F24E0699, 33F24G0596, 33F24H0057, 33F24J0350, 33F24J0458, 33F24K0615, 33F24M0126, 33F25A0338, 33F25B0039, 33F25B0131, 33F25D0192, 33F25D0281, 33F25E1109, 33F25F0496, 33F25J0764, 33F26B0054; ASK-04020-MW/10801902142983, 10801902193275/33F23M0188, 33F24B0447, 33F24C0744, 33F24E0725, 33F24G0231, 33F24G0669, 33F24H0344, 33F24L0005, 33F24L0024, 33F25A0062, 33F25B0064, 33F25D0290, 33F25D0729, 33F25E0428, 33F25H0328, 33F26B0089, 33F26B0263; ASK-04510-MM5/10801902193275/33F24K0360, 33F25A0237, 33F25B0546; ASK-00520-JH/10801902138788, 10801902193275/33F24D0201, 33F24F0686, 33F24J0128, 33F24K0373, 33F25A0204, 33F25B0541, 33F25D0324, 33F25D0645, 33F25H0429, 33F25H0507, 33F25J0195, 33F26A1380, 33F26B0159, 33F26C0192; ASK-00520-UHC/10801902139839, 10801902193275/33F23L0771, 33F24A0775, 33F24B0219, 33F24C0125, 33F24D0093, 33F24E0383, 33F24G0386, 33F24J0284, 33F24K0149, 33F24L0712, 33F25A0495, 33F25C0125, 33F25C0826, 33F25E0099, 33F25H0047, 33F25J0851, 33F25L0392, 33F26B0540; ASK-00820-CL/10801902193275, 10801902193916/33F24G0275, 33F24J0285, 33F24K0152, 33F24L0590, 33F25A0497, 33F25C0797, 33F25E0102, 33F25H0050, 33F25J0853, 33F25L0385, 33F26B0536; ASK-00820-WC/10801902193275/33F24G0150, 33F24G0227, 33F24G0691, 33F24H0253, 33F24K0624, 33F25B0091, 33F25B0334, 33F25J0574, 33F26B0113; ASK-01218-HM/10801902193275/33F24G0276, 33F24K0551, 33F24L0215, 33F25A0296, 33F25B0543, 33F25E0450, 33F25F0364, 33F25G0163, 33F25G0208, 33F25H0499, 33F25J0100, 33F25J0139; ASK-01220-HMH/10801902193275/33F25B0245, 33F25B0544, 33F25C0698, 33F25D0388; ASK-01220-NWM/10801902193275/33F24H0181, 33F24J0154, 33F24K0497, 33F25F0157, 33F25H0658; ASK-01220-UH/10801902193275/33F24G0391, 33F24J0286, 33F24J0541, 33F24K0154, 33F24L0663, 33F25C0126, 33F25E0104, 33F25E0955, 33F25H0052, 33F25J0494, 33F25J0855, 33F25L0459, 33F25M0952; ASK-01618-AU/10801902205909, 10801902193275/33F24F0213, 33F24K0673, 33F25C0653, 33F25E1171, 33F25L0062, 33F26A0233; ASK-01618-CL/10801902195934, 10801902193275/33F24E0648, 33F24K0355, 33F25A0224,33F25B0493, 33F25D0327, 33F25E0588, 33F25F0158, 33F25J0140, 33F25M0112, 33F26C0366; ASK-01618-JH/10801902138801, 10801902193275/33F24D0584, 33F24K0490, 33F24L0844, 33F25B0494, 33F25D0530, 33F25H0834, 33F25K0264, 33F25K0357, 33S25D0530; ASK-01618-PH/10801902193275/33F24K0749, 33F24L0837, 33F25C0251, 33F25E0019, 33F25G0220; ASK-01618-RU/10801902202304, 10801902193275/33F24B0869, 33F24D1027, 33F25A0102, 33F25C0713, 33F25J0792, 33F25M0618; ASK-04018-HF/10801902193275/33F24H0156, 33F24L0397, 33F25D0391, 33F25G0401, 33F25K0069, 33F25M0142; ASK-04018-NS/10801902193275/33F25E1176, 33F25G0103; ASK-04018-ST/10801902117639, 10801902193275/33F24A0112, 33F24A0826, 33F24B0237, 33F24C0140, 33F24E0402, 33F24E0403, 33F24G0281, 33F24K0163, 33F25A0504, 33F25C0780, 33F25E0115, 33F25G0104, 33F25J0498, 33F25M0917, 33F26B1011; ASK-04120-BGH/10801902117936, 10801902193275/33F24D0518, 33F24G0262, 33F24J0474, 33F25A0150, 33F25C0740, 33F25E1207, 33F25H0096, 33F25K0331; ASK-04500-SM/30801902118012, 10801902193275/33F24A0117, 33F24A1163, 33F24D0059, 33F24D0968, 33F24E0782, 33F24G0263, 33F24J0302, 33F25C0500, 33F25E0162, 33F25H0738, 33F25L0209, 33F25M0617, 33F26B0020, 33F26B0746; ASK-04500-UCH/10801902139464, 10801902193275/33F24E0454, 33F24G0446, 33F24J0588, 33F24K0207, 33F24L0715, 33F25C0155, 33F25C0924, 33F25E0163, 33F25H0739, 33F25L0332, 33F26B0655; ASK-04510-EUH2/10801902193275, 10801902213386/33F24J0303, 33F24L0728, 33F25C0156, 33F25C0803, 33F25E0164, 33F25H0103, 33F25J0522, 33F25L0343, 33F25M0850, 33F26B0660; ASK-04510-MS4/10801902193275, 10801902139709/33F24K0212, 33F24L0764, 33F25C0860, 33F25E0169, 33F25E0994, 33F25J0526, 33F25L0423, 33F26B0654; ASK-04510-UPM/10801902118087, 10801902193275/33F24B0144, 33F24E0101, 33F24E0102, 33F24G0456, 33F24J0595, 33F24K0216, 33F24L0675, 33F25A0544, 33F25C0947, 33F25E0174, 33F25H0107, 33F25J0529, 33F25J0738, 33F25L0022, 33F26B0647, 33F26B0665, 33F26C0617; SAC-00520-1A/10801902140644, 10801902193275/33F24C0780, 33F24E0772, 33F24G0025, 33F24G0675, 33F24H0061, 33F24J0190, 33F24J0207, 33F24J0415, 33F24M0010, 33F25A0097, 33F25B0052, 33F25B0126, 33F25B0410, 33F25C0540, 33F25D0185, 33F25E0408, 33F25E0472, 33F25G0530, 33F25H0832, 33F25J0045, 33F25J1013, 33F25M0704, 33F26B0259; SAC-00520-X1A/10801902193275, 10801902140583/33F24J0208, 33F25A0098, 33F25B0023, 33F25B0127, 33F25B0287, 33F25D0086, 33F25E1180, 33F25F0288, 33F25F0425, 33F25H0347, 33F25H0866, 33F25L0177, 33F26B0058, 33F26B0279; SAC-00522-1A/10801902140606, 10801902193275/33F23L0976, 33F24B0461, 33F24C0783, 33F24E0775, 33F24G0243, 33F24J0242, 33F24J0416, 33F24M0122, 33F25A0389, 33F25B0076, 33F25E0382, 33F25H0348, 33F26B0257; SAC-00522-X1A/10801902193275/33F24L0536, 33F26B0059; SAC-00820-1A/10801902140637, 10801902193275/33F24B0463, 33F24C0785, 33F24E0777, 33F24F0081, 33F24G0136, 33F24H0059, 33F24H0352, 33F24H0388, 33F24L0057, 33F24M0011, 33F24M0123, 33F25A0134, 33F25B0109, 33F25B0282, 33F25B0646, 33F25C0543, 33F25C0568, 33F25D0094, 33F25D0186, 33F25D0302, 33F25E0364, 33F25F0045, 33F25J0581, 33F25J0980, 33F25K0298, 33F25K0338; SAC-00820-X1A/10801902193275, 10801902140620/33F25C0491, 33F25C0544, 33F25D0073, 33F25E0409, 33F25F0055, 33F25H0801, 33F25J0660, 33F25K0337, 33F25L0193, 33F25M0697, 33F26B0068, 33F26B0702; SAC-01218-1A/10801902199734, 10801902193275/33F24A1699, 33F24D0559, 33F24E0668, 33F24F1031, 33F25A0203, 33F25C0455, 33F25D0580, 33F25J0189, 33F26C0035; SAC-01218-X1A/10801902193275, 10801902199741/33F24J0138, 33F24L0960, 33F25A0294, 33F25B0537, 33F25C0479, 33F25E0768, 33F25H0618, 33F25J0451, 33F26A1374, 33F26B0775; SAC-01220-1A/10801902199758, 10801902193275/33F24C0971, 33F24D0361, 33F24F0986, 33F24L0509, 33F25A0221, 33F25B0481, 33F25C0374, 33F25D0635, 33F25E0711, 33F25G0297, 33F25J0133, 33F26A1362, 33F26B0458, 33F26C0680; SAC-01220-X1A/10801902193275, 10801902140989/33F24J0163, 33F24L0148, 33F25A0194, 33F25B0470, 33F25B0680, 33F25D0636, 33F25E0841, 33F25G0411, 33F25J0259, 33F26A1449, 33F26B0202, 33F26C0168; SAC-01618-1A/10801902199765, 10801902193275/33F24A0983, 33F24A1565, 33F24C0373, 33F24C1010, 33F24D0323, 33F24D0875, 33F24F0992, 33F24K0364, 33F24L0394, 33F24L1126, 33F25A0295, 33F25B0510, 33F25C0250, 33F25D0258, 33F25D0385, 33F25D0581, 33F25E0712, 33F25E0903, 33F25F0231, 33F25G0402, 33F25J0123, 33F25J0340, 33F26A1356, 33F26A1509, 33F26B0941, 33F26D0311; SAC-01618-X1A/10801902193275, 10801902145489/33F24J0144, 33F24L0395, 33F25A0222, 33F25B0511, 33F25D0259, 33F25D0321, 33F25D0458, 33F25E0770, 33F25F0232, 33F25G0264, 33F25G0383, 33F25J0134, 33F25J0452, 33F26A1435, 33F26B0842, 33F26B0939, 33F26B0940; UM-04018/10801902192063, 10801902193275/33F24A0359, 33F24A0360, 33F24A0361, 33F24A1061, 33F24A1062, 33F24B0162, 33F24B0163, 33F24B0164, 33F24C0053, 33F24D0042, 33F24D0043, 33F24H0463, 33F24H0464, 33F24J0466, 33F24K0306, 33F24K0311, 33F24K0543, 33F24L0723, 33F24L0761, 33F25A0608, 33F25C0209, 33F25E0284, 33F25E0297, 33F25E0742, 33F25E1061, 33F25E1069; ASK-04020-ABM/10801902193275, 10801902218947/33F24J0341, 33F24J0551, 33F24L0700, 33F25C0923, 33F25E0117, 33F25J0500, 33F25L0468, 33F26B0995; ASK-04020-BGH/10801902117660, 10801902193275/33F24A0814, 33F24C0142, 33F24D0109, 33F24E0406, 33F24G0404, 33F24J0554, 33F24L0634, 33F25A0507, 33F25C0809, 33F25E0120, 33F25H0064, 33F25J0867, 33F25L0386, 33F25M0890; ASK-04020-LOL/10801902193275, 10801902144765/33F24G0417, 33F24J0566, 33F24K0180, 33F24L0780, 33F25C0993, 33F25H0077, 33F25H0733, 33F25J0670, 33F25L0425, 33F26C0318, 33S24B0254, 33S24C0155; ASK-04020-MHS/20801902117711, 10801902193275/33F24A0380, 33F24A1033, 33F24B0255, 33F24C0157, 33F24D0121, 33F24E0420, 33F24H0476, 33F24J0568, 33F24K0181, 33F25C0990, 33F25E0137, 33F25G0111, 33F25H0078, 33F25J0505, 33F25L0377, 33F26B0526, 33S24A1033, 33S24B0255, 33S24C0157, 33S24D0121, 33X24K0003; ASK-04020-MIB3/10801902193275/33F24L0687, 33F25C0859, 33F25E0981, 33F25J0878, 33F26A0967; ASK-04020-PMC1/10801902193275/33F25C0489; ASK-04020-URMC/10801902117868, 10801902193275/33F24A0142, 33F24A0870, 33F24B0274, 33F24C0173, 33F24D0136, 33F24E0442, 33F24G0436, 33F24L0644, 33F25A0530, 33F25E0151, 33F25H0091, 33F25J0888; ASK-04220-FMH1/10801902193275/33F24K0203, 33F25A0535, 33F25E0158, 33F25J0890; NA-04020-1A/10801902119916, 10801902193275/33F24A1057, 33F24B0153, 33F24C0045, 33F24D0039, 33F24G0549, 33F24J0333, 33F24K0293, 33F24L0678, 33F25A0597, 33F25C0900, 33F25E0267, 33F25E1047, 33F25G0150, 33F25H0174, 33F25H0666, 33F25J0664, 33F25K0403, 33F25L0023, 33F25L0436, 33F25M0936, 33F26B0577; NA-04020-B/10801902193275, 10801902221312/33F24L0072, 33F25A0598, 33F25C0763, 33F25E0268, 33F25E1048, 33F25H0175, 33F25H0667, 33F25J0632, 33F26B0530; NA-04020-C/10801902193275, 10801902221329/33F24L0073, 33F25A0599, 33F25C0926, 33F25E0269, 33F25E1049, 33F25G0151, 33F25H0176, 33F25H0668, 33F26B0529; ASK-04550-NYP/10801902130836, 10801902193275/33F24F0685, 33F24H0144, 33F24K0424, 33F25A0166, 33F25B0170, 33F25B0495, 33F25D0337, 33F25G0355, 33F25H0431, 33F25H0639, 33F26A1367, 33F26A1542, 33F26C0585; ASK-04300-PHP1/10801902143805, 10801902193275/33F24F0619, 33F24H0147, 33F24K0072, 33F24M0047, 33F25C0649, 33F25K0314, 33F25L0029, 33F25M0066; ASK-04301-TJ/20801902114987, 10801902193275/33F24D0733, 33F24F0798, 33F25A0235, 33F25B0516; ASK-04001-VAMC1/10801902158854, 10801902193275/33F24E0400, 33F24G0400, 33F24K0161, 33F25A0502, 33F25E0114, 33F25J0863, 33F25L0387, 33F26B1016; ASK-04020-WBH/10801902117899/33F24C0174, 33F24D0138, 33F24E0445, 33F24G0438, 33F24J0582, 33F24L0793;", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2391-2026%22", "url": "https://recallledger.net/recalls/device-z-2391-2026-description-ref-ra-cath-kit-20-ga-x-1-3-4in-ak-04020-spc-ra-cath-ki/"}, {"id": "fda-device-z-2390-2026", "source": "FDA", "category": "device", "recall_number": "Z-2390-2026", "title": "Description/REF: SAC KIT: 18 GA X 12CM W BIO/SAC-01218-B recall (ARROW INTERNATIONAL, LLC)", "product": "Description/REF: SAC KIT: 18 GA X 12CM W BIO/SAC-01218-B; SAC KIT: 18 GA X 12CM W CHG/SAC-01218-C; SAC KIT: 18 GA X 16CM W BIO/SAC-01618-B", "reason": "Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.", "hazard_level": "Class I", "company": "ARROW INTERNATIONAL, LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-21", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "0", "codes": "REF(Material)/UDI-DI/Lot(Batch): SAC-01218-B/10801902225303/33F26C0515; SAC-01218-C/10801902225273/33F26C0517; SAC-01618-B/10801902225310/33F26C0518", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2390-2026%22", "url": "https://recallledger.net/recalls/device-z-2390-2026-description-ref-sac-kit-18-ga-x-12cm-w-bio-sac-01218-b-sac-kit-18/"}, {"id": "fda-device-z-2389-2026", "source": "FDA", "category": "device", "recall_number": "Z-2389-2026", "title": "Description/REF: SPINAL ANESTHESIA KIT/ASA-24090-SB recall (ARROW INTERNATIONAL, LLC)", "product": "Description/REF: SPINAL ANESTHESIA KIT/ASA-24090-SB; SPINAL ANESTHESIA KIT/ASA-24103-SB; SPINAL ANESTHESIA KIT/ASA-25090-SB; SPINAL ANESTHESIA KIT: 24 GA X 9 CM/ASK-24090-SA; SPINAL ANESTHESIA KIT: 25 GA X 9 CM/ASK-24090-SPH; SPINAL ANESTHESIA KIT/ASK-25090-BIDMC; SPINAL ANESTHESIA KIT/ASK-25090-UF", "reason": "Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.", "hazard_level": "Class I", "company": "ARROW INTERNATIONAL, LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-21", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "79,614", "codes": "REF(Material)/UDI-DI/Lot(Batch): ASA-24090-SB/10801902193275, 10801902201994/33F24G0383, 33F24K0145, 33F24L0550, 33F25A0491, 33F25C0838, 33F25E0094, 33F25H0044, 33F25J0490, 33F25L0444, 33S25E0094; ASA-24103-SB/10801902202007, 10801902193275/33F24E0380, 33F24E0381, 33F24G0274, 33F24K0146, 33F24L0696, 33F25A0492, 33F25C0123, 33F25C0774, 33F25E0095, 33F25G0097, 33F25H0045, 33F25J0491, 33F25L0329, 33F26B0494; ASA-25090-SB/10801902202014, 10801902193275/33F24E0089, 33F24E0090, 33F24G0384, 33F24K0147, 33F24L0545, 33F24L0755, 33F25A0493, 33F25A0621, 33F25B0374, 33F25C0844, 33F25E0097, 33F25G0098, 33F25H0046, 33F25J0850, 33F25K0257; ASK-24090-SA/10801902202281, 10801902193275/33F24D0396, 33F24E0544, 33F24L0589, 33F25C0182, 33F25C0965, 33F25E0228, 33F25H0146, 33F25J0922, 33F26B0573; ASK-24090-SPH/10801902202274, 10801902193275/33F24D0397, 33F24G0505, 33F24K0260, 33F24L0654, 33F25A0575, 33F25C0943, 33F25E1026, 33F25H0753, 33F25K0410, 33F26B0501; ASK-25090-BIDMC/10801902210217/33F24E0546, 33F24E0547, 33F24L0636, 33F25C0183, 33F25C0831, 33F25E0230, 33F25J0923, 33F25L0357; ASK-25090-UF/10801902206692, 10801902193275/33F24E0548, 33F24L0602, 33F25C0806, 33F25E0231, 33F25G0138, 33F25J0557, 33F25M0957;", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2389-2026%22", "url": "https://recallledger.net/recalls/device-z-2389-2026-description-ref-spinal-anesthesia-kit-asa-24090-sb-spinal-anesthesia/"}, {"id": "fda-device-z-2388-2026", "source": "FDA", "category": "device", "recall_number": "Z-2388-2026", "title": "Description/REF: HEMODIALYSIS KIT: 2-LUMEN 12 FR X 20 CM/AK-15122-F recall (ARROW INTERNATIONAL, LLC)", "product": "Description/REF: HEMODIALYSIS KIT: 2-LUMEN 12 FR X 20 CM/AK-15122-F, AHDC KIT: 3L 12 FR X 16 CM/ASK-12123-UOC1, AHDC KIT: 3-L 12 FR X 16 CM/ASK-12123-UPM, AHDC KIT: 3L 12 FR X 20 CM/ASK-15123-UOC1, AHDC KIT: 3-L 12 FR X 20 CM/ASK-15123-UPM, AHDC KIT: 3-L 12 FR X 16 CM/CDC-12123-P1A, AHDC KIT: 3-L 12 FR X 16 CM/CDC-12123-XP1A, AHDC KIT: 3-L 12 FR X 16 CM/CDC-12123-XPCN1A, AHDC KIT: 3-L 12 FR X 16 CM/CDC-12123-XPN1A, AHDC KIT: 3-L 12 FR X 20 CM/CDC-15123-P1A, AHDC KIT: 3-L 12 FR X 20 CM/CDC-15123-XPCN1A, AHDC KIT: 3-L 12 FR X 20 CM/CDC-15123-XPN1A, AHDC KIT: 3-L 12 FR X 25 CM/CDC-16123-XPCN1A, HEMODIALYSIS KIT 2L: 12 FR X 20CM AGB/AK-25122-CDC, HEMODIALYSIS KIT: 2-LUMEN 14 FR X 20 CM/AK-25142-F, HEMODIALYSIS KIT: 2L 12 FR X 6 IN/ASK-22122-MM1, HEMODIALYSIS KIT: 2L 12 FR X 6 IN/ASK-22122-MM2, AHDC KIT: 2L 14 FR X 15 CM/ASK-22142-UOC1, AHDC AGB KIT: 2-L 14 FR X 15 CM/ASK-22142-UPM, HEMODIALYSIS KIT: 2L 14 FR X 20 CM/ASK-25142-UNC1, AHDC KIT: 2L 14 FR X 20 CM/ASK-25142-UOC1, AHDC AGB KIT: 2L 14 FR X 20 CM/ASK-25142-UPM, HEMODIALYSIS KIT 2L: 14 FR X 25 CM AGB/ASK-26142-UNC1, HEMODIALYSIS KIT: 2LUMEN 12 FR X 16 CM/AU-22122-F, HEMODIALYSIS KIT: 2L 12 FR X 16 CM AGB/CDC-22122-1A, AHDC AGB U-BEND KIT: 2-L 12 FR X 16 CM/CDC-22122-XCN1A-U, AHDC AGB KIT: 2-L 12 FR X 16 CM/CDC-22122-XN1A, AHDC AGB U-BEND KIT: 2-L 12 FR X 16 CM/CDC-22122-XN1A-U, HEMODIALYSIS KIT 2L: 14 FR X 15 CM AGB/CDC-22142-1A, HEMODIALYSIS KIT: 2L 14 FR X 15 CM AGB/CDC-22142-XC1A, AHDC AGB KIT: 2-L 14 FR X 15 CM/CDC-22142-XCN1A, AHDC AGB CURVED KIT: 2-L 14 FR X 15 CM/CDC-22142-XCN1A-C, AHDC AGB KIT: 2-L 14 FR X 15 CM/CDC-22142-XN1A, AHDC AGB CURVED KIT: 2-L 14 FR X 15 CM/CDC-22142-XN1A-C, AHDC AGB U-BEND KIT: 2-L 12 FR X 13 CM/CDC-23122-XCN1A-U, AHDC AGB U-BEND KIT: 2-L 12 FR X 13 CM/CDC-23122-XN1A-U, HEMODIALYSIS KIT: 2L 12 FR X 13 CM AGB/CDC-23122-XU1A, HEMODIALYSIS KIT: 2L 12 FR X 20 CM AGB/CDC-25122-1A, HEMODIALYSIS KIT: 2L 12 FR X 20 CM AGB/CDC-25122-X1A, AHDC AGB KIT: 2-L 12 FR X 20 CM/CDC-25122-XCN1A, AHDC AGB U-BEND KIT: 2-L 12 FR X 20 CM/CDC-25122-XCN1A-U, AHDC AGB KIT: 2-L 12 FR X 20 CM/CDC-25122-XN1A, HEMODIALYSIS KIT: 2L 12 FR X 20 CM AGB/CDC-25122-XU1A, HEMODIALYSIS KIT 2L: 14 FR X 20 CM AGB/CDC-25142-1A, HEMODIALYSIS KIT: 2L 14 FR X 20 CM AGB/CDC-25142-XC1A, AHDC AGB KIT: 2-L 14 FR X 20 CM/CDC-25142-XCN1A, AHDC AGB CURVED KIT: 2-L 14 FR X 20 CM/CDC-25142-XCN1A-C, AHDC AGB KIT: 2-L 14 FR X 20 CM/CDC-25142-XN1A, AHDC AGB CURVED KIT: 2-L 14 FR X 20 CM/CDC-25142-XN1A-C, HEMODIALYSIS KIT: 2L 12 FR X 25 CM AGB/CDC-26122-1A, AHDC AGB KIT: 2-L 12 FR X 25 CM/CDC-26122-XCN1A, AHDC AGB KIT: 2-L 12 FR X 25 CM/CDC-26122-XN1A, HEMODIALYSIS KIT 2L: 14 FR X 25 CM AGB/CDC-26142-1A, HEMODIALYSIS KIT: 2L 14 FR X 25 CM AGB/CDC-26142-X1A, AHDC AGB KIT: 2-L 14 FR X 25 CM/CDC-26142-XCN1A, AHDC AGB KIT: 2-L 14 FR X 25 CM/CDC-26142-XN1A, HEMODIALYSIS KIT: 2-LUMEN 12 FR X 20 CM/AK-25122-F, AHDC AGB KIT: 2-L 12 FR X 16 CM/CDC-22122-XCN1A, LBCVC AGB KIT: 3-L 12 FR X 16 CM/CDC-22123-XCN1A, LBCVC AGB KIT: 3-L 12 FR X 20 CM/CDC-25123-XCN1A, LBCVC AGB KIT:3-L 12 FR X 20 CM/CDC-25123-XN1A", "reason": "Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.", "hazard_level": "Class I", "company": "ARROW INTERNATIONAL, LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-21", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "62,719", "codes": "REF(Material)/UDI-DI/Lot(Batch): AK-15122-F/10801902197136, 10801902193275, 10801902168525/33F24E0348, 33F24J0280, 33F24K0119, 33F24L0601, 33F25A0477, 33F25C0908, 33F24A0850; ASK-12123-UOC1/10801902193275/33F25B0430, 33F25D0119; ASK-12123-UPM/10801902193275, 10801902222463/33F25E0535, 33F25G0188, 33F25G0189, 33F26C0333, 33F25D0262; ASK-15123-UOC1/10801902193275/33F25C0378, 33F25D0121; ASK-15123-UPM/10801902193275, 10801902159950/33F25E0718, 33F25H0447, 33F26A1389, 33F24E0649; CDC-12123-P1A/40801902111768, 10801902193275/33F24D0632, 33F24F0758, 33F24L0465, 33F25A0281, 33F25E0794; CDC-12123-XP1A/10801902193275, 30801902111785, 10801902213416/33F25J0723, 33F26A1382, 33F26B0433, 36F25A0007, 36F25B0009, 36F25E0018, 33F24D0299; CDC-12123-XPCN1A/10801902213416, 10801902193275/33F24D0950, 33F24K0417, 33F24L0466, 33F25A0216, 33F25B0667, 33F25D0436, 33F25D0666, 33F25E0693, 33F25G0239, 33F25J0247, 33F26A1556, 33F26B0801, 33F26C0767, 33F25B0668; CDC-12123-XPN1A/10801902193275, 10801902213409/33F25D0554, 33F25G0240, 33F25J0312, 33F26B0214,33F26C0199, 33F25A0181; CDC-15123-P1A/10801902193275/33F25D0437, 33F25H0547,33F25B0613; CDC-15123-XPCN1A/10801902213430, 10801902193275/33F24F0107, 33F24F0998, 33F24K0403, 33F24L0834, 33F25A0283, 33F25B0527, 33F25E0650, 33F25E0745, 33F25F0085, 33F25H0596, 33F25J0314, 33F26A1464, 33F26B0883, 33F25B0669; CDC-15123-XPN1A/0801902193275, 10801902213423, 10801902116793/33F25D0439, 33F25G0238, 33F25H0597, 33F25J0315, 33F26A1468, 33F26B0826, 33F24C0461; CDC-16123-XPCN1A/10801902193275/33F25B0671, 33F25D0440, 33F25E0651, 33F25G0236, 33F25H0529, 33F25J0316, 33F25G0237, AK-25122-CDC/10801902193275/33F24G0370, 33F24K0135, 33F25C0120, 33F25C0969, 33F25E0942, 33F24G0371; AK-25142-F/10801902193275, 70801902123205, 10801902167795/33F25C0863, 33F25E0087, 33F25H0038, 33F25J0846, 33F26B0531, 33F24D0089; ASK-22122-MM1/10801902193275/33F25E0546; ASK-22122-MM2/10801902193275, 10801902221923, 10801902144956/33F25G0172, 33F25L0031, 33F25M0310, 33F26A1652, 33F26B0151, 33F26B0450, 33F24F0854; ASK-22142-UOC1/10801902193275/33F25C0545, 33F25D0122; ASK-22142-UPM/10801902193275, 10801902222487, 10801902202281/33F25D0594, 33F25F0116, 33F25G0187, 33F26A1390, 33F26B0205, 33F24D0396; ASK-25142-UNC1/10801902193275/33F25C0655, 33F24K0561; ASK-25142-UOC1/10801902193275/33F25B0362, 33F25D0123; ASK-25142-UPM/10801902193275/33F25E0595, 33F25H0446, 33F25J0381, 33F26A1446, 33F25J0092; ASK-26142-UNC1/10801902193275/33F25B0427, 33F25K0058; AU-22122-F/10801902193275/33F24K0269, 33F25A0584, 33F25C0862, 33F25E0245, 33F25J0567; CDC-22122-1A/20801902123484, 10801902193275/, CDC-22122-XCN1A-U/33F24F0996, 33F24L0374, 33F25C0461; CDC-22122-XN1A/10801902193275/33F25C0239, 33F25E0875, 33F25J0419; CDC-22122-XN1A-U/10801902193275, 10801902213621/33F25A0309, 33F25E0876, 33F26B0217; CDC-22142-1A/50801902123515, 10801902193275/33F24D0928, 33F24F0103, 33F24F0896, 33F24L0111, 33F24L0955, 33F25B0500, 33F25D0447, 33F25E0654, 33F25G0278, 33F25H0577, 33F25J0319; CDC-22142-XC1A/10801902193275/33F25A0284, 33F25J0180; CDC-22142-XCN1A/10801902193275, 10801902213539/33F25A0285, 33F25B0529, 33F25D0449, 33F25E0655, 33F25E0818, 33F25F0214, 33F25G0233, 33F26A1477, 33F26B0898, 33R25J0455; CDC-22142-XCN1A-C/10801902193275/33F24L0473, 33F25B0615, 33F25F0213; CDC-22142-XN1A/10801902193275, 10801902213522/33F25C0240, 33F25E0578, 33F25F0215, 33F25H0528, 33F25J0321, 33F26A1383, 33F26B0215, 33F26C0016; CDC-22142-XN1A-C/10801902193275/33F25B0485, 33F25E0879; CDC-23122-XCN1A-U/10801902193275/33F24L0279, 33F25D0492; CDC-23122-XN1A-U/10801902193275/33F25E0579; CDC-23122-XU1A/10801902193275/33F25D0493, 33F25H0432, 33F25J0248; CDC-25122-1A/10801902193275/33F25B0619, 33F25E0881; CDC-25122-X1A/10801902193275/33F25E0882, 33F25J0422; CDC-25122-XCN1A/10801902213492, 10801902193275/33F24F0929, 33F25C0242, 33F25D0498, 33F25E0883, 33F25G0234, 33F26B0439, 33F26C0214; CDC-25122-XCN1A-U/10801902193275/33F24L1041, 33F25B0620, 33F25F0121, 33F25G0226; CDC-25122-XN1A/10801902193275, 10801902213485/33F25C0243, 33F25E0884, 33F25K0183, 33R25E0884; CDC-25122-XU1A/10801902193275/33F25B0621, 33F25E0886, 33F25H0568; CDC-25142-1A/50801902123584, 10801902193275/33F24F0837, 33F24K0457, 33F24L0113, 33F24L1031, 33F25B0622, 33F25D0503, 33F25E0889, 33F25F0106, 33F25J0127; CDC-25142-XC1A/10801902193275/33F25B0467; CDC-25142-XCN1A/10801902193275, 10801902213553/33F25A0312, 33F25E0657, 33F25E0821, 33F25G0231, 33F25H0527, 33F25J0428, 33F26B0452, 33F26C0133; CDC-25142-XCN1A-C/10801902193275/33F24L0377, 33F25D0238; CDC-25142-XN1A/10801902193275, 10801902213546/33F25B0624, 33F25D0504, 33F25E0823, 33F25G0232, 33F26B0437; CDC-25142-XN1A-C/10801902193275/33F24L0485, 33F25B0676; CDC-26122-1A/60801902123611, 10801902193275/33F24F0084, 33F24K0475, 33F25G0389; CDC-26122-XCN1A/10801902213515, 10801902193275/33F24F1028, 33F24L0117, 33F25D0308, 33F25D0557, 33F25F0219; CDC-26122-XN1A/10801902193275/33F25E0451; CDC-26142-1A/10801902193275/33F24L0488, 33F24L1025, 33F25C0368, 33F25E0891, 33F25H0406, 33F25J0116; CDC-26142-X1A/10801902193275/33F25D0558, 33F25E0892; CDC-26142-XCN1A/10801902193275, 10801902213577/33F24L0941, 33F25B0530, 33F25D0507, 33F25E0699, 33F25H0525, 33F26B0396, 33F26B0895, 33F26C0780; CDC-26142-XN1A/10801902193275, 10801902213560/33F24L0927, 33F25E0580, 33F25H0526, 33F26B0393; AK-25122-F/ CDC-22122-XCN1A/10801902193275/33F24G0371, 33F24L0742, 33F25C0822, 33F25E0084, 33F25J0483, 33F25L0400; CDC-22123-XCN1A/10801902213591, 10801902193275/33F24D0842,33F24F1018, 33F24L0110, 33F25C0205, 33F25D0613, 33F25E0878, 33F26B0455; CDC-25123-XCN1A/10801902213614, 10801902193275/33F24D0818, 33F24L0483, 33F25C0244, 33F25D0502, 33F25E0888, 33F25G0228, 33F25J0425, 33F26B0395, 33F26B0894; CDC-25123-XN1A/10801902193275/33F25C0332, 33F25G0229", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2388-2026%22", "url": "https://recallledger.net/recalls/device-z-2388-2026-description-ref-hemodialysis-kit-2-lumen-12-fr-x-20-cm-ak-15122-f-a/"}, {"id": "fda-device-z-2387-2026", "source": "FDA", "category": "device", "recall_number": "Z-2387-2026", "title": "Description/REF: PI MIDLINE 2L: 5FR X 20CM/CDC-32052-MPKC recall (ARROW INTERNATIONAL, LLC)", "product": "Description/REF: PI MIDLINE 2L: 5FR X 20CM/CDC-32052-MPKC", "reason": "Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.", "hazard_level": "Class I", "company": "ARROW INTERNATIONAL, LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-21", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "90", "codes": "REF(Material)/UDI-DI/Lot(Batch): CDC-32052-MPKC/10801902193275/33F24L0236", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2387-2026%22", "url": "https://recallledger.net/recalls/device-z-2387-2026-description-ref-pi-midline-2l-5fr-x-20cm-cdc-32052-mpkc/"}, {"id": "fda-device-z-2386-2026", "source": "FDA", "category": "device", "recall_number": "Z-2386-2026", "title": "Description/REF: PARACENTESIS KIT/ASK-00376-JHH recall (ARROW INTERNATIONAL, LLC)", "product": "Description/REF: PARACENTESIS KIT/ASK-00376-JHH", "reason": "Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.", "hazard_level": "Class I", "company": "ARROW INTERNATIONAL, LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-21", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "180", "codes": "REF(Material)/UDI-DI/Lot(Batch): ASK-00376-JHH/10801902193275/33F25G0629, 33F24K0592", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2386-2026%22", "url": "https://recallledger.net/recalls/device-z-2386-2026-description-ref-paracentesis-kit-ask-00376-jhh/"}, {"id": "fda-device-z-2385-2026", "source": "FDA", "category": "device", "recall_number": "Z-2385-2026", "title": "Description/REF: ACCESS TRAY/GU-04020 recall (ARROW INTERNATIONAL, LLC)", "product": "Description/REF: ACCESS TRAY/GU-04020; PSI KIT: 8.5 FR/AK-09803-CDC; PSI KIT: 9 FR/AK-09903-CDC; PSI KIT: 8.5 FR X 4 IN (10 CM)/ASK-09810-PCMH1; PSI KIT: 9 FR X 10 CM/ASK-09903-KH; PSI KIT: 9 FR X 10 CM/ASK-09903-PHP1; PSI KIT: 9 FR X 4 IN (10 CM)/ASK-09903-UPA; PSI KIT: 9 FR X 4 1/8 IN (10 CM)/ASK-09903-YNH; PSI KIT: 9 FR X 4 1/8 IN (10 CM)/ASK-09907-SL; PSI KIT: 8.5 FR X 4-1/8IN (10 CM)/NA-09803-CDC; PSI KIT: 9 FR X 4-1/8IN (10 CM)/NA-09903-CDC; PSI KIT: 9 FR X 4 IN (10 CM)/ASK-09903-ECL4; PSI KIT: 9 FR X 4 1/8 IN (10 CM)/ASK-09903-MGH3; MULTI-LUMEN/PSI KIT/AK-11142-SPCS; MAC KIT: 2-L 9 FR DISTAL X 11.5 CM/CDC-11242-1A; MULTI-LUMEN/PSI KIT/AK-11142-D; MULTILUMEN/PSI KIT: 9 FR X 4 IN (10 CM)/ASK-11142-MGH4; MULTI-LUMEN/PSI KIT/NA-11242-CDC; MULTI-LUMEN/PSI KIT/AK-21142-SK; MAC KIT: 2L 9 FR DISTAL X 10 CM AGB/ASK-21142-LMDTG; MULTI LUMEN/PSI KIT: 9 FR X 4 IN (10 CM)/ASK-21142-RH; MULTILUMEN/PSI KIT 9 FR X 11.5 CM/ASK-21242-IMC; MAC KIT: 2L 9 FR DISTAL X 11.5 CM AGB/ASK-21242-LMDTG; MAC KIT: 2L 9 FR DISTAL X 11.5 CM/ASK-21242-UMD; MAC KIT: 2L 9 FR DISTAL X 11.5 CM/ASK-21242-UU3; MAC KIT: 2L 9 FR DISTAL X 11.5 CM/ASK-21242-VCU; MAC KIT: 2L 9 FR DISTAL X 11.5 CM AGB/CDC-21242-1A; MAC KIT: 2L 9 FR DISTAL X 11.5 CM AGB/CDC-21242-X1A; MULTI-LUMEN/PSI KIT/AK-21242-CDC; 2L MAC KIT: 9 FR DISTAL X 4 IN (10 CM)/ASK-21142-FH4; MULTI LUMEN/PSI KIT: 9 FR X 4 IN (10 CM)/ASK-21142-GH1; 2L MAC KIT: 9 FR DISTAL X 4 IN (10 CM)/ASK-21142-SUU; 2-L MAC KIT: 9 FR DISTAL X 4 IN (10 CM)/ASK-21142-UPMC4; MAC KIT: 2L 9 FR DISTAL X 11.5 CM/ASK-21242-UKL; MAC KIT: 2L 9 FR DISTAL X 11.5 CM/ASK-21242-UMF; MULTILUMEN/PSI KIT: 9 FR X 4 1/2 IN/ASK-21242-UR1; PSI KIT: 8.5 FR/AK-29803-CDC; PSI KIT: 9 FR/AK-29903-CDC; PSI KIT: 9 FR/AK-29907-CDC; PSI KIT: 8.5 FR X 4IN (10 CM)/ASK-09804-UN1; PSI KIT: 9 FR/ASK-09903-UM; PSI KIT: 8.5 FR X 10 CM ANTIMICROBIAL/ASK-29803-LMDT; PSI KIT: 8.5 FR X 10 CM ANTIMICROBIAL/ASK-29803-LMDTG; PSI KIT: 9 FR X 4 1/8 (10 CM)/ASK-29903-BID1; PSI KIT: 9 FR X 10 CM ANTIMICROBIAL/ASK-29903-LMDTG; PSI KIT: 9 FR X 10 CM ANTIMICROBIAL/ASK-29903-UMD; PSI KIT: 9 FR X 4 IN (10 CM)/ASK-29903-UR1; PSI KIT: 8.5 FR X 10 CM ANTIMICROBIAL/CDC-29803-X1A; PSI KIT: 8.5 FR X 10 CM/ASK-29803-ECL; PSI KIT: 8.5 FR X 4 IN (10 CM)/ASK-29803-UPM3; PSI KIT: 9 FR X 10 CM/ASK-29903-ECL; PSI KIT: 9FR X 4IN (10 CM) ANTIMICROBIAL/ASK-29903-UPM3; PSI KIT: 9 FR X 4 IN (10 CM)/ASK-09907-TG1", "reason": "Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.", "hazard_level": "Class I", "company": "ARROW INTERNATIONAL, LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-21", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "426,041", "codes": "REF(Material)/UDI-DI/Lot(Batch): GU-04020/30801902118807, 10801902193275, 30801902118807, 30801902118807/33F24C0753, 33F24E0736, 33F24G0154, 33F24G0648, 33F24H0377, 33F25A0059, 33F25A0072, 33F25A0395, 33F25F0260, 33F25G0736, 33F25H0298, 33F25J0603, 33F26B0084, 33F26B0314, 33F26C0578, 33F24D0036; AK-09803-CDC/20801902121756, 10801902193275, 10801902117417/33F24B0126, 33F24B0127, 33F24C0021, 33F24D0021, 33F24E0072, 33F24G0338, 33F24G0587, 33F24J0506, 33F24K0105, 33F24L0722, 33F25A0468, 33F25C0107, 33F25C0953, 33F25E0054, 33F25E0921, 33F25G0086, 33F25H0023, 33F25J0828, 33F25K0255, 33F25K0364, 33F25L0328, 33F24A0239; AK-09903-CDC/10801902117417, 10801902193275, 20801902121916/33F24A0356, 33F24B0128, 33F24B0129,33F24C0022, 33F24D0022, 33F24E0074, 33F24E0075, 33F24G0340, 33F24G0588, 33F24J0507, 33F24K0107, 33F24L0676, 33F24L0759, 33F25A0470, 33F25C0108, 33F25C0730, 33F25E0056, 33F25E0923, 33F25H0025, 33F25J0471, 33F25K0031, 33F25L0237, 33F25M0920, 33F26A1053, 33F24A0386; ASK-09810-PCMH1/10801902193275/33F25K0051, 33F24J0109; ASK-09903-KH/10801902119350, 10801902193275/33F24D0713, 33F24K0385, 33F24L1060, 33F25D0340, 33F25E0778, 33F25H0567, 33F25M0163, 33F26A1407, 33F25E1184; ASK-09903-PHP1/10801902193275, 10801902115222/33F24J0115, 33F25H0497, 33F26A0410, 33F24F0625; ASK-09903-UPA/10801902193275, 10801902118193/33F24K0387, 33F24L0855, 33F24A0787; ASK-09903-YNH/10801902118193, 10801902193275, 10801902118209/33F24E0527, 33F24H0478, 33F24L0682, 33F25H0135, 33F25J0915, 33F24A0110; ASK-09907-SL/10801902118209, 10801902193275/33F24D0053, 33F24D0967, 33F24G0265, 33F25E0215, 33F25E0454, 33F25G0680, 33F25J0551, 33F25K0328, 33F25L0206, 33F26C0312, 33F25B0188; NA-09803-CDC/10801902119930, 10801902193275, 10801902119947/33F24C0756, 33F24E0739, 33F25A0342, 33F25J0615, 33F26B0028, 33F24A1327; NA-09903-CDC/10801902119947, 10801902193275, 10801902119954/33F24E0740, 33F24H0381, 33F24J0199, 33F24J0361, 33F24L0020, 33F25B0278, 33F25C0551, 33F25E0340, 33F25E0400, 33F25E0468, 33F25F0419, 33F25H0708, 33F26A1655, 33F26B0023, 33F24A0113; ASK-09903-ECL4/10801902193275, 10801902224344/33F26A1582, 33F26B0399, 33F25E0534; ASK-09903-MGH3/10801902193275, 10801902189841, 10801902212006/33F25C0264, 33F25G0338, 33F25J0360, 33F25K0130, 33F26B0126, 33F26C0004, 33F24D0780; AK-11142-SPCS/10801902196412, 10801902193275, 60801902123093/33F24A0382, 33F24A1019, 33F24C0024, 33F24E0078, 33F24E0154, 33F24G0343, 33F24J0510, 33F24K0110, 33F24L0673, 33F25A0472, 33F25C0381, 33F25C0389, 33F25C0952, 33F25E0059, 33F25H0027, 33F25J0831, 33F25K0302, 33F25L0365, 33F26B0514, 33S24J0510, 33F24D0075; CDC-11242-1A/60801902116736, 10801902193275, 40801902111768/33F24D0431, 33F24E0213, 33F24F0140, 33F24F0220, 33F24G0103, 33F24H0392, 33F24H0425, 33F24H0450, 33F24L0011, 33F25B0018, 33F25B0096, 33F25D0705, 33F25E1120, 33F25F0024, 33F25F0414, 33F25G0043, 33F25G0486, 33F25J0016, 33F25J0992, 33F25K0308, 33F25M0481, 33F24C1001; AK-11142-D/20801902121916, 10801902193275, 10801902196412/33F24A1018, 33F24C0023,33F24E0077, 33F24G0342,33F24J0509, 33F24K0109, 33F24L0615, 33F25A0471, 33F25C0842, 33F25E0058, 33F25G0088, 33F25J0472, 33F25K0301, 33F25L0467, 33F26B0593, 33F26B0958, 33F24A0252; ASK-11142-MGH4/10801902193275, 10801902189865, 10801902182545/33F25D0466, 33F25F0113, 33F25L0130, 33F25M0398, 33F26A1539, 33F26B0680, 33F24D0736; NA-11242-CDC/10801902119954, 10801902193275, 10801902119978/33F24A0817, 33F24A1218, 33F24B0399, 33F24C0270, 33F24G0554, 33F24J0663, 33F24L0743, 33F25C0197, 33F25C0870, 33F25E0273, 33F25H0179, 33F25H0761, 33F25L0419, 33F26B0562, 33F24C0271; AK-21142-SK/10801902193275, 30801902122248, 30801902122255/33F24G0356, 33F24G0589, 33F24J0520, 33F24K0122, 33F24L0670, 33F25A0480, 33F25C0720, 33F25E0071, 33F25H0030, 33F25J0837, 33F25L0473, 33F25M0964, 33F26A1097, 33F26B0956, 33R24L0670, 33F24D0023; ASK-21142-LMDTG/10801902193275/33F25K0417, 33F25F0007; ASK-21142-RH/10801902193275/10801902129953/33F24J0108, 33F24L0165, 33F24M0172, 33F25B0422, 33F25E1172, 33F25H0776, 33F25K0424, 33F26C0337, 33F25A0245; ASK-21242-IMC/10801902193275, 10801902118407/33F24G0500, 33F24J0631, 33F24K0255, 33F24L0609, 33F25A0572, 33F25E0223, 33F25H0142, 33F25J0921, 33F26B0543, 33F25C0696; ASK-21242-LMDTG/10801902193275, 10801902220827/33F25G0202, 33F25H0414, 33F25K0382, 33F25M0130, 33F26C0378, 33F24H0123; ASK-21242-UMD/10801902193275/33F24K0476, 33F24L0315, 33F25B0196, 33F25C0279, 33F25D0476, 33F25H0492, 33F25J0378, 33F25M0150, 33F26A1365, 33F25B0551; ASK-21242-UU3/10801902193275/33F24G0503, 33F24L0652, 33F25C0181, 33F25E0226, 33F25H0144, 33F25J0556, 33F24K0077; ASK-21242-VCU/10801902193275, 10801902112962/33F24K0694, 33F25G0171, 33F25H0495, 33F25J0379, 33F26C0494, 33F25C0439; CDC-21242-1A/50801902116821, 10801902193275/33F24D0486, 33F24D0981, 33F24E0227, 33F24F0175, 33F24G0104, 33F24H0296, 33F24H0305, 33F24H0331, 33F24H0357, 33F24H0393, 33F24H0427, 33F24M0019, 33F24M0055, 33F25A0131, 33F25A0367, 33F25B0019, 33F25C0511, 33F25D0706, 33F25E0417, 33F25E1122, 33F25F0416, 33F25G0066, 33F25G0476, 33F25G0711, 33F25H0852, 33F25J0964, 33F25K0352, 33F25L0229, 33F26A1614, 33F26A1624, 33F26A1649, 33F24H0332; CDC-21242-X1A/10801902193275, 30801902116834, 10801902196511/33F25J0291, 33F25J0672, 33F25J0678, 33F25J0690, 33F25J0700, 33F25J0708, 33F25J0724, 33F25L0067, 33F26A1616, 33F26A1625, 33F26B0642, 36F25B0014, 36F25E0020, 36F25G0029, 36F25H0016, 36F25J0005, 33F24C0518; AK-21242-CDC/30801902122255, 10801902193275, 30801902122262/33F24E0082, 33F24E0083, 33F24J0521, 33F24K0123, 33F24L0618, 33F25A0481, 33F25C0946, 33F25E0072, 33F25H0031, 33F25K0037, 33F25K0414, 33F25L0372, 33F26B0520, 33F26C0626, 33F24E0352; ASK-21142-FH4/10801902193275/33F24L0683; ASK-21142-GH1/10801902193275/33F25C0180, 33F25E1023, 33F25H0141, 33F25H0752, 33F25J0920, 33F25L0455, 33F25B0276; ASK-21142-SUU/10801902193275/33F25J0096, 33F25C0275; ASK-21142-UPMC4/10801902193275/33F25A0247; ASK-21242-UKL/10801902114065, 10801902193275, 10801902136487/33F24F0710, 33F24K0467, 33F24L0314, 33F25B0195, 33F25C0278, 33F25D0475, 33F25G0412, 33F25J0149, 33F25M0202, 33F26A1551, 33F26C0010, 33F26C0759, 33F24F0849; ASK-21242-UMF/10801902193275, 10801902129502/33F25D0477, 33F25H0487, 33F25J0150, 33F25K0096, 33F24D0715; ASK-21242-UR1/10801902193275, 10801902119435, 10801902118902/33F25E0225, 33F25J0555, 33F25L0427, 33F25M0928, 33F26C0261, 33F24E0542; AK-29803-CDC/10801902193275, 20801902117506/33F24G0378, 33F24J0283, 33F24J0533, 33F24K0141, 33F24L0620, 33F25A0488, 33F25C0901, 33F25E0090, 33F25G0095, 33F25H0039, 33F25J0487, 33F25L0389, 33F25M0893, 33F26A1021, 33F26B0537, 33F26C0262, 33F24G0379; AK-29903-CDC/10801902193275, 10801902117516, 10801902117523/33F24J0345, 33F24J0534, 33F24K0142,33F24L0672, 33F25A0489, 33F25C0904, 33F25E0091, 33F25G0096, 33F25H0040, 33F25J0488, 33F25L0382, 33F25M0889, 33F26B0533, 33F24D0091; AK-29907-CDC/10801902117523, 10801902193275/33F24E0377, 33F24J0535, 33F24L0606, 33F25C0122, 33F25C0854, 33F25E0092, 33F25H0041, 33F25J0848, 33F26B0503, 33F25A0146; ASK-09804-UN1/10801902193275, 10801902145847/33F25H0485, 33F26A0248, 33F24B0018; ASK-09903-UM/10801902193275, 10801902118186/33F25B0432, 33F25F0361, 33F25L0136, 33F24D0545; ASK-29803-LMDT/10801902193275, 10801902220810/33F25H0367, 33F25J0153, 33F25K0258, 33F25K0418, 33F26A1354, 33F26C0357, 33F25G0464; ASK-29803-LMDTG/10801902193275, 10801902220858/33F25H0413, 33F25H0585, 33F25K0207, 33F25K0419, 33F25M0198, 33F25M0440, 33F26C0170, 33F24G0607; ASK-29903-BID1/10801902193275/33F25K0066, 33F26A0251, 33F24H0139; ASK-29903-LMDTG/10801902193275, 10801902220735/33F25L0025, 33F25M0338, 33F26C0021, 33F24H0124; ASK-29903-UMD/10801902193275/33F25C0583, 33F26A0409, 33F24K0402; ASK-29903-UR1/10801902193275/33F25J0796, 33F24J0107; CDC-29803-X1A/10801902193275, 30801902117022, 10801902193114/33F25F0334, 33F25H0878, 33F25J0292, 33F25K0016, 33F25K0315, 33F25M0088, 33F26A1415, 33F26B0473, 36F25E0019, 36F25G0020, 36F25H0013, 33F24E0214; ASK-29803-ECL/10801902193275, 10801902200478/33F26A1576, 33F24D0625; ASK-29803-UPM3/10801902193275/33F25B0236; ASK-29903-ECL/10801902193275/33F26A1580, 33F25D0235; ASK-29903-UPM3/10801902193275/33F25J0558; ASK-09907-TG1/10801902118216/33F24D1025", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2385-2026%22", "url": "https://recallledger.net/recalls/device-z-2385-2026-description-ref-access-tray-gu-04020-psi-kit-8-5-fr-ak-09803-cdc-p/"}, {"id": "fda-device-z-2384-2026", "source": "FDA", "category": "device", "recall_number": "Z-2384-2026", "title": "Description/REF: ACCESS TRAY/ASK-04001-JHH recall (ARROW INTERNATIONAL, LLC)", "product": "Description/REF: ACCESS TRAY/ASK-04001-JHH; ACCESS TRAY/ASK-04001-LMDTG; PI CVC KIT: 3 LUMEN 7 FR X 6 IN (16 CM)/ASK-12703-PSPH1; 3L CVC KIT: 7 FR X 16 CM/ASK-12703-WMC2; MULTILUMEN PI CVC KIT: 3L 7 FR X 20CM/ASK-15703-LMDT1; MULTILUMEN PI CVC KIT: 3L 7 FR X 20CM/ASK-15703-LMDTG1; MULTILUMEN PI CVC KIT: 3L 7 FR X 8 IN/ASK-15703-PVH; 1L CVC KIT: 16 GA X 8 IN (20CM)/ASK-24301-JHH1; CVC KIT: 16 GA X 16 CM/CDC-24306-1A; CVC KIT: 3-L 7 FR X 30 CM ANTIMICROBIAL/CDC-24703-X1A; LBCVC KIT: 3L 12 FR X 20 CM AGB/CDC-25123-1A; CVC KIT: 2L 8 FR X 6IN (16 CM)/ASK-42802-ECL3; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-ACH; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-BJC1; MULTI LUMEN PI CVC KIT: 3L 7 FR X 16 CM/ASK-42703-DU1; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-EMC; MULTI LUMEN PI CVC KIT: 3L 7 FR X 6IN/ASK-42703-LMDT1; MULTI LUMEN PI CVC KIT: 3L 7 FR X 6 IN/ASK-42703-LMDTG1; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-MCY1; MULTILUMEN PI CVC KIT: 3L 7 FR X 6 IN/ASK-42703-NS1; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-PAGP1; PI CVC KIT: 3L 7 FR X 6 IN (16 CM)/ASK-42703-PAM1; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-PAMC2; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-PAU1; MULTI LUMEN PI CVC KIT: 3L 7 FR X 16/ASK-42703-PB1; PI CVC KIT: 3L 7 FR X 16CM AGB+/ASK-42703-PBSWH2; MULTI LUMEN PI CVC KIT: 3L 7 FR X 16 IN/ASK-42703-PCAM1; MULTILUMEN PI CVC KIT: 3L 7 FR X 16 CM/ASK-42703-PCSJ2; MULTI LUMEN PI CVC KIT: 3L 7 FR X 6 IN/ASK-42703-PECL2; MULTI LUMEN PI CVC KIT: 3L 7 FR X 6 IN/ASK-42703-PGM4; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-PHHN1; MULTI LUMEN CVC KIT: 3L 7 FR X 6 IN/ASK-42703-PLC; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-PMEM; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-PMHC1; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-PNHS1; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-POHU2; MULTILUMEN PI CVC KIT: 3L 7 FR X 6/ASK-42703-POSU2; MULTILUMEN CVC KIT 7 FR X 6 IN (16 CM)/ASK-42703-PTJH; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-PUCH2; PI CVC KIT: 3L 7 FR X 6 IN (16 CM) AGB+/ASK-42703-PUCI1; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-PUHC2; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-PUMH; MULTI-LUMEN PI CVC KIT: 3-L 7 FR/ASK-42703-PUPM1; MULTI LUMEN PI CVC KIT: 3L 7 FR X 6 IN/ASK-42703-SHUF2; MULTI LUMEN PI CVC KIT: 3L 7 FR/ASK-42703-SL1; CVC KIT: 3 LUMEN 7 FR X 6 IN (16 CM)/ASK-42703-UMC; PI CVC KIT: 3L 7 FR X 6 IN (16 CM) AGB+/ASK-42703-WHH; CVC/PSI KIT: 2 LUMEN 8 FR X 6 IN/ASK-42802-CHM; CVC KIT: 2L 8 FR X 16 CM/ASK-42802-LMDT1; PI CATHETER 2L: 8FR X 16CM AGB+/ASK-42802-MCY1; PI CVC KIT: 2L 8FR X 16CM AGB+/ASK-42802-PBSWH2; MULTILUMEN CVC KIT: 2L 8 FR X 6/ASK-42802-POSU2; PI CVC KIT: 2L 8 FR X 16 CM AGB+/ASK-42802-PUNCC2; PI CVC KIT: 2-L 8 FR/ASK-42802-PUPM1; PI CVC KIT: 2L 8 FR/ASK-42802-TGH1; PI CVC KIT: 4L 8.5 FR X 16 CM AGB+/ASK-42854-BJC1; CVC KIT: 4L 8.5 FR X (16CM) AGB+/ASK-42854-PBMH; PI CVC KIT: 4L 8.5FR X 16CM AGB+/ASK-42854-PMM; PI CVC KIT: 4L 8.5 FR X 16 CM AGB+/ASK-42854-PUCH2; PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-ACH; 3L CVC KIT: 7 FR X 20 CM AGB+/ASK-45703-ARM; PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-BJC1; PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-BLH; MULTI LUMEN PI CVC KIT: 3L 7 FR X 20 CM/ASK-45703-DU1; PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-HHC4; PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-LMDT1; PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-LMDTG1; PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-MCY1; PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-NO; PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-NS1; MULTI LUMEN PI CVC KIT: 3L 7 FR X 8 IN/ASK-45703-PADV1; PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-PAGP1; MULTI LUMEN CVC KIT: 3L 7 FR X 8 IN/ASK-45703-PAMC1; MULTI LUMEN CVC KIT: 3L 7 FR X 8 IN/ASK-45703-PAU1; PI CVC KIT: 3L 7FR X 20CM AGB+/ASK-45703-PBSWH2; PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-PCAM1; MULTILUMEN PI CVC KIT: 3L 7 FR X 20 CM/ASK-45703-PCSJ2; PI CVC KIT: 3L 7 FR X 8 IN (20 CM) AGB+/ASK-45703-PDM1; MULTI LUMEN PI CVC KIT: 3L 7 FR X 20 CM/ASK-45703-PECL2; MULTI LUMEN PI CVC KIT: 3L 7 FR X 8 IN/A", "reason": "Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.", "hazard_level": "Class I", "company": "ARROW INTERNATIONAL, LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-21", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "1,061,069", "codes": "REF(Material)/UDI-DI/Lot(Batch): ASK-04001-JHH/10801902193275/33F24K0748, 33F26A1669, 33F25G0558; ASK-04001-LMDTG/10801902193275, 10801902218442/33F26A0405, 33F24E0333; ASK-12703-PSPH1/10801902214338, 10801902193275, 10801902214338/33F24F0787, 33F24L0304, 33F25A0242, 33F25C0268, 33F25D0470, 33F25E0537, 33F25E0854, 33F25J0365, 33F25M0247, 33F26A1555, 33F26B0855, 33F26C0742, 33F24K0672; ASK-12703-WMC2/10801902193275/33F24K0493, 33F24L0305, 33F25B0156, 33F25E0593, 33F25H0483, 33F25J0367, 33F25M0218, 33F24K0545; ASK-15703-LMDT1/10801902193275/33F24J0164, 33F24L0307, 33F25B0192, 33F25C0230; ASK-15703-LMDTG1/10801902193275/33F25D0537, 33F25E0670, 33F25G0295, 33F25J0146, 33F25K0093, 33F25M0138, 33F26B0131, 33F25E0312; ASK-15703-PVH/10801902133226, 10801902193275, 10801902210217/33F24D0809, 33F24F0669, 33F24K0462, 33F24L0226, 33F25A0167, 33F25B0193, 33F25B0547, 33F25D0265, 33F25D0653, 33F25G0169, 33F25G0404, 33F25J0369, 33F26A1459, 33F24M0270; ASK-24301-JHH1/10801902193275, 10801902214819, 10801902210217/33F25A0170, 33F25B0552, 33F25E0547, 33F25G0222, 33F25L0056, 33F26B0421, 33F24E0546; CDC-24306-1A/30801902116919, 10801902193275, 30801902116919/33F24D0786, 33F24E0620, 33F24F0926, 33F24K0446, 33F24L0990, 33F25A0310, 33F25D0495, 33F25E0880, 33F25J0323, 33F26B0377, 33F26C0693, 33F24L1111; CDC-24703-X1A/10801902193275/33F25D0497, 33F25E0748, 33F25G0318, 33F25H0570, 33F25J0325, 33F26A1563, 33F25B0619; CDC-25123-1A/10801902193275, 10801902191622/33F24H0012, 33F24L0481, 33F25C0445, 33F25D0500, 33F25F0382, 33F25G0258, 33F26A1560, 33F26B0394, 33F25B0675; ASK-42802-ECL3/10801902193275/33F25E0567, 33F25F0128, 33F25H0464, 33F25J0286, 33F26A1399; ASK-42703-ACH/10801902193275, 30801902119514/33F24L0327, 33F24L1064, 33F25C0292, 33F25E0675, 33F25H0420, 33F25J0267, 33F25L0122, 33F25M0091, 33F26A1505, 33F24D0032; ASK-42703-BJC1/10801902193275, 10801902202519/33F24K0500, 33F24L0328, 33F25B0556, 33F25G0173, 33F25J0268, 33F26A1513, 33F26B0767, 33F25C0744; ASK-42703-DU1/10801902193275, 1080190216099/33F25B0141, 33F25C0232, 33F25E0786, 33F25J0105, 33F25M0014, 33F26C0342, 33F24F0060; ASK-42703-EMC/10801902160475, 10801902118421/33F24F0881, 33F25A0214, 33F25C0293, 33F25D0596, 33F25H0632, 33F25M0115, 33F26C0343, 33F24F0132; ASK-42703-LMDT1/10801902205657, 10801902193275/33F24F0688, 33F24J0157, 33F24L0228, 33F24L0329, 33F24L1096, 33F25A0252, 33F25B0557, 33F25C0352, 33F25E0557, 33F25E0722, 33F25G0400, 33F25K0139, 33F26A1370, 33F26B0210, 33F25C0294; ASK-42703-LMDTG1/10801902193275, 10801902205695, 10801902220896/33F25E0558, 33F25E0860, 33F25G0271, 33F25G0399, 33F25H0419, 33F26B0387, 33F24G0070; ASK-42703-MCY1/10801902193275, 0801902220896/33F24H0198, 33F24K0425, 33F25A0198, 33F25B0651, 33F25C0353, 33F25D0405, 33F25E0676, 33F25H0452, 33F25J0220, 33F25M0183, 33F26A1479, 33F26B0863, 33F25H0409; ASK-42703-NS1/10801902193275, 10801902216479/33F25A0300, 33F25B0652, 33F25C0375, 33F25E0723, 33F25H0459, 33F25J0221, 33F26A1579, 33F26B0825, 33F25C0354; ASK-42703-PAGP1/10801902193275, 10801902158717, 10801902136685/33F25D0406, 33F25E0560, 33F25E0790, 33F25H0560, 33F25L0114, 33F26A1353, 33F26A1506, 33F26B0751, 33F24D0181; ASK-42703-PAM1/10801902136685, 10801902193275/33F24E0310, 33F24L0895, 33F25A0256, 33F25B0496, 33F25C0477; ASK-42703-PAMC2/10801902193275, 10801902217131/33F25F0188, 33F25J0270, 33F26C0161, 33F24K0400; ASK-42703-PAU1/10801902193275/33F24L0414, 33F25B0143, 33F25C0474, 33F25G0397, 33F25M0313, 33F26A1349, 33F25B0232; ASK-42703-PB1/10801902193275, 10801902220377/33F25E0458, 33F25K0427, 33F24F0065; ASK-42703-PBSWH2/10801902220377, 10801902193275, 10801902220377, 10801902203189/33F24F0651, 33F24K0368, 33F24L0230, 33F24L0415, 33F24L1079, 33F25B0167, 33F25C0440, 33F25D0539, 33F25E0014, 33F25E0596, 33F25G0205, 33F25H0511, 33F25J0222, 33F25K0112, 33F25M0394, 33F26B0412, 33F24D0720; ASK-42703-PCAM1/10801902203189, 10801902193275, 10801902141030/33F24F0675, 33F24L1058, 33F25B0560, 33F25C0355, 33F25D0351, 33F25E0725, 33F25G0366, 33F25J0386, 33F25M0388, 33F26B0791, 33F24F0874; ASK-42703-PCSJ2/10801902193275, 10801902211672/33F25H0468, 33F25J0271, 33F26B0389, 33F26C0179, 33S24L0906, 33F25B0445; ASK-42703-PECL2/10801902193275/33F25H0466, 33F25J0272, 33F26A0011; ASK-42703-PGM4/10801902193275, 10801902221824/33F25B0653, 33F25D0541, 33F25J0106, 33F25J0387, 33F25K0140, 33F26B0749, 33F26C0027, 33F25E1195; ASK-42703-PHHN1/10801902193275, 10801902144734/33F25H0486, 33F25K0064, 33F25M0673, 33F26A0249, 33F26B0906, 33F25E0009; ASK-42703-PLC/10801902193275/33F25D0407, 33F25E0791, 33F25F0099, 33F25H0606, 33F26A1393, 33F25E1196; ASK-42703-PMEM/10801902193275, 10801902142167/33F25G0554, 33F25K0054, 33F25L0256, 33F26C0050, 33F24L0418; ASK-42703-PMHC1/10801902193275/10801902135244/33F25E0561, 33F25H0430, 33F25H0638, 33F25J0388, 33F25M0232, 33F26B0135, 33F26B0796, 33F25F0363; ASK-42703-PNHS1/10801902193275, 10801902225495/33F25D0542, 33F25E0599, 33F25H0498, 33F25H0650, 33F26D0066; ASK-42703-POHU2/10801902193275, 10801902212020/33F25E0562, 33F25G0284, 33F25J0389, 33F26A1421, 33F24F0662; ASK-42703-POSU2/10801902193275/33F24K0401, 33F24L0419, 33F24L0949, 33F25B0446, 33F25D0758; ASK-42703-PTJH/10801902193275, 10801902219012/33F24L0190, 33F25A0015, 33F25B0366, 33F25C0658, 33F25E0316, 33F24E0660; ASK-42703-PUCH2/10801902219012, 10801902193275, 10801902219012, 10801902135022/ ASK-42703-PUCI1/33F24F1025, 33F24L0336, 33F24L1009, 33F25B0476, 33F25C0356, 33F25E0021, 33F25F0189, 33F25H0455, 33F25J0275, 33F25K0142, 33F25M0120, 33F26A1518, 33F26B0182, 33F26B0781, 33F24F0850; ASK-42703-PUHC2/10801902193275, 10801902159608/33F25D0353, 33F25E0602, 33F25G0288, 33F25H0635, 33F25J0277, 33F25K0143, 33F26B0386, 33F26C0149, 33F24D0765; ASK-42703-PUMH/10801902129465, 10801902193275, 10801902159592/33F24F0697, 33F24K0709, 33F24L0997, 33F25C0301, 33F25E0677, 33F25J0278, 33F26A0256, 33F26B0789, 33F26C0227, 33F24D0698; ASK-42703-PUPM1/10801902159592, 10801902193275, 10801902225150/33F24F0761, 33F24K0499, 33F24L1074, 33F25B0519, 33F25C0357, 33F25D0354, 33F25D0598, 33F25E0678, 33F25G0346, 33F25J0279, 33F25M0126, 33F26B0363; ASK-42703-SHUF2/10801902193275, 10801902208368/33F25D0355, 33F25E0792, 33F25H0473, 33F25J0280, 33F25M0204, 33F26A1501, 33F26B0832, 33F24L0339; ASK-42703-SL1/10801902193275, 10801902205206/33F25B0483, 33F25C0443, 33F25D0482, 33F25E0793, 33F25G0306, 33F25J0281, 33F26A1437, 33F24D0631; ASK-42703-UMC/10801902193275, 10801902205206/33F24K0363, 33F24L0340, 33F25B0568,33F25E0801, 33F25G0328, 33F25J0282, 33F25M0194, 33F26A1444, 33F26B0769, 33F26C0221, 33F25B0158; ASK-42703-WHH/10801902193275, 10801902159189, 30801902119576/33F25E0565, 33F25G0350, 33F25J0283, 33F26B0777, 33F24E0552; ASK-42802-CHM/10801902193275/33F24H0178, 33F24K0480, 33F24L0859, 33F25D0236, 33F25F0190, 33F25H0518, 33F25J0284, 33F25M0139, 33F26B0175, 33F25E0005; ASK-42802-LMDT1/10801902205664, 10801902193275/33F24F0737, 33F24K0381, 33F24L0250, 33F24L0423, 33F25B0570, 33F25C0377, 33F25F0129, 33F25G0281, 33F25J0158, 33F25K0146, 33F26C0156, 33F25F0533; ASK-42802-MCY1/10801902193275, 10801902220384/33F24K0328, 33F24K0754, 33F24F0964; ASK-42802-PBSWH2/10801902193275, 10801902220384/33F24H0200, 33F24K0408, 33F24L0424, 33F24L1006, 33F25B0477, 33F25D0357, 33F25G0203, 33F25G0204, 33F25H0659, 33F25J0390, 33F25M0195, 33F25M0335, 33F26B0424, 33F24F0759; ASK-42802-POSU2/10801902193275/33F24K0473, 33F25D0759; ASK-42802-PUNCC2/10801902164251, 10801902193275, 10801902159585/33F24F0948, 33F24L0425, 33F25H0443, 33F25J0394, 33F24D0660; ASK-42802-PUPM1/10801902159585, 10801902193275, 10801902225143/33F24F0668, 33F24K0422, 33F24L0341, 33F24L1042, 33F25C0305, 33F25E0679, 33F25F0194, 33F25J0159, 33F25M0123, 33F26B0364; ASK-42802-TGH1/10801902213829, 10801902193275, 10801902213829/33F24L1054, 33F25B0521, 33F25D0311, 33F25E0604, 33F25G0225, 33F25J0288, 33F25L0204, 33F26A1543, 33F26B0844, 33F26C0224, 33F25C0306; ASK-42854-BJC1/10801902202540, 10801902193275, 10801902202540/33F24F0644, 33F24K0348, 33F24L0232, 33F25A0260, 33F25B0571, 33F25D0358, 33F25D0601, 33F25E0863, 33F25G0367, 33F26A1524, 33F26B0764, 33F26C0140, 33F24H0126; ASK-42854-PBMH/10801902193275, 40801902131469/33F26A0241, 33F24E0639; ASK-42854-PMM/40801902131469, 10801902193275/33F24F1014, 33F24L1013, 33F25C0307, 33F25D0546, 33F25E0802, 33F25H0480, 33F25J0398, 33F25A0019; ASK-42854-PUCH2/10801902193275, 10801902219050/33F25K0065, 33F26B0902, 33F24L0347; ASK-45703-ACH/10801902193275, 10801902203257, 30801902119644/33F25B0235, 33F25E0007, 33F25F0237, 33F25K0046, 33F25M0675, 33F26B0221, 33F24D0033; ASK-45703-ARM/10801902193275, 1080190215812/33F24L0903, 33F25B0449, 33F25D0363, 33F25E0682, 33F25H0479, 33F25J0228, 33F25K0150, 33F26A1423, 33F26B0849, 33F25F0004; ASK-45703-BJC1/10801902193275, 10801902202533, 10801902213782/33F24K0426, 33F24L0826, 33F25B0450, 33F25B0577, 33F25D0547, 33F25F0104, 33F25F0199, 33F25M0096, 33F26A1348, 33F26B0378, 33F26B0750, 33F24F0776; ASK-45703-BLH/10801902193275, 10801902213782, 10801902135381/33F24L1067, 33F25J0110, 33F25K0071, 33F25K0151, 33F25M0331, 33F26A1457, 33F26B0776, 33F24F0165; ASK-45703-DU1/10801902193275, 10801902160970, 10801902160468/33F25B0451, 33F25D0548, 33F25E0683, 33F25H0558, 33F26A1451, 33F26B0208, 33F26B0707, 33F26B0845, 33F24D0579; ASK-45703-HHC4/10801902193275, 10801902211467, 10801902205671/33F25D0364 ,33F25D0661, 33F25E0867, 33F25G0246, 33F25H0598, 33F25J0229, 33F25M0152, 33F26A1537, 33F26B0818, 33S25E0867, 33F24F0873; ASK-45703-LMDT1/10801902193275, 10801902205671/33F24K0440, 33F24L0432, 33F24L0919, 33F25B0160, 33F25D0365, 33F25D0603, 33F25E0608, 33F25G0326, 33F25H0475, 33F25J0230, 33F25M0153, 33F26A1552, 33F26B0880, 33F25B0453; ASK-45703-LMDTG1/10801902193275, 10801902205749, 10801902220902/33F25B0579, 33F25E0018, 33F25E0609, 33F25F0200, 33F25G0398, 33F25J0401, 33F25M0190, 33F25M0332, 33F26B0482, 33F26C0226, 33F24G0072; ASK-45703-MCY1/10801902193275/33F24J0132, 33F24K0445, 33F24L0433, 33F24L1028, 33F25B0657, 33F25E0022, 33F25E0610, 33F25F0201, 33F25H0657, 33F25M0144, 33F26A1573, 33F25L0143; ASK-45703-NO/10801902205213, 10801902193275, 10801902216417/33F24F0844, 33F24L0352, 33F25B0581, 33F25E0611, 33F24D0769; ASK-45703-NS1/10801902216417, 10801902193275, 10801902216417/33F24F0835, 33F24L0434, 33F24L1047, 33F25E0612, 33F25F0130, 33F25G0214, 33F25M0176, 33F26A1544, 33F26B0864, 33F25F0006; ASK-45703-PADV1/10801902193275/33F24J0146, 33F24K0458, 33F24L0353, 33F25C0311, 33F25E0423, 33F25E0684, 33F25H0561, 33F25M0127, 33F26A0775, 33F25A0265; ASK-45703-PAGP1/10801902193275, 10801902158724/33F25E0613, 33F25F0202, 33F25G0409, 33F25J0297, 33F26A1339, 33F26C0125, 33F25B0658; ASK-45703-PAMC1/10801902193275, 10801902217148, 10801902208344/33F25D0549, 33F25E0728, 33F25J0298, 33F25K0152, 33F26B0199, 33F24D0738; ASK-45703-PAU1/10801902208344, 10801902193275, 10801902220353/33F24F0783, 33F24L0354, 33F25D0483, 33F25E0729, 33F25H0534, 33F25J0404, 33F24F0070; ASK-45703-PBSWH2/10801902220353, 10801902193275, 10801902220353, 10801902203158/33F24F0937, 33F24L0437, 33F24L1112, 33F25A0306, 33F25B0659, 33F25E0614, 33F25E0803, 33F25F0080, 33F25H0368, 33F25H0513, 33F25K0153, 33F25M0191, 33F26C0157, 33F24F0660; ASK-45703-PCAM1/10801902193275/33F24L0355, 33F25C0312, 33F25E0016, 33F25E0804, 33F25J0162, 33F26A1447, 33F24K0479; ASK-45703-PCSJ2/10801902193275, 10801902211689, 10801902202861/33F25G0245, 33F25J0165, 33F25K0155, 33F26A1546, 33F26B0853, 33F24D0896; ASK-45703-PDM1/10801902202861, 10801902193275/33F24F0747, 33F25A0268, 33F25B0584, 33F25D0368, 33F25D0604, 33F25E0617, 33F25G0330, 33F25H0612, 33F25J0166, 33F25M0196, 33F26A1460, 33F25B0585; ASK-45703-PECL2/10801902193275/33F25D0369, 33F25D0605, 33F25E0619, 33F25G0242, 33F25J0168, 33F26A0013; ASK-45703-PGM4/10801902193275, 10801902221817/33F25B0660, 33F25D0412, 33F25J0169, 33F25K0078, 33F26C0176, 33F24M0174; ASK-45703-PGVH/10801902193275, 10801902200508/33F25E0310, 33F25H0781, 33F24F0101; ASK-45703-PHF4/)10801902200508, 10801902193275/33F24F0887, 33F24L0253, 33F24L0439, 33F25A0269, 33F25B0586, 33F25C0314, 33F25D0606, 33F25E0575, 33F25F0118, 33F25M0060, 33F25M0170, 33F26A1480, 33F26B0877, 33F25B0587; ASK-45703-PHUMC1/10801902193275, 10801902201017/33F25K0047, 33F25L0137, 33F26C0116, 33F25B0588; ASK-45703-PJHH1/10801902214833, 10801902193275/33F24D0929, 33F24F0765, 33F24L0254, 33F25B0162, 33F25B0589, 33F25E0013, 33F25E0023, 33F25E0622, 33F25G0223, 33F25J0171, 33F26A1461, 33F26B0798, 33F26C0195, 33F25A0271; ASK-45703-PMEM/10801902142174, 10801902193275/33F26C0051, 33F25B0591; ASK-45703-PMHC1/10801902193275, 10801902135237/33F25D0485, 33F25F0146, 33F25H0562, 33F25K0405, 33F26A1462, 33F26B0871, 33F25A0272; ASK-45703-PNHS1/10801902193275, 10801902193275/33F25C0317, 33F25E0732, 33F25G0293, 33F25H0649, 33F26D0067; ASK-45703-PNO2/10801902193275, 10801902205220, 10801902212082/33F25E0685, 33F25H0536, 33F25K0073, 33F25K0157, 33F26A1373, 33F26B0154, 33F26C0006, 33F24F0731; ASK-45703-POSU2/10801902193275/33F24K0404, 33F24L0868, 33F25B0457, 33F25B0594, 33F25D0760; ASK-45703-PPHPB1/10801902143850, 10801902193275/33F24F0721, 33F24K0379, 33F24L0444, 33F24L0849, 33F25B0595, 33F25D0487, 33F25E0805, 33F25H0496, 33F25J0299, 33F25K0158, 33F25E0444; ASK-45703-PRGK1/10801902193275, 10801902136654/33F25E0577, 33F25E0806, 33F25G0267, 33F25G0353, 33F25J0300, 33F26A1439, 33F26B0865, 33F24L0869; ASK-45703-PSAU1/10801902193275, 10801902159462/33F25L0262, 33F26C0049, 33F24H0106; ASK-45703-PSCH1/10801902193275/33F25B0241, 33F25E0010, 33F25H0777, 33F24M0274; ASK-45703-PSFR1/10801902193275/33F25H0451, 33F25H0654, 33F25M0145, 33F26A1540, 33F25C0483; ASK-45703-PSHS2/10801902193275/33F25E0808, 33F25H0517, 33F24L0873; ASK-45703-PSJR1/10801902193275, 10801902221053, 10801902125207/33F25D0371, 33F25E0625, 33F25G0198, 33F25M0162, 33F26C0128, 33F24F0626; ASK-45703-PSSM1/10801902193275, 10801902119749/33F24K0571, 33F25A0022, 33F25A0432, 33F25B0231, 33F25B0436, 33F25C0656, 33F25G0556, 33F26A0245, 33F24D0917; ASK-45703-PUCH2/10801902219029, 10801902193275, 10801902135046/33F24F0960, 33F24L0447, 33F24L1029, 33F25C0362, 33F25E0734, 33F25H0661, 33F25M0171, 33F26A1527, 33F26B0763, 33F24D0665; ASK-45703-PUCI1/10801902193275, 10801902135046/33F24J0172, 33F24L0363, 33F25B0460, 33F25C0321, 33F25E0626, 33F25F0205, 33F25J0304, 33F25M0187, 33F26C0013, 33F24L0971; ASK-45703-PUHC2/10801902193275, 10801902159615, 10801902118674/33F25A0277, 33F25E0627, 33F25G0302, 33F25J0232, 33F25M0119, 33F26B0128, 33F26B0879, 33F24D0730; ASK-45703-PUMC/10801902193275, 10801902113228/33F25C0322, 33F25E0688, 33F25H0648, 33F25M0122, 33F26B0130, 33F25F0376; ASK-45703-PUMH/10801902193275, 10801902129489, 10801902156355/33F25A0010, 33F25D0029, 33F25G0009, 33F25K0055, 33F25L0257, 33F26C0118, 33F24D0694; ASK-45703-PUN1/10801902156355, 10801902193275, 10801902164268/33F24F0769, 33F24L0948, 33F25B0462, 33F25C0323, 33F25E0689, 33F25M0131, 33F26C0130, 33F24D0696; ASK-45703-PUNMH/10801902193275, 10801902144161, 10801902159554/33F24L0264, 33F24L0366, 33F25B0599, 33F25D0374, 33F25E0691, 33F25G0305, 33F25J0406, 33F25K0161, 33F25M0222, 33F26B0716, 33F26B0870, 33F24D0848; ASK-45703-PUPM1/10801902159554, 10801902193275, 10801902159554, 10801902225181/33F24F0689, 33F24L0265, 33F24L1128, 33F25A0278, 33F25B0600, 33F25C0324, 33F25E0629, 33F25E0869, 33F25G0408, 33F25H0633, 33S25E0869,, 33F26B0365; ASK-45703-PUWH/10801902193275, 10801902112948/33F24M0046, 33F25A0023, 33F25A0429, 33F25E1174, 33F25G0266, 33F25H0779, 33F25K0049, 33F25L0131, 33F26A1132, 33F24D0310; ASK-45703-PVCU1/10801902112948, 10801902193275/33F24D0869, 33F24L0451, 33F24L0924, 33F25B0602, 33F25D0552, 33F25F0131, 33F25G0304, 33F25J0305, 33F26B0797, 33F25B0463; ASK-45703-PWH1/10801902213904/33F24E0561; ASK-45703-PYNH1/10801902193275/33F24G0519, 33F24K0268, 33F25C0184, 33F25C0909, 33F25E0244, 33F25L0336, 33F25M0843, 33F25G0261; ASK-45703-RR/10801902206944, 10801902193275/33F24F0961, 33F24K0447, 33F24L0452, 33F24L0879, 33F25B0603, 33F25D0608, 33F25E0871, 33F25K0087, 33F25M0395, 33F26A1425, 33F26A1426, 33F26C0695, 33F25B0604; ASK-45703-SHUF2/10801902193275, 10801902208351, 10801902202366/33F25E0631, 33F25F0206, 33F25G0396, 33F25J0174, 33F26B0778, 33F24F0771; ASK-45703-SL1/10801902193275, 10801902202366, 10801902203127/33F24L0453, 33F25B0464, 33F25D0413, 33F25E0809, 33F25H0538, 33F25J0409, 33F26A1410, 33F26B0173, 33F24D0583; ASK-45703-TC/10801902203127, 10801902193275/33F24F0877, 33F24L0454, 33F25B0146, 33F25H0539, 33F26B0186, 33F24L0163; ASK-45854-BJC1/10801902193275, 10801902202557/33F24L0164, 33F24L1019, 33F25B0605, 33F25E0810, 33F26C0137, 33F25B0465; ASK-45854-LMDTG1/10801902193275, 10801902205763/33F25D0376, 33F25D0662, 33F25E0735, 33F25H0535, 33F25J0411, 33F26A1409, 33F26C0126, 33F24H0216; ASK-45854-MCY1/10801902193275/33F24K0494, 33F25L0145; ASK-45854-PBMH/10801902193275/33F25M0676, 33F24L0456; ASK-45854-PBSWH2/10801902193275, 10801902220360/33F25A0307, 33F25C0364, 33F25E0736, 33F25H0512, 33F25J0412, 33F26B0788, 33F25B0606; ASK-45854-PECL2/10801902193275, 10801902224269/33F25K0056, 33F25M0678, 33F26B0227; ASK-45854-PNHS1/10801902193275, 10801902225471/33F25C0326, 33F25D0489, 33F25J0235, 33F26A1351, 33F26D0065; ASK-45854-PPHPB1/10801902193275/33F24H0170, 33F24L0370, 33F25B0607, 33F25C0475, 33F25E0692, 33F25H0581, 33F25J0306, 33F25D0031; ASK-45854-PSHS2/10801902193275/33F25F0371, 33F25K0062, 33F25M0679; ASK-45854-PUN1/10801902193275, 10801902159578/33F25H0484, 33F24D0717; ASK-45854-PUPM1/10801902159578, 10801902193275, 10801902225167/33F24E0665, 33F24F0898, 33F24L1007,33F25B0163, 33F25B0608, 33F25D0414, 33F25E0811, 33F25H0559, 33F25M0011, 33F26B0366; ASK-45854-PUR1/10801902193275/33F24M0178, 33F25B0429, 33F25E1200, 33F25K0057, 33F26A0250, 33F26A1394; ASK-46702-PJHH1/10801902193275, 10801902214888, 10801902116700/33F24L0835, 33F25D0490, 33F25J0307, 33F26C0351, 33F24F1020; CDC-42854-XPCN1A/10801902162134, 10801902193275/33F24F0702, 33F24K0345, 33F24L0130,33F24L0387,33F24L1147, 33F25B0631, 33F25C0334, 33F25D0565, 33F25E0703, 33F25E0897, 33F25G0344, 33F25J0254, 33F26A1476, 33F26B0897, 33F26C0067, 33F25B0534; CDC-42854-XPN1A/10801902193275, 10801902162141/33F25C0335, 33F25D0566, 33F25D0673, 33F26B0810, 33F26B0944, 33F24J0098; CDC-45854-XPCN1A/10801902162158, 10801902193275/33F24E0224, 33F24F0217, 33F24F0245, 33F24G0110, 33F24H0071, 33F24H0430, 33F24J0227, 33F24M0059, 33F24M0117, 33F25A0370, 33F25B0320, 33F25E1128, 33F25F0014, 33F25G0068, 33F25H0291, 33F25J0620, 33F25J0977, 33F25L0089, 33F26A1621, 33F26A1631, 33F26B0625, 33F25A0319; CDC-45854-XPN1A/10801902193275, 10801902162165/33F25B0633, 33F25C0336, 33F25D0572, 33F25E0758, 33F25G0259, 33F25G0342, 33F25J0331, 33F26A0419, 33F26A1569, 33F26C0215, 33F25B0634; AK-42703-CDC/10801902193275/33F25C0802, 33F25H0042, 33F25J0849, 33F25L0415, 33F25B0538; AK-45703-ACDC/10801902167825, 10801902193275, 10801902167825/33F24C0123, 33F24E0379, 33F24G0382, 33F24J0536, 33F24K0144, 33F24L0547, 33F24L1161, 33F25A0490, 33F25C0824, 33F25E0093, 33F25E0949, 33F25G0756, 33F25H0043, 33F25J0489, 33F25L0418, 33F25M0677, 33F26A1054, 33F26A1256, 33F26B0561, 33F26B0976, 33F25B0513; CDC-42703-P1A/10801902170863, 10801902193275/33F24D0984,33F24E0263, 33F24E0840, 33F24F0157, 33F24F0174, 33F24F0234, 33F24H0403, 33F24H0437, 33F24H0459, 33F24J0255, 33F24K0045, 33F24M0042, 33F24M0078, 33F24M0136, 33F25A0386, 33F25B0048, 33F25B0120, 33F25C0220, 33F25C0580, 33F25D0737, 33F25E1104, 33F25G0438, 33F25G0661, 33F25G0764, 33F25H0211, 33F25H0337, 33F25H0819, 33F25J0965, 33F25L0013, 33F25M0513, 33F26B0641, 33F26B1041, 33F26C0322, 33S25G0438, 33F24M0049; CDC-42703-XP1A/10801902193275, 20801902117087, 10801902162080/33F25K0249, 33F25K0386, 33F25L0091, 33F25L0227, 33F25L0271, 33F25L0301, 33F25M0514, 33F25M0526, 33F25M0546, 33F25M0573, 36F25B0028, 36F25B0066, 36F25D0016, 36F25D0017, 33F24C1215; CDC-42703-XPCN1A/10801902162080, 10801902193275/33F24C1227, 33F24E0237, 33F24E0837, 33F24F0001, 33F24F0161, 33F24F0242,33F24F0243,33F24G0209,33F24G0210, 33F24G0211, 33F24G0212, 33F24H0336, 33F24H0362, 33F24H0404, 33F24J0197, 33F24J0222, 33F24J0259, 33F24K0006, 33F24K0654, 33F24M0023, 33F24M0024, 33F24M0025, 33F24M0058, 33F24M0093, 33F24M0138, 33F24M0151, 33F24M0198, 33F25B0277, 33F25B0376, 33F25B0377, 33F25D0063, 33F25E0797, 33F25E0798, 33F25E1188, 33F25F0067, 33F25F0068, 33F25H0882, 33F25J0680, 33F25J0692, 33F25J0696, 33F25J0701,33F25J0704, 33F25J0709, 33F25J0713, 33F25J0714, 33F25J0716, 33F25J0720, 33F25J0727, 33F25J0731, 33F25K0320, 33F25K0387, 33F25K0388, 33F25K0389, 33F25L0165, 33F25L0183, 33F25L0197, 33F25L0280, 33F25L0294, 33F25M0015, 33F25M0018, 33F25M0024, 33F25M0027, 33F25M0036, 33F25M0574, 33F26A1664, 33F26B0626, 33F26B0627, 33F26C0430, 33F26C0431, 33F26C0432, 36F25B0067, 36F25C0003, 36F25C0004, 36F25D0018, 36F25D0019,36F25D0020, 36F25D0029,36F25E0002, 36F25E0003, 36F25E0004, 36F25E0013, 36F25E0027, 36F25G0001, 36F25G0004, 36F25G0005, 36F25G0008, 36F25G0014, 36F25H0020, 36F25H0021, 36F25H0022, 36F25J0004, 36F25J0006, 33F25F0069; CDC-42802-XPCN1A/10801902162103, 10801902193275/33F24D0791, 33F24F0096, 33F24F0768, 33F24K0367, 33F24L0126, 33F24L0383, 33F24L0893, 33F25A0317, 33F25B0533, 33F25D0563, 33F25D0616, 33F25D0637, 33F25E0702, 33F25E0828, 33F25E0895, 33F25F0220, 33F25H0628, 33F25J0438, 33F26A1567, 33F26C0551, 33F25C0246; CDC-42802-XPN1A/10801902193275, 10801902162097, 10801902170887/33F25D0617, 33F25D0671, 33F25E0896, 33F26A1568, 33F26B0811, 33F26B0945, 33F24D0858; CDC-42854-P1A/10801902170887, 10801902193275, 10801902170887/33F24F0749, 33F24L0128, 33F24L0385, 33F25C0371, 33F25D0672, 33F25E0753, 33F25G0300, 33F25H0548, 33F25J0182, 33F25K0189, 33F25M0081, 33F26A1474, 33F26B0709, 33F26B0806, 33F25H0877; CDC-45703-P1A/10801902171525/33F24D0988, 33F24E0239, 33F24E0252, 33F24E0841, 33F24F0164, 33F24F0225, 33F24G0208, 33F24G0253, 33F24H0079, 33F24H0308, 33F24H0337, 33F24J0225, 33F24J0262, 33F24K0049, 33F24K0690, 33F24L0015, 33F24M0033, 33F24M0034, 33F24M0080, 33F24M0094, 33F24M0140, 33F24M0152, 33F25A0369, 33F25A0387, 33F25B0230, 33F25B0300, 33F25B0345, 33F25C0534, 33F25D0725, 33F25E0419, 33F25E1127, 33F25E1157, 33F25F0026, 33F25F0053, 33F25G0036, 33F25G0055, 33F25G0517, 33F25H0364, 33F25H0784, 33F25J0591, 33F25K0244, 33F25L0053, 33F25L0235, 33F24H0376; CDC-45703-XPB1A/10801902193275, 10801902168372/33F25D0377, 33F25H0553, 33F25J0329, 33F26B0885, 33F24D0499; CDC-45703-XPCN1A/10801902161243, 10801902193275, 10801902161243/33F24E0212, 33F24E0216, 33F24E0217, 33F24E0230, 33F24E0231, 33F24E0243, 33F24E0244, 33F24E0255, 33F24E0256, 33F24E0827, 33F24F0237, 33F24F0240, 33F24F0241, 33F24G0214,33F24G0215, 33F24G0216, 33F24G0256, 33F24G0257, 33F24G0258, 33F24H0083, 33F24H0311, 33F24H0312, 33F24H0313, 33F24H0314, 33F24H0340, 33F24H0366, 33F24H0407, 33F24H0440, 33F24H0462, 33F24K0635, 33F24K0636, 33F24K0637, 33F24K0646, 33F24K0647, 33F24K0653, 33F24M0026, 33F24M0027, 33F24M0028, 33F24M0029, 33F24M0030, 33F24M0031, 33F24M0184, 33F24M0195, 33F24M0196, 33F24M0201, 33F24M0202, 33F25C0589, 33F25C0691, 33F25C0716, 33F25C0717, 33F25E0787, 33F25E0789, 33F25E0799, 33F25E0800, 33F25E1181, 33F25E1182, 33F25E1183, 33F25E1185, 33F25E1186, 33F25E1187, 33F25F0061, 33F25F0063, 33F25F0065, 33F25F0329, 33F25F0330, 33F25F0331, 33F25F0343, 33F25F0344, 33F25F0345, 33F25J0086, 33F25J0087, 33F25J0088, 33F25J0290, 33F25J0293, 33F25J0663, 33F25J0674, 33F25J0675, 33F25J0676, 33F25J0677, 33F25J0683, 33F25J0685, 33F25J0686, 33F25J0694, 33F25J0698, 33F25J0699, 33F25J0703, 33F25J0706, 33F25J0707, 33F25J0719, 33F25K0306, 33F25K0307, 33F25K0391, 33F25K0392, 33F25K0393, 33F25L0001, 33F25L0051, 33F25L0052, 33F25L0065, 33F25L0080, 33F25L0087, 33F25L0088, 33F25L0215, 33F25L0247, 33F25L0282, 33F25L0300, 33F25L0321, 33F25L0326, 33F25M0004, 33F25M0022, 33F25M0023, 33F25M0030, 33F25M0038,33F25M0473, 33F25M0516, 33F25M0535, 33F26A0211, 33F26A1640, 33F26A1641, 33F26A1642, 33F26A1643, 33F26B0612, 33F26B0613, 33F26B0614, 33F26B0615, 33F26B0616, 33F26B0617, 33F26B0618, 33F26B0619, 33F26C0321, 33F26C0543, 33F26C0553, 33F26C0564, 33F26C0568, 33F26C0844, 33F26C0861, 33F26C0877, 33F26C0878, 33F26C0879, 33F26C0880, 33R24M0184, 33X25H0001, 33X25K0005, 36F25C0001, 36F25C0002, 36F25C0009, 36F25C0012, 36F25D0007, 36F25D0012, 36F25D0024, 36F25D0025, 36F25D0026, 36F25D0036, 36F25D0037, 36F25E0005, 36F25E0006, 36F25E0010, 36F25E0011, 36F25E0024, 36F25E0025, 36F25G0006, 36F25G0007, 36F25G0009, 36F25G0010, 36F25G0016, 36F25G0017, 36F25G0018, 36F25H0023, 36F25H0024, 33F25E0795; CDC-45703-XPN1A/10801902193275, 10801902162042/33F25F0333, 33F25F0338, 33F25J0294, 33F25J0673, 33F25J0684, 33F25J0780, 33F25L0249, 33F25M0684,33F25M0775, 33F26A0311, 33F26B0608, 33F26B0609, 33F26B0610, 33F26B0611, 33F26B0685, 33F26B1036, 33F26B1055, 33F26B1057, 33F26B1058, 36F25D0027, 36F25D0033, 36F25D0039,36F25D0040, 36F25E0007, 36F25E0012, 36F25E0014, 36F25E0015, 36F25E0022, 36F25E0023, 36F25G0011, 36F25G0015, 36F25G0026, 36F25G0027, 36F25G0028, 36F25H0003, 36F25H0004, 36F25H0005, 36F25H0012, 36F25H0018, 36F25H0019, 36F25H0025, 36F25H0027, 36F25J0001,36F25J0002, 33F25B0505; CDC-45802-XP1A/10801902193275, 10801902162110/33F25D0568, 33F25E0755, 33F25G0275, 33F25H0434, 33F25J0119, 33F25L0107, 33F25M0347, 33F26A1473, 33F24D0771; CDC-45802-XPCN1A/10801902193275, 10801902162110/33F24K0407, 33F24L0495, 33F25B0490, 33F25D0569, 33F25E0756, 33F25G0380, 33F25J0120, 33F26B0890, 33F25A0290; CDC-46702-XP1A/10801902193275, 10801902168389/33F25E0447, 33F25E0706, 33F25J0332, 33F26A1471, 33F26B0218, 33F25B0506; CDC-47702-XP1A/10801902193275, 10801902168396, 20801902118787/33F25D0573, 33F25F0133, 33F25H0441, 33F25J0185, 33F25K0192, 33F25M0409, 33F26B0710, 33F26B0804, 33F26C0779, 33F24A0137; ASK-45703-PTJH/20801902116400/33F25A0016, 33F25C0585;", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2384-2026%22", "url": "https://recallledger.net/recalls/device-z-2384-2026-description-ref-access-tray-ask-04001-jhh-access-tray-ask-04001-lmdt/"}, {"id": "fda-device-z-2383-2026", "source": "FDA", "category": "device", "recall_number": "Z-2383-2026", "title": "Description/REF: PACING/PSI KIT: 5 FR 2L/ASK-07155-MGU recall (ARROW INTERNATIONAL, LLC)", "product": "Description/REF: PACING/PSI KIT: 5 FR 2L/ASK-07155-MGU", "reason": "Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.", "hazard_level": "Class I", "company": "ARROW INTERNATIONAL, LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-21", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "95", "codes": "REF(Material)/UDI-DI/Lot(Batch): ASK-07155-MGU/10801902210217/33F25C0798", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2383-2026%22", "url": "https://recallledger.net/recalls/device-z-2383-2026-description-ref-pacing-psi-kit-5-fr-2l-ask-07155-mgu/"}, {"id": "fda-device-z-2382-2026", "source": "FDA", "category": "device", "recall_number": "Z-2382-2026", "title": "Description/REF: DRAINAGE KIT/AK-01600 recall (ARROW INTERNATIONAL, LLC)", "product": "Description/REF: DRAINAGE KIT/AK-01600, DRAINAGE KIT/AK-01601, DRAINAGE KIT/ASK-01601-MM, THORACENTESIS KIT/AK-01000-T, THORACENTESIS KIT/AK-01000, THORACENTESIS KIT/ASK-01000-CHP, DRAINAGE KIT/ASK-01000-NW, THORACENTESIS KIT/ASK-01000-UPMS, PNEUMOTHORAX KIT/AK-01500, PNEUMOTHORAX KIT (NO HEIMLICH VALVE)/ASK-01500, PNEUMOTHORAX KIT/ASK-01500-JCM", "reason": "Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.", "hazard_level": "Class I", "company": "ARROW INTERNATIONAL, LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-21", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "444,943", "codes": "REF(Material)/UDI-DI/Lot(Batch): AK-01600/50801902120156, 10801902193275, 50801902120156, 60801902120160/33F24A0376, 33F24A1008, 33F24C0091, 33F24D0067, 33F24E0321, 33F24G0322, 33F24L0062, 33F24L0811, 33F24M0267, 33F25C0101, 33F25C0988, 33F25E0035, 33F25H0010, 33F25J0819, 33F26B0492, 33F24A0044; AK-01601/60801902120160, 10801902193275, 10801902190915/33F24A0783, 33F24A1070, 33F24C0092, 33F24E0322, 33F24G0323, 33F24J0273, 33F24L0651, 33F25C0102, 33F25C0916, 33F25E0036, 33F25G0078, 33F25J0460, 33F25L0371, 33F24B0427; ASK-01601-MM/10801902125726, 10801902193275, 10801902125726, 10801902205909/33F24F0656, 33F24K0319, 33F24M0166, 33F25A0163, 33F25E0587, 33F25G0164, 33F25L0116, 33F26A1377, 33F26C0174, 33F24F0213; AK-01000-T/10801902145120, 10801902193275, 10801902194029/33F24C0090, 33F24D0066, 33F24E0319, 33F24G0320, 33F24K0085, 33F24L0792, 33F25C0872, 33F25E0033, 33F25J0459, 33F25L0367, 33F24A0015; AK-01000/10801902197952, 10801902193275, 10801902197952, 10801902145120/33F24A0017, 33F24A0018, 33F24A0348, 33F24A0349, 33F24A0350, 33F24A0351, 33F24A1005, 33F24A1006, 33F24D0005, 33F24D0006, 33F24D0007, 33F24D0008, 33F24D0009, 33F24D0010, 33F24D0011, 33F24D0012, 33F24E0032, 33F24E0033, 33F24E0034, 33F24E0035, 33F24E0036, 33F24E0037, 33F24E0038, 33F24E0041, 33F24E0042, 33F24E0167, 33F24E0168, 33F24E0169, 33F24E0170, 33F24E0171, 33F24G0319, 33F24G0567, 33F24G0568, 33F24J0487, 33F24J0673, 33F24K0084, 33F24K0308, 33F24K0312, 33F24L0626, 33F24L0726, 33F24L0782, 33F24L0787, 33F25A0454, 33F25A0611, 33F25A0612, 33F25C0100,33F25C0211,33F25C0905,33F25C0954, 33F25E0032,33F25E0286, 33F25E0287, 33F25E0908, 33F25E1063, 33F25E1064, 33F25G0076, 33F25G0157, 33F25H0008, 33F25H0188, 33F25H0189, 33F25H0190, 33F25H0191, 33F25H0192, 33F25J0458, 33F25J0740, 33F25J0741, 33F25J0788, 33F25J0799, 33F25J0800, 33F25K0250, 33F25K0251, 33F25K0360, 33F25K0361, 33F25K0362, 33F25K0363, 33F25L0019, 33F25L0020, 33F25L0100, 33F25L0101, 33F25L0268, 33F25L0485, 33F25L0487, 33F25M0831, 33F25M0860, 33F26A0217, 33F26A0218, 33F26A0693, 33F26A0988, 33F26B0505, 33F26B0506, 33F26C0574, 33F24A0794; ASK-01000-CHP/10801902193275, 30801902120190, 10801902203134/33F24G0228, 33F24J0192, 33F24K0020, 33F24L0021, 33F24L0523, 33F24M0063, 33F25B0010, 33F25B0061, 33F25B0132, 33F25C0405, 33F25D0198, 33F25H0277, 33F25H0810, 33F25J0995, 33F26A1273, 33F26B0695, 33F24E0388; ASK-01000-NW/10801902193275, 10801902114867/33F24G0390, 33F24K0153, 33F25B0693, 33F25C0873, 33F25H0051, 33F25J0854, 33F25M0921, 33F24A0645; ASK-01000-UPMS/10801902114867, 10801902193275/33F24B0805, 33F24C0930, 33F24D0683, 33F24H0186, 33F24L0214, 33F24L0912, 33F25B0542, 33F25D0325, 33F25D0527, 33F25F0156,33F25J0099, 33F25J0196, 33F25L0270, 33F26A1392, 33F24G0276; AK-01500/10801902194029, 10801902193275, 50801902120156/33F24E0044, 33F24E0172, 33F24E0173, 33F24G0321, 33F24G0569, 33F24J0488, 33F24K0086, 33F24K0573, 33F24L0724, 33F25A0455, 33F25C0722, 33F25D0126, 33F25E0034, 33F25E0909, 33F25G0077, 33F25G0549, 33F25H0009, 33F25H0720, 33F25J0818, 33F25L0384, 33F26B0535, 33F26C0263, 33R24E0044, 33F23K0711; ASK-01500/10801902156232, 10801902193275, 30801902120206/33F24A0777, 33F24C0130, 33F24E0391, 33F24G0392, 33F24J0542, 33F24L0765, 33F25C0127, 33F25C0735, 33F25E0105, 33F25H0053, 33F25J0495, 33F25L0335, 33F24A1274; ASK-01500-JCM/30801902120206, 10801902193275, 10801902125726", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2382-2026%22", "url": "https://recallledger.net/recalls/device-z-2382-2026-description-ref-drainage-kit-ak-01600-drainage-kit-ak-01601-drainag/"}, {"id": "fda-device-z-2381-2026", "source": "FDA", "category": "device", "recall_number": "Z-2381-2026", "title": "Description/REF: HEMODIALYSIS KIT: 2-LUMEN 12 FR X 16 CM/AK-12122-F recall (ARROW INTERNATIONAL, LLC)", "product": "Description/REF: HEMODIALYSIS KIT: 2-LUMEN 12 FR X 16 CM/AK-12122-F", "reason": "Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.", "hazard_level": "Class I", "company": "ARROW INTERNATIONAL, LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-21", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "1,945", "codes": "REF(Material)/UDI-DI/Lot(Batch): AK-12122-F/10801902197129, 10801902193275, 10801902197129, 10801902168464/33F24B0184, 33F24D0076, 33F24F0321, 33F24G0345, 33F24K0111, 33F25A0474, 33F25C0915, 33F25E0061, 33F25E0924, 33F25J0832, 33F25L0404, 33F26B0552, 33F24A0102", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2381-2026%22", "url": "https://recallledger.net/recalls/device-z-2381-2026-description-ref-hemodialysis-kit-2-lumen-12-fr-x-16-cm-ak-12122-f/"}, {"id": "fda-device-z-2380-2026", "source": "FDA", "category": "device", "recall_number": "Z-2380-2026", "title": "Description/REF: PERITONEAL LAVAGE CATH KIT:8FR/AK-09000 recall (ARROW INTERNATIONAL, LLC)", "product": "Description/REF: PERITONEAL LAVAGE CATH KIT:8FR/AK-09000", "reason": "Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.", "hazard_level": "Class I", "company": "ARROW INTERNATIONAL, LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-21", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "7560", "codes": "REF(Material)/UDI-DI/Lot(Batch): AK-09000/30801902121722, 10801902193275, 20801902121756/33F24B0178, 33F24C0097, 33F24E0336, 33F24F0311, 33F24G0335, 33F24K0101, 33F24L0795, 33F25E0919, 33F25G0467, 33F25G0758, 33F25H0722, 33F25J0468, 33F25L0463, 33F26A0389, 33F24A0368", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2380-2026%22", "url": "https://recallledger.net/recalls/device-z-2380-2026-description-ref-peritoneal-lavage-cath-kit-8fr-ak-09000/"}, {"id": "fda-device-z-2379-2026", "source": "FDA", "category": "device", "recall_number": "Z-2379-2026", "title": "Description/REF: PI JACC KIT: 2L 5.5 FR X 15 CM CG+/ASK-41552-LTAC recall (ARROW INTERNATIONAL, LLC)", "product": "Description/REF: PI JACC KIT: 2L 5.5 FR X 15 CM CG+/ASK-41552-LTAC; PI JACC KIT: 3L 6 FR X 20 CM CG+/ASK-42063-LTAC; AGBA PI JACC KIT: 1-L 4.5 FR X 15 CM/CDC-41541-JX1A; AGBA PI JACC KIT: 2-L 5.5 FR X 15 CM/CDC-41552-JX1A; AGBA PI JACC KIT: 3-L 6 FR X 15 CM/CDC-41563-JX1A; AGBA PI JACC KIT: 1-L 4.5 FR X 20 CM/CDC-42041-JX1A; AGBA PI JACC KIT: 2-L 5.5 FR X 20 CM/CDC-42052-JX1A; AGBA PI JACC KIT: 3-L 6 FR X 20 CM/CDC-42063-JX1A", "reason": "Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.", "hazard_level": "Class I", "company": "ARROW INTERNATIONAL, LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-21", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "1,516", "codes": "REF(Material)/UDI-DI/Lot(Batch): ASK-41552-LTAC/10801902193275/33F24J0142, 33F24H0002; ASK-42063-LTAC/10801902214925/33F24F1005; CDC-41541-JX1A/10801902193275/33F25H0768; CDC-41552-JX1A/10801902193275, 10801902201505/33F25A0185, 33F25E0826, 33F24D0561; CDC-41563-JX1A/10801902193275/33F25B0150; CDC-42041-JX1A/10801902193275, 10801902188288/33F25E0751, 33F26C0353, 33F25A0186; CDC-42052-JX1A/10801902193275/33F25G0312, 33F24J0131; CDC-42063-JX1A/10801902193275/33F25C0447, 33F25D0516, 33F25E0752, 33F25J0436, 33F25C0370", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2379-2026%22", "url": "https://recallledger.net/recalls/device-z-2379-2026-description-ref-pi-jacc-kit-2l-5-5-fr-x-15-cm-cg-ask-41552-ltac-pi/"}, {"id": "fda-device-z-2378-2026", "source": "FDA", "category": "device", "recall_number": "Z-2378-2026", "title": "Description/REF: PI PICC: 3: 6FR x 55CM w CHG/ DLX-35563-HPKC recall (ARROW INTERNATIONAL, LLC)", "product": "Description/REF: PI PICC: 3: 6FR x 55CM w CHG/ DLX-35563-HPKC; AGBA PICC: 2L 5.5 FR X 45 CM/ASK-44552-ABKB; AGBA PICC/DELTA KIT: 5.5 FR X 55 CM/ASK-45552-MHBV; AGBA PICC: 1L 4.5FR x 55CM w Biopatch/DLX-45541-HPKB; PICC/DELTA KIT: 2L 5.5 FR X 50 CM/ASK-45052-MC; AGBA PI PICC KIT: 1L 4.5FR 40CM/CDC-44041-HPK1A; AGBA PI PICC KIT 2-LUMEN: 5.5 FR X 40CM/CDC-44052-HPK1A; AGBA PICC/DELTA FG: 2-L 5.5 FR X 40 CM/CDC-44052-VPS2; PI AGBA PICC KIT: 3-L 6 FR X 50 CM/CDC-45063-HPK1A; AGBA PICC/DELTA KIT: 1-L 4.5 FR X 55 CM/CDC-45541-VPS2; AGBA PICC/DELTA FG: 2-L 5.5 FR X 55 CM/CDC-45552-VPS2; PICC/VPS 1L 4.5 FR/ASK-45541-CHS; PI AGBA PICC KIT: 1L 4.5 FR X 55 CM VPS/ASK-45541-UOI2; PICC KIT: 2L 5.5FR 55CM AGBA VPS/ASK-45552-CHS; PI AGBA PICC KIT: 2L 5.5 FR X 55 CM VPS/ASK-45552-UOI2; PICC KIT: 3L 6FR 55CM AGBA/ASK-45563-CHS; PI JACC KIT: 3L 6 FR X 25 CM CG+/ASK-42563-LTAC; PI JACC KIT: 1-L 4.5 FR X 25 CM CG+/CDC-42541-JX1A; PI JACC KIT: 2-L 5.5 FR X 25 CM CG+/CDC-42552-JX1A; PI JACC KIT: 3-L 6 FR X 25 CM CG+/CDC-42563-JX1A; PI JACC KIT: 2-L 5.5 FR X 30 CM CG+/CDC-43052-JX1A; PI JACC KIT: 3-LUMEN: 6 FR X 30 CM CG+/CDC-43063-JX1A; PICC KIT: 2-L 4 FR X 55 CM/CDC-05542-PK1A", "reason": "Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.", "hazard_level": "Class I", "company": "ARROW INTERNATIONAL, LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-21", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "3,481", "codes": "REF(Material)/UDI-DI/Lot(Batch): DLX-35563-HPKC/10801902193275/33F25D0520; ASK-44552-ABKB/10801902140798, 10801902216677/33X25K0002, 33S24A0529; ASK-45552-MHBV/10801902193275/33F25K0372, 33F25M0199, 33F26A1534, 33F24L0348; DLX-45541-HPKB/10801902193275, 10801902208849/33F25G0393, 33F25L0055, 33F26A1570, 33F24D0604; ASK-45052-MC/10801902216660/33S24A1242; CDC-44041-HPK1A/10801902193275/33F24K0430; CDC-44052-HPK1A/10801902193275/33F25D0241; CDC-44052-VPS2/10801902193275/33F25E0514; CDC-45063-HPK1A/10801902193275/33F25D0242; CDC-45541-VPS2/50801902120781, 10801902193275/33S24A0211, 33F25C0699; CDC-45552-VPS2/10801902193275/33F25E0704; ASK-45541-CHS/10801902193275/33F26A1422, 33F24L0897; ASK-45541-UOI2/10801902193275/33F24L0991; ASK-45552-CHS/10801902193275/33F26A1395, 33F25G0260; ASK-45552-UOI2/10801902193275/33F24L0431; ASK-45563-CHS/10801902193275/33F25A0199; ASK-42563-LTAC/10801902203271/33F24F0852; CDC-42541-JX1A/10801902193275/33F26A1469, 33F24J0135; CDC-42552-JX1A/10801902193275/33F25D0561, 33F24L0285; CDC-42563-JX1A/10801902193275, 10801902170863/33F25C0702, 33F25D0562, 33F25G0311, 33F25J0437, 33F24D0507; CDC-43052-JX1A/10801902193275/33F25M0062, 33F24J0120; CDC-43063-JX1A/10801902193275, 10801902188332/33F25G0003, 33F26B0805, 33F25D0240; CDC-05542-PK1A/10801902193275, 50801902116715/33F25H0436, 33F25H0576, 33F24D0325", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2378-2026%22", "url": "https://recallledger.net/recalls/device-z-2378-2026-description-ref-pi-picc-3-6fr-x-55cm-w-chg-dlx-35563-hpkc-agba-pi/"}, {"id": "fda-device-z-2377-2026", "source": "FDA", "category": "device", "recall_number": "Z-2377-2026", "title": "Description/REF: ARTERIAL LINE KIT: SL 20 GA X 5 IN/ASK-04510-MM6 RA CATH KIT: 20 GA X... recall (ARROW INTERNATIONAL, LLC)", "product": "Description/REF: ARTERIAL LINE KIT: SL 20 GA X 5 IN/ASK-04510-MM6 RA CATH KIT: 20 GA X 1-3/4IN/NA-04020-X1ASP ACCESS TRAY/ASK-04001-MS RA CATH KIT: 20 GA X 8 CM/ASK-00820-UM1 VESSEL CATH KIT: 20GA X 5IN/AK-04550-S CVC KIT: 1-LUMEN 5 FR X 20 CM/AK-04301-SP CVC KIT: 16 GA X 6IN (16 CM)/AK-04306-SP CVC KIT: 16GA X 6 IN/AK-04800-S CVC KIT: 2-LUMEN 4 FR X 5 CM/AK-12402 CVC KIT: 3-LUMEN 7 FR X 16 CM/AK-12703-CDC CVC KIT: 2L 4 FR X 13 CM/AK-14402 CVC KIT: 2-LUMEN 5 FR X 13 CM/AK-14502 CVC KIT: 3-LUMEN 5.5 FR X 30 CM/AK-14553 CVC KIT: 3-LUMEN 7 FR X 30 CM/AK-14703-SP CVC KIT: 2-LUMEN 4 FR X 8 CM/AK-15402 CVC KIT: 3-LUMEN 5.5 FR X 8 CM/AK-15553 CVC KIT: 2-LUMEN 4 FR X 30 CM/AK-16402 CVC KIT: 3-LUMEN 5.5 FR X 13 CM/AK-16553 CVC KIT: 5 FR X 20 CM/ASK-04301-HH2 CVC KIT 3L: 7 FR X 6 IN (16 CM)/ASK-12703-MGH3", "reason": "Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.", "hazard_level": "Class I", "company": "ARROW INTERNATIONAL, LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-21", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "126,530", "codes": "REF(Material)/UDI-DI/Lot(Batch): ASK-04510-MM6/10801902193275, 10801902221909/33F25E0590, 33F25G0196, 33F25M0005, 33F25M0149, 33F26A0302, 33F26C0723, 33F24K0212; NA-04020-X1ASP/10801902193275/33F25J0575, 33F25J0756, 33F26B0065, 33F26B0027; ASK-04001-MS/10801902193275/33F24K0706, 33F25F0375, 33F25F0005; ASK-00820-UM1/10801902193275/33F24G0150; AK-04550-S/10801902196719, 10801902193275, 60801902121709/33F24A0029, 33F24A0355, 33F24A1014, 33F24A1619, 33F24B0112, 33F24C0548, 33F24D0017, 33F24E0174, 33F24G0328, 33F24G0576, 33F24J0276, 33F24J0494, 33F24K0092, 33F24L0720, 33F25A0458, 33F25C0950 33F25E0041, 33F25E0911, 33F25G0080, 33F25H0013, 33F25J0820, 33F25L0402, 33F26B0550, 33F26C0267, 33F23M0175; AK-04301-SP/10801902121650, 10801902193275, 10801902121674/33F24A1010, 33F24C0093, 33F24D0068, 33F24E0325, 33F24G0325, 33F24J0274, 33F24K0090, 33F24L0809, 33F25C0757, 33F25E0038, 33F25G0760, 33F25H0721, 33F25J0462, 33F25L0239, 33F25M0888, 33F24A0146; AK-04306-SP/10801902121674, 10801902193275, 10801902192230/33F24A0846, 33F24B0174, 33F24C0094, 33F24E0327, 33F24E0329, 33F24J0275, 33F24J0492, 33F24L0717, 33F25B0249, 33F25C0783, 33F25E0039, 33F25J0463, 33F25L0054, 33F25L0345, 33F26B0684, 33F23J0175; AK-04800-S/60801902121709, 10801902193275, 10801902209501/33F24B0437, 33F24C0735, 33F24E0708, 33F24G0120, 33F24G0647, 33F24H0415, 33F24J0448, 33F24L0037, 33F24M0128, 33F25A0396, 33F25B0111, 33F25D0028, 33F25G0509, 33F25H0326, 33F25J0997, 33F26C0274, 33F24C0013; AK-12402/10801902168471, 10801902193275, 10801902168488/33F24E0342, 33F24F0325, 33F24G0347, 33F24J0512, 33F24K0113, 33F24L0750, 33F25C0109, 33F25C0964, 33F25E0063, 33F25E0926, 33F25J0474, 33F24A0408; AK-12703-CDC/10801902168488, 10801902193275, 10801902168495/33F24A1020, 33F24B0187, 33F24C0104, 33F24D0078, 33F24G0348, 33F24J0513, 33F24K0114, 33F24L0596, 33F25C0110, 33F25C0759, 33F25J0834, 33F25M0948, 33F24A0401; AK-14402/10801902168495, 10801902193275, 10801902168495, 10801902168518/33F24E0177, 33F24E0343, 33F24F0328, 33F24G0349, 33F24J0514, 33F24K0115, 33F25B0369, 33F25C0875, 33F25E0064, 33F25E0928, 33F25H0029, 33F25J0475, 33F26B0564, 33F24A0813; AK-14502/10801902168518, 10801902193275, 30801902122040/33F24E0344, 33F24G0350, 33F24K0116, 33F24L0656, 33F25C0878, 33F25E0065, 33F25G0089, 33F25J0476, 33F26B0568, 33F24A0849; AK-14553/30801902122040, 10801902193275, 10801902122077/33F24B0190, 33F24C0107, 33F24E0345, 33F24E0346, 33F24F0332, 33F24G0351, 33F24K0117, 33F24L0689, 33F25C0112, 33F25C0848, 33F25G0090, 33F25J0835, 33F24B0191; AK-14703-SP/10801902122077, 10801902193275, 10801902197136/33F24E0347, 33F24G0352, 33F24J0516, 33F24K0118, 33F24L0737, 33F25A0476, 33F25C0887, 33F25E0067, 33F25E0929, 33F25J0477, 33F25L0399, 33F25M0905, 33F24D0079; AK-15402/10801902168532, 10801902193275, 10801902168532, 10801902168549/33F24B0194, 33F24E0350, 33F24G0354, 33F24H0034, 33F24J0518, 33F24K0120, 33F24L0751, 33F25A0479, 33F25C0799, 33F25E0069, 33F25E0932, 33F25H0723, 33F25J0836, 33F25L0348, 33F26C0317, 33F24A1268; AK-15553/10801902168549, 10801902193275, 10801902168549, 10801902168563/33F24E0714, 33F24G0226, 33F24G0687, 33F24H0249, 33F24J0353, 33F25B0332, 33F25D0195, 33F25H0796, 33F25J0081, 33F26B0287, 33F24A1269; AK-16402/10801902168563, 10801902193275, 10801902168563, 10801902168570/33F24C0738, 33F24E0715, 33F24H0065, 33F24H0416, 33F24J0212, 33F24J0426, 33F25A0046, 33F25C0087, 33F25C0604, 33F25G0458, 33F25J0082, 33F26A1658, 33F26B0069, 33F26C0446, 33F24A0796; AK-16553/10801902168570, 10801902193275, 30801902122248/33F24E0178, 33F24E0351, 33F24G0355, 33F24J0519, 33F24K0121, 33F24L0790, 33F25C0980, 33F25E0070, 33F25J0478, 33F24C0025; ASK-04301-HH2/10801902193275, 20801902114987/33F25H0640, 33F25K0070, 33F25K0090, 33F24D0733; ASK-12703-MGH3/10801902193275, 10801902115260/33F25D0263, 33F24F0838", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2377-2026%22", "url": "https://recallledger.net/recalls/device-z-2377-2026-description-ref-arterial-line-kit-sl-20-ga-x-5-in-ask-04510-mm6-ra-c/"}, {"id": "fda-device-z-2376-2026", "source": "FDA", "category": "device", "recall_number": "Z-2376-2026", "title": "Description/REF: CVC/PSI KIT: 2 LUMEN 8 FR X 6 IN/ASK-42802-PLH recall (ARROW INTERNATIONAL, LLC)", "product": "Description/REF: CVC/PSI KIT: 2 LUMEN 8 FR X 6 IN/ASK-42802-PLH; CVC KIT: 3-LUMEN 12 FR X 16 CM/AK-12123-F; CVC KIT: 3-LUMEN 12 FR X 20 CM/AK-15123-F; 3L CVC KIT: 7 FR X 16 CM/ASK-12703-PMAH; 3L PI CVC KIT: 7 FR X 16 CM/ASK-12703-PNM; 3L CVC KIT: 7 FR X 16 CM/ASK-12703-PUMH; MULTILUMEN PI CVC KIT: 3L 7 FR X 8 IN/ASK-15703-PRH; MULTILUMEN PI CVC KIT: 3L 7 FR X 20 CM/CDC-15703-P1A; PI CVC KIT: 3-L 7 FR X 6IN (16 CM)/NA-12703-PCDC; PI CVC KIT: 3-L 7 FR X 8IN (20 CM)/NA-15703-PCDC; CVC KIT: 3-LUMEN 5.5 FR X 8 CM/AK-25553; 2-L CVC KIT: 4 FR X 5 CM/CDC-22402-X1A; 2-L CVC KIT: 5 FR X 5 CM/CDC-22502-X1A; 2-L CVC KIT: 4 FR X 8 CM/CDC-25402-X1A; 2-L CVC KIT: 5 FR X 8 CM/CDC-25502-X1A; 3-L CVC KIT: 5.5 FR X 8 CM/CDC-25553-X1A; 3-L CVC KIT: 5.5 FR X 13 CM/CDC-26553-X1A; CVC KIT 3L: 12 FR X 16 CM AGB/AK-22123-CDC; CVC KIT: 3-LUMEN 12 FR X 16 CM/AK-22123-F; CVC KIT: 2-LUMEN 4 FR X 5 CM/AK-22402; CVC KIT: 2-LUMEN 5 FR X 5 CM/AK-22502; CVC KIT: 16 GA X 8IN/AK-24301-SK; CVC KIT: 2-LUMEN 4 FR X 13 CM/AK-24402; CVC KIT: 3-LUMEN 7 FR X 30 CM/AK-24703-ASK; CVC KIT 3L: 12FR X 20 CM AGB/AK-25123-CDC; CVC KIT: 3-LUMEN 12 FR X 20 CM/AK-25123-F; CVC KIT: 2-LUMEN 4 FR X 8 CM/AK-25402; CVC KIT: 2-LUMEN 5 FR X 8 CM/AK-25502; CVC KIT: 3-LUMEN 5.5 FR X 13 CM/AK-26553; LBCVC KIT: 3L 12 FR X 16 CM AGB/CDC-22123-1A; LBCVC KIT: 3L 12 FR X 16 CM AGB/CDC-22123-X1A; CVC KIT: 16 GA X 20 CM/CDC-24301-1A; PI CVC KIT: 2L 7 FR X 16 CM AGB/AK-22702-P1A; PI CVC KIT: 2L 7 FR X 16 CM AGB/CDC-22702-XP1A; CVC KIT: 3L 7 FR X 20 CM/ASK-45703-CPR; MULTILUMEN PI CVC KIT: 3L 7 FR X 16 CM/ASK-42703-AKP1A; MULTI-LUMEN PI CVC KIT: 3-L 7 FR X 6IN/ASK-42703-KH; PI CVC KIT: 3L 7FR X 16CM AGB+/ASK-42703-MGH1; MULTI LUMEN PI CVC KIT: 3L 7 FR X 6IN/ASK-42703-PCCH2; PI CVC KIT: 3LUMEN 7 FR X 6IN (16 CM)/ASK-42703-PFS1; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-PNO2; MULTI LUMEN PI CVC KIT: 3L 7 FR/ASK-42703-PSCH1; MULTILUMEN PI CVC KIT: 2L 8 FR X 16 CM/ASK-42802-AKP1A; CVC KIT: 2L 8 FR X 16CM/ASK-42802-LMDTG1; PI CVC KIT: 2L 8 FR X 6 IN (16 CM) AGB+/ASK-42802-PUCI1; PI CVC KIT: 2L 8 FR X 16 CM AGB+/ASK-42802-PUMH; PI CVC KIT: 2L 8 FR X 16 CM AGB+/ASK-42802-UMM; PI CVC KIT: 4-L 8.5 FR X 6 IN/ASK-42854-AKP1A; PI CVC KIT: 4L 8.5FR X 16CM AGB+/ASK-42854-MGH; MULTILUMEN PI CVC KIT: 3L 7 FR X 20 CM/ASK-45703-AKP1A; PI CVC KIT: 3L 7 FR X 20CM AGB+/ASK-45703-MGH; MULTI LUMEN PI CVC KIT: 3L 7 FR X 8 IN/ASK-45703-PCCH2; MULTI LUMEN PI CVC KIT: 3L 7 FR X 8 IN/ASK-45703-PECL1; PI CVC KIT: 3 LUMEN 7 FR X 8 IN (20 CM)/ASK-45703-PFS1; PI CVC KIT: 3L 7 FR X 8 IN (20 CM) AGB+/ASK-45703-PHM1; PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-PHU; PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-PMSG1; MULTILUMEN PI CVC KIT: 3L 7 FR X 20 CM/ASK-45703-PNCB; MULTILUMEN CVC KIT: 3L 7 FR X 20 CM/ASK-45703-PPCM; PI CVC KIT: 3-LUMEN 7 FR X 8 IN (20 CM)/ASK-45703-PRH; MULTILUMEN PI CVC KIT: 3L 7 FR X 8 IN/ASK-45703-PSJ2; PI CVC KIT: 3L 7 FR X 20 CM/ASK-45703-PSVM; MULTI LUMEN PI CVC KIT: 3L 7 FR X 20 CM/ASK-45703-PUHS; PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-PUKL; PI CVC KIT: 3L 7FR X 20CM AGB+/ASK-45703-PUMF1; PI CVC KIT: 3L 7 FR X 8 IN (20 CM)/ASK-45703-PUR1; PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-RHR1; MULTILUMEN PI CVC KIT: 3L 7 FR X 20 CM/ASK-45703-WA; MULTI LUMEN PI CVC KIT: 2L 8 FR X 8 IN/ASK-45802-AKP1A; PI CVC KIT: 4L 8.5 FR X 20 CM/ASK-45854-AKP1A; PI CVC KIT: 4L 8.5FR X 20CM AGB+/ASK-45854-MGH; PI CVC KIT: 4L 8.5 FR X 8IN/ASK-45854-PCCH2; CVC KIT: 4L 8.5 FR X 20 CM AGB/ASK-45854-PNM; MULTI LUMEN CVC KIT: 4L 8.5 FR X 8 IN/ASK-45854-PPCM; PI CVC KIT: 4L 8.5 FR X 20 CM AGB+/ASK-45854-PUCH2; MULTILUMEN PI CVC KIT: 2L 7 FR X 20 CM/ASK-46702-PWBH1; MULTILUMEN CVC KIT: 2L 8 FR X 16 CM/CDC-42802-P1A; PI CVC KIT: 3-L 7 FR X 20 CM AGB/CDC-45703-PA1A; CVC KIT: 2L 8 FR X 6IN (16 CM)/ASK-42802-ECL4; PI CVC KIT: 3-L 7 FR X 16 CM AGB+/AK-42703-P1A; PI CVC KIT: 2-L 8 FR X 16 CM AGB+/AK-42802-P1A; PI CVC KIT: 4-L 8.5 FR X 16 CM AGB+/AK-42854-P1A; PI CVC KIT: 3-L 7 FR X 20 CM AGB+/AK-45703-P1A; PI CVC KIT: 2-L 8 FR X 20 CM AGB", "reason": "Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.", "hazard_level": "Class I", "company": "ARROW INTERNATIONAL, LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-21", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "308,263", "codes": "REF(Material)/UDI-DI/Lot(Batch): ASK-42802-PLH/10801902193275, 10801902133110, 10801902212013/33F25L0140 33F26B0222, 33F24F0799; AK-12123-F/10801902168464, 10801902193275, 10801902186338/33F24B0185, 33F24C0102, 33F24D0077, 33F24F0323, 33F24G0346, 33F24K0112, 33F25C0929, 33F25E0062, 33F25H0028, 33F25J0833, 33F24G0129; AK-15123-F/10801902168525, 10801902193275, 10801902186499/33F24C0108, 33F24E0349, 33F24G0353, 33F24L0650, 33F25A0478, 33F25C0779, 33F25E0068, 33F25M0946, 33F24E0713; ASK-12703-PMAH/10801902193275/33F24J0116; ASK-12703-PNM/10801902193275, 10801902214338/33F24L0197, 33F24D0725; ASK-12703-PUMH/10801902193275, 10801902164602/33F25L0030, 33F24F0914; ASK-15703-PRH/10801902193275, 10801902133226/33F25C0271, 33F25F0168, 33F25J0101, 33F25J0368, 33F26A1500, 33F24C0858; CDC-15703-P1A/10801902116793, 10801902193275/33F24D0980, 33F24E0236, 33F24E0832, 33F24G0252, 33F24H0074, 33F24H0401, 33F24H0457, 33F24J0195, 33F24K0024, 33F24M0016, 33F24M0017, 33F24M0064, 33F25B0116, 33F25C0577, 33F25D0719, 33F25G0427, 33F25G0441, 33F25G0663, 33F25H0361, 33F25J1039, 33F25M0495, 33F25M0512, 33F25B0670; NA-12703-PCDC/10801902193275, 10801902119978, 10801902119985/33F24G0555, 33F24K0298, 33F25A0602, 33F25E1055, 33F25H0180, 33F25J0942, 33F25L0474, 33F26B0598, 33F24D0414; NA-15703-PCDC/10801902119985, 10801902193275, 10801902119985, 10801902210217/33F24F0191, 33F24G0556, 33F24J0336, 33F24K0572, 33F25A0157, 33F25C0200, 33F25C0833, 33F25E0275, 33F25H0181, 33F25H0762, 33F25J0943, 33F25L0456, 33F26B0587, 33F25A0603; AK-25553/10801902193275, 10801902167801/33F24H0250, 33F24M0062, 33F25A0382, 33F25B0310, 33F25C0069, 33F25C0506, 33F26C0405, 33F24G0377; CDC-22402-X1A/)10801902193275/33F25K0177, 33F26B0893, 33F25E1192; CDC-22502-X1A/10801902193275/33F25F0216, 33F25C0331; CDC-25402-X1A/10801902193275, 20801902116974/33F25A0287, 33F25D0505, 33F25E0824, 33F25H0569, 33F26A1470, 33F26B0216, 33F24L0486; CDC-25502-X1A/10801902193275/33F24L0980, 33F25D0506, 33F25E0698, 33F25G0315, 33F25J0429, 33F26A1472, 33F24L0832; CDC-25553-X1A/10801902193275, 10801902168129, 60801902123611/33F25E0890, 33F25E1191, 33F26A1384, 33F26B0708, 33F24F0084; CDC-26553-X1A/10801902193275, 10801902168136, 50801902117019/33F25E0749, 33F25E1190, 33F25J0432, 33F26B0807, 33F26C0210, 33F26D0063, 33F24D0807; AK-22123-CDC/10801902193275, 10801902167740/33F24K0127, 33F25A0483, 33F25E0076, 33F25E0938, 33F25H0032, 33F25J0480, 33F25K0398, 33F25M0960, 33F24E0358; AK-22123-F/10801902193275/33F24G0362, 33F24J0526, 33F24K0128, 33F24L0762, 33F25C0963, 33F25E0939, 33F25H0033, 33F24G0363; AK-22402/10801902193275, 10801902167764/33F24L0704, 33F25A0484, 33F25C0817, 33F25E0079, 33F25H0035, 33F25L0373, 33F25M0879, 33F24B0203; AK-22502/10801902193275, 10801902167764/33F24E0363, 33F24G0366, 33F24K0131, 33F24L0708, 33F25C0885, 33F25J0842, 33F24K0487; AK-24301-SK/10801902193275/33F24G0367, 33F24J0528, 33F24K0132, 33F24L0680, 33F25C0118, 33F25C0775, 33F25E0080, 33F25G0092, 33F25H0036, 33F25H0724, 33F25J0482, 33F25L0411, 33F25M0915, 33F24K0133; AK-24402/10801902193275/33F24L0059, 33F24L0727, 33F25C0119, 33F25C0976, 33F25E0081, 33F24K0134; AK-24703-ASK/10801902193275, 10801902118971, 60801902123178/33F24L0778, 33F25C0928, 33F25E0082, 33F25H0037, 33F25J0843, 33F26B0495, 33F24F0281; AK-25123-CDC/10801902193275/33F24K0136, 33F24L0730; AK-25123-F/10801902193275/33F25C0913, 33F25E0085, 33F25E0943, 33F25J0484, 33F26B0496, 33F24G0374; AK-25402/10801902193275, 10801902167795/33F24G0376, 33F24J0282, 33F24K0139, 33F24L0752, 33F25C0121, 33F25C0968, 33F25G0093, 33F25J0486, 33F25L0381, 33F26B0532, 33F24G0688; AK-25502/10801902193275, 10801902180381/33F24H0051, 33F24M0001, 33F25A0125, 33F25B0333, 33F25F0256, 33F25F0500, 33F25H0807, 33F25K0228, 33F25L0163, 33F26A0051, 33F26B0266, 33F24G0689; AK-26553/10801902193275, 20801902117506/33F24K0140, 33F24L0776, 33F25E0089, 33F25G0094, 33F25J0847, 33F25L0410, 33F25M0914, 33F24D0024; CDC-22123-1A/10801902168044, 10801902193275/33F24F0943, 33F24L0472, 33F25A0325, 33F25B0672, 33F25E0653, 33F25E0877, 33F25M0114, 33F25M0424, 33F26A1508, 33F25A0326; CDC-22123-X1A/10801902193275, 20801902116851, 20801902116851,10801902213591/33F25B0673, 33F25D0446, 33F25D0667, 33F25F0212, 33F25G0413, 33F25J0317, 33F25M0396, 33F26B0442, 33F24D0842; CDC-24301-1A/30801902116902, 10801902193275, 30801902116902, 30801902116919/33F24D0874, 33F24F0076, 33F24F0863, 33F24K0501, 33F24L0979, 33F25B0617, 33F25D0494, 33F25D0668, 33F25E0697, 33F25E0820, 33F25H0571, 33F25J0249, 33F25K0181, 33F25L0084, 33F25L0104, 33F26A1413, 33F26B0784, 33S25E0697, 33F24C0702; AK-22702-P1A/10801902193275, 30801902122378/33F25D0322, 33F25H0424, 33F25J0097, 33F25K0085, 33F24E0364; CDC-22702-XP1A/10801902193275, 30801902116896/33F25D0451, 33F25F0217, 33F25H0573, 33F25J0322, 33F26A1386, 33F26B0706, 33F25K0180; ASK-45703-CPR/10801902193275/33F24J0477, 33F24L1068; ASK-42703-AKP1A/10801902193275, 10801902202519/33F24J0324, 33F25A0577, 33F25C0841, 33F25E0233, 33F25E1027, 33F25G0140, 33F25H0148, 33F25H0754, 33F25J0924, 33F25M0869, 33F24F0754; ASK-42703-KH/10801902193275, 10801902205657/33F24G0269, 33F24L0087, 33F25E0235, 33F25G0141, 33F25L0213, 33F24D0891; ASK-42703-MGH1/10801902193275, 10801902223682, 10801902193275/33F25J0735, 33F26C0344, 33F25E0509; ASK-42703-PCCH2/10801902193275, 10801902141030/33F24L0231, 33F24L0416, 33F24L0945, 33F25B0443, 33F25B0561, 33F25D0352, 33F25E0726, 33F25G0316, 33F25J0155, 33F25M0013, 33F26B0792, 33F26C0228, 33F25D0540; ASK-42703-PFS1/10801902193275/33F25E0598, 33F25B0275; ASK-42703-PNO2/10801902193275/33F26A1661, 33F24L0335; ASK-42703-PSCH1/10801902137330, 10801902193275/33F24F1038, 33F24H0204, 33F25B0566, 33F25H0491, 33F25J0274, 33F25M0092, 33F26B0124, 33F24H0100; ASK-42802-AKP1A/10801902193275, 10801902217155/33F24G0511, 33F24K0264, 33F24L0745, 33F25C0931, 33F25H0150, 33F25J0561, 33F25L0481, 33F25M0971, 33F24F0676; ASK-42802-LMDTG1/10801902193275, 10801902205701/33F26A1254, 33F26B0814, 33F24H0215; ASK-42802-PUCI1/10801902193275/33F24L0195; ASK-42802-PUMH/10801902193275, 10801902164251/33F25H0493, 33F25K0059, 33F25L0141, 33F25M0674, 33F24D0712; ASK-42802-UMM/10801902159653, 10801902193275/33F24F1027, 33F24G0513; ASK-42854-AKP1A/10801902193275, 10801902202540/33F24J0635, 33F24K0265, 33F24L0610, 33F25A0580, 33F25E0239, 33F25H0152, 33F25J0562, 33F24E0632; ASK-42854-MGH/10801902223668, 10801902193275/33F26C0876, 33F25E1198; ASK-45703-AKP1A/10801902193275, 10801902158120/33F24G0515, 33F24J0636, 33F24K0266, 33F24L0577, 33F25A0581, 33F25C0843, 33F25E0241, 33F25G0142, 33F25H0154, 33F25J0564, 33F25L0238, 33F25M0902, 33F24F0106; ASK-45703-MGH/10801902223675/33F26C0875, 33F25B0580; ASK-45703-PCCH2/10801902193275, 10801902141047, 10801902193275/33F24L0356, 33F24L1092, 33F25B0582, 33F25D0550, 33F25E0615, 33F25G0352, 33F25J0163, 33F25K0154, 33F26B0772, 33F24L0088; ASK-45703-PECL1/10801902193275, 10801902130386/33F25E0618, 33F25F0204, 33F25G0289, 33F25J0167, 33F25M0192, 33F26B0191, 33F26B0765, 33F25C0313; ASK-45703-PFS1/10801902193275/33F25E0510, 33F25B0274; ASK-45703-PHM1/10801902193275, 10801902116229/33F25E0620, 33F25G0290, 33F25H0572, 33F25J0405, 33F26B0715, 33F26B0854, 33F25K0313; ASK-45703-PHU/10801902193275/33F25L0135, 33F26A0243, 33F25G0685; ASK-45703-PMSG1/10801902193275, 30801902116315/33F25E1199, 33F25F0357, 33F26A0411, 33F24D0674; ASK-45703-PNCB/30801902116315, 10801902193275/33F24F0818, 33F24L0256, 33F24L1075, 33F25B0592, 33F25D0486, 33F25E0731, 33F25H0433, 33F25M0159, 33F25M0426, 33F26B0760, 33F25B0456; ASK-45703-PPCM/10801902193275, 10801902116335/33F25F0358, 33F25G0688, 33F25K0048, 33F25L0028, 33F26B0903, 33F24K0067; ASK-45703-PRH/10801902193275, 10801902116359, 10801902116373/33F25A0275, 33F25C0318, 33F25E0807, 33F25G0358, 33F25J0301, 33F26A1420, 33F26B0799, 33F24E0560; ASK-45703-PSJ2/10801902193275, 10801902119732/33F25C0319, 33F25E0733, 33F25G0357, 33F25H0641, 33F25J0302, 33F26A1507, 33F26B0878, 33F24L0259; ASK-45703-PSVM/10801902119749, 10801902193275, 10801902119749/33F24F0755, 33F24L0446, 33F25B0459, 33F25C0320, 33F25D0551, 33F25F0120, 33F25G0356, 33F25J0303, 33F26A1523, 33F26B0762, 33F25D0237; ASK-45703-PUHS/10801902193275, 10801902114058/33F24L0942, 33F25B0596, 33F25E0687, 33F25G0303, 33F25H0642, 33F26A1424, 33F24F0717; ASK-45703-PUKL/10801902193275, 10801902114058, 10801902193275/33F24H0185, 33F24K0433, 33F24L0262, 33F25B0597, 33F25D0372, 33F25E0628, 33F25H0566, 33F25J0173, 33F26B0233, 33S25E0628, 33F25B0461; ASK-45703-PUMF1/10801902193275/33F25K0060, 33F25L0134, 33F26A0235, 33F24K0567; ASK-45703-PUR1/10801902116465, 10801902193275/33F24F0790, 33F24H0206, 33F24L0266, 33F24L0922, 33F25B0601, 33F25D0375, 33F25E0630, 33F25E0870, 33F25J0408, 33F25M0128,33F26A1432, 33F26B0836, 33F24G0616; ASK-45703-RHR1/10801902116465, 10801902193275/33F24F0790, 33F24H0206, 33F24L0266,33F24L0922, 33F25B0601,33F25D0375, 33F25E0630, 33F25E0870, 33F25J0408, 33F25M0128, 33F26A1432, 33F26B0836, 33F24G0616; ASK-45703-WA/10801902193275, 10801902116564, 30801902119774/33F25A0443, 33F25E0011, 33F25K0309, 33F26B0909, 33F24C0746; ASK-45802-AKP1A/10801902193275, 30801902119774/33F24L0023, 33F26A1657, 33F26B0277, 33F25D0034; ASK-45854-AKP1A/10801902193275, 30801902119781/33F24G0671, 33F24L0039, 33F25A0366, 33F25B0094, 33F25D0715, 33F25G0495, 33F25J0033, 33F25K0349, 33F25L0226, 33F26A1654, 33F26B0025, 33F26B0698, 33F24J0130; ASK-45854-MGH/10801902223699, 10801902193275/33F26C0688, 33F25C0363; ASK-45854-PCCH2/10801902193275/33F25J0234, 33F25E1175; ASK-45854-PNM/10801902193275/33F24K0570, 33F25B0431, 33F25E0006, 33F25F0377, 33F25H0780, 33F25L0261; ASK-45854-PPCM/10801902143867/33F24F0736; ASK-45854-PUCH2/10801902193275/33F24M0177; ASK-46702-PWBH1/10801902193275/33F24K0321, 33F24K0269; CDC-42802-P1A/10801902170870, 10801902193275, 10801902170870/33F24F0244, 33F24H0070, 33F24H0426, 33F24J0223, 33F24J0468,33F24L0009,33F24M0079, 33F24M0139, 33F25B0319, 33F25C0533, 33F25E1094, 33F25E1156,33F25F0384, 33F25H0338, 33F25J0766, 33F25J0990, 33F25L0086, 33F25M0016, 33F26A1619, 33F26B1051, 33F25H0880; CDC-45703-PA1A/10801902193275, 30801902117190, 10801902117202/33F24M0081, 33F25F0241, 33F26A1656, 33F26B0334, 33F24C1072; ASK-42802-ECL4/10801902224283, 10801902205664/33F26B0489, 33F24D0651; AK-42703-P1A/10801902193275, 10801902171372/33F25D0323, 33F25D0585, 33F25F0122, 33F25F0153, 33F25G0376, 33F25J0135, 33F26B0459, 33F24L1104; AK-42802-P1A/10801902193275/33F25B0539, 33F25D0386, 33F25F0137, 33F25J0136, 33F25B0512; AK-42854-P1A/10801902193275, 10801902168167, 10801902119152/33F25E0664, 33F25H0442, 33F25J0341, 33F26B0752, 33F23H0557; AK-45703-P1A/10801902193275, 10801902171389/33F25C0341, 33F25D0387, 33F25D0643, 33F25F0154, 33F25G0257, 33F25G0375, 33F25J0137, 33F25J0342, 33F26A1416, 33F26B0150, 33F26B0766, 33F25C0191; AK-45802-P1A/10801902193275, 10801902168181/33F25E0665, 33F25J0191, 33F26B0754, 33F25A0223; AK-45854-P1A/10801902193275, 10801902168198/33F25D0459, 33F25F0138, 33F26B0145, 33F25B0540; AK-47702-P1A/10801902193275/33F25E0502, 33F25G0162, 33F25H0407, 33F25J0343, 33F24G0383; ASK-42703-PECL3/10801902193275/33F26A1397, 33F25B0562; ASK-42703-PUPM3/10801902225150, 10801902156966/33F26C0238, 33F24F0977; ASK-42802-PUPM3/10801902225143, 10801902193275/33F26C0239, 33F25B0498; ASK-45703-PECL3/10801902193275, 10801902224313/33F26A1577, 33F26B0773, 33F25C0234; ASK-45703-PUPM3/10801902225181, 10801902116465/33F26C0219, 33F24D0840; ASK-45854-PECL3/10801902193275/33F24L0191; ASK-45854-PUPM3/10801902225167, 10801902193275/33F26C0240, 33F24H0111; ASK-45854-SMW/10801902224436, 10801902214888/33F26B0830, 33F24F0872; CDC-42802-XP1A/10801902193275, 10801902168365, 10801902162103/33F25J0295, 33F25J0728, 33F25K0304, 33F25K0390, 33F25L0228, 33F25M0037, 33F25M0485, 33F25M0717, 33F26A1630, 36F25C0008, 36F25D0001, 36F25D0034, 36F25E0001, 36F25G0022, 36F25H0015, 33F24D0258; CDC-42854-XP1A/10801902193275, 20801902117148, 10801902162134/33F25J0681, 33F26A0390, 33F26C0209, 33F26D0062, 36F25D0003, 36F25H0014, 33F24D0827; CDC-45703-XP1A/10801902193275, 20801902117216/33F25G0286, 33F25H0876,33F25J0089,33F25J0682, 33F25J0702, 33F25J0705, 33F25J0711,33F25J0718, 33F25J0729, 33F25J0733, 33F25K0305, 33F25L0063,33F25L0093, 33F25L0094, 33F25L0231, 33F25L0252, 33F25L0253, 33F25L0254, 33F25L0286, 33F25L0302, 33F25L0322, 33F25M0487, 33F26A0062, 33F26B0637, 33F26B0638, 33F26D0185, 36F25A0008, 36F25A0014, 36F25D0010, 36F25D0011, 36F25D0014, 36F25D0021, 36F25D0022, 36F25D0023, 36F25D0028, 36F25D0041, 33F25C0372; CDC-45854-XP1A/10801902193275, 10801902169720, 10801902162158/33F25J0695, 33F25J0730, 33F25K0394, 33F26A1620, 33F26B0572, 33F26B0735, 36F25G0003, 36F25G0021, 36F25G0024, 36F25H0011, 36F25H0017, 33F24D0424 ASK-42703-PGM3/10801902213751/33F24F0951, 33F24K0743; ASK-42802-UH1/10801902156386/33F24H0122; ASK-45703-PGM3/10801902213768/33F24D0844, 33F24F0840;", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2376-2026%22", "url": "https://recallledger.net/recalls/device-z-2376-2026-description-ref-cvc-psi-kit-2-lumen-8-fr-x-6-in-ask-42802-plh-cvc-k/"}, {"id": "fda-device-z-2375-2026", "source": "FDA", "category": "device", "recall_number": "Z-2375-2026", "title": "Description/REF: PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-PNHS2 recall (ARROW INTERNATIONAL, LLC)", "product": "Description/REF: PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-PNHS2; PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-PNHS2; PI CVC KIT: 4L 8.5 FR X 20 CM AGB+/ASK-45854-PNHS2", "reason": "Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.", "hazard_level": "Class I", "company": "ARROW INTERNATIONAL, LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-21", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "0", "codes": "REF(Material)/UDI-DI/Lot(Batch): ASK-42703-PNHS2/10801902193275/33F25J0107; ASK-45703-PNHS2/10801902193275/33F25B0593; ASK-45854-PNHS2/10801902193275/33F24H0128", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2375-2026%22", "url": "https://recallledger.net/recalls/device-z-2375-2026-description-ref-pi-cvc-kit-3l-7-fr-x-16-cm-agb-ask-42703-pnhs2-p/"}, {"id": "fda-device-z-2374-2026", "source": "FDA", "category": "device", "recall_number": "Z-2374-2026", "title": "Description/REF: AHDC KIT: 3-L 12 FR X 16 CM/AK-12123-PCDC recall (ARROW INTERNATIONAL, LLC)", "product": "Description/REF: AHDC KIT: 3-L 12 FR X 16 CM/AK-12123-PCDC; AHDC KIT: 3-L 12 FR X 20 CM/AK-15123-PCDC; AHDC KIT: 3-L 12 FR X 20 CM/CDC-15123-XP1A; AHDC KIT: 3-L 12 FR X 25 CM/CDC-16123-XP1A; AHDC KIT: 3-L 12 FR X 25 CM/CDC-16123-XPN1A; AHDC AGB U-BEND KIT: 2-L 12 FR X 20 CM/CDC-25122-XN1A-U; LBCVC AGB KIT: 3-L 12 FR X 16 CM/CDC-22123-XN1A", "reason": "Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.", "hazard_level": "Class I", "company": "ARROW INTERNATIONAL, LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-21", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "4,270", "codes": "REF(Material)/UDI-DI/Lot(Batch): AK-12123-PCDC/10801902193275, 10801902168471/33F24J0419, 33F25B0015, 33F25F0022, 33F25G0482, 33F25J0029, 33F25K0268, 33F26B0056, 33F24E0175; AK-15123-PCDC/10801902186499, 10801902193275, 10801902168532/33F24G0140, 33F24J0449, 33F24M0074, 33F25B0040, 33F25J0604, 33F24A0767; CDC-15123-XP1A/10801902193275, 30801902111822, 10801902213430/33F25D0438, 33F25E0649, 33F25H0579, 33F25J0313, 33F26B0161, 33F26C0198, 33F24D0355; CDC-16123-XP1A/10801902193275, 40801902111867/33F25D0612, 33F25G0291, 33F25H0578, 33F26C0190, 33F24L0469; CDC-16123-XPN1A/10801902193275, 10801902196498/33F25J0113, 33F24D0974; CDC-25122-XN1A-U/10801902193275/33F25J0114, 33F25B0621; CDC-22123-XN1A/50801902123515/33F24D0928", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2374-2026%22", "url": "https://recallledger.net/recalls/device-z-2374-2026-description-ref-ahdc-kit-3-l-12-fr-x-16-cm-ak-12123-pcdc-ahdc-kit/"}, {"id": "fda-device-z-2373-2026", "source": "FDA", "category": "device", "recall_number": "Z-2373-2026", "title": "Description/REF: HEMODIALYSIS KIT: 2-LUMEN 8 FR X 11 CM/AK-11802-F recall (ARROW INTERNATIONAL, LLC)", "product": "Description/REF: HEMODIALYSIS KIT: 2-LUMEN 8 FR X 11 CM/AK-11802-F; HEMODIALYSIS KIT: 2-LUMEN 12 FR X 16 CM/AK-22122; HEMODIALYSIS KIT 2L: 14 FR X 15CM AGB/AK-22142-CDC; HEMODIALYSIS KIT 2L: 14 FR X 20CM AGB/AK-25142-CDC; HEMODIALYSIS KIT: 2L 14 FR X 15 CM/ASK-22142-UMD; HEMODIALYSIS KIT: 2L 14 FR X 15 CM/ASK-22142-UNC; HEMODIALYSIS KIT: 2L 14 FR X 20 CM/ASK-25142-UMD; HEMODIALYSIS KIT 2L: 14 FR X 20 CM AGB/ASK-25142-UN1; HEMODIALYSIS KIT: 2L 14 FR X 25 CM/ASK-26142-UMD; HEMODIALYSIS KIT: 2LUMEN 12 FR X 13 CM/AU-23122-F; HEMODIALYSIS KIT: 2LUMEN 12 FR X 20 CM/AU-25122-F; HEMODIALYSIS KIT: 2L 12 FR X 16 CM AGB/CDC-22122-X1A; HEMODIALYSIS KIT: 2L 12 FR X 16 CM AGB/CDC-22122-XU1A; HEMODIALYSIS KIT: 2L 14 FR X 15 CM AGB/CDC-22142-X1A; HEMODIALYSIS KIT: 2L 12 FR X 25 CM AGB/CDC-26122-X1A; HEMODIALYSIS KIT 2L: 12 FR X 16CM AGB/AK-22122-CDC; HEMODIALYSIS KIT: 2-LUMEN 12 FR X 16 CM/AK-22122-F; HEMODIALYSIS KIT: 2-LUMEN 14 FR X 15 CM/AK-22142-F; AHDC AGB U-BEND KIT: 2-L 12 FR X 16 CM/CDC-22122-CN1AU; AHDC AGB CURVED KIT: 2-L 14 FR X 15 CM/CDC-22142-CN1AC; AHDC AGB U-BEND KIT: 2-L 12 FR X 13 CM/CDC-23122-CN1AU; AHDC AGB U-BEND KIT: 2-L 12 FR X 20 CM/CDC-25122-CN1AU; AHDC AGB CURVED KIT: 2-L 14 FR X 20 CM/CDC-25142-CN1AC;", "reason": "Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.", "hazard_level": "Class I", "company": "ARROW INTERNATIONAL, LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-21", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "15,425", "codes": "REF(Material)/UDI-DI/Lot(Batch): AK-11802-F/10801902193275, 10801902197129/33F24G0344, 33F24J0511, 33F24L0637, 33F25A0473, 33F25E0060, 33F25J0473, 33F24A0848; AK-22122/10801902193275/33F24H0232, 33F24J0523; AK-22142-CDC/10801902193275/33F24J0527, 33F24K0129, 33F24L0649, 33F25C0115, 33F25C0959, 33F25E0940, 33F25J0481, 33F25L0428, 33F24G0364; AK-25142-CDC/10801902193275, 50801902123195/33F25A0486, 33F25C0892, 33F25E0086, 33F25E0944, 33F25J0485, 33F25J0845, 33F25L0374, 33F26B0521, 33F25A0487; ASK-22142-UMD/10801902193275, 10801902136470, 10801902143690/33F25F0362, 33F25J0094, 33F26A0244, 33F26B0137, 33F24F0041; ASK-22142-UNC/10801902193275/33F25G0269, 33F24K0560; ASK-25142-UMD/10801902193275, 10801902136500/33F25B0239, 33F25E0308, 33F25G0686, 33F25K0425, 33F26A0246, 33F26C0047, 33F24K0696; ASK-25142-UN1/10801902193275, 10801902156379/33F24L1157, 33F26B0908, 33F25B0420; ASK-26142-UMD/10801902193275, 33F26A0408, 33F25B0427; AU-23122-F/10801902193275/33F25C0877, 33F25H0157, 33F24L0038; AU-25122-F/10801902193275, 70801902123328, 10801902210071/33F25G0562, 33R24L0038, 33F24D0400; CDC-22122-X1A/10801902193275, 10801902213478/33F25E0694, 33F25G0268, 33F24D0693; CDC-22122-XU1A/10801902193275, 10801902168044/33F25E0652, 33F25H0643, 33F24D0830; CDC-22142-X1A/10801902193275/33F25A0284; CDC-26122-X1A/10801902213515/33F24F1028; AK-22122-CDC/10801902193275, 10801902198492/33F24K0125, 33F24L0647, 33F25C0114, 33F25E0936, 33F25G0091, 33F24E0355; AK-22122-F/10801902193275/33F24G0360, 33F24J0524, 33F24K0126, 33F25A0482, 33F25E0075, 33F25E0937, 33F25J0839, 33F25L0413, 33F24G0361; AK-22142-F/10801902193275/33F24L0662, 33F25C0117, 33F25C0865, 33F25H0034, 33F25J0841, 33F24K0130; CDC-22122-CN1AU/10801902193275, 10801902222265/33F26A1388, 33F26B0398, 33F24L0966; CDC-22142-CN1AC/10801902193275/33F26A1550, 33F25J0455; CDC-23122-CN1AU/10801902193275, 10801902222319/33F26A0008, 33F26A1478, 33F26B0397, 33F24L0279; CDC-25122-CN1AU/10801902193275/33F25M0346, 33F25E0882; CDC-25142-CN1AC/30801902123597/36F25B0018", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2373-2026%22", "url": "https://recallledger.net/recalls/device-z-2373-2026-description-ref-hemodialysis-kit-2-lumen-8-fr-x-11-cm-ak-11802-f/"}, {"id": "fda-device-z-2372-2026", "source": "FDA", "category": "device", "recall_number": "Z-2372-2026", "title": "Description/REF: HEMODIALYSIS KIT: 2L 14 FR X 20 CM AGB\tCDC-25142-X1A recall (ARROW INTERNATIONAL, LLC)", "product": "Description/REF: HEMODIALYSIS KIT: 2L 14 FR X 20 CM AGB\tCDC-25142-X1A", "reason": "Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.", "hazard_level": "Class I", "company": "ARROW INTERNATIONAL, LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-21", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "1180", "codes": "REF(Material)/UDI-DI/Lot(Batch): CDC-25142-X1A/30801902123597, 10801902193275/36F25E0021, 33F25B0467", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2372-2026%22", "url": "https://recallledger.net/recalls/device-z-2372-2026-description-ref-hemodialysis-kit-2l-14-fr-x-20-cm-agb-cdc-25142-x1a/"}, {"id": "fda-device-z-2371-2026", "source": "FDA", "category": "device", "recall_number": "Z-2371-2026", "title": "Description/REF: EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05502-VM1 recall (ARROW INTERNATIONAL, LLC)", "product": "Description/REF: EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05502-VM1; EPIDURAL CATHETERIZATION KIT: 19 GA/AK-05501; EPIDURAL CATHETERIZATION KIT/AK-05502; EPIDURAL CATHETERIZATION KIT/AK-05502D; EPIDURAL CATHETERIZATION KIT/AK-05503; EPIDURAL CATHETERIZATION KIT/AK-05503-L; SPINAL ANES/EPIDURAL CATH KIT/AK-05560; SPINAL ANES/EPIDURAL CATH KIT/ASK-02520-SBMC1; EPIDURAL CATHETERIZATION KIT/ASK-05400-BW1; EPIDURAL CATHETERIZATION KIT/ASK-05400-GH; SPINAL ANES/EPIDURAL CATH KIT/ASK-05401-LMC; EPIDURAL CATHETERIZATION KIT/ASK-05401-NM; SPINAL ANES/EPIDURAL CATH KIT/ASK-05500-BID1; EPIDURAL CATHETERIZATION KIT: 19 GA/ASK-05500-JHH1; EPIDURAL CATHETERIZATION KIT: 19 GA/ASK-05500-MCV1; EPIDURAL CATHETER KIT: 19GA X 90CM\tASK-05500-MVH; EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05500-UMC; 19 GA X 35.5 IN EPIDURAL CATHETER KIT/ASK-05502-MLH; SPINAL ANES/EPIDURAL CATH KIT/ASK-05560-JMH1; SPINAL ANES/EPIDURAL CATH KIT/ASK-05560-MKD2; SPINAL ANES/EPIDURAL CATH KIT/ASK-05560-OM1; EPIDURAL CATHETERIZATION KIT/ASK-17019-SM; EPIDURAL CATHETERIZATION KIT/BP-05501; EPIDURAL CATHETERIZATION KIT/CK-05401; EPIDURAL CATHETERIZATION KIT/HS-05501; EPIDURAL CATHETERIZATION KIT/MM-05501; EPIDURAL CATHETERIZATION KIT: 19 GA/MP-17019-TK; EPIDURAL CATHETERIZATION KIT: 19 GA/MP-17019-TKD; EPIDURAL CATHETERIZATION KIT: 19 GA/MP-17019-TKL; EPIDURAL CATHETERIZATION KIT/MSO-05401-JMH; EPIDURAL CATHETERIZATION KIT/NM-05401; EPIDURAL CATHETERIZATION KIT/SJ-05501; EPIDURAL CATHETERIZATION KIT/SM-05401; EPIDURAL CATHETER KIT: 19 GA X 90 CM/TM-05401; EPIDURAL CATHETERIZATION KIT/TM-05502; SPINAL ANES/EPIDURAL CATH KIT/UI-05502; SPINAL ANES/EPIDURAL CATH KIT: 19 GA/ASK-05400-SHM; EPIDURAL CATH KIT: 19 GA/ASK-05400-UOM; EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05500-MR; EPIDURAL CATHETERIZATION KIT: 19 GA/ASK-05500-TM; EPIDURAL CATHETERIZATION KIT/ASK-05501-BHL1; EPIDURAL CATHETERIZATION KIT/ASK-05501-GH; EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05501-SM; EPIDURAL CATHETERIZATION KIT/ASK-05502-BSM; EPIDURAL CATHETERIZATION KIT/ASK-05502-MGH1; EPIDURAL CATHETERIZATION KIT/ASK-05503-BWB1; EPIDURAL CATHETERIZATION KIT/ASK-05503-HMH; EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05503-SPH; EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05503-UPM1; SPINAL ANES/EPIDURAL CATH KIT/ASK-05560-UCI2; EPIDURAL CATHETERIZATION KIT: 19 GA/ASK-17019-UMP; EPIDURAL CATHETERIZATION KIT/MH-05503-1; EPIDURAL CATHETERIZATION KIT/ASK-05401-VB2; Epidural Catheterization Kit: 19GA/ASK-05500-SC1; Epidural Catheterization Kit: 19GA/ASK-05500-SC3; EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05501-AFH1; EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05501-BMC; EPIDURAL CATHETERIZATION KIT/ASK-05502-NY; EPIDURAL CATHETERIZATION KIT/ASK-17019-RMH", "reason": "Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.", "hazard_level": "Class I", "company": "ARROW INTERNATIONAL, LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-21", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "1,525,831", "codes": "REF(Material)/UDI-DI/Lot(Batch): ASK-05502-VM1/10801902210217, 10801902209938/33F25C0168, 33F25C0880, 33F25E0202, 33F25G0134, 33F25H0126, 33F26C0297, 33F24C0216; AK-05501/)10801902210217, 10801902209501, 10801902209518/33F24E0057, 33F24E0058, 33F24J0496, 33F24K0094, 33F24L0564, 33F25A0460, 33F25A0617, 33F25C0728,33F25E0043, 33F25E0913, 33F25G0081, 33F25H0015, 33F25J0465, 33F25J0822, 33F25K0254, 33F25L0376, 33F26C0300, 33F24B0119; AK-05502/10801902209518, 10801902210217, 10801902209525/33F24C0015, 33F24G0581, 33F24G0582, 33F24G0583, 33F24J0497, 33F24J0678, 33F24J0679, 33F24J0680, 33F24J0681, 33F24K0095, 33F24K0310, 33F24L0580, 33F24L0624, 33F24L0628, 33F24L0630, 33F24L0757, 33F24L0785, 33F25A0461, 33F25A0618, 33F25A0619, 33F25A0620, 33F25C0103, 33F25C0724, 33F25C0725, 33F25C0741, 33F25C0791, 33F25E0044, 33F25E0291, 33F25E0292, 33F25E0293, 33F25E0914, 33F25E1067, 33F25G0082, 33F25G0159, 33F25H0016, 33F25H0197, 33F25H0198, 33F25H0199, 33F25J0466, 33F25J0643, 33F25J0790, 33F25J0805, 33F25J0806, 33F25J0807, 33F25J0808, 33F25K0024, 33F25K0252, 33F25K0358, 33F25K0359, 33F25L0099, 33F25L0266, 33F25L0267, 33F25M0970, 33F25M0978, 33F26A1100, 33F24C0096; AK-05502D/10801902210217, 10801902209532/33F24G0331, 33F24J0498, 33F24K0096, 33F24L0713, 33F25A0462, 33F25C0745, 33F25E0045, 33F25H0017, 33F25J0467, 33F25L0366, 33F24C0017; AK-05503/10801902210217, 10801902209549/33F24J0277, 33F24J0499, 33F24K0097, 33F24L0674, 33F25A0463, 33F25C0949, 33F25E0046, 33F25E0915, 33F25H0018, 33F25J0823, 33F25L0406, 33F25M0912, 33F24C0018; AK-05503-L/10801902209549, 10801902210217, 10801902209549/33F24C0019, 33F24E0066, 33F24J0682, 33F24K0098, 33F24L0613, 33F24L0758, 33F25A0464, 33F25C0104, 33F25C0731, 33F25C0793, 33F25E0047, 33F25E0916, 33F25G0083, 33F25H0019, 33F25H0200, 33F25J0791, 33F25J0809, 33F25K0026, 33F25K0253, 33F25L0057, 33F25L0352, 33F25M0861, 33F26A0989, 33F24J0278; AK-05560/10801902210217, 10801902209556, 30801902121722/33F24J0501, 33F24K0099, 33F24L0552, 33F25A0145, 33F25A0465, 33F25C0743, 33F25E0048, 33F25E0917, 33F25G0084, 33F25H0020, 33F25J0737, 33F25J0824, 33F25M0895, 33F26B0538, 33F26C0592, 33F24A0812; ASK-02520-SBMC1/10801902209570, 10801902210217, 10801902193275/33F24D0103, 33F24F0275, 33F24G0396, 33F25A0137; ASK-05400-BW1/10801902209617, 10801902209631/33F24D0153, 33F24E0474, 33F24G0461, 33F24J0307, 33F24L0556, 33F25B0246, 33F25C0729, 33F25E0178, 33F25G0121, 33F25J0899, 33F25L0042, 33F25L0450, 33F24C0196; ASK-05400-GH/10801902209631, 10801902210217, 10801902202199/33F24D0154, 33F24E0480, 33F24G0292, 33F24J0310, 33F24J0600, 33F24L0597, 33F25A0153, 33F25C0161, 33F25C0754, 33F25E0181, 33F25G0123, 33F25J0532, 33F25L0391, 33F25M0897, 33F24D0155; ASK-05401-LMC/10801902210217, 10801902209662/33F24J0603, 33F25F0240, 33F25G0754, 33F25J0534, 33F24D0031; ASK-05401-NM/10801902210217/33F24E0104, 33F24G0295, 33F24J0311, 33F24J0604, 33F24K0223, 33F24L0559, 33F25A0548, 33F25C0840, 33F25E0184, 33F25G0125, 33F25H0113, 33F25J0535, 33F25L0024, 33F25L0361, 33F24E0027; ASK-05500-BID1/10801902210217/33F24E0490, 33F24G0297, 33F24H0488, 33F24J0607, 33F24L0594, 33F25A0551, 33F25C0823, 33F25E0187, 33F25G0127, 33F25J0536, 33F25L0438, 33F24K0228; ASK-05500-JHH1/10801902210217, 10801902209716, 10801902209723/33F24L0572, 33F25B0379, 33F25D0215, 33F25E0190, 33F25G0129, 33F25H0744, 33F25J0538, 33F25K0407, 33F25M0955, 33S24L0572, 33F24C0203; ASK-05500-MCV1/10801902210217/33F24E0494, 33F24E0495, 33F24G0470, 33F24J0611, 33F24K0229, 33F24L0707, 33F25A0554, 33F25C0784, 33F25E0191, 33F25E1005, 33F25G0761, 33F25H0115, 33F24E0496; ASK-05500-MVH/10801902209730, 10801902210217/33F24D0380, 33F24E0498, 33F24G0472, 33F24L0681; ASK-05500-UMC/10801902209754, 10801902210217/33F24D0382, 33F24J0316, 33F24K0233, 33F24L0085, 33F24L0772, 33F25C0166, 33F25C0737, 33F25E0196, 33F25E0317, 33F25E1008, 33F25H0120, 33F25J0540, 33F25L0397, 33F25M0904, 33F24E0502; ASK-05502-MLH/10801902210217/33F24J0618, 33F24K0239, 33F24L0555, 33F25A0562, 33F25C0996, 33F25E0201, 33F25H0125, 33F25J0544, 33F25L0440, 33F26B0977, 33F24L0583; ASK-05560-JMH1/10801902210217, 10801902209983/33F24G0483, 33F24L0773, 33F25A0566, 33F25C0894, 33F25E1014, 33F25H0130, 33F25J0548, 33F24E0519; ASK-05560-MKD2/10801902193275, 10801902210217/33F24K0246, 33F25G0468, 33F24J0476; ASK-05560-OM1/10801902210217, 10801902210002/33F24K0550, 33F25A0155, 33F25C0171, 33F25F0383, 33F25G0560, 33F25H0131, 33F25H0746, 33F25J0784, 33F25L0006, 33F25M0903, 33F24D0391; ASK-17019-SM/10801902210217, 10801902211221/33F25G0137, 33F25H0136, 33F25J0553, 33F25L0465, 33F24B0348; BP-05501/10801902210217, 10801902193275/33F24E0156, 33F24J0642, 33F24K0270, 33F25B0689, 33F25C0868, 33F25E1034, 33F25G0145, 33F25H0158, 33F25J0568, 33F25L0369, 33F26B0518, 33F25C0444; CK-05401/10801902202144, 10801902210217, 10801902193275/33F24C0256, 33F25A0591, 33F25C0972, 33F25E0256, 33F25E1040, 33F25H0756, 33F25J0935, 33F25L0244, 33F26B0620, 33F25D0674; HS-05501/10801902210217, 10801902202090/33F24E0580, 33F24J0329, 33F24B0389; MM-05501/10801902210217/33F24J0655, 33F24K0287, 33F24L0788, 33F25J0628, 33F25L0445, 33F24C0263; MP-17019-TK/10801902210217/33F24D0409, 33F24J0390, 33F24K0288, 33F24L0546, 33F25A0595, 33F25C0727, 33F25E0262, 33F25E1045, 33F25H0170, 33F25J0629, 33F25L0441, 33F25M0939, 33F24D0410; MP-17019-TKD/10801902210217, 10801902210224/33F24J0657, 33F24L0698, 33F25C0760, 33F25E0263, 33F25H0171, 33F25J0938, 33F24B0152; MP-17019-TKL/10801902210224, 10801902210217/33F24D0038, 33F24K0289, 33F24L0614, 33F25C0190, 33F25C0839, 33F25E0264, 33F25G0149, 33F25J0630, 33F25K0380, 33F24K0290; MSO-05401-JMH/10801902210217/33F25C0193, 33F25H0172, 33F25J0631, 33F25L0375, 33F25M0880, 33F24D0413; NM-05401/10801902210217, 10801902210262, 10801902140644/33F25J0944, 33F25M0968, 33F26B0600, 33F24C0780; SJ-05501/10801902210330, 10801902210217, 10801902202496/33F24C0049, 33F24C0050, 33F24J0382, 33F24J0383, 33F24J0384, 33F24J0385, 33F24J0386, 33F24K0552, 33F24K0553, 33F24K0554, 33F24K0555, 33F24K0556, 33F24K0557, 33F24L0625, 33F24L0721, 33F24L0760, 33F24L0786, 33F25A0605, 33F25A0623, 33F25A0624, 33F25C0202, 33F25C0789, 33F25C0790, 33F25C0945, 33F25C0997, 33F25E0278, 33F25E0295, 33F25E0296, 33F25E1057, 33F25E1068, 33F25G0154, 33F25G0160, 33F25H0183, 33F25H0202, 33F25H0203, 33F25J0639, 33F25J0644, 33F25J0798, 33F25J0811, 33F25J0812, 33F25J0813, 33F26B0601, 33F26C0299, 33F26C0307, 33F24A1336; SM-05401/10801902210217, 10801902210354, 10801902193275/33F24G0561, 33F24K0302, 33F24L0607, 33F25C0204, 33F25C0805, 33F25E0279, 33F25E1058, 33F25H0184, 33F25J0948, 33F26A1030, 33F24G0270; TM-05401/10801902210217, 30801902202155, 10801902210361/33F24D0418, 33F24G0563, 33F24J0669, 33F24L0089, 33F24L0741, 33F25C0207, 33F25C0918, 33F25E0282, 33F25E1059, 33F25J0950, 33F25L0447, 33F26C0308, 33F24B0410; TM-05502/10801902210378/33F24B0411; UI-05502/10801902210217/33F24G0565, 33F24J0670, 33F24L0562, 33F25A0607, 33F25C0881, 33F25E0283, 33F25E1060, 33F25G0752, 33F25H0186, 33F25J0951, 33F24A0359; ASK-05400-SHM/10801902210217/33F24E0482, 33F24G0465, 33F24J0601, 33F24K0221, 33F24L0800, 33F25C0162, 33F25C0888, 33F25E0182, 33F25H0741, 33F25L0457, 33F24E0483; ASK-05400-UOM/10801902210217/33F25G0124, 33F25H0742, 33F25K0263, 33F24G0294; ASK-05500-MR/10801902210217, 10801902209730/33F24E0497, 33F24G0471, 33F24K0230, 33F25A0555, 33F25C0796, 33F25E0192, 33F25H0116, 33F25K0408, 33F25M0854, 33F24C0204; ASK-05500-TM/10801902210217, 10801902209747, 10801902209754/33F25C0165, 33F25E1007, 33F25M0871, 33F26C0256, 33F24C0206; ASK-05501-BHL1/10801902210217/33F24L0566, 33F25A0558, 33F25C0810, 33F25E0197, 33F25E1009, 33F25H0121, 33F25J0541, 33F25L0439, 33F24E0503; ASK-05501-GH/10801902210217, 10801902210392/33F24K0235, 33F25A0559, 33F25E0198, 33F25H0122, 33F25J0542, 33F24D0384; ASK-05501-SM/10801902210217, 10801902210392, 10801902214857/33F24E0505, 33F24K0236, 33F25A0560, 33F25C0808, 33F25E0199, 33F25E1010, 33F25H0123, 33F25J0907, 33F26C0304, 33F24C0210; ASK-05502-BSM/10801902209853, 10801902210217/33F24D0385, 33F24E0508, 33F24G0301, 33F24K0237, 33F25A0154, 33F25B0687, 33F25H0124, 33F25J0543, 33F25K0409, 33F25L0466, 33F26B0592, 33F24E0509; ASK-05502-MGH1/10801902210217, 10801902209860/33F24J0617, 33F24L0569, 33F25B0247, 33F25C0938, 33F25E0304, 33F25G0133, 33F25J0909, 33F25L0098, 33F26B0545, 33F24J0318; ASK-05503-BWB1/10801902210217, 10801902209938, 10801902209952/33F24E0514, 33F24G0481, 33F24J0619, 33F24K0241, 33F24L0690, 33F25C0169, 33F25C0756, 33F25E1011, 33F25J0545, 33F25L0453, 33F26B0584, 33F24C0217; ASK-05503-HMH/10801902210217, 10801902209952, 10801902209969/33F24L0643, 33F25A0563, 33F25C0170, 33F25C0765, 33F25E1012, 33F25G0135, 33F25H0127, 33F25J0546, 33F25L0451, 33F26A1079, 33F24C0218; ASK-05503-SPH/10801902210217, 10801902209969, 10801902211405/33F24E0516, 33F24J0620, 33F24K0243, 33F24L0598, 33F25A0564, 33F25E0204, 33F25L0458, 33F25M0951, 33F24C0219; ASK-05503-UPM1/10801902211405, 10801902210217, 10801902209976/33F24D0389, 33F24E0160, 33F24J0621, 33F24K0244, 33F24L0549, 33F25A0565, 33F25C0992, 33F25E0205, 33F25E1013, 33F25H0129, 33F25J0547, 33F25L0454, 33F24D0390; ASK-05560-UCI2/10801902210217, 10801902193275/33F24G0485, 33F24J0623, 33F24L0593, 33F25A0567, 33F25C0893, 33F25E0206, 33F25E1015, 33F25H0132, 33F25J0911, 33F25L0061; ASK-17019-UMP/10801902210217, 10801902211221, 10801902210057/33F24J0628, 33F24K0250, 33F25B0694, 33F25E0216, 33F25H0137, 33F25J0916, 33F26B1000, 33F24B0350; MH-05503-1/10801902210217/33F25H0169, 33F24G0542 ASK-05401-VB2/10801902214840/33F24C0199, 33F24D0374, 33F24E0486, 33F24G0296, 33F24J0312, 33F24J0605, 33F24K0224, 33F24L0733, 33F25A0549; ASK-05500-SC1 /10801902202250/33F24B0319, 33F24C0205, 33F24D0381, 33F24E0499, 33F24G0299, 33F24J0315, 33F24J0613, 33F24K0232, 33F24L0567, 33F25A0557, 33F25C0884, 33F25E0194; ASK-05500-SC3/10801902223651/33F25G0751, 33F25H0118, 33F26B0644; ASK-05501-AFH1/10801902209761/33F24G0475; ASK-05501-BMC/10801902209785/33F24J0479; ASK-05502-NY/10801902209884/33F24E0512; ASK-17019-RMH/10801902214918/33F24B0346, 33F24E0531", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2371-2026%22", "url": "https://recallledger.net/recalls/device-z-2371-2026-description-ref-epidural-catheter-kit-19-ga-x-90-cm-ask-05502-vm1/"}, {"id": "fda-device-z-2370-2026", "source": "FDA", "category": "device", "recall_number": "Z-2370-2026", "title": "Description/REF: PI AGBA PICC KIT: 3L 6 FR X 40 CM W/VPS/ASK-44063-NS AGBA... recall (ARROW INTERNATIONAL, LLC)", "product": "Description/REF: PI AGBA PICC KIT: 3L 6 FR X 40 CM W/VPS/ASK-44063-NS AGBA PICC/DELTA: 2L 5.5 FR X 50 CM/ASK-45052-NS AGBA PICC/DELTA KIT: 1L 4.5 FR X 55 CM/ASK-45541-MHBV PICC KIT: 2L 5.5 FR X 55 CM CG+ VPS/ASK-45552-RH AGBA PICC NaviCurve: 2L 5.5FR x 55CM BP/DLX-45552-CURVB AGBA PICC NaviCurve: 2L 5.5FR x 55CM TCG/DLX-45552-CURVC AGBA PICC: 2L 5.5FR x 55CM w Biopatch/DLX-45552-HPKB AGBA PICC NaviCurve: 3L 6FR x 55CM BP/DLX-45563-CURVB PI PICC KIT: 4 FR X 50 CM/ASK-35041-NH PI PICC KIT: 2-L 5 FR X 50 CM/ASK-35052-NH PI PICC G4 Stylet: 1L 4FR x 55CM w CHG/DLX-35541-VPSC PI PICC NaviCurve: 2L 5FR x 55CM w BP/DLX-35552-CURVB PI PICC NaviCurve: 3L 6FR x 55CM w BP/DLX-35563-CURVB PI PICC G4 Stylet: 3L 6FR x 55CM w BP/DLX-35563-VPSB AGBA PI PICC KIT: 2L 5.5 FR X 55CM/CDC-45552-HPK1A PI AGBA PICC KIT: 3-L 6 FR X 55 CM/CDC-45563-HPK1A PI AGBA PICC KIT: 1L 4.5 FR X 55 CM VPS/ASK-45541-UOI1 PICC KIT: 1L 4.5 FR X 55 CM VPS/ASK-45541-VFH1 PI AGBA PICC KIT: 2L 5.5 FR X 55 CM VPS/ASK-45552-UOI1 PICC KIT: 2L 5.5 FR X 55 CM VPS/ASK-45552-VFH1 PI AGBA PICC KIT: 3L 6 FR X 55 CM W/VPS/ASK-45563-UWH1 AGBA PICC NaviCurve: 1L 4.5FR x 55CM BP/DLX-45541-CURVB AGBA PICC NaviCurve: 1L 4.5FR x 55CM TCG/DLX-45541-CURVC AGBA PICC G4 Stylet: 1L 4.5FR x 55CM TCG/DLX-45541-VPSC AGBA PICC G4 Stylet: 2L 5.5FR x 55CM BP/DLX-45552-VPSB AGBA PICC G4 Stylet: 2L 5.5FR x 55CM TCG/DLX-45552-VPSC PI PICC:1L 4FR X 50CM PRELOAD VPS STYLET/CDC-35041-VPS PICC KIT: 3 FR X 55 CM/CDC-05531-PK1A", "reason": "Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.", "hazard_level": "Class I", "company": "ARROW INTERNATIONAL, LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-21", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "37,738", "codes": "REF(Material)/UDI-DI/Lot(Batch): ASK-44063-NS/10801902193275/33F25F0100; ASK-45052-NS/10801902193275/33F24L0864 ASK-45541-MHBV/10801902193275, 10801902167696/33F25D0410, 33F26C0012, 33S24A0690, 33F25B0574; ASK-45552-RH/10801902193275/33F25B0575, 33F25D0361, 33F25F0197, 33F25K0373, 33F25A0082; DLX-45552-CURVB/10801902193275, 10801902208702/33F25E0506, 33F25E0833, 33F26C0038, 33S24B0518, 33F24L0982; DLX-45552-CURVC/10801902193275, 10801902208733/33F25B0386, 33F25D0381, 33F25D0624, 33F25E0765, 33F25F0225, 33F25H0602, 33F26C0182, 33F25B0390; DLX-45552-HPKB/10801902193275, 10801902208825, 10801902208856/33F25D0454, 33F25D0677, 33F25E0834, 33F25J0446, 33F25M0172, 33F26B0867, 33S24A0586, 33S24A1370, 33F24F0097; DLX-45563-CURVB/10801902193275/33F25C0339, 33F25E0836, 33F25A0321; ASK-35041-NH/10801902221077, 10801902193275/33F26B0140 33F25G0460; ASK-35052-NH/10801902193275/33F25H0412, 33F24L1080; DLX-35541-VPSC/10801902193275/33F25C0449, 33F25D0245, 33F25H0501, 33F24L1148; DLX-35552-CURVB/10801902193275, 10801902208764/33F25C0214, 33F25E0511 ,33F25E0832 ,33F26C0120 33F26C0732, 33F25C0373; DLX-35563-CURVB/10801902193275, 10801902208771/33F25C0337, 33F26B0155, 33F25D0453; DLX-35563-VPSB/10801902193275/33F25C0395; CDC-45552-HPK1A/10801902193275, 10801902188462/33F25D0067, 33F25D0243, 33F25E0452, 33F25E0658, 33F25E0829, 33F26B0891, 33F26C0202, 33S23K0168, 33S24A0419, 33S24A0523, 33S24A1387, 33F25K0317; CDC-45563-HPK1A/10801902193275, 10801902188479/33F25G0283, 33F25H0626, 33S24A0543, 33F24D0497; ASK-45541-UOI1/10801902193275, 10801902221664/33F25H0411, 33F25J0399, 33S24A1368, 33F26A0226; ASK-45541-VFH1/10801902193275, 10801902218886/33F25B0655, 33F25E0573, 33F25G0210, 33F26A1533, 33F26B0841, 33F25G0584; ASK-45552-UOI1/10801902193275/33F26A0227; ASK-45552-VFH1/10801902193275/33F25D0362, 33F25E0866, 33F25J0226, 33F25M0180, 33F26A1455, 33F25H0408; ASK-45563-UWH1/10801902193275/33F25D0660, 33F25J0227, 33F24K0066; DLX-45541-CURVB/10801902193275/33F25B0385, 33F25D0250, 33F25E0760, 33F25J0336, 33F25K0194, 33F24L1115; DLX-45541-CURVC/10801902193275/33F25B0507, 33F25C0216, 33F25E0761, 33F25F0223, 33F25G0362, 33F25J0337, 33F25E0762; DLX-45541-VPSC/10801902193275, 10801902208610/33F24L0390, 33F24L1130, 33F25C0247, 33F25D0251, 33F25D0380, 33F25D0623, 33F25E0764, 33F25E0900, 33F25F0224, 33F25H0604, 33F25J0445, 33F26A1541, 33F26B0460, 33F26C0220, 33F26C0717, 33F25B0387; DLX-45552-VPSB/10801902193275/33F25C0249, 33F25D0253, 33F25D0314, 33F25D0382, 33F24L0392; DLX-45552-VPSC/10801902193275, 10801902208634/33F24L0939, 33F25B0508, 33F25D0254, 33F25D0315, 33F25D0383,33F25D0626, 33F25E0581, 33F25E0709, 33F25E0835, 33F25J0129, 33F25J0257, 33F25M0167, 33F26B0712, 33F26B0937, 33F25B0388; CDC-35041-VPS/10801902186741, 10801902193275/33X25K0001, 33F25E0425; CDC-05531-PK1A/10801902193275, 60801902123420/33F25C0641, 33F25D0435, 33F25E0646, 33F25J0416, 33F26B0711, 33F25D0765", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2370-2026%22", "url": "https://recallledger.net/recalls/device-z-2370-2026-description-ref-pi-agba-picc-kit-3l-6-fr-x-40-cm-w-vps-ask-44063-ns/"}, {"id": "fda-device-z-2369-2026", "source": "FDA", "category": "device", "recall_number": "Z-2369-2026", "title": "Description/REF: PSI KIT: 7 FR X 4IN ANTIMICROBIAL/ASK-09701-UMH recall (ARROW INTERNATIONAL, LLC)", "product": "Description/REF: PSI KIT: 7 FR X 4IN ANTIMICROBIAL/ASK-09701-UMH; PSI KIT: 8.5 FR X 4 1/8 IN (10 CM)/ASK-09803-OSU4; PSI/CVC KIT: 9 FR/7 FR X 6IN (16CM)/ASK-09903-AMC1; PSI KIT: 9 FR X 4 1/8 IN (10 CM)/ASK-09903-CMC1; PSI KIT: 9 FR X 4 1/8 IN (10 CM)/ASK-09903-OSU4; PSI KIT: 9 FR X 4 1/8 IN (10CM)/ASK-09903-PCMH1; PSI KIT: 8.5 FR X 10 CM/CDC-09803-1A; PSI KIT: 9 FR X 4 IN (10 CM)/ASK-09903-ECL3; MAC KIT: 2L 9 FR DISTAL X 11.5 CM/ASK-11242-PHP2; MULTI LUMEN/PSI KIT/ASK-11142-NSU; MULTI-LUMEN/PSI KIT/AK-21242-X; MAC KIT: 2L 9 FR DISTAL X 10 CM AGB/ASK-21142-DMC; MAC KIT: 2L 9 FR DISTAL X 10 CM AGB/ASK-21142-GMC1; MULTILUMEN/PSI KIT: 9 FR X 4 IN (10 CM)/ASK-21142-HF5; MAC KIT: 2L 9 FR DISTAL X 10 CM AGB/ASK-21142-LMDT; 2L MAC KIT: 9 FR DISTAL X 4IN (10 CM)/ASK-21142-UCL1; 2-L MAC KIT: 9 FR DISTAL X 4 IN (10 CM)/ASK-21142-UPMC2; MAC KIT: 2L 9 FR DISTAL X 11.5 CM/ASK-21242-SL1; MAC KIT: 2L 9 FR DISTAL X 11.5 CM/ASK-21242-UMH; MAC KIT: 2L 9 FR DISTAL X 11.5 CM/ASK-21242-UN1; MAC KIT: 2-L 9 FR DISTAL X 10 CM AGB/CDC-21142-XCN1A; MAC KIT: 2-L 9 FR DISTAL X 10 CM AGB/CDC-21142-XN1A; MAC KIT: 2-L 9 FR DISTAL X 11.5 CM AGB/CDC-21242-XCN1A; MAC KIT: 2-L 9 FR DISTAL X 11.5 CM AGB/CDC-21242-XN1A; 2L MAC KIT: 9 FR DISTAL X 4 IN/ASK-21142-CO1; 2L MAC KIT: 9 FR DISTAL X 4 IN (10 CM)/ASK-21142-FH3; 2L MAC KIT: 9 FR DISTAL X 4 IN (10 CM)/ASK-21142-OHSU3; MULTILUMEN/PSI KIT: 9 FR X 4 IN (10 CM)/ASK-21142-SG2; MULTILUMEN/MAC KIT: 9 FR X 4 IN (10 CM)/ASK-21142-UOI1; 2 LUMEN/PSI KIT: 9 FR X 4 IN (10 CM)/ASK-21142-WHC2; MAC KIT: 2L 9 FR DISTAL X 11.5 CM/ASK-21242-BID1; AGB MAC KIT: 2L 9 FR DISTAL/ASK-21242-BSWH2; MAC KIT: 2L 9 FR DISTAL X 11.5 CM/ASK-21242-DU1; MULTILUMEN/PSI KIT 9 FR X 11.5 CM/ASK-21242-PCMH1; MAC KIT: 2L 9 FR DISTAL X 11.5 CM/ASK-21242-UCH2; AGB MAC KIT: 2L 9 FR DISTAL X 11.5 CM/ASK-21242-UHC2; PSI KIT: 8.5 FR X 10 CM ANTIMICROBIAL/ASK-29803-BSWH2; PSI KIT: 8.5 FR X 4 IN (10 CM)/ASK-29803-HHC; PSI KIT: 8.5 FR X 4 IN (10 CM)/ASK-29803-MCY1; PSI KIT: 8.5 FR X 4 IN (10 CM)/ASK-29803-UPM1; PSI KIT: 8.5 FR X 4 1/8 IN (10 CM)/ASK-29804-VCU; PSI KIT: 9 FR X 10 CM ANTIMICROBIAL/ASK-29903-MCY1; PSI KIT: 9 FR/ASK-29903-MHI; PSI KIT: 9 FR X 4 IN (10 CM)/ASK-29903-OHU4; PSI KIT: 9 FR X 4 IN (10 CM)/ASK-29903-UCH2; PSI KIT: 9 FR X 10 CM ANTIMICROBIAL/ASK-29903-UCL1; PSI KIT: 9 FR X 10 CM ANTIMICROBIAL/ASK-29903-UHC4; PSI KIT: 9FR X 4IN (10 CM) ANTIMICROBIAL/ASK-29903-UPM1; PSI KIT: 9 FR X 4 1/8 IN (10 CM)/ASK-29907-LGH; PSI KIT: 8.5 FR X 10 CM ANTIMICROBIAL/CDC-29803-1A; PSI KIT: 9 FR X 10 CM ANTIMICROBIAL/CDC-29903-1A; PSI KIT: 9 FR X 10 CM ANTIMICROBIAL/CDC-29903-X1A; PSI KIT: 9 FR X 10 CM ANTIMICROBIAL/CDC-29903-XCN1A; PSI KIT: 9 FR X 10 CM ANTIMICROBIAL/CDC-29903-XN1A; PSI KIT: 9 FR X 10 CM ANTIMICROBIAL/ASK-29903-AHH; PSI KIT: 8.5 FR X 10 CM ANTIMICROBIAL/CDC-29803-XN1A; PSI ACCESS TRAY/ASK-04001-MM2; MAC KIT: 2L 9 FR DISTAL X 10 CM AGB/ASK-21142-GMC; MULTI LUMEN/PSI KIT: 9 FR DISTAL X 4 1/2/ASK-21242-OSU3", "reason": "Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.", "hazard_level": "Class I", "company": "ARROW INTERNATIONAL, LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-21", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "348,684", "codes": "REF(Material)/UDI-DI/Lot(Batch): ASK-09701-UMH/10801902193275, 10801902139365, 10801902143874/33F24M0171, 33F25A0444, 33F25G0008, 33F25K0039, 33F25L0133, 33F26B0369, 33F23K0811; ASK-09803-OSU4/10801902212075, 10801902193275/33F24F0994, 33F24K0428, 33F25B0183, 33F25D0761; ASK-09903-AMC1/1080190219327, 10801902161830, 10801902136678/33F25A0437, 33F25E0024, 33F25G0690, 33F25L0142, 33F26C0117, 33F24B0612; ASK-09903-CMC1/10801902136678, 10801902193275/33F24D0050, 33F24D0965, 33F24F0130, 33F24J0321, 33F24J0627, 33F24L0585, 33F25A0110, 33F25C0176, 33F25C0588, 33F25E0212, 33F25E1020, 33F25F0324, 33F25G0753, 33F25L0208, 33F26A0396, 33F26A1255, 33F25E0716; ASK-09903-OSU4/10801902212006, 10801902193275/33F24G0022, 33F24L0298, 33F25D0762; ASK-09903-PCMH1/10801902193275, 20801902115205/33F25L0139, 33F26B0136, 33F24H0108; CDC-09803-1A/50801902116715, 10801902193275, 60801902116729/33F24D0892, 33F24F0766, 33F24L0274, 33F25B0147, 33F25C0497, 33F25C0498, 33F25D0553, 33F25E0647, 33F25F0209, 33F25H0574, 33F25L0121, 33F25M0410, 33F24D0504; ASK-09903-ECL3/10801902193275/33F25G0241, 33F25H0530, 33F25J0357, 33F26A0015; ASK-11242-PHP2/10801902193275, 10801902196436/33F24J0117, 33F24K0727, 33F25A0009, 33F25E0003, 33F25F0359, 33F25K0040, 33F25L0132, 33F26B0223, 33F26D0016, 33F24K0544; ASK-11142-NSU/10801902182545, 10801902193275/33F24E0326, 33F24K0354, 33F24L0244, 33F24L0300, 33F25B0189, 33F25C0228, 33F25D0467, 33F25E0591, 33F25G0272, 33F25G0405, 33F25H0629, 33F25J0363, 33F26A1572, 33F26B0816, 33F24L0840; AK-21242-X/10801902193275, 30801902122262, 80801902123127/33F24G0358, 33F24J0522, 33F24K0124, 33F24L0749, 33F25B0683, 33F25E0073, 33F25J0479, 33F25L0443, 33F26C0301, 33F24D0371; ASK-21142-DMC/10801902193275, 10801902218930, 10801902206685/33F25B0242, 33F25M0671, 33F26A0237, 33F26B0946, 33F24D0718; ASK-21142-GMC1/10801902193275, 10801902200492/33F25B0642, 33F25E0719, 33F25H0582, 33F25M0147, 33F26C0335, 33F24F0098; ASK-21142-HF5/10801902200492, 10801902193275, 10801902200492/33F24F0921, 33F24K0350, 33F24L0245, 33F25A0168, 33F25C0272, 33F25D0344, 33F25F0103, 33F25G0282, 33F25H0614, 33F25J0371, 33F26A1525, 33F26C0040, 33F24L0309; ASK-21142-LMDT/10801902193275, 10801902220728/33F25A0041, 33F25B0381, 33F25D0346, 33F25F0172, 33F25K0416, 33F25M0343, 33F26B0189, 33F26C0139, 33F25K0206; ASK-21142-UCL1/10801902193275/33F25E0541, 33F25G0391, 33F25J0102, 33F25J0373, 33F25M0235, 33F26A1375, 33F24H0098; ASK-21142-UPMC2/10801902159479, 10801902193275, 10801902225365/33F24F0879, 33F24J0161, 33F24L0310, 33F24L1023, 33F25C0276, 33F25E0780, 33F25G0348, 33F25J0209, 33F26A1371, 33F26A1547, 33R25G0348, 33F26C0490; ASK-21242-SL1/10801902193275/33F26A1347, 33F25E0314; ASK-21242-UMH/10801902129502, 10801902193275, 10801902156348/33F24E0637, 33F24F0895, 33F24L0317, 33F25B0197, 33F25C0280, 33F25D0478, 33F25F0178, 33F25H0564, 33F25L0106, 33F26A1517, 33F24F0618; ASK-21242-UN1/10801902193275, 10801902156348/33F24H0146, 33F25A0438, 33F25D0032, 33F25E0315, 33F25F0236, 33F25H0778, 33F25K0044, 33F26A0252, 33F26B0219, 33F26C0048, 33F25C0816; CDC-21142-XCN1A/10801902196498, 10801902193275/33F24E0226, 33F24E0242, 33F24E0254, 33F24F0250, 33F24G0203, 33F24H0356, 33F24H0391, 33F24J0220, 33F24L0078, 33F24M0018, 33F24M0054, 33F24M0206, 33F25A0130, 33F25A0385, 33F25B0068, 33F25B0340, 33F25C0076, 33F25C0510, 33F25D0697, 33F25D0733, 33F25E1092, 33F25E1101, 33F25F0435, 33F25G0027, 33F25H0334, 33F25H0814, 33F25J1006, 33F25K0310, 33F25L0090, 33F25L0277, 33F26A1615, 33F26A1622, 33F26A1623, 33F26A1645, 33F25B0528; CDC-21142-XN1A/10801902193275, 10801902196504, 50801902116821/33F25D0441, 33F25E0816, 33F25F0210, 33F25J0418, 33F26B0438, 33F26B0809, 33F26C0018, 33F24D0429; CDC-21242-XCN1A/10801902196511, 10801902193275, 10801902196511/33F24D0427, 33F24D0493, 33F24D0502, 33F24E0257, 33F24E0833, 33F24G0147, 33F24G0162, 33F24G0202, 33F24G0249, 33F24G0620, 33F24H0067, 33F24H0330, 33F24H0355, 33F24H0390, 33F24H0423, 33F24H0449, 33F24J0252, 33F24K0013, 33F24K0041, 33F24K0629, 33F24L0158, 33F24M0056, 33F24M0066, 33F24M0091, 33F25A0132, 33F25A0373, 33F25B0028, 33F25B0097, 33F25B0135, 33F25C0217, 33F25C0529, 33F25C0692, 33F25D0690,33F25D0692, 33F25D0698, 33F25D0707, 33F25D0721, 33F25D0734, 33F25D0754, 33F25E0415, 33F25E1102, 33F25E1123, 33F25E1152, 33F25F0030, 33F25F0039, 33F25F0484, 33F25F0525, 33F25H0335, 33F25H0872, 33F25J0747, 33F25J0774, 33F25K0292, 33F25K0353, 33F25L0092, 33F25L0236, 33F25L0298, 33F26A1617, 33F26A1626, 33F26A1632, 33F26A1635, 33F26B0621, 33F26B0622, 33F26B1039, 33F26D0229, 33F26D0230, 33X25J0002, 33F24H0395; CDC-21242-XN1A/10801902193275, 10801902196528, 20801902123484/33F25A0378, 33F25B0029, 33F25B0098, 33F25B0341, 33F25C0420, 33F25C0530, 33F25E1093, 33F25E1124, 33F25H0286, 33F25H0362, 33F25J0775, 33F25J1040, 33F26A1618, 33F26A1627, 33F26C0453, 33F26C0881, 33X25J0001, 33F24F0996; ASK-21142-CO1/10801902214291, 10801902193275/33F24F0767, 33F24K0423, 33F25B0548, 33F25D0266, 33F25F0170, 33F25H0592, 33F25K0136, 33F26A1450, 33F26C0489, 33F24J0113; ASK-21142-FH3/10801902206685, 10801902193275/33F24E0615, 33F24F0988, 33F24K0455, 33F24L0308, 33F24L0896, 33F25A0244, 33F25B0549, 33F25E0539, 33F25F0171, 33F25G0254, 33F25H0607, 33F26A1574; ASK-21142-OHSU3/10801902193275, 10801902188899, 10801902129953/33F25E1194, 33F25G0692, 33F25K0041, 33F25K0422, 33F26B0907, 33F24F0049; ASK-21142-SG2/10801902193275/33F25B0550, 33F25C0274, 33F25E0540, 33F25F0174, 33F25H0533, 33F25J0208, 33F26B0198, 33F26B0786, 33F25G0695; ASK-21142-UOI1/10801902193275, 10801902158878, 10801902159479/33F24J0014, 33F25A0013, 33F25B0425, 33F25E0012, 33F25G0553, 33F25H0773, 33F25K0042, 33F25L0259, 33F26A0236, 33F26C0115, 33F24D0800; ASK-21142-WHC2/10801902193275, 10801902134964/33F25B0643, 33F25D0473, 33F25E0857, 33F25F0114, 33F25J0210, 33F26C0338, 33F24H0148; ASK-21242-BID1/10801902193275, 10801902219135, 10801902220339/33F24L1014, 33F25B0644, 33F25E0594, 33F25F0091, 33F25F0346, 33F25H0454, 33F25J0211, 33F26C0376, 33F24F0067; ASK-21242-BSWH2/10801902220339, 10801902193275, 10801902160987/33F24F0965, 33F24K0451, 33F24L0311, 33F25A0298,33F25B0645, 33F25D0347, 33F25E0542, 33F25E0858, 33F25G0206, 33F25H0515, 33F25J0212, 33F25K0094, 33F25M0326, 33F26A1445, 33F26C0152, 33F24D0321; ASK-21242-DU1/10801902160987, 10801902193275, 10801902118407/33F24D0797, 33F24F0859, 33F24J0149, 33F24L1085, 33F25B0440, 33F25C0277, 33F25D0400, 33F25E0859, 33F25H0557, 33F25J0213, 33F25K0095, 33F24E0539; ASK-21242-PCMH1/10801902160987, 10801902193275, 10801902118407/33F24D0797, 33F24F0859, 33F24J0149, 33F24L1085, 33F25B0440, 33F25C0277, 33F25D0400, 33F25E0859, 33F25H0557, 33F25J0213, 33F25K0095, 33F24E0539; ASK-21242-UCH2/10801902219036, 10801902193275/33F24F0756, 33F24L1051, 33F25C0343, 33F25D0474, 33F25F0177, 33F25H0586, 33F25J0375, 33F26A1495, 33F26C0180, 33F26C0502, 33F25D0224; ASK-21242-UHC2/10801902193275, 10801902159639, 10801902114065/33F25D0349, 33F25F0115, 33F25G0349, 33F25H0634, 33F25J0377, 33F26C0173, 33F24D0662; ASK-29803-BSWH2/10801902220346, 10801902193275/33F24F1006, 33F24K0461, 33F24L0407, 33F25B0472, 33F25B0648, 33F25C0344, 33F25F0092, 33F25F0142, 33F25H0514, 33F25J0382, 33F25M0186, 33F26A1428, 33F26B0834, 33F26A0014; ASK-29803-HHC/10801902193275, 10801902211443/33F25A0213, 33F25B0442, 33F25F0181, 33F25G0247, 33F25J0152, 33F26B0174, 33F25E0548; ASK-29803-MCY1/10801902193275/33F24H0203, 33F24K0386, 33F24L0409, 33F25B0649, 33F25E0720, 33F25G0200, 33F25E0549; ASK-29803-UPM1/10801902193275, 10801902225136/33F24L0227, 33F24L0876, 33F25C0284, 33F25E0782, 33F25G0392, 33F25K0097, 33F25L0117, 33F26A1584, 33F26C0510; ASK-29804-VCU/10801902193275, 10801902112986/33F25E0551, 33F25F0360, 33F26B0225, 33F24L0889; ASK-29903-MCY1/10801902193275, 10801902221039, 10801902217087/33F24L0322, 33F25C0348, 33F25D0481, 33F25F0182, 33F25G0199, 33F25J0264, 33F26A1571, 33F26B0869, 33F24D0590; ASK-29903-MHI/10801902217087, 10801902193275/33F24F0808, 33F24L0831, 33F25B0474, 33F25E0555, 33F25H0458, 33F25J0265, 33F26C0341, 33F25F0008; ASK-29903-OHU4/10801902193275/33F25E0449, 33F25C0289; ASK-29903-UCH2/10801902193275/33F24K0489, 33F24L0410, 33F24L1024, 33F25C0350, 33F25F0183, 33F25H0587, 33F26A1458, 33F25H0438; ASK-29903-UCL1/10801902193275, 10801902144512/33F25J0385, 33F26B0713, 33F25B0200; ASK-29903-UHC4/10801902193275, 10801902159622/33F25F0184, 33F25H0470, 33F25J0154, 33F26B0123, 33F26C0025, 33F24H0118; ASK-29903-UPM1/10801902193275, 10801902159530, 10801902225174/33F24L0326, 33F25B0555, 33F25E0674, 33F25F0185, 33F25G0263, 33F25G0347, 33F25J0217, 33F25M0113, 33F26B0178, 33F26C0511; ASK-29907-LGH/10801902193275/33F25A0008, 33F25D0033, 33F25G0684, 33F25L0260, 33F25G0459; CDC-29803-1A/50801902117019, 10801902193275/33F24F0800, 33F24J0177, 33F24L0119, 33F24L1142, 33F25B0678, 33F25D0509, 33F25E0750, 33F25G0277, 33F25G0388, 33F25J0181, 33F26A1385, 33F26B0435, 33F25E0796; CDC-29903-1A/60801902117030, 10801902193275/33F24F0742, 33F24K0372, 33F24L0121, 33F24L1146, 33F25A0289, 33F25B0531, 33F25F0086, 33F25G0177, 33F25G0319, 33F25H0575, 33F25J0253 ,33F25M0106, 33F26A1491, 33F25J0671; CDC-29903-X1A/10801902193275, 20801902117049, 10801902193190/33F25J0679, 33F25J0726, 33F25K0187, 33F26A1553, 33F26C0352, 36F25B0022, 36F25G0002, 36F25G0019, 36F25G0025, 36F25H0007, 33F24E0229; CDC-29903-XCN1A/10801902193190, 10801902193275/33F24F0025, 33F24F0160, 33F24G0207, 33F24G0248, 33F24H0075, 33F24H0432, 33F24J0254, 33F24K0042, 33F24K0692, 33F24M0076, 33F24M0135, 33F25A0133, 33F25B0020, 33F25B0069, 33F25B0119, 33F25B0318, 33F25C0512, 33F25D0691, 33F25D0699, 33F25D0723, 33F25D0755, 33F25E1125, 33F25F0040, 33F25F0402, 33F25G0488, 33F25J0656, 33F25J0777, 33F25K0312, 33F25L0012, 33F25L0315, 33F25M0045, 33F26A1629, 33F26B0527, 33F26B0926, 33F26C0073, 33F26C0086, 33F26C0100, 33F26C0550, 33F25A0314; CDC-29903-XN1A/10801902193275, 10801902193206/33F25B0532, 33F25D0511, 33F25E0701, 33F25E0894, 33F25H0423, 33F25H0623, 33F25J0326, 33F26A1475, 33F26B0734, 33F26C0019, 33F25C0701; ASK-29903-AHH/10801902193275/33F25B0553, 33F25F0143, 33F25G0384, 33F25H0489, 33F25M0239, 33F24L0166; CDC-29803-XN1A/10801902193275, 10801902193121, 60801902117030/33F25D0510, 33F25E0700, 33F25E0893, 33F25G0337, 33F25J0252, 33F25M0400, 33F26B0152, 33F26B0733, 33F26B0820, 33F26C0009, 33F26C0582, 33F24D0888; ASK-04001-MM2/10801902193275, 10801902160086, 10801902114881/33F25B0428, 33F26B0220, 33F24D0538; ASK-21142-GMC/10801902189674/33F24K0062, 33F24K0670, 33F24M0044, 33F25A0105; ASK-21242-OSU3/10801902211986/33F24F0720, 33F24K0338, 33F24L0312;", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2369-2026%22", "url": "https://recallledger.net/recalls/device-z-2369-2026-description-ref-psi-kit-7-fr-x-4in-antimicrobial-ask-09701-umh-ps/"}, {"id": "fda-device-z-2368-2026", "source": "FDA", "category": "device", "recall_number": "Z-2368-2026", "title": "Description/REF: RA CATH KIT: 20 GA X 1 3/4 IN/TJ-04020-1 recall (ARROW INTERNATIONAL, LLC)", "product": "Description/REF: RA CATH KIT: 20 GA X 1 3/4 IN/TJ-04020-1; RA CATH KIT: 20 GA X 1 1/2IN/NA-04220-S1A; ARTERIAL LINE KIT/AK-04510-S; ARTERIAL CATH KIT: 18 GA X 6IN (16 CM)/ASK-04018-HUMC; ARTERIAL LINE KIT: 18 GA X 6 IN (16 CM)/ASK-04018-OH1; RA CATH KIT: 20 GA X 1 3/4IN (4.45 CM)/ASK-04020-BID; RA CATH KIT: 20 GA X 1-3/4IN/ASK-04020-MAR; ARTERIAL LINE KIT: 20 GA X 5 IN/ASK-04020-PM4; RA CATH KIT: 20 GA X 1 1/2IN (3.81 CM)/ASK-04120-HF3; RA CATH SET: 20 GA X 2 1/2 IN (6.35 CM)/ASK-04120-UR; ARTERIAL CATH KIT: 20 GA X 3 1/16 IN/ASK-04125-MGH; ARTERIAL CATH KIT: 20 GA X 5 IN/ASK-04500-HFH4; ARTERIAL LINE KIT: 20GA X 5IN/ASK-04510-BID2; ARTERIAL LINE KIT: 20GA X 5IN (12 CM)/ASK-04510-EHP1; ARTERIAL LINE KIT/ASK-04510-FEM1; ARTERIAL LINE KIT: 20 GA X 5 IN (12 CM)/ASK-04510-HFH; ARTERIAL CATH KIT: 20 GA X 5 IN/ASK-04510-HFH4; ARTERIAL LINE KIT/ASK-04510-SE; ARTERIAL LINE KIT: 20 GA X 5 IN (12CM)/ASK-04510-TGH2; RA CATH KIT: 20 GA X 12 CM/NA-04550-1A; RA CATH KIT: 20 GA X 12 CM/NA-04550-X1A; RA CATH KIT: 18 GA X 1-3/4IN/AK-04018; RA CATH KIT: 20 GA X 1-3/4IN/AK-04020; RA CATH KIT: 20 GA X 1-3/4IN/AK-04020-C; RA CATH KIT: 20 GA X 1-1/2IN/AK-04120; RA CATH KIT: 22 GA X 1-3/8IN/AK-04122; RA CATH KIT: 20 GA X 1-1/2IN/AK-04220; RA CATH KIT: 20 GA X 1 3/4 IN (4.45 CM)/ASK-04020-AH; RA CATH KIT: 20 GA X 1 3/4 IN/ASK-04020-ATH; RA CATH KIT: 20 GA X 1 3/4IN (4.45CM)/ASK-04020-AU2; RA CATH KIT: 20 GA X 1 3/4 IN/ASK-04020-BHS; ARTERIAL CATHETERIZATION KIT/ASK-04020-BIDB2; RA CATH KIT: 20 GA X 4.45 CM/ASK-04020-CCD1; ARTERIAL CATHETERIZATION KIT/ASK-04020-CR; ART LINE KIT: 20 GA X 1 3/4 IN (4.45 CM)/ASK-04020-EUH2; RA CATH KIT: 20 GA X 1 3/4 IN/ASK-04020-FAM1; RA CATH KIT: 20 GA X 1 3/4 IN/ASK-04020-FMC; RA CATH KIT: 20 GA X 1-3/4IN/ASK-04020-KSF2; RA CATH KIT: 20 GA X 1 3/4 IN (4.5 CM)/ASK-04020-LHC2; RA CATH KIT: 20 GA X 1 3/4 IN (4.5 CM)/ASK-04020-LHC3; RA CATH KIT: 20 GA X 1 3/4 IN/ASK-04020-LM; RA CATH KIT: 20 GA X 1 3/4IN/ASK-04020-MCH1; RA CATH KIT: 20 GA X 1-3/4IN (4.45 CM)/ASK-04020-MIH1; RA CATH KIT: 20 GA X 4.45 CM/ASK-04020-NWMX; RA CATH KIT: 20 GA X 1-3/4IN/ASK-04020-PHP; RA CATH KIT: 20 GA X 1-3/4 IN (4.45CM)/ASK-04020-RIHM; RA CATH KIT: 20 GA X 1 3/4 IN/ASK-04020-RMC1; RA CATH KIT: 20 GA X 1-3/4IN/ASK-04020-RU; RA CATH KIT: 20 GA X 1 3/4 IN (4.45 CM)/ASK-04020-SE; RA CATH KIT: 20 GA X 1-3/4IN/ASK-04020-SHM; RA CATH KIT: 20 GA X 1 3/4 IN/ASK-04020-SRMC1; RA CATH KIT: 20 GA X 1 3/4 IN (4.45 CM)/ASK-04020-UCL1; RA CATH KIT: 20 GA X 4.45 CM/ASK-04020-UMI; RA CATH KIT: 20 GA X 1-3/4 IN (4.45CM)/ASK-04020-UN; RA CATH KIT: 20 GA X 1-3/4IN (4.45 CM)/ASK-04020-UNC; RA CATH KIT: 20 GA X 1-3/4IN (4.45 CM)/ASK-04020-UNC1; RA CATH SET: 20 GA X 1-1/2IN (3.81CM)/ASK-04220-PSU; RA CATH KIT: 20 GA X 1-1/2 IN (3.81 CM)/ASK-04220-UCL1; RA CATH KIT: 20 GA X 1-3/4IN/NA-04020-S1A; CVC KIT: 20 GA X 5 IN (12CM)/ASK-04550-JMC1; ARTERIAL ACCESS TRAY/ASK-04001-BW2; ARTERIAL ACCESS TRAY WITH .025 IN SWG/ASK-04001-WUH1; ARTERIAL LINE KIT/ASK-04510-HUM", "reason": "Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.", "hazard_level": "Class I", "company": "ARROW INTERNATIONAL, LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-21", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "785,999", "codes": "REF(Material)/UDI-DI/Lot(Batch): TJ-04020-1/10801902193275, 30801902202155/33F24J0338, 33F25A0158, 33F25C0753, 33F25E0281, 33F24B0409; NA-04220-S1A/10801902193275/33F25E1052, 33F24G0553; AK-04510-S/10801902192230, 10801902193275, 10801902196719/33F24A0337, 33F24A0338, 33F24A0339, 33F24A0341, 33F24A0342, 33F24A0343, 33F24A1012, 33F24B0107, 33F24B0108, 33F24B0109, 33F24B0110, 33F24B0111, 33F24C0010, 33F24C0011, 33F24D0015, 33F24D0016, 33F24E0046, 33F24E0047, 33F24G0327, 33F24G0570, 33F24G0571, 33F24G0572, 33F24G0573, 33F24G0574, 33F24G0575, 33F24J0493, 33F24J0674, 33F24J0675, 33F24J0676, 33F24J0677, 33F24K0091, 33F24K0309, 33F24K0313, 33F24L0623, 33F24L0627, 33F24L0629, 33F24L0631, 33F24L0754, 33F24L0783, 33F25A0457, 33F25A0613, 33F25A0614, 33F25A0615, 33F25A0616, 33F25C0738, 33F25C0751, 33F25C0794, 33F25C0846, 33F25C0907, 33F25C0955, 33F25C0956, 33F25E0040, 33F25E0288, 33F25E0289, 33F25E0290, 33F25E0910, 33F25E1065, 33F25E1066, 33F25G0079, 33F25G0158, 33F25H0012, 33F25H0193, 33F25H0194, 33F25H0195, 33F25H0196, 33F25J0464, 33F25J0642, 33F25J0789, 33F25J0801, 33F25J0802, 33F25J0803, 33F25J0804, 33F25L0486, 33F25L0488, 33F26B0668, 33F26B0669, 33F26B0671, 33F26B0672, 33F23L0360; ASK-04018-HUMC/10801902193275/33F25B0360, 33F25K0050, 33F25M0680, 33F25E1176; ASK-04018-OH1/10801902117622, 10801902193275, 10801902117622, 10801902117639/33F24F0741, 33F24L0218, 33F24L0865, 33F25B0173, 33F25C0253, 33F25E0667, 33F25F0162, 33F25J0143, 33F26A1440, 33F26B0794, 33F24A0112; ASK-04020-BID/10801902211429, 10801902193275, 10801902211429/33F24D0870, 33F24E0650, 33F24F0646, 33F24L0220, 33F24L0399, 33F25B0175, 33F25D0335, 33F25E0668, 33F25G0248, 33F25L0123, 33F26A0254, 33F26A1441, 33S23J0777, 33F24G0405; ASK-04020-MAR/10801902193275, 10801902159776/33F24J0567, 33F24L0586, 33F25A0519, 33F25E0136, 33F25E0979, 33F25G0675, 33F25J0504, 33F25L0210, 33F26B0742, 33F25K0032; ASK-04020-PM4/10801902138498, 10801902193275, 10801902138498, 30801902158896/33F24E0428, 33F24E0429, 33F24G0424, 33F24K0188, 33F24L0789, 33F25C0142, 33F25C0821, 33F25E0142, 33F25H0085, 33F25J0883, 33F25L0470, 33F26B0659, 33F24F0095; ASK-04120-HF3/10801902200447, 10801902193275, 10801902200447, 10801902117943/33F24D0857, 33F24F0638, 33F24H0168, 33F24K0389, 33F24L0289, 33F25D0336, 33F25F0126, 33F25F0163, 33F25H0616, 33F25J0202, 33F25M0158, 33F25M0362, 33F26A1429, 33F26B0127, 33S24A1516, 33S24C0854, 33F24A0136; ASK-04120-UR/10801902117943, 10801902193275, 10801902117943/33F24A0769, 33F24B0278, 33F24C0175, 33F24D0140, 33F24E0447, 33F24G0287, 33F24K0201, 33F25B0692, 33F25C0962, 33F25E0156, 33F25H0097, 33F25J0889, 33F25L0383, 33F26C0309, 33F24G0441; ASK-04125-MGH/10801902193275, 10801902139976/33F24J0584, 33F25C0985, 33F25D0307, 33F25E0157, 33F25E0990, 33F25H0098, 33F25J0519, 33F25L0421, 33F26A1057, 33F26B0983, 33F24K0203; ASK-04500-HFH4/10801902200461, 10801902193275, 10801902118001/33F24E0651, 33F24F0722, 33F24L0292, 33F25C0437, 33F25D0228, 33F25E0775, 33F25F0109, 33F25F0164, 33F25H0615, 33F25M0345, 33F26A1363, 33F26B0405, 33S24C0436, 33S24L0292, 33F24A0141; ASK-04510-BID2/10801902193275, 10801902211412, 10801902115024/33F24J0171, 33F25A0165, 33F25C0438, 33F25D0229, 33F25E0852, 33F25G0249, 33F25J0204, 33F25M0233, 33F26A1443, 33F26B0410, 33F24F0820; ASK-04510-EHP1/10801902193275, 10801902115024/33F24L0293, 33F25C0192, 33F25D0230, 33F25E0589, 33F25E0853, 33F25H0646, 33F25L0125, 33F26A0255, 33F26A1520, 33F26B0838, 33F24J0303; ASK-04510-FEM1/10801902214796, 10801902193275/33F24A0831, 33F24B0286, 33F24C0185, 33F24E0456, 33F24E0457, 33F24G0448, 33F24J0304, 33F24L0771, 33F25A0539, 33F25E0165, 33F25G0118, 33F25J0523, 33F26A1051, 33F26B0658, 33F24J0591; ASK-04510-HFH/10801902115031, 10801902193275, 10801902200454/33F24G0053, 33F24L0022, 33F24M0108, 33F24M0190, 33F25A0126, 33F25A0356, 33F25A0384, 33F25B0043, 33F25D0200, 33F25H0329, 33F25H0848, 33F25J0613, 33F26A1358, 33F26B0677, 33F24D0865; ASK-04510-HFH4/10801902200454, 10801902193275/33F24F0865, 33F24J0167, 33F24L0965, 33F25A0236, 33F25C0260, 33F25E0776, 33F25G0332, 33F25J0205, 33F25M0276, 33F26A0305, 33F26B0194, 33F24J0306; ASK-04510-SE/10801902193275, 20801902214038, 10801902217018/33F24K0213, 33F24L0592, 33F25B0251, 33F25C0159, 33F25E0171, 33F25J0527, 33F25L0333, 33F26B0664, 33F24A0873; ASK-04510-TGH2/10801902217018, 10801902193275, 10801902118070/33F24B0292, 33F24C0188, 33F24E0463, 33F24G0289, 33F24K0214, 33F24L0633, 33F25A0542, 33F25C0879, 33F25E0172, 33F25G0120, 33F25J0528, 33F25L0354, 33F25M0862, 33F24C0189; NA-04550-1A/30801902117367, 10801902193275, 33F24A1562, 33F24C0709, 33F24D0331, 33F24E0628, 33F24F0946, 33F24K0382, 33F24L0144, 33F24L1015, 33F25C0223, 33F25D0320, 33F25E0512, 33F25E0663, 33F25E0839, 33F25J0187, 33F25K0199, 33F24K0374; NA-04550-X1A/10801902193275, 30801902117374, 10801902119930/33F24K0704, 33F24L0145, 33F24L1138, 33F25C0465, 33F25C0472, 33F25D0633, 33F25G0387, 33F25J0188, 33F25K0200, 33F26C0354, 33F26C0763, 33F24A1326; AK-04018/10801902190915, 10801902193275, 10801902190939/33F24E0696, 33F24L0051, 33F25A0353, 33F25B0078, 33F25D0714, 33F25G0732, 33F25J0593, 33F26B0039, 33F24A1251; AK-04020/10801902190939, 10801902193275, 60801902121549, 10801902121551/33F24C0727, 33F24C1254, 33F24D0439, 33F24E0697, 33F24F0010, 33F24G0049, 33F24G0116, 33F24G0220, 33F24G0645, 33F24G0646, 33F24G0680, 33F24H0064, 33F24J0013, 33F24J0457, 33F24K0033, 33F24M0004,33F24M0052, 33F24M0070, 33F24M0103,33F24M0146,33F25A0084, 33F25A0335, 33F25A0346, 33F25A0362, 33F25A0397, 33F25B0080, 33F25B0307, 33F25B0414, 33F25C0058, 33F25C0097, 33F25C0494, 33F25C0575, 33F25D0027, 33F25D0083, 33F25D0102, 33F25D0296, 33F25D0703, 33F25F0293, 33F25F0398, 33F25G0493, 33F25H0322, 33F25H0842, 33F25J0037, 33F25J0767, 33F25K0276, 33F25L0154, 33F25L0169, 33F25L0218, 33F26A1264, 33F26A1290, 33F26A1313, 33F26B0291, 33F24C0728, 33F24C0729, 33F24E0699, 33F24G0596, 33F24H0057, 33F24J0350, 33F24J0458, 33F24K0615, 33F24M0126, 33F25A0338, 33F25B0039, 33F25B0131, 33F25D0192, 33F25D0281, 33F25E1109, 33F25F0496, 33F25J0764, 33F26B0054, 33F23M0173; AK-04020-C/60801902121549, 10801902193275, 10801902121551/33F24G0050, 33F24G0595, 33F24G0619, 33F24G0681, 33F24H0060, 33F24H0085, 33F24H0244, 33F24J0421, 33F24J0471, 33F24L0074, 33F24L0517, 33F24M0051, 33F24M0102, 33F24M0145,33F25A0354,33F25B0013, 33F25B0079, 33F25B0130, 33F25B0279, 33F25C0096, 33F25C0411, 33F25C0523, 33F25C0595, 33F25D0014, 33F25D0082, 33F25D0169, 33F25E0404, 33F25E1088, 33F25E1164, 33F25F0430, 33F25J1033, 33F25K0343, 33F25L0175, 33F25M0472, 33F26A0212, 33F26A1275, 33F26B0053, 33F26B0290, 33F23M0171; AK-04120/10801902190922, 10801902193275, 20801902121572/33F24A1254, 33F24B0432, 33F24C0731, 33F24D0440, 33F24E0701, 33F24H0444, 33F24J0006, 33F24K0623, 33F24L0035, 33F24M0127, 33F25A0129, 33F25B0057, 33F25B0328, 33F25E1096, 33F25F0405, 33F25F0522, 33F25G0511, 33F25J1067, 33F26C0419, 33F24C0789; AK-04122/20801902121572, 10801902193275, 10801902121582/33F24G0051, 33F24G0148, 33F24G0682, 33F24K0535, 33F24M0071, 33F25A0092, 33F25A0380, 33F25B0005, 33F25D0108, 33F25J0762, 33F25K0003, 33F24A1009; AK-04220/10801902190946, 10801902193275, 10801902121636/33F24C0733, 33F24E0703, 33F24G0117, 33F24G0223, 33F24G0683, 33F24H0246, 33F24H0414, 33F24J0009, 33F24J0447, 33F24M0003, 33F24M0086, 33F25C0085, 33F25D0171, 33F25G0065, 33F25J0059, 33F26C0392, 33F24A1257; ASK-04020-AH/10801902193275, 10801902114898/33F24L0219, 33F24L0398, 33F24L0950, 33F25B0174, 33F25C0436, 33F25D0332, 33F25D0648, 33F25E0848, 33F25H0647, 33F25J0350, 33F26C0572, 33F24G0403; ASK-04020-ATH/10801902193275, 10801902193237, 10801902205916/33F24J0553, 33F24K0167, 33F24L0777, 33F25C0133, 33F25C0982, 33F25E0964, 33F25G0106, 33F25G0670, 33F25H0063, 33F25H0727, 33F25L0242, 33F25L0452, 33F25M0947, 33F26B0583, 33F24D0856; ASK-04020-AU2/10801902205916, 10801902193275, 10801902117660/33F24E0645, 33F24F1044, 33F24K0365, 33F24L1020, 33F25A0230, 33F25C0225, 33F25D0333, 33F25E0523, 33F25E0849, 33F25H0474, 33F25J0199, 33F25L0120, 33F25M0208, 33F26A1419, 33F26B0449, 33F26C0030, 33F24A0814; ASK-04020-BHS/10801902193275, 30801902144578, 10801902211429/33F25A0231, 33F25D0589, 33F25E0850, 33F25F0095, 33F25G0320, 33F25J0200, 33F26A1514, 33R24D0228, 33S24C0678, 33S24C1077, 33F24D0277; ASK-04020-BIDB2/10801902193275/33F24K0168, 33F25A0508, 33F25C0134, 33F25C0835, 33F25E0121, 33F25G0107, 33F25H0065, 33F25H0728, 33F25J0669, 33F25K0399, 33F25L0429, 33F25M0929, 33F24J0365; ASK-04020-CCD1/10801902193275/33F24J0289, 33F24J0556, 33F24L0641, 33F25A0510, 33F25C0772, 33F25E0123, 33F25G0108, 33F25H0730, 33F25M0874, 33F24G0282; ASK-04020-CR/10801902193275, 10801902206814/33F24K0169, 33F24L0679, 33F25A0511, 33F25C0785, 33F25E0124, 33F25E0969, 33F25G0109, 33F25G0669, 33F25H0067, 33F25H0731, 33F25J0868, 33F25L0241, 33F25M0881, 33F26B0523, 33F24G0407; ASK-04020-EUH2/10801902193275, 10801902213379, 10801902193244/33F24J0290, 33F24J0557, 33F24L0753, 33F25A0512, 33F25C0930, 33F25E0125, 33F25H0068, 33F25J0869, 33F25M0894, 33F26B0236, 33F23H0888; ASK-04020-FAM1/10801902193275/ 33F24H0374, 33F24J0181, 33F24L0734, 33F25C0135, 33F25C0781, 33F25E0126, 33F25E0970, 33F25J0502, 33F24G0408; ASK-04020-FMC/10801902193275, 10801902121384/33F24J0558, 33F24K0171, 33F25A0513, 33F25C0773, 33F25E0127, 33F25E0971, 33F25H0069, 33F25J0870, 33F25L0388, 33F25M0892, 33F24A0828; ASK-04020-KSF2/10801902193275/33F25A0516, 33F25C0851, 33F25E0132, 33F25H0075, 33F25J0876, 33F25M0906, 33F24K0178; ASK-04020-LHC2/10801902193275, 10801902225525/33F24L0716, 33F25A0517, 33F25C0734, 33F25E0133, 33F25J0503, 33F25L0491, 33F25M0922, 33F26C0672; ASK-04020-LHC3/10801902193275, 10801902225525/33F24L0716, 33F25A0517, 33F25C0734, 33F25E0133, 33F25J0503, 33F25L0491, 33F25M0922, 33F26C0672, 33F24L0653; ASK-04020-LM/10801902193275/33F25B0690, 33F25E0977, 33F25H0076, 33F25J0877, 33F25L0422, 33F25M0925, 33F24G0417; ASK-04020-MCH1/10801902193275, 20801902117711/33F24L0920, 33F24A0380; ASK-04020-MIH1/10801902193275/33F24L0744, 33F25A0522, 33F25C0978, 33F25E0138, 33F25H0080, 33F25J0879, 33F26A0996, 33F25A0442; ASK-04020-NWMX/10801902193275/33F24K0186, 33F25J0882, 33F25L0363, 33F25M0872, 33F24G0423; ASK-04020-PHP/10801902193275, 10801902138498/33F24K0187, 33F25A0148, 33F25C0401, 33F25D0283, 33F25E1145, 33F25J1027, 33F24C0164; ASK-04020-RIHM/10801902193275/33F24L0243, 33F24L1034, 33F25B0177, 33F25C0256, 33F25D0462, 33F25E0525, 33F25E0773, 33F25G0317, 33F25H0645, 33F25J0351, 33F26A1408, 33F24M0095; ASK-04020-RMC1/10801902193275/33F25J0509, 33F25L0464, 33F24L0747; ASK-04020-RU/10801902193275/33F25A0524, 33F25C0807, 33F25E0143, 33F25G0112, 33F25J0510, 33F25M0863, 33F24G0427; ASK-04020-SE/10801902193275, 10801902213263, 10801902138757/33F24L0611, 33F25A0525, 33F25C0849, 33F25E0144, 33F25E0984, 33F25J0511, 33F26B0999, 33F24E0433; ASK-04020-SHM/10801902193275/33F24G0428, 33F24J0576, 33F24K0190, 33F24L0684, 33F25A0526, 33F25C0971, 33F25E0145, 33F25G0113, 33F25J0512, 33F25L0378, 33F25M0883, 33F25C0143; ASK-04020-SRMC1/10801902193275, 10801902117837/33F24J0296, 33F24K0192, 33F24L0710, 33F25C0144, 33F25C0820, 33F25E0146, 33F25H0086, 33F25J0884, 33F25M0842, 33F24A0868; ASK-04020-UCL1/10801902193275, 10801902144550/33F24K0412, 33F24L1081, 33F25A0233, 33F25C0257, 33F25D0393, 33F25E0774, 33F25G0360, 33F25J0201, 33F26B0160, 33F24G0178; ASK-04020-UMI/10801902193275, 10801902145571/33F24L1123, 33F24E0726; ASK-04020-UN/10801902145571, 10801902193275, 60801902117849/33F24K0021, 33F24L0533, 33F24M0053, 33F24M0107, 33F25A0089, 33F25B0016, 33F25B0092, 33F25B0314, 33F25D0015, 33F25D0113, 33F25D0172, 33F25E1146, 33F25H0797, 33F25K0230, 33F26B0090, 33F26B0262, 33F24A0373; ASK-04020-UNC/60801902117849, 10801902193275, 10801902143782/33F24A1035, 33F24B0270, 33F24C0170, 33F24G0432, 33F24J0297, 33F24J0577, 33F24L0799, 33F25A0527, 33F25C0145, 33F25C0994, 33F25E0147, 33F25H0088, 33F25J0513, 33F25L0359, 33F25M0868, 33F26A0993, 33F26B0975, 33F24F0461; ASK-04020-UNC1/10801902193275, 10801902143782, 10801902117851/33F24G0286, 33F24J0298, 33F24K0194, 33F24L0806, 33F25C0146, 33F25E0148, 33F25H0089, 33F25J0514, 33F25L0469, 33F25M0959, 33F26C0599, 33F24A0255; ASK-04220-PSU/10801902193275/33F25A0152, 33F25H0737, 33F24K0495; ASK-04220-UCL1/10801902193275, 10801902159127, 10801902143805/33F24L0290, 33F25A0206, 33F25C0226, 33F25D0463, 33F25E0669, 33F25G0351, 33F25H0428, 33F25J0352, 33F26B0153, 33F24F0619; NA-04020-S1A/10801902193275, 10801902139396/33F25A0600, 33F25C0195, 33F25C0786, 33F25E0270, 33F25E1050, 33F25G0152, 33F25H0177, 33F25H0759, 33F25J0633, 33F25K0404, 33F25L0472, 33F25M0962, 33F26B0595, 33F24J0683; ASK-04550-JMC1/10801902193275, 10801902130836/33F25C0837, 33F25E0175, 33F25E0997, 33F25L0146, 33F24F0685; ASK-04001-BW2/10801902193275, 10801902221602/33F25A0500, 33F25E0110, 33F25H0057, 33F25J0496, 33F25L0360, 33F26A0994, 33S23M0157, 33F25A0226; ASK-04001-WUH1/10801902193275, 10801902220834, 10801902119268/33F24J0549, 33F24K0162, 33F24L0685, 33F25H0061, 33F25J0864, 33F26B0683, 33F26B1021, 33F24A0078; ASK-04510-HUM/10801902115048/33F24C0956, 33F24D0699, 33F24E0647, 33F24F0911, 33F24L0885", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2368-2026%22", "url": "https://recallledger.net/recalls/device-z-2368-2026-description-ref-ra-cath-kit-20-ga-x-1-3-4-in-tj-04020-1-ra-cath-k/"}, {"id": "fda-device-z-2367-2026", "source": "FDA", "category": "device", "recall_number": "Z-2367-2026", "title": "Description/REF: AGBA PICC G4 Stylet: 3L 6FR x 55CM BP/DLX-45563-VPSB recall (ARROW INTERNATIONAL, LLC)", "product": "Description/REF: AGBA PICC G4 Stylet: 3L 6FR x 55CM BP/DLX-45563-VPSB; AGBA PICC G4 Stylet: 3L 6FR x 55CM TCG/DLX-45563-VPSC; ARROW(R) VPS(R) ACCESS KIT/ASK-04001-UCHD1; ARROW(R) VPS(R) ACCESS KIT/ASK-04001-UCHS1; ARROW(R) VPS(R) ACCESS KIT/ASK-04001-DU13; ARROW(R) VPS(R) ACCESS KIT/ASK-04001-UNHS1", "reason": "Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.", "hazard_level": "Class I", "company": "ARROW INTERNATIONAL, LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-21", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "11,358", "codes": "REF(Material)/UDI-DI/Lot(Batch): DLX-45563-VPSB/10801902193275/33F25C0704, 33F25D0316, 33F25D0627, 33F25M0094, 33F24L0860; DLX-45563-VPSC/10801902193275, 10801902208658, 10801902210118/33F25B0509, 33F25C0340, 33F25D0255, 33F25D0628, 33F25E0767, 33F25E0901, 33F25F0227, 33F25J0448, 33F25K0036, 33F26C0104, 33F26C0107, 33F24C0257; ASK-04001-UCHD1/10801902193275, 10801902219005/33F25H0415, 33F25J0349, 33F26B0440, 33F24L0396; ASK-04001-UCHS1/10801902193275, 10801902219067/33F24L1083, 33F25D0331, 33F25E0521, 33F25E0846, 33F25K0068, 33F25K0107, 33F25M0133, 33F26A1417, 33F26C0029, 33F24K0406; ASK-04001-DU13/10801902193275, 10801902201970/33F25B0514, 33F25C0703, 33F25F0090, 33F25F0124, 33F25H0421, 33F25J0197, 33F26A1372, 33F26B0850, 33F26C0369, 33R25A0227, 33F24K0314; ASK-04001-UNHS1/10801902193275, 10801902211887, 10801902158854/33F25A0229, 33F25C0714, 33F25D0390, 33F25E0847, 33F25G0244, 33F25M0129, 33F26A1139, 33F26C0370, 33F24E0400", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2367-2026%22", "url": "https://recallledger.net/recalls/device-z-2367-2026-description-ref-agba-picc-g4-stylet-3l-6fr-x-55cm-bp-dlx-45563-vpsb/"}, {"id": "fda-device-z-2366-2026", "source": "FDA", "category": "device", "recall_number": "Z-2366-2026", "title": "Description/REF: PACING PSI KIT: 6 FR/AI-06210-KS recall (ARROW INTERNATIONAL, LLC)", "product": "Description/REF: PACING PSI KIT: 6 FR/AI-06210-KS, PACING PSI KIT: 5 FR 2-L/AI-07155-KS, PACING PSI KIT: 5 FR 2L/ASK-07155-UPM", "reason": "Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.", "hazard_level": "Class I", "company": "ARROW INTERNATIONAL, LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-21", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "15,915", "codes": "REF(Material)/UDI-DI/Lot(Batch): AI-06210-KS/10801902210217, 10801902211504/33F24G0127, 33F24H0302, 33F25E0321, 33F26A1322, 33F25B0008; AI-07155-KS/10801902210217, 10801902211481, 10801902197938/33F25B0056, 33F25C0574, 33F25D0190, 33F25D0688, 33F25E0387, 33F25E0467, 33F25E1140, 33F25E1211, 33F25G0708, 33F25H0269, 33F25H0319, 33F25H0357, 33F25J0606, 33F25L0085, 33F25L0313, 33F26A0018, 33F26A1258, 33F26A1305, 33F26B0256, 33F26B0731, 33F26B0938, 33F26C0063, 33F26C0271, 33F26C0537, 33F24D0003; ASK-07155-UPM/10801902210217, 10801902203172/33F25E0208, 33F25H0134, 33F25J0913, 33F25M0051, 33F23L0622", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2366-2026%22", "url": "https://recallledger.net/recalls/device-z-2366-2026-description-ref-pacing-psi-kit-6-fr-ai-06210-ks-pacing-psi-kit-5/"}, {"id": "fda-device-z-2365-2026", "source": "FDA", "category": "device", "recall_number": "Z-2365-2026", "title": "Description/REF: BIOPSY SYSTEM COMPREHENSIVE KIT/ASK-09458-AH recall (ARROW INTERNATIONAL, LLC)", "product": "Description/REF: BIOPSY SYSTEM COMPREHENSIVE KIT/ASK-09458-AH, ASK-09458-COC, ASK-09458-EUH, ASK-09458-SD, ASK-09458-VU", "reason": "Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.", "hazard_level": "Class I", "company": "ARROW INTERNATIONAL, LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-21", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "14,840", "codes": "REF(Material)/UDI-DI/Lot(Batch): ASK-09458-AH/10801902203172, 10801902193275, 10801902203172/33F24C0359, 33F24C1122, 33F24E0323, 33F24F0780, 33F24K0397, 33F25A0208, 33F25B0518, 33F25D0001, 33F25D0338, 33F25D0465, 33F25E0528, 33F25H0610, 33F25J0353, 33F25K0076, 33F25K0091, 33F25M0173, 33F26A1538, 33F26B0819, 33F24H0227; ASK-09458-COC/10801902193275, 10801902221084, 10801902216394/33F24K0755, 33F25C0380, 33F25D0590, 33F25H0583, 33F25J0354, 33F25K0125, 33F25M0243, 33F25M0393, 33F26A1535, 33F26B0404, 33F24F0732; ASK-09458-EUH/10801902193275, 10801902216394/33F24L0908, 33F25E0715, 33F25F0096, 33F25G0215, 33F25J0144, 33F25M0118, 33F26A1515, 33F26B0862, 33F24H0125; ASK-09458-SD/10801902193275, 10801902215014/33F25D0398, 33F25F0165, 33F25M0692, 33F26C0488; ASK-09458-VU/10801902217261, 10801902193275, 10801902217261, 10801902193275/33F24C0832, 33F24D0624, 33F24F0650, 33F24K0752, 33F24L0916, 33F25D0534, 33F25E0531, 33F25F0141, 33F25H0588, 33F25K0127, 33F25M0177, 33F26B0134, 33F26B0477, 33F26C0487, 33F24H0099", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2365-2026%22", "url": "https://recallledger.net/recalls/device-z-2365-2026-description-ref-biopsy-system-comprehensive-kit-ask-09458-ah-ask-09/"}, {"id": "fda-device-z-2364-2026", "source": "FDA", "category": "device", "recall_number": "Z-2364-2026", "title": "Description/REF: ACCESS TRAY/ASK-04001-SUH-S recall (ARROW INTERNATIONAL, LLC)", "product": "Description/REF: ACCESS TRAY/ASK-04001-SUH-S; ACCESS TRAY/ASK-04001-VM1; STIMUCATH SFTY KIT: 19G CTH, 17Gx4CM NDL/AB-19604-KS; STIMUCATH SFTY KIT: 19G CTH, 17Gx8CM NDL/AB-19608-KS; STIMUCATH SFTY KIT: 20G CTH, 18Gx8CM NDL/AB-20608-KS; STIMUCATH KIT: 19G CATH, 17G x 9CM NDL/AB-05060-PK; FLEXBLOCK ULTRASOUND KIT: 17Gx9CM NS NDL/ASK-19609-VCU; CONTINUOUS NERVE BLOCK KIT/ASK-19600-CC2; CONTINUOUS NERVE BLOCK KIT 19 GA X 60/ASK-19608-CC; CONTINUOUS NERVE BLOCK KIT 19GA X 60CM/ASK-19608-KP; CONTINUOUS NERVE BLOCK KIT 19GA X 60CM/ASK-19608-SHC; FLEXBLOCK KIT:ECHO CATH, 17Gx8CM STM NDL/FB-19608-K; FLEXBLOCK ULTRASOUND KIT: 17Gx8CM STM ND/FB-19608-KU; FLEXBLOCK KIT:ECHO CATH, 17Gx9CM NS NDL/FB-19609-K; FLEXBLOCK ULTRASOUND KIT: 17Gx9CM NS NDL/FB-19609-KU; CONTINUOUS PERIPHERAL NERVE BLOCK KIT/ASK-19608-US1; EPIDURAL CATHETERIZATION KIT/ASK-05001-SLR1; EPIDURAL CATHETERIZATION KIT/MH-05001; EPIDURAL CATHETERIZATION KIT/WJ-05401; SPINAL ANES/EPIDURAL CATH 19GA X 90CM/ASK-05501-USC1; EPIDURAL NEEDLE KIT/LG-03000; EPIDURAL ANESTHESIA KIT/MTO-03000-VM; EPIDURAL ANESTHESIA KIT/SM-03001; Anesthesia conduction kit/FB-19611-K", "reason": "Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.", "hazard_level": "Class I", "company": "ARROW INTERNATIONAL, LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-21", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "205,685", "codes": "REF(Material)/UDI-DI/Lot(Batch): ASK-04001-SUH-S/10801902210217, 10801902193275/33F25C0766, 33F25E0112, 33F25G0101, 33F25H0058, 33F25H0725, 33F25J0862, 33F25M0836, 33F25F0160; ASK-04001-VM1/10801902210217, 10801902202106, 10801902193275/33F24L0599, 33F26A0962, 33F24G0280; AB-19604-KS/10801902210217, 10801902209471/33F24L0608, 33F25G0474, 33F25J0814, 33F25M0887, 33F24D0064; AB-19608-KS/10801902210217, 10801902209471/33F24E0312, 33F24F0295, 33F24G0316, 33F24K0082, 33F24L0714, 33F25E0027, 33F25E0904, 33F25H0003, 33F25J0815, 33F25L0337, 33F26B0498, 33F24E0314; AB-20608-KS/)10801902210217/33F25H0004, 33F25J0816, 33F24D0437; AB-05060-PK/10801902209433, 10801902210217/33F24D0002, 33F24E0029, 33F24G0315, 33F24J0484, 33F24K0081, 33F25A0451, 33F25C0747, 33F25E0026, 33F25J0646, 33F24E0028; ASK-19609-VCU/10801902210217, 10801902206876, 10801902214291/33F24E0536, 33F24J0630, 33F24L0605, 33F25C0179, 33F25E0220, 33F25H0140, 33F26B1003, 33F24D0628; ASK-19600-CC2/10801902210057, 10801902210217, 10801902210064/33F24D0393, 33F24E0533, 33F24G0494, 33F24K0251, 33F24L0665, 33F25C0177, 33F25E0217, 33F25H0138, 33F24C0230; ASK-19608-CC/10801902210217, 10801902210064, 10801902202236/33F24G0309, 33F24K0252, 33F24L0639, 33F25B0691, 33F25C0178, 33F25C0761, 33F25E0218, 33F25E1022, 33F25H0750, 33F25J0918, 33F26B0230, 33F24D0394; ASK-19608-KP/10801902210217/33F24G0495, 33F24G0086; ASK-19608-SHC/10801902210217, 40801902202220, 10801902202243/33F24G0496, 33F24J0629, 33F24K0253, 33F24L0573, 33F25A0571, 33F25C0733, 33F25E0219, 33F25G0757, 33F25H0139, 33F25J0919, 33F25K0400, 33F25L0480, 33F26B0606, 33F24C0231; FB-19608-K/10801902210217, 10801902210125/33F24G0533, 33F24J0650, 33F24K0279, 33F24L0568, 33F25C0186, 33F25C0748, 33F25E0257, 33F25G0147, 33F25H0164, 33F25J0623, 33F25L0340, 33F25M0847, 33F24C0258; FB-19608-KU/10801902210217, 10801902210132/33F24E0026, 33F24E0574, 33F24G0312, 33F24J0328, 33F24L0557, 33F24M0268, 33F25C0187, 33F25C0940, 33F25E0258, 33F25H0165, 33F25J0624, 33F25L0344, 33F25M0851, 33F23G0580; FB-19609-K/10801902210132, 10801902210217, 10801902210132, 10801902210149/33F24C0259, 33F24D0407, 33F24E0575, 33F24G0534, 33F24K0281, 33F24L0805, 33F25C0721, 33F25E1042, 33F25J0625, 33F25L0351, 33F25M0856, 33F26B0504, 33F24B0386; FB-19609-KU/10801902210149, 10801902210217, 10801902210149, 10801902193275/33F24C0260, 33F24E0576, 33F24E0577, 33F24G0535, 33F24L0763, 33F25A0592, 33F25E0259, 33F25E1043, 33F25H0758, 33F25K0402, 33F25L0471, 33F26B0594, 33F26C0480, 33S24L0763, 33F24L0738; ASK-19608-US1/10801902210217/33F24E0535, 33F24K0254, 33F24L0770, 33F24E0014; ASK-05001-SLR1/10801902210217, 10801902209617/33F24J0596, 33F24L0560, 33F25A0546, 33F25C0939, 33F25E0177, 33F25E0998, 33F25J0530, 33F24C0194; MH-05001/10801902210217/33F24G0540, 33F24J0331, 33F24J0654, 33F25E0261, 33F25H0168, 33F25J0937, 33F25L0478, 33F24K0286; WJ-05401/10801902210385, 10801902210217, 10801902210385/33F24B0166, 33F24C0054, 33F24J0672, 33F24K0307, 33F24L0548, 33F25A0609, 33F25A0625, 33F25C0723, 33F25E0285, 33F25E1062, 33F25G0156, 33F25H0187, 33F25J0640, 33F25J0952, 33F25L0414, 33F26B0559, 33F26C0858; ASK-05501-USC1/10801902210217, 10801902214857, 10801902209853/33F24E0506, 33F24E0507, 33F24G0478, 33F24L0561, 33F25A0561, 33F25C0167, 33F25C0769, 33F25E0200, 33F25G0132, 33F25H0745, 33F25J0908, 33F25L0412, 33F26B0557, 33F24C0211; LG-03000/10801902210217/33F24L0668, 33F24E0581; MTO-03000-VM/10801902210217, 10801902202076, 10801902119916/33F24E0586, 33F24G0547, 33F24J0658, 33F24K0291, 33F24L0632, 33F25A0596, 33F25C0869, 33F25E0265, 33F25H0173, 33F25J0939, 33F25L0380, 33F26C0306, 33F24A1057; SM-03001/10801902210217, 10801902202496, 10801902210354/33F24E0779, 33F24J0243, 33F24J0434, 33F24M0012, 33F25A0099, 33F25B0035, 33F25B0128, 33F25C0410, 33F25C0521, 33F25F0421, 33F25G0531, 33F25J0053, 33F25L0171, 33F26B0643, 33F24C0276; FB-19611-K/10801902210156/33F24F0014", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2364-2026%22", "url": "https://recallledger.net/recalls/device-z-2364-2026-description-ref-access-tray-ask-04001-suh-s-access-tray-ask-04001/"}, {"id": "fda-device-z-2363-2026", "source": "FDA", "category": "device", "recall_number": "Z-2363-2026", "title": "PARACENTESIS KIT recall (ARROW INTERNATIONAL, LLC)", "product": "PARACENTESIS KIT, REF: AK-00376, ASK-00376-VCU", "reason": "Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.", "hazard_level": "Class I", "company": "ARROW INTERNATIONAL, LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-21", "report_date": "2026-06-24", "status": "Ongoing", "distribution": "US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "50,724", "codes": "REF(Material)/UDI-DI/Lot(Batch): AK-00376/10801902197938, 10801902193275, 10801902197938, 10801902197952/33F24D0004, 33F24E0166, 33F24G0318, 33F24J0486, 33F24K0083, 33F24L0725, 33F25A0453, 33F25A0610, 33F25C0749, 33F25C0906, 33F25E0031, 33F25G0075, 33F25H0007, 33F25H0719, 33F25J0739, 33F25J0817, 33F25L0462, 33F25M0954, 33F26B0949, 33F26C0575, 33F24A0016; ASK-00376-VCU/10801902193275, 10801902138788/33F24L0522, 33F24M0088, 33F25C0060, 33F25D0282, 33F25F0257, 33F25G0746, 33F25J0602, 33F24D0201", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2363-2026%22", "url": "https://recallledger.net/recalls/device-z-2363-2026-paracentesis-kit-ref-ak-00376-ask-00376-vcu/"}, {"id": "fda-food-h-0937-2026", "source": "FDA", "category": "food", "recall_number": "H-0937-2026", "title": "Flan Cake [image] Custard Cake The Original recall (Galaxy RG Corp)", "product": "Flan Cake [image] Custard Cake The Original, Net Wt. 30 oz, packaged in a transparent and rigid plastic clamshell container, one unit per container. KEEP REFRIGERATED. UPC 824790852959", "reason": "Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).", "hazard_level": "Class II", "company": "Galaxy RG Corp", "company_location": "Miami, FL, United States", "date": "2026-04-03", "report_date": "2026-06-17", "status": "Terminated", "distribution": "FL and TX.", "states": ["FL", "TX"], "nationwide": false, "quantity": "423 (30-oz) units", "codes": "Expiration Date: From 04/03/2026 to 05/03/2026 Lot#034320462, 034320562, 034320662, 034320962, 034321062, 034321162, 034321262, 034321362, 034321662, 034321762, 034321862, 034321962, 034322062, 034322362, 034322462, 034322562, 034322662, 034322762, 034323062, 034323162, 044320162, 044320262, 044320362", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0937-2026%22", "url": "https://recallledger.net/recalls/food-h-0937-2026-flan-cake-image-custard-cake-the-original-net-wt-30-oz-packaged-i/"}, {"id": "fda-food-h-0936-2026", "source": "FDA", "category": "food", "recall_number": "H-0936-2026", "title": "Cheesecake de Guava [image] Guava Cheesecake The Original recall (Galaxy RG Corp)", "product": "Cheesecake de Guava [image] Guava Cheesecake The Original, Net Wt. 26 oz, packaged in a transparent and rigid plastic clamshell container, one unit per container. KEEP REFRIGERATED. UPC 824790853116", "reason": "Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).", "hazard_level": "Class II", "company": "Galaxy RG Corp", "company_location": "Miami, FL, United States", "date": "2026-04-03", "report_date": "2026-06-17", "status": "Terminated", "distribution": "FL and TX.", "states": ["FL", "TX"], "nationwide": false, "quantity": "375 (26-oz) units", "codes": "Expiration Date: From 04/03/2026 to 05/03/2026 Lot#034320462, 034320562, 034320662, 034320962, 034321062, 034321162, 034321262, 034321362, 034321662, 034321762, 034321862, 034321962, 034322062, 034322362, 034322462, 034322562, 034322662, 034322762, 034323062, 034323162, 044320162, 044320262, 044320362", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0936-2026%22", "url": "https://recallledger.net/recalls/food-h-0936-2026-cheesecake-de-guava-image-guava-cheesecake-the-original-net-wt-26/"}, {"id": "fda-food-h-0935-2026", "source": "FDA", "category": "food", "recall_number": "H-0935-2026", "title": "Cheesecake de Fresa [image] Strawberry Cheesecake The Original recall (Galaxy RG Corp)", "product": "Cheesecake de Fresa [image] Strawberry Cheesecake The Original, Net Wt. 26 oz, packaged in a transparent and rigid plastic clamshell container, one unit per container. KEEP REFRIGERATED. UPC 824790852843", "reason": "Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).", "hazard_level": "Class II", "company": "Galaxy RG Corp", "company_location": "Miami, FL, United States", "date": "2026-04-03", "report_date": "2026-06-17", "status": "Terminated", "distribution": "FL and TX.", "states": ["FL", "TX"], "nationwide": false, "quantity": "149 (26-oz) units", "codes": "Expiration Date: From 04/03/2026 to 05/03/2026 Lot#034320462, 034320562, 034320662, 034320962, 034321062, 034321162, 034321262, 034321362, 034321662, 034321762, 034321862, 034321962, 034322062, 034322362, 034322462, 034322562, 034322662, 034322762, 034323062, 034323162, 044320162, 044320262, 044320362", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0935-2026%22", "url": "https://recallledger.net/recalls/food-h-0935-2026-cheesecake-de-fresa-image-strawberry-cheesecake-the-original-net-wt/"}, {"id": "fda-food-h-0934-2026", "source": "FDA", "category": "food", "recall_number": "H-0934-2026", "title": "Cheesecake de Mango [image] Mango Cheesecake The Original recall (Galaxy RG Corp)", "product": "Cheesecake de Mango [image] Mango Cheesecake The Original, Net Wt. 26 oz, packaged in a transparent and rigid plastic clamshell container, one unit per container. KEEP REFRIGERATED. UPC 824790852836", "reason": "Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).", "hazard_level": "Class II", "company": "Galaxy RG Corp", "company_location": "Miami, FL, United States", "date": "2026-04-03", "report_date": "2026-06-17", "status": "Terminated", "distribution": "FL and TX.", "states": ["FL", "TX"], "nationwide": false, "quantity": "93 (26-oz) units", "codes": "Expiration Date: From 04/03/2026 to 05/03/2026 Lot#034320462, 034320562, 034320662, 034320962, 034321062, 034321162, 034321262, 034321362, 034321662, 034321762, 034321862, 034321962, 034322062, 034322362, 034322462, 034322562, 034322662, 034322762, 034323062, 034323162, 044320162, 044320262, 044320362", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0934-2026%22", "url": "https://recallledger.net/recalls/food-h-0934-2026-cheesecake-de-mango-image-mango-cheesecake-the-original-net-wt-26/"}, {"id": "fda-food-h-0933-2026", "source": "FDA", "category": "food", "recall_number": "H-0933-2026", "title": "Cheesecake de Dulce de Leche [image] Caramel Cheesecake The Original recall (Galaxy RG Corp)", "product": "Cheesecake de Dulce de Leche [image] Caramel Cheesecake The Original, Net Wt. 26 oz, packaged in a transparent and rigid plastic clamshell container, one unit per container. KEEP REFRIGERATED. UPC 824790852829", "reason": "Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).", "hazard_level": "Class II", "company": "Galaxy RG Corp", "company_location": "Miami, FL, United States", "date": "2026-04-03", "report_date": "2026-06-17", "status": "Terminated", "distribution": "FL and TX.", "states": ["FL", "TX"], "nationwide": false, "quantity": "498 (26-oz) units", "codes": "Expiration Date: From 04/03/2026 to 05/03/2026 Lot#034320462, 034320562, 034320662, 034320962, 034321062, 034321162, 034321262, 034321362, 034321662, 034321762, 034321862, 034321962, 034322062, 034322362, 034322462, 034322562, 034322662, 034322762, 034323062, 034323162, 044320162, 044320262, 044320362", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0933-2026%22", "url": "https://recallledger.net/recalls/food-h-0933-2026-cheesecake-de-dulce-de-leche-image-caramel-cheesecake-the-original/"}, {"id": "fda-food-h-0932-2026", "source": "FDA", "category": "food", "recall_number": "H-0932-2026", "title": "Marquesita de Chocolate y Vainilla [image] Delighted Flavored Cakes The Original recall (Galaxy RG Corp)", "product": "Marquesita de Chocolate y Vainilla [image] Delighted Flavored Cakes The Original, Net Wt. 16 oz, packaged in a transparent and rigid plastic clamshell container, one unit per container. KEEP REFRIGERATED. UPC 824790852706", "reason": "Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).", "hazard_level": "Class II", "company": "Galaxy RG Corp", "company_location": "Miami, FL, United States", "date": "2026-04-03", "report_date": "2026-06-17", "status": "Terminated", "distribution": "FL and TX.", "states": ["FL", "TX"], "nationwide": false, "quantity": "809 (16-oz) units", "codes": "Expiration Date: From 04/03/2026 to 05/03/2026 Lot#034320462, 034320562, 034320662, 034320962, 034321062, 034321162, 034321262, 034321362, 034321662, 034321762, 034321862, 034321962, 034322062, 034322362, 034322462, 034322562, 034322662, 034322762, 034323062, 034323162, 044320162, 044320262, 044320362", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0932-2026%22", "url": "https://recallledger.net/recalls/food-h-0932-2026-marquesita-de-chocolate-y-vainilla-image-delighted-flavored-cakes-th/"}, {"id": "fda-food-h-0931-2026", "source": "FDA", "category": "food", "recall_number": "H-0931-2026", "title": "Marquesita de Dulceleche [image] Delighted Flavored Cakes The Original recall (Galaxy RG Corp)", "product": "Marquesita de Dulceleche [image] Delighted Flavored Cakes The Original, Net Wt. 16 oz, packaged in a transparent and rigid plastic clamshell container, one unit per container. KEEP REFRIGERATED. UPC 824790852706", "reason": "Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).", "hazard_level": "Class II", "company": "Galaxy RG Corp", "company_location": "Miami, FL, United States", "date": "2026-04-03", "report_date": "2026-06-17", "status": "Terminated", "distribution": "FL and TX.", "states": ["FL", "TX"], "nationwide": false, "quantity": "877 (16-oz) units", "codes": "Expiration Date: From 04/03/2026 to 05/03/2026 Lot#034320462, 034320562, 034320662, 034320962, 034321062, 034321162, 034321262, 034321362, 034321662, 034321762, 034321862, 034321962, 034322062, 034322362, 034322462, 034322562, 034322662, 034322762, 034323062, 034323162, 044320162, 044320262, 044320362", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0931-2026%22", "url": "https://recallledger.net/recalls/food-h-0931-2026-marquesita-de-dulceleche-image-delighted-flavored-cakes-the-original/"}, {"id": "fda-food-h-0930-2026", "source": "FDA", "category": "food", "recall_number": "H-0930-2026", "title": "Marquesita de Fresa [image] Delighted Flavored Cakes The Original recall (Galaxy RG Corp)", "product": "Marquesita de Fresa [image] Delighted Flavored Cakes The Original, Net Wt. 16 oz, packaged in a transparent and rigid plastic clamshell container, one unit per container. KEEP REFRIGERATED. UPC 824790852706", "reason": "Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).", "hazard_level": "Class II", "company": "Galaxy RG Corp", "company_location": "Miami, FL, United States", "date": "2026-04-03", "report_date": "2026-06-17", "status": "Terminated", "distribution": "FL and TX.", "states": ["FL", "TX"], "nationwide": false, "quantity": "629 (16-oz) units", "codes": "Expiration Date: From 04/03/2026 to 05/03/2026 Lot#034320462, 034320562, 034320662, 034320962, 034321062, 034321162, 034321262, 034321362, 034321662, 034321762, 034321862, 034321962, 034322062, 034322362, 034322462, 034322562, 034322662, 034322762, 034323062, 034323162, 044320162, 044320262, 044320362", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0930-2026%22", "url": "https://recallledger.net/recalls/food-h-0930-2026-marquesita-de-fresa-image-delighted-flavored-cakes-the-original-net/"}, {"id": "fda-food-h-0929-2026", "source": "FDA", "category": "food", "recall_number": "H-0929-2026", "title": "Marquesita de Mango [image] Delighted Flavored Cakes The Original recall (Galaxy RG Corp)", "product": "Marquesita de Mango [image] Delighted Flavored Cakes The Original, Net Wt. 16 oz, packaged in a transparent and rigid plastic clamshell container, one unit per container. KEEP REFRIGERATED. UPC 824790852706", "reason": "Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).", "hazard_level": "Class II", "company": "Galaxy RG Corp", "company_location": "Miami, FL, United States", "date": "2026-04-03", "report_date": "2026-06-17", "status": "Terminated", "distribution": "FL and TX.", "states": ["FL", "TX"], "nationwide": false, "quantity": "442 (16-oz) units", "codes": "Expiration Date: From 04/03/2026 to 05/03/2026 Lot#034320462, 034320562, 034320662, 034320962, 034321062, 034321162, 034321262, 034321362, 034321662, 034321762, 034321862, 034321962, 034322062, 034322362, 034322462, 034322562, 034322662, 034322762, 034323062, 034323162, 044320162, 044320262, 044320362", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0929-2026%22", "url": "https://recallledger.net/recalls/food-h-0929-2026-marquesita-de-mango-image-delighted-flavored-cakes-the-original-net/"}, {"id": "fda-food-h-0928-2026", "source": "FDA", "category": "food", "recall_number": "H-0928-2026", "title": "Marquesita de Guava [image] Delighted Flavored Cakes The Original recall (Galaxy RG Corp)", "product": "Marquesita de Guava [image] Delighted Flavored Cakes The Original, Net Wt. 16 oz, packaged in a transparent and rigid plastic clamshell container, one unit per container. KEEP REFRIGERATED. UPC 824790852706", "reason": "Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).", "hazard_level": "Class II", "company": "Galaxy RG Corp", "company_location": "Miami, FL, United States", "date": "2026-04-03", "report_date": "2026-06-17", "status": "Terminated", "distribution": "FL and TX.", "states": ["FL", "TX"], "nationwide": false, "quantity": "1,316 (16-oz) units", "codes": "Expiration Date: From 04/03/2026 to 05/03/2026 Lot#034320462, 034320562, 034320662, 034320962, 034321062, 034321162, 034321262, 034321362, 034321662, 034321762, 034321862, 034321962, 034322062, 034322362, 034322462, 034322562, 034322662, 034322762, 034323062, 034323162, 044320162, 044320262, 044320362", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0928-2026%22", "url": "https://recallledger.net/recalls/food-h-0928-2026-marquesita-de-guava-image-delighted-flavored-cakes-the-original-net/"}, {"id": "fda-food-h-0927-2026", "source": "FDA", "category": "food", "recall_number": "H-0927-2026", "title": "Tiramisu [image] Cofee Cake The Original recall (Galaxy RG Corp)", "product": "Tiramisu [image] Cofee Cake The Original, Net Wt. 30 oz, packaged in a transparent and rigid plastic clamshell container, one unit per container. KEEP REFRIGERATED. UPC 824790850320", "reason": "Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).", "hazard_level": "Class II", "company": "Galaxy RG Corp", "company_location": "Miami, FL, United States", "date": "2026-04-03", "report_date": "2026-06-17", "status": "Terminated", "distribution": "FL and TX.", "states": ["FL", "TX"], "nationwide": false, "quantity": "221 (30-oz) units", "codes": "Expiration Date: From 04/03/2026 to 05/03/2026 Lot#034320462, 034320562, 034320662, 034320962, 034321062, 034321162, 034321262, 034321362, 034321662, 034321762, 034321862, 034321962, 034322062, 034322362, 034322462, 034322562, 034322662, 034322762, 034323062, 034323162, 044320162, 044320262, 044320362", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0927-2026%22", "url": "https://recallledger.net/recalls/food-h-0927-2026-tiramisu-image-cofee-cake-the-original-net-wt-30-oz-packaged-in-a/"}, {"id": "fda-food-h-0926-2026", "source": "FDA", "category": "food", "recall_number": "H-0926-2026", "title": "Cake de Mango [image] Mango Cake The Original recall (Galaxy RG Corp)", "product": "Cake de Mango [image] Mango Cake The Original, Net Wt. 47 oz, packaged in a rigid plastic clamshell container with a transparent dome lid and tray base, one unit per container. KEEP REFRIGERATED. UPC 824790852805", "reason": "Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).", "hazard_level": "Class II", "company": "Galaxy RG Corp", "company_location": "Miami, FL, United States", "date": "2026-04-03", "report_date": "2026-06-17", "status": "Terminated", "distribution": "FL and TX.", "states": ["FL", "TX"], "nationwide": false, "quantity": "257 (47-oz) units", "codes": "Expiration Date: From 04/03/2026 to 05/03/2026 Lot#034320462, 034320562, 034320662, 034320962, 034321062, 034321162, 034321262, 034321362, 034321662, 034321762, 034321862, 034321962, 034322062, 034322362, 034322462, 034322562, 034322662, 034322762, 034323062, 034323162, 044320162, 044320262, 044320362", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0926-2026%22", "url": "https://recallledger.net/recalls/food-h-0926-2026-cake-de-mango-image-mango-cake-the-original-net-wt-47-oz-packaged/"}, {"id": "fda-food-h-0925-2026", "source": "FDA", "category": "food", "recall_number": "H-0925-2026", "title": "Cake de Guayaba [image] Guava Cake The Original recall (Galaxy RG Corp)", "product": "Cake de Guayaba [image] Guava Cake The Original, Net Wt. 47 oz, packaged in a plastic container, one unit per container. KEEP REFRIGERATED. UPC 824790852782", "reason": "Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).", "hazard_level": "Class II", "company": "Galaxy RG Corp", "company_location": "Miami, FL, United States", "date": "2026-04-03", "report_date": "2026-06-17", "status": "Terminated", "distribution": "FL and TX.", "states": ["FL", "TX"], "nationwide": false, "quantity": "311 (47-oz) units", "codes": "Expiration Date: From 04/03/2026 to 05/03/2026 Lot#034320462, 034320562, 034320662, 034320962, 034321062, 034321162, 034321262, 034321362, 034321662, 034321762, 034321862, 034321962, 034322062, 034322362, 034322462, 034322562, 034322662, 034322762, 034323062, 034323162, 044320162, 044320262, 044320362", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0925-2026%22", "url": "https://recallledger.net/recalls/food-h-0925-2026-cake-de-guayaba-image-guava-cake-the-original-net-wt-47-oz-packag/"}, {"id": "fda-food-h-0924-2026", "source": "FDA", "category": "food", "recall_number": "H-0924-2026", "title": "Cake de Fresa y Chocolate [image] Stawberry & Chocolate Cake The Original recall (Galaxy RG Corp)", "product": "Cake de Fresa y Chocolate [image] Stawberry & Chocolate Cake The Original, Net Wt. 48 oz, packaged in a rigid plastic clamshell container with a transparent dome lid and tray base, one unit per container. KEEP REFRIGERATED. UPC 824790852980", "reason": "Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).", "hazard_level": "Class II", "company": "Galaxy RG Corp", "company_location": "Miami, FL, United States", "date": "2026-04-03", "report_date": "2026-06-17", "status": "Terminated", "distribution": "FL and TX.", "states": ["FL", "TX"], "nationwide": false, "quantity": "190 (48-oz) units", "codes": "Expiration Date: From 04/03/2026 to 05/03/2026 Lot#034320462, 034320562, 034320662, 034320962, 034321062, 034321162, 034321262, 034321362, 034321662, 034321762, 034321862, 034321962, 034322062, 034322362, 034322462, 034322562, 034322662, 034322762, 034323062, 034323162, 044320162, 044320262, 044320362", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0924-2026%22", "url": "https://recallledger.net/recalls/food-h-0924-2026-cake-de-fresa-y-chocolate-image-stawberry-chocolate-cake-the-origi/"}, {"id": "fda-food-h-0923-2026", "source": "FDA", "category": "food", "recall_number": "H-0923-2026", "title": "Cake de Coco [image] Coconut Cake The Original recall (Galaxy RG Corp)", "product": "Cake de Coco [image] Coconut Cake The Original, Net Wt. 47 oz, packaged in a rigid plastic clamshell container with a transparent dome lid and tray base, one unit per container. KEEP REFRIGERATED. UPC 824790852775", "reason": "Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).", "hazard_level": "Class II", "company": "Galaxy RG Corp", "company_location": "Miami, FL, United States", "date": "2026-04-03", "report_date": "2026-06-17", "status": "Terminated", "distribution": "FL and TX.", "states": ["FL", "TX"], "nationwide": false, "quantity": "241 (47-oz) units", "codes": "Expiration Date: From 04/03/2026 to 05/03/2026 Lot#034320462, 034320562, 034320662, 034320962, 034321062, 034321162, 034321262, 034321362, 034321662, 034321762, 034321862, 034321962, 034322062, 034322362, 034322462, 034322562, 034322662, 034322762, 034323062, 034323162, 044320162, 044320262, 044320362", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0923-2026%22", "url": "https://recallledger.net/recalls/food-h-0923-2026-cake-de-coco-image-coconut-cake-the-original-net-wt-47-oz-package/"}, {"id": "fda-food-h-0922-2026", "source": "FDA", "category": "food", "recall_number": "H-0922-2026", "title": "Cake de Capuchino [image] Capuchino Cake The Original recall (Galaxy RG Corp)", "product": "Cake de Capuchino [image] Capuchino Cake The Original, Net Wt. 63 oz, packaged in a transparent and rigid plastic clamshell container with a transparent dome lid and tray base, one unit per container. KEEP REFRIGERATED. UPC 824790850375", "reason": "Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).", "hazard_level": "Class II", "company": "Galaxy RG Corp", "company_location": "Miami, FL, United States", "date": "2026-04-03", "report_date": "2026-06-17", "status": "Terminated", "distribution": "FL and TX.", "states": ["FL", "TX"], "nationwide": false, "quantity": "3,786 (63-oz) units", "codes": "Expiration Date: From 04/03/2026 to 05/03/2026 Lot#034320462, 034320562, 034320662, 034320962, 034321062, 034321162, 034321262, 034321362, 034321662, 034321762, 034321862, 034321962, 034322062, 034322362, 034322462, 034322562, 034322662, 034322762, 034323062, 034323162, 044320162, 044320262, 044320362", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0922-2026%22", "url": "https://recallledger.net/recalls/food-h-0922-2026-cake-de-capuchino-image-capuchino-cake-the-original-net-wt-63-oz/"}, {"id": "fda-food-h-0921-2026", "source": "FDA", "category": "food", "recall_number": "H-0921-2026", "title": "Capuchino [image] Syrup Cone Cake The Original recall (Galaxy RG Corp)", "product": "Capuchino [image] Syrup Cone Cake The Original, Net Wt. 13 oz, packaged in a transparent and rigid plastic clamshell container, one unit per container. KEEP REFRIGERATED. UPC 824790852119", "reason": "Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).", "hazard_level": "Class II", "company": "Galaxy RG Corp", "company_location": "Miami, FL, United States", "date": "2026-04-03", "report_date": "2026-06-17", "status": "Terminated", "distribution": "FL and TX.", "states": ["FL", "TX"], "nationwide": false, "quantity": "3,028 (13-oz) units", "codes": "Expiration Date: From 04/03/2026 to 05/03/2026 Lot#034320462, 034320562, 034320662, 034320962, 034321062, 034321162, 034321262, 034321362, 034321662, 034321762, 034321862, 034321962, 034322062, 034322362, 034322462, 034322562, 034322662, 034322762, 034323062, 034323162, 044320162, 044320262, 044320362", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0921-2026%22", "url": "https://recallledger.net/recalls/food-h-0921-2026-capuchino-image-syrup-cone-cake-the-original-net-wt-13-oz-package/"}, {"id": "fda-food-h-0920-2026", "source": "FDA", "category": "food", "recall_number": "H-0920-2026", "title": "Rollitos de DulceLeche [image] Caramel Rolls The Original recall (Galaxy RG Corp)", "product": "Rollitos de DulceLeche [image] Caramel Rolls The Original, Net Wt. 15 oz, packaged in a transparent and rigid plastic clamshell container, one unit per container. KEEP REFRIGERATED. UPC 824790852454", "reason": "Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).", "hazard_level": "Class II", "company": "Galaxy RG Corp", "company_location": "Miami, FL, United States", "date": "2026-04-03", "report_date": "2026-06-17", "status": "Terminated", "distribution": "FL and TX.", "states": ["FL", "TX"], "nationwide": false, "quantity": "1,334 (15-oz) units", "codes": "Expiration Date: From 04/03/2026 to 05/03/2026 Lot#034320462, 034320562, 034320662, 034320962, 034321062, 034321162, 034321262, 034321362, 034321662, 034321762, 034321862, 034321962, 034322062, 034322362, 034322462, 034322562, 034322662, 034322762, 034323062, 034323162, 044320162, 044320262, 044320362", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0920-2026%22", "url": "https://recallledger.net/recalls/food-h-0920-2026-rollitos-de-dulceleche-image-caramel-rolls-the-original-net-wt-15/"}, {"id": "fda-food-h-0919-2026", "source": "FDA", "category": "food", "recall_number": "H-0919-2026", "title": "Rollitos de Guava [image] Guava Rolls The Original recall (Galaxy RG Corp)", "product": "Rollitos de Guava [image] Guava Rolls The Original, Net Wt. 15 oz, packaged in a transparent and rigid plastic clamshell container, one unit per container. KEEP REFRIGERATED. UPC 824790852454", "reason": "Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).", "hazard_level": "Class II", "company": "Galaxy RG Corp", "company_location": "Miami, FL, United States", "date": "2026-04-03", "report_date": "2026-06-17", "status": "Terminated", "distribution": "FL and TX.", "states": ["FL", "TX"], "nationwide": false, "quantity": "7,856 (15-oz) units", "codes": "Expiration Date: From 04/03/2026 to 05/03/2026 Lot#034320462, 034320562, 034320662, 034320962, 034321062, 034321162, 034321262, 034321362, 034321662, 034321762, 034321862, 034321962, 034322062, 034322362, 034322462, 034322562, 034322662, 034322762, 034323062, 034323162, 044320162, 044320262, 044320362", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0919-2026%22", "url": "https://recallledger.net/recalls/food-h-0919-2026-rollitos-de-guava-image-guava-rolls-the-original-net-wt-15-oz-pac/"}, {"id": "fda-food-h-0918-2026", "source": "FDA", "category": "food", "recall_number": "H-0918-2026", "title": "Jumbo Napolitano [image] Jumbo Neapolitan recall (Galaxy RG Corp)", "product": "Jumbo Napolitano [image] Jumbo Neapolitan, Net Wt. 26 oz, packaged in a rigid plastic clamshell container with a transparent dome lid and tray base, one unit per container. KEEP REFRIGERATED. UPC 824790853086", "reason": "Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).", "hazard_level": "Class II", "company": "Galaxy RG Corp", "company_location": "Miami, FL, United States", "date": "2026-04-03", "report_date": "2026-06-17", "status": "Terminated", "distribution": "FL and TX.", "states": ["FL", "TX"], "nationwide": false, "quantity": "2,598 (26-oz) units", "codes": "Expiration Date: From 04/03/2026 to 05/03/2026 Lot#034320462, 034320562, 034320662, 034320962, 034321062, 034321162, 034321262, 034321362, 034321662, 034321762, 034321862, 034321962, 034322062, 034322362, 034322462, 034322562, 034322662, 034322762, 034323062, 034323162, 044320162, 044320262, 044320362", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0918-2026%22", "url": "https://recallledger.net/recalls/food-h-0918-2026-jumbo-napolitano-image-jumbo-neapolitan-net-wt-26-oz-packaged-in/"}, {"id": "fda-food-h-0917-2026", "source": "FDA", "category": "food", "recall_number": "H-0917-2026", "title": "Napolitano [image] Neapolitan The Original recall (Galaxy RG Corp)", "product": "Napolitano [image] Neapolitan The Original, Net Wt. 22 oz, packaged in a transparent and rigid plastic clamshell container, one unit per container. KEEP REFRIGERATED. UPC 824790852256", "reason": "Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).", "hazard_level": "Class II", "company": "Galaxy RG Corp", "company_location": "Miami, FL, United States", "date": "2026-04-03", "report_date": "2026-06-17", "status": "Terminated", "distribution": "FL and TX.", "states": ["FL", "TX"], "nationwide": false, "quantity": "5,960 (22-oz) units", "codes": "Expiration Date: From 04/03/2026 to 05/03/2026 Lot#034320462, 034320562, 034320662, 034320962, 034321062, 034321162, 034321262, 034321362, 034321662, 034321762, 034321862, 034321962, 034322062, 034322362, 034322462, 034322562, 034322662, 034322762, 034323062, 034323162, 044320162, 044320262, 044320362", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0917-2026%22", "url": "https://recallledger.net/recalls/food-h-0917-2026-napolitano-image-neapolitan-the-original-net-wt-22-oz-packaged-in/"}, {"id": "fda-food-h-0916-2026", "source": "FDA", "category": "food", "recall_number": "H-0916-2026", "title": "Jumbo Brazo Gitano Caramelo [image] Jumbo Caramel Roll The Original recall (Galaxy RG Corp)", "product": "Jumbo Brazo Gitano Caramelo [image] Jumbo Caramel Roll The Original, Net Wt. 40 oz, packaged in a rigid plastic clamshell container with a transparent dome lid, one unit per container. KEEP REFRIGERATED. UPC 824790852645", "reason": "Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).", "hazard_level": "Class II", "company": "Galaxy RG Corp", "company_location": "Miami, FL, United States", "date": "2026-04-03", "report_date": "2026-06-17", "status": "Terminated", "distribution": "FL and TX.", "states": ["FL", "TX"], "nationwide": false, "quantity": "1,116 (40-oz) units", "codes": "Expiration Date: From 04/03/2026 to 05/03/2026 Lot#034320462, 034320562, 034320662, 034320962, 034321062, 034321162, 034321262, 034321362, 034321662, 034321762, 034321862, 034321962, 034322062, 034322362, 034322462, 034322562, 034322662, 034322762, 034323062, 034323162, 044320162, 044320262, 044320362", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0916-2026%22", "url": "https://recallledger.net/recalls/food-h-0916-2026-jumbo-brazo-gitano-caramelo-image-jumbo-caramel-roll-the-original-n/"}, {"id": "fda-food-h-0915-2026", "source": "FDA", "category": "food", "recall_number": "H-0915-2026", "title": "Brazo Gitano [image] Caramel Sweet Roll The Original recall (Galaxy RG Corp)", "product": "Brazo Gitano [image] Caramel Sweet Roll The Original, Net Wt. 24 oz, packaged in a rigid plastic clamshell container with a transparent dome lid and tray base, one unit per container. KEEP REFRIGERATED. UPC 882479852232", "reason": "Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).", "hazard_level": "Class II", "company": "Galaxy RG Corp", "company_location": "Miami, FL, United States", "date": "2026-04-03", "report_date": "2026-06-17", "status": "Terminated", "distribution": "FL and TX.", "states": ["FL", "TX"], "nationwide": false, "quantity": "2,273 (24-oz) units", "codes": "Expiration Date: From 04/03/2026 to 05/03/2026 Lot#034320462, 034320562, 034320662, 034320962, 034321062, 034321162, 034321262, 034321362, 034321662, 034321762, 034321862, 034321962, 034322062, 034322362, 034322462, 034322562, 034322662, 034322762, 034323062, 034323162, 044320162, 044320262, 044320362", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0915-2026%22", "url": "https://recallledger.net/recalls/food-h-0915-2026-brazo-gitano-image-caramel-sweet-roll-the-original-net-wt-24-oz-p/"}, {"id": "fda-device-z-2410-2026", "source": "FDA", "category": "device", "recall_number": "Z-2410-2026", "title": "Halyard recall (AVID Medical, Inc.)", "product": "Halyard, Eye Bag Pack. Kit Code: UIEB48-01.", "reason": "Inadvertent distribution of sealed pouches that had not undergone validated sterilization.", "hazard_level": "Class II", "company": "AVID Medical, Inc.", "company_location": "Toano, VA, United States", "date": "2026-04-30", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "US Nationwide distribution in the state of Iowa.", "states": ["IA"], "nationwide": true, "quantity": "60 kits", "codes": "Kit Code: UIEB48-01. UDI-DI: 10809160484098. Lot Number: UIEB48-01. Expiration Date: 8/7/2028.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2410-2026%22", "url": "https://recallledger.net/recalls/device-z-2410-2026-halyard-eye-bag-pack-kit-code-uieb48-01/"}, {"id": "fda-device-z-2409-2026", "source": "FDA", "category": "device", "recall_number": "Z-2409-2026", "title": "Halyard recall (AVID Medical, Inc.)", "product": "Halyard, Drape Pack. Kit Code: LMDP36-01.", "reason": "Inadvertent distribution of sealed pouches that had not undergone validated sterilization.", "hazard_level": "Class II", "company": "AVID Medical, Inc.", "company_location": "Toano, VA, United States", "date": "2026-04-30", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "US Nationwide distribution in the state of Iowa.", "states": ["IA"], "nationwide": true, "quantity": "72 kits", "codes": "Kit Code: LMDP36-01.UDI-DI: 10809160479148. Lot Number: LMDP36-01. Expiration Date: 9/10/2028", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2409-2026%22", "url": "https://recallledger.net/recalls/device-z-2409-2026-halyard-drape-pack-kit-code-lmdp36-01/"}, {"id": "fda-device-z-2408-2026", "source": "FDA", "category": "device", "recall_number": "Z-2408-2026", "title": "Halyard recall (AVID Medical, Inc.)", "product": "Halyard, Towel Six Pack. Kit Code: AMTS70-01.", "reason": "Inadvertent distribution of sealed pouches that had not undergone validated sterilization.", "hazard_level": "Class II", "company": "AVID Medical, Inc.", "company_location": "Toano, VA, United States", "date": "2026-04-30", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "US Nationwide distribution in the state of Iowa.", "states": ["IA"], "nationwide": true, "quantity": "224 kits", "codes": "Kit Code: AMTS70-01. UDI-DI: 10809160469972. Lot Number: AMTS70-01. Expiration Date: 9/2/2028.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2408-2026%22", "url": "https://recallledger.net/recalls/device-z-2408-2026-halyard-towel-six-pack-kit-code-amts70-01/"}, {"id": "fda-device-z-2407-2026", "source": "FDA", "category": "device", "recall_number": "Z-2407-2026", "title": "Halyard recall (AVID Medical, Inc.)", "product": "Halyard, Pain Pack. Kit Code: AMPK48-01.", "reason": "Inadvertent distribution of sealed pouches that had not undergone validated sterilization.", "hazard_level": "Class II", "company": "AVID Medical, Inc.", "company_location": "Toano, VA, United States", "date": "2026-04-30", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "US Nationwide distribution in the state of Iowa.", "states": ["IA"], "nationwide": true, "quantity": "120 kits", "codes": "Kit Code: AMPK48-01. UDI-DI: 10809160472798. Lot Number: 334669. Expiration Date: 8/27/2028.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2407-2026%22", "url": "https://recallledger.net/recalls/device-z-2407-2026-halyard-pain-pack-kit-code-ampk48-01/"}, {"id": "fda-device-z-2404-2026", "source": "FDA", "category": "device", "recall_number": "Z-2404-2026", "title": "Boston Scientific Model SC-4318 recall (Boston Scientific Neuromodulation Corporation)", "product": "Boston Scientific Model SC-4318, Clik X Anchor REF: M365SC43180", "reason": "Sterile anchors my lack sterility assurance.", "hazard_level": "Class II", "company": "Boston Scientific Neuromodulation Corporation", "company_location": "Valencia, CA, United States", "date": "2026-04-29", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "US Nationwide distribution in the states of MD, UT, FL, LA, SC, OK.", "states": ["FL", "LA", "MD", "OK", "SC", "UT"], "nationwide": true, "quantity": "43 units", "codes": "GTIN: 08714729905318/Lot # 35107836", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2404-2026%22", "url": "https://recallledger.net/recalls/device-z-2404-2026-boston-scientific-model-sc-4318-clik-x-anchor-ref-m365sc43180/"}, {"id": "fda-device-z-2403-2026", "source": "FDA", "category": "device", "recall_number": "Z-2403-2026", "title": "Boston Scientific TCN Electrodes: REF: TCN-5 recall (Boston Scientific Neuromodulation Corporation)", "product": "Boston Scientific TCN Electrodes: REF: TCN-5, TCN Electrode, NITINOL, 5 cm x 0.45 mm (0.0175 in); REF:TCN-10, TCN Electrode, NITINOL, 10 cm x 0.45 mm (0.0175 in) REF:TCN-15, TCN Electrode, NITINOL, 15 cm x 0.45 mm (0.0175 in); REF:TCN-20, TCN Electrode, NITINOL, 20 cm x 0.45 mm (0.0175 in) REF: TCN-5-3m, TCN Electrode, NITINOL, 3M CABLE, 5 cm x 0.45 mm (0.0175 in) REF: TCN-10-3M, TCN Electrode, NITINOL, 3M CABLE, 10 cm x 0.45 mm (0.0175 in); REF: TCN-15-3M, TCN Electrode, NITINOL, 3M CABLE, 15 cm x 0.45 mm (0.0175 in) REF: TCN-20-3M, TCN Electrode, NITINOL, 3M CABLE, 20 cm x 0.45 mm (0.0175 in)", "reason": "Reusable electrodes may not meet expected performance levels.", "hazard_level": "Class II", "company": "Boston Scientific Neuromodulation Corporation", "company_location": "Valencia, CA, United States", "date": "2026-04-29", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "Worldwide distribution - US Nationwide and the countries of PE, MX, PR, CO, MY, CA.", "states": ["CA", "CO", "PR"], "nationwide": true, "quantity": "49,251 units", "codes": "All Lots: / UDI: TCN-10: 00813250013054; TCN-10-3M: 00813250017502; TCN-15: 00813250013061; TCN-15-3M: 00813250017519; TCN-20: 00813250013078; TCN-20-3M: 00813250017526; TCN-5: 00813250013047; TCN-5-3M:00813250017533", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2403-2026%22", "url": "https://recallledger.net/recalls/device-z-2403-2026-boston-scientific-tcn-electrodes-ref-tcn-5-tcn-electrode-nitinol/"}, {"id": "fda-device-z-2402-2026", "source": "FDA", "category": "device", "recall_number": "Z-2402-2026", "title": "Boston Scientific CSK Electrodes: REF: CSK-TC10 recall (Boston Scientific Neuromodulation Corporation)", "product": "Boston Scientific CSK Electrodes: REF: CSK-TC10, CSK Electrode, STAINLESS STEEL, 10 cm x 28 ga (0.36 mm) REF: CSK-TC10-3M,CSK Electrode, STAINLESS STEEL, 3M Cable, 10 cm x 28 ga (0.36 mm); REF: CSK-TC15, CSK Electrode, STAINLESS STEEL, 15 cm x 28 ga (0.36 mm); REF: CSK-TC15-3M, CSK Electrode, STAINLESS STEEL, 3M Cable, 15 cm x 28 ga (0.36 mm) REF: CSK-TC20, CSK Electrode, STAINLESS STEEL, 20 cm x 28 ga (0.36 mm) REF: CSK-TC5,CSK Electrode, STAINLESS STEEL, 5 cm x 28 ga (0.36 mm); REF: CSK-TC5-3M, CSK Electrode, STAINLESS STEEL, 3M Cable, 5 cm x 28 ga (0.36 mm)", "reason": "Reusable electrodes may not meet expected performance levels.", "hazard_level": "Class II", "company": "Boston Scientific Neuromodulation Corporation", "company_location": "Valencia, CA, United States", "date": "2026-04-29", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "Worldwide distribution - US Nationwide and the countries of PE, MX, PR, CO, MY, CA.", "states": ["CA", "CO", "PR"], "nationwide": true, "quantity": "31,923 units", "codes": "All Lots: / UDI: CSK-TC10:00813250010107; CSK-TC10-3M: 00813250011524; CSK-TC15 00813250010114; CSK-TC15-3M: 00813250011548 CSK-TC20: 0081325001140; CSK-TC5: 00813250010091; CSK-TC5-3M: 00813250011531;", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2402-2026%22", "url": "https://recallledger.net/recalls/device-z-2402-2026-boston-scientific-csk-electrodes-ref-csk-tc10-csk-electrode-stain/"}, {"id": "fda-device-z-2362-2026", "source": "FDA", "category": "device", "recall_number": "Z-2362-2026", "title": "Brand Name: EXENT Analyser Product Name: EXENT Analyser Model/Catalog Number:... recall (The Binding Site Group, Ltd.)", "product": "Brand Name: EXENT Analyser Product Name: EXENT Analyser Model/Catalog Number: IE800.A Software Version: 1.0.20 Product Description: The EXENT Analyser is an automated analyser intended for the qualitative and quantitative in vitro measurement of analytes in human body fluids used in conjunction with the EXENT assays.", "reason": "It was reported that plates 2 and 3 were marked as passed , although it appeared that QC had not been performed on these plates, despite samples being measured. The potential clinical hazards include false or missed detection of M-protein (false positive); and falsely elevated or decreased M-protein concentration.", "hazard_level": "Class II", "company": "The Binding Site Group, Ltd.", "company_location": "Birmingham, N/A, United Kingdom", "date": "2026-04-16", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "US Nationwide distribution.", "states": [], "nationwide": true, "quantity": "1", "codes": "Lot Code: Model No; IE800A; EXENT Analyser; UDI; 05051700020886, Serial Number; 101150, Software version; v1.0.20.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2362-2026%22", "url": "https://recallledger.net/recalls/device-z-2362-2026-brand-name-exent-analyser-product-name-exent-analyser-model-catalo/"}, {"id": "fda-device-z-2361-2026", "source": "FDA", "category": "device", "recall_number": "Z-2361-2026", "title": "Medartis APTUS recall (Medartis AG)", "product": "Medartis APTUS, 5.0 headedCCS Long Thread 50/20mm, REF A-8216.50/1, 1/Pkg; Cannulated Compression Screws for bone fixation", "reason": "The cannulation of the CCS screw is not centered.", "hazard_level": "Class II", "company": "Medartis AG", "company_location": "Basel Town, N/A, Switzerland", "date": "2026-04-24", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "US Nationwide distribution in the states of LA, TX. IN, CA, NC.", "states": ["CA", "IN", "LA", "NC", "TX"], "nationwide": true, "quantity": "13 units", "codes": "UDI/DI 07630037887706, Lot Numbers: 25444702, 24425542, 24404471, 25441997", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2361-2026%22", "url": "https://recallledger.net/recalls/device-z-2361-2026-medartis-aptus-5-0-headedccs-long-thread-50-20mm-ref-a-8216-50-1-1/"}, {"id": "fda-device-z-2352-2026", "source": "FDA", "category": "device", "recall_number": "Z-2352-2026", "title": "Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit... recall (Avanos Medical, Inc.)", "product": "Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 24 Fr PULL Model/Catalog Number: 8180-24", "reason": "Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.", "hazard_level": "Class II", "company": "Avanos Medical, Inc.", "company_location": "Alpharetta, GA, United States", "date": "2026-04-30", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "US Nationwide distribution.", "states": [], "nationwide": true, "quantity": "1,205 kits", "codes": "UDI-DI 10350770007868, Lot Numbers 30371319, 30374055, 30383058, 30386936", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2352-2026%22", "url": "https://recallledger.net/recalls/device-z-2352-2026-product-name-mic-safety-percutaneous-endoscopic-gastrostomy-peg-kit-w/"}, {"id": "fda-device-z-2351-2026", "source": "FDA", "category": "device", "recall_number": "Z-2351-2026", "title": "Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit... recall (Avanos Medical, Inc.)", "product": "Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 20 Fr PULL Model/Catalog Number: 8180-20", "reason": "Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.", "hazard_level": "Class II", "company": "Avanos Medical, Inc.", "company_location": "Alpharetta, GA, United States", "date": "2026-04-30", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "US Nationwide distribution.", "states": [], "nationwide": true, "quantity": "6,005 kits", "codes": "Lot Code: Model No 8180-20, UDI-DI 10350770007851, Lot Numbers 20133232, 30371326, 30378749, 30378751, 30379686, 30383063, 30383057, 80403339, 80403342", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2351-2026%22", "url": "https://recallledger.net/recalls/device-z-2351-2026-product-name-mic-safety-percutaneous-endoscopic-gastrostomy-peg-kit-w/"}, {"id": "fda-device-z-2350-2026", "source": "FDA", "category": "device", "recall_number": "Z-2350-2026", "title": "Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit... recall (Avanos Medical, Inc.)", "product": "Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 14 Fr PULL Model/Catalog Number: 8180-14", "reason": "Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.", "hazard_level": "Class II", "company": "Avanos Medical, Inc.", "company_location": "Alpharetta, GA, United States", "date": "2026-04-30", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "US Nationwide distribution.", "states": [], "nationwide": true, "quantity": "218 kits", "codes": "UDI-DI 10350770007844, Lot Numbers 30371318, 30375469, 30383056", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2350-2026%22", "url": "https://recallledger.net/recalls/device-z-2350-2026-product-name-mic-safety-percutaneous-endoscopic-gastrostomy-peg-kit-w/"}, {"id": "fda-device-z-2349-2026", "source": "FDA", "category": "device", "recall_number": "Z-2349-2026", "title": "Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit... recall (Avanos Medical, Inc.)", "product": "Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 24 Fr PUSH OTW Model/Catalog Number: 8170-24", "reason": "Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.", "hazard_level": "Class II", "company": "Avanos Medical, Inc.", "company_location": "Alpharetta, GA, United States", "date": "2026-04-30", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "US Nationwide distribution.", "states": [], "nationwide": true, "quantity": "234 kits", "codes": "UDI-DI 10350770007837, Lot Numbers 30371847, 30374834, 30378748, 30380347", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2349-2026%22", "url": "https://recallledger.net/recalls/device-z-2349-2026-product-name-mic-safety-percutaneous-endoscopic-gastrostomy-peg-kit-w/"}, {"id": "fda-device-z-2348-2026", "source": "FDA", "category": "device", "recall_number": "Z-2348-2026", "title": "Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit... recall (Avanos Medical, Inc.)", "product": "Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 20 Fr PUSH OTW Model/Catalog Number: 8170-20", "reason": "Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.", "hazard_level": "Class II", "company": "Avanos Medical, Inc.", "company_location": "Alpharetta, GA, United States", "date": "2026-04-30", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "US Nationwide distribution.", "states": [], "nationwide": true, "quantity": "1,615 kits", "codes": "UDI-DI 10350770007820, Lot Numbers 30371324, 30374833, 30384889, 80403350", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2348-2026%22", "url": "https://recallledger.net/recalls/device-z-2348-2026-product-name-mic-safety-percutaneous-endoscopic-gastrostomy-peg-kit-w/"}, {"id": "fda-device-z-2347-2026", "source": "FDA", "category": "device", "recall_number": "Z-2347-2026", "title": "Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit... recall (Avanos Medical, Inc.)", "product": "Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 14 Fr PUSH OTW Model/Catalog Number: 8170-14 Product Description: Feeding Tube Kit Component: No", "reason": "Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.", "hazard_level": "Class II", "company": "Avanos Medical, Inc.", "company_location": "Alpharetta, GA, United States", "date": "2026-04-30", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "US Nationwide distribution.", "states": [], "nationwide": true, "quantity": "53 kits", "codes": "UDI-DI 10350770007813, Lot Number 30370718", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2347-2026%22", "url": "https://recallledger.net/recalls/device-z-2347-2026-product-name-mic-safety-percutaneous-endoscopic-gastrostomy-peg-kit-w/"}, {"id": "fda-device-z-2346-2026", "source": "FDA", "category": "device", "recall_number": "Z-2346-2026", "title": "Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PULL ... recall (Avanos Medical, Inc.)", "product": "Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PULL Model/Catalog Number: 7180-24", "reason": "Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.", "hazard_level": "Class II", "company": "Avanos Medical, Inc.", "company_location": "Alpharetta, GA, United States", "date": "2026-04-30", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "US Nationwide distribution.", "states": [], "nationwide": true, "quantity": "1,006 kits", "codes": "UDI-DI 10350770007806, Lot Numbers 30371316, 30377829, 80403341", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2346-2026%22", "url": "https://recallledger.net/recalls/device-z-2346-2026-product-name-mic-safety-percutaneous-endoscopic-gastrostomy-peg-kit/"}, {"id": "fda-device-z-2345-2026", "source": "FDA", "category": "device", "recall_number": "Z-2345-2026", "title": "Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PULL ... recall (Avanos Medical, Inc.)", "product": "Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PULL Model/Catalog Number: 7180-20", "reason": "Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.", "hazard_level": "Class II", "company": "Avanos Medical, Inc.", "company_location": "Alpharetta, GA, United States", "date": "2026-04-30", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "US Nationwide distribution.", "states": [], "nationwide": true, "quantity": "3,184 kits", "codes": "UDI-DI 10350770007783, Lot Numbers 30371313, 30371314, 30373295, 30373296, 30374832, 30378735, 80403340", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2345-2026%22", "url": "https://recallledger.net/recalls/device-z-2345-2026-product-name-mic-safety-percutaneous-endoscopic-gastrostomy-peg-kit/"}, {"id": "fda-device-z-2344-2026", "source": "FDA", "category": "device", "recall_number": "Z-2344-2026", "title": "Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PULL ... recall (Avanos Medical, Inc.)", "product": "Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PULL Model/Catalog Number: 7180-14", "reason": "Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.", "hazard_level": "Class II", "company": "Avanos Medical, Inc.", "company_location": "Alpharetta, GA, United States", "date": "2026-04-30", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "US Nationwide distribution.", "states": [], "nationwide": true, "quantity": "208 kits", "codes": "UDI-DI 10350770007769, Lot Numbers 30371312 and 30373421", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2344-2026%22", "url": "https://recallledger.net/recalls/device-z-2344-2026-product-name-mic-safety-percutaneous-endoscopic-gastrostomy-peg-kit/"}, {"id": "fda-device-z-2343-2026", "source": "FDA", "category": "device", "recall_number": "Z-2343-2026", "title": "Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PUSH OTW ... recall (Avanos Medical, Inc.)", "product": "Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PUSH OTW Model/Catalog Number: 7170-24 Product Description: Feeding Tube Kit Component: No", "reason": "Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.", "hazard_level": "Class II", "company": "Avanos Medical, Inc.", "company_location": "Alpharetta, GA, United States", "date": "2026-04-30", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "US Nationwide distribution.", "states": [], "nationwide": true, "quantity": "132 kits", "codes": "UDI-DI: 10350770007790, Lot Numbers 30370715, 30371329, 30375466", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2343-2026%22", "url": "https://recallledger.net/recalls/device-z-2343-2026-product-name-mic-safety-percutaneous-endoscopic-gastrostomy-peg-kit/"}, {"id": "fda-device-z-2342-2026", "source": "FDA", "category": "device", "recall_number": "Z-2342-2026", "title": "Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PUSH OTW ... recall (Avanos Medical, Inc.)", "product": "Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PUSH OTW Model/Catalog Number: 7170-20 Product Description: Feeding Tube Kit Component: No", "reason": "Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were 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Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PUSH OTW Model/Catalog Number: 7170-14 Product Description: Feeding Tube Kit", "reason": "Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.", "hazard_level": "Class II", "company": "Avanos Medical, Inc.", "company_location": "Alpharetta, GA, United States", "date": "2026-04-30", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "US Nationwide distribution.", "states": [], "nationwide": true, "quantity": "22 kits", "codes": "UDI-DI 10350770007752, Lot Number 30370713", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2341-2026%22", "url": "https://recallledger.net/recalls/device-z-2341-2026-product-name-mic-safety-percutaneous-endoscopic-gastrostomy-peg-kit/"}, {"id": "fda-device-z-2340-2026", "source": "FDA", "category": "device", "recall_number": "Z-2340-2026", "title": "Product Name: CORFLO Safety PEG Kit with ENFit Connector Model/Catalog Number:... recall (Avanos Medical, Inc.)", "product": "Product Name: CORFLO Safety PEG Kit with ENFit Connector Model/Catalog Number: 50-6316 Product Description: Feeding Tube Kit Component: No", "reason": "Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.", "hazard_level": "Class II", "company": "Avanos Medical, Inc.", "company_location": "Alpharetta, GA, United States", "date": "2026-04-30", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "US Nationwide distribution.", "states": [], "nationwide": true, "quantity": "54 kits", "codes": "UDI-DI 10350770007530, Lot Numbers 30365233, 30367015, 30372821, 30378386", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2340-2026%22", "url": "https://recallledger.net/recalls/device-z-2340-2026-product-name-corflo-safety-peg-kit-with-enfit-connector-model-catalo/"}, {"id": "fda-device-z-2339-2026", "source": "FDA", "category": "device", "recall_number": "Z-2339-2026", "title": "Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-6312 recall (Avanos Medical, Inc.)", "product": "Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-6312", "reason": "Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.", "hazard_level": "Class II", "company": "Avanos Medical, Inc.", "company_location": "Alpharetta, GA, United States", "date": "2026-04-30", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "US Nationwide distribution.", "states": [], "nationwide": true, "quantity": "43 kits", "codes": "UDI-DI 10350770007523, Lot Numbers 30365232, 30367019, 30380107", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2339-2026%22", "url": "https://recallledger.net/recalls/device-z-2339-2026-product-name-corflo-safety-peg-kit-with-enfit-connector-model-cata/"}, {"id": "fda-device-z-2338-2026", "source": "FDA", "category": "device", "recall_number": "Z-2338-2026", "title": "Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-5320 recall (Avanos Medical, Inc.)", "product": "Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-5320", "reason": "Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.", "hazard_level": "Class II", "company": "Avanos Medical, Inc.", "company_location": "Alpharetta, GA, United States", "date": "2026-04-30", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "US Nationwide distribution.", "states": [], "nationwide": true, "quantity": "72 kits", "codes": "UDI-DI 10350770007516, Lot Numbers 30365231, 30371022, 30373824, 30378385, 30383807, 30385321", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2338-2026%22", "url": "https://recallledger.net/recalls/device-z-2338-2026-product-name-corflo-safety-peg-kit-with-enfit-connector-model-cata/"}, {"id": "fda-device-z-2337-2026", "source": "FDA", "category": "device", "recall_number": "Z-2337-2026", "title": "Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-4320 recall (Avanos Medical, Inc.)", "product": "Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-4320", "reason": "Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.", "hazard_level": "Class II", "company": "Avanos Medical, Inc.", "company_location": "Alpharetta, GA, United States", "date": "2026-04-30", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "US Nationwide distribution.", "states": [], "nationwide": true, "quantity": "49 kits", "codes": "UDI-DI 10350770007578, Lot Numbers 30365230, 30367013, 30373825", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2337-2026%22", "url": "https://recallledger.net/recalls/device-z-2337-2026-product-name-corflo-safety-peg-kit-with-enfit-connector-model-cata/"}, {"id": "fda-device-z-2336-2026", "source": "FDA", "category": "device", "recall_number": "Z-2336-2026", "title": "Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6316 recall (Avanos Medical, Inc.)", "product": "Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6316", "reason": "Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.", "hazard_level": "Class II", "company": "Avanos Medical, Inc.", "company_location": "Alpharetta, GA, United States", "date": "2026-04-30", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "US Nationwide distribution.", "states": [], "nationwide": true, "quantity": "41 kits", "codes": "Lot Code: Model No 30-6316, UDI-DI 10350770007561, Lot Numbers 30365229 and 30376100", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2336-2026%22", "url": "https://recallledger.net/recalls/device-z-2336-2026-product-name-corflo-safety-peg-kit-model-catalog-number-30-6316/"}, {"id": "fda-device-z-2335-2026", "source": "FDA", "category": "device", "recall_number": "Z-2335-2026", "title": "Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6312 recall (Avanos Medical, Inc.)", "product": "Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6312", "reason": "Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.", "hazard_level": "Class II", "company": "Avanos Medical, Inc.", "company_location": "Alpharetta, GA, United States", "date": "2026-04-30", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "US Nationwide distribution.", "states": [], "nationwide": true, "quantity": "31 kits", "codes": "Lot Code: Model No 30-6312, UDI-DI 10350770007547, Lot Number 30365228", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2335-2026%22", "url": "https://recallledger.net/recalls/device-z-2335-2026-product-name-corflo-safety-peg-kit-model-catalog-number-30-6312/"}, {"id": "fda-device-z-2334-2026", "source": "FDA", "category": "device", "recall_number": "Z-2334-2026", "title": "Brand Name: CORFLO Product Name: CORFLO Safety PEG Kit Model/Catalog Number: 30-5320 recall (Avanos Medical, Inc.)", "product": "Brand Name: CORFLO Product Name: CORFLO Safety PEG Kit Model/Catalog Number: 30-5320", "reason": "Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.", "hazard_level": "Class II", "company": "Avanos Medical, Inc.", "company_location": "Alpharetta, GA, United States", "date": "2026-04-30", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "US Nationwide distribution.", "states": [], "nationwide": true, "quantity": "61 kits", "codes": "UDI-DI 10350770007554, Lot Numbers 30365227, 30368642, 30374529, 30376099, 30380696, and 30387248", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2334-2026%22", "url": "https://recallledger.net/recalls/device-z-2334-2026-brand-name-corflo-product-name-corflo-safety-peg-kit-model-catalog/"}, {"id": "fda-device-z-2333-2026", "source": "FDA", "category": "device", "recall_number": "Z-2333-2026", "title": "Brand Name: CORFLO Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-4320 recall (Avanos Medical, Inc.)", "product": "Brand Name: CORFLO Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-4320", "reason": "Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.", "hazard_level": "Class II", "company": "Avanos Medical, Inc.", "company_location": "Alpharetta, GA, United States", "date": "2026-04-30", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "US Nationwide distribution.", "states": [], "nationwide": true, "quantity": "231 kits", "codes": "UDI-DI 10350770007585, Lot Numbers 30365226 and 30382750", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2333-2026%22", "url": "https://recallledger.net/recalls/device-z-2333-2026-brand-name-corflo-product-name-corflo-safety-peg-kit-model-catalo/"}, {"id": "fda-device-z-2332-2026", "source": "FDA", "category": "device", "recall_number": "Z-2332-2026", "title": "Brand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE recall (HF Acquisition Co LLC)", "product": "Brand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 12 TESTS Product Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 12 TESTS Model/Catalog Number: 1023770 Software Version: N/A Product Description: The SporeTraq Mail-In Spore Testing Service includes 12 bacterial Spore Strips provided by Mesa Labs. The Spore Strip (single species G. stearothermophilus ATCC#7953 or dual species G. stearothermophilus ATCC #7953 and B. atrophaeus ATCC #9372) is intended for use in testing the efficacy of sterilizer systems used in healthcare facilities. The Spore Strips are compatible with Steam sterilization, Chemiclave¿ sterilization, Ethylene Oxide sterilization, or Dry Heat sterilization processes. The test strip is placed in the customer s sterilizer during their sterilization cycle and upon completion the sterilized test strip along with the control strip is returned to Mesa Labs for lab testing in the return envelope. Spore test results are digitally stored in HealthFirst s OnTraq smart automation tracking and reporting system for easy and secure access to a paperless archive from any device with internet access. Component: N/A", "reason": "Due to incorrect incubation process being performed on product.", "hazard_level": "Class II", "company": "HF Acquisition Co LLC", "company_location": "Mukilteo, WA, United States", "date": "2026-04-13", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "U.S. Nationwide distribution including in the states of AR, AZ, CA, CO, CT, DE, FL, GA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, VT, WA, and WI.", "states": ["AR", "AZ", "CA", "CO", "CT", "DE", "FL", "GA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "MI", "MN", "MO", "MS", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI"], "nationwide": true, "quantity": "0", "codes": "Lot Code: Please see attached spreadsheet listing products that were not incubated per the following requirements : a. Spore strips used in steam sterilizers are incubated for 24 hours b. Spore strips used in chemiclave sterilizers are incubated for 72 hours c. Spore strips used in dry heat or ethylene oxide sterilizers are incubated for 7 days As noted in the previous recall scope question, HealthFirst's Field Correction scope will be expanded to include notifications to all customers in possession of 1023780 SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 52 TESTS,1023770 SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 12 TESTS or other products serviced by Mesa Labs.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2332-2026%22", "url": "https://recallledger.net/recalls/device-z-2332-2026-brand-name-sporetraq-mail-in-spore-testing-service-12-tests-product/"}, {"id": "fda-device-z-2331-2026", "source": "FDA", "category": "device", "recall_number": "Z-2331-2026", "title": "Brand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE recall (HF Acquisition Co LLC)", "product": "Brand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 52 TESTS Product Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 52 TESTS Model/Catalog Number: 1023780 Software Version: N/A Product Description: The SporeTraq Mail-In Spore Testing Service includes 52 bacterial Spore Strips provided by Mesa Labs. The Spore Strip (single species G. stearothermophilus ATCC#7953 or dual species G. stearothermophilus ATCC #7953 and B. atrophaeus ATCC #9372) is intended for use in testing the efficacy of sterilizer systems used in healthcare facilities. The Spore Strips are compatible with Steam sterilization, Chemiclave¿ sterilization, Ethylene Oxide sterilization, or Dry Heat sterilization processes. The test strip is placed in the customer s sterilizer during their sterilization cycle and upon completion the sterilized test strip along with the control strip is returned to Mesa Labs for lab testing in the return envelope. Spore test results are digitally stored in HealthFirst s OnTraq smart automation tracking and reporting system for easy and secure access to a paperless archive from any device with internet access. Component: N/A", "reason": "Due to incorrect incubation process being performed on product.", "hazard_level": "Class II", "company": "HF Acquisition Co LLC", "company_location": "Mukilteo, WA, United States", "date": "2026-04-13", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "U.S. Nationwide distribution including in the states of AR, AZ, CA, CO, CT, DE, FL, GA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, VT, WA, and WI.", "states": ["AR", "AZ", "CA", "CO", "CT", "DE", "FL", "GA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "MI", "MN", "MO", "MS", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI"], "nationwide": true, "quantity": "2210", "codes": "Lot Code: Please see attached spreadsheet listing products that were not incubated per the following requirements : a. Spore strips used in steam sterilizers are incubated for 24 hours b. Spore strips used in chemiclave sterilizers are incubated for 72 hours c. Spore strips used in dry heat or ethylene oxide sterilizers are incubated for 7 days As noted in the recall scope question, HealthFirst's Field Correction scope will be expanded to include notifications to all customers in possession of 1023780 SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 52 TESTS,1023770 SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 12 TESTS or other products serviced by Mesa Labs. Product/Item Number: 1023780 UDI-DI code: 00850065007496 Lot Numbers: DSS-122 DSS-125 DSS-128 DSS-131 DSS-134", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2331-2026%22", "url": "https://recallledger.net/recalls/device-z-2331-2026-brand-name-sporetraq-mail-in-spore-testing-service-52-tests-product/"}, {"id": "fda-device-z-2324-2026", "source": "FDA", "category": "device", "recall_number": "Z-2324-2026", "title": "TDC VELOCE\" recall (D.O.R.C. Dutch Opthalmic Research Center Intl B.V.)", "product": "TDC VELOCE\", 27G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT27, 9311.27G01, 9311.27G02, 9311.27K01, 9311.27K02, 9311.27K03, 9627.G0101, 9627.G0201, 9311.27G01-00;", "reason": "An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.", "hazard_level": "Class II", "company": "D.O.R.C. Dutch Opthalmic Research Center Intl B.V.", "company_location": "Zuidland, N/A, Netherlands", "date": "2026-04-30", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "Worldwide - US Nationwide and the countries of AUSTRALIA, AUSTRIA, BELGIUM, BULGARIA, CZECHIA, FINLAND, FRANCE, GERMANY, GREAT BRITAIN, HONG KONG, IRELAND, ITALY, JAPAN, NETHERLANDS, NEW ZEALAND, POLAND, SLOVENIA, SOUTH AFRICA, SPAIN, SWEDEN, TAIWAN, TURKEY.", "states": [], "nationwide": true, "quantity": "261 boxes totaling 1566 units", "codes": "1. Article Number: 9268.VIT27; UDI-DI: 08717872031880; 2. Article Number: 9311.27G01; UDI-DI: 08717872035123; 3. Article Number: 9311.27G02; UDI-DI: 08717872035352; 4. Article Number: 9311.27K01; UDI-DI: N/A; 5. Article Number: 9311.27K02; UDI-DI: N/A; 6. Article Number: 9311.27K03; UDI-DI: N/A; 7. Article Number: 9627.G0101; UDI-DI: N/A; 8. Article Number: 9627.G0201; UDI-DI: N/A; 9. Article Number: 9311.27G01-00; UDI-DI: 08717872035321; Lot Numbers: 202511001, 202601070, 51682-*-*-1, 51683-*-*-1, 54025-*-*-1, 54995-*-*-1, 56258-*-*-1, 56259-*-*-1, 64307-*-*-1, 64310-*-*-1, 69018-*-*-1, 75718-*-*-1, 76781-*-*-1, 76810-*-*-1, 77842-*-*-1, 79461-*-*-1, 80339-*-*-1, 80964-*-*-1, 81336-*-*-1, 82214-*-*-1, 82743-*-*-1, 83585-*-*-1, 84581-*-*-1, 85452001, 86070001, 87206001, 90383001, 97231001;", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2324-2026%22", "url": "https://recallledger.net/recalls/device-z-2324-2026-tdc-veloce-27g-two-dimensional-cutter-20k-cpm-article-numbers-9/"}, {"id": "fda-device-z-2323-2026", "source": "FDA", "category": "device", "recall_number": "Z-2323-2026", "title": "TDC VELOCE\" recall (D.O.R.C. Dutch Opthalmic Research Center Intl B.V.)", "product": "TDC VELOCE\", 25G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT25, 9311.25G01, 9311.25G02, 9311.25K01, 9311.25K02, 9311.25K03, 9625.G0201;", "reason": "An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.", "hazard_level": "Class II", "company": "D.O.R.C. Dutch Opthalmic Research Center Intl B.V.", "company_location": "Zuidland, N/A, Netherlands", "date": "2026-04-30", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "Worldwide - US Nationwide and the countries of AUSTRALIA, AUSTRIA, BELGIUM, BULGARIA, CZECHIA, FINLAND, FRANCE, GERMANY, GREAT BRITAIN, HONG KONG, IRELAND, ITALY, JAPAN, NETHERLANDS, NEW ZEALAND, POLAND, SLOVENIA, SOUTH AFRICA, SPAIN, SWEDEN, TAIWAN, TURKEY.", "states": [], "nationwide": true, "quantity": "2068 boxes totaling 12408 units", "codes": "1. Article Number: 9268.VIT25; UDI-DI: 08717872031873; 2. Article Number: 9311.25G01; UDI-DI: 08717872035116; 3. Article Number: 9311.25G02; UDI-DI: 08717872035345; 4. Article Number: 9311.25K01; UDI-DI: N/A; 5. Article Number: 9311.25K02; UDI-DI: N/A; 6. Article Number: 9311.25K03; UDI-DI: N/A; 7. Article Number: 9625.G0201; UDI-DI: N/A; Lot Numbers: 101118001, 101799001, 101800001, 102675001, 102676001, 103507001, 103508001, 103509001, 104360001, 50489-*-*-1, 54992-*-*-1, 54993-*-*-1, 54994-*-*-1, 56251-*-*-1, 56254-*-*-1, 56255-*-*-1, 56256-*-*-1, 56257-*-*-1, 57683-*-*-1, 58588-*-*-1, 58589-*-*-1, 60300-*-*-1, 65315-*-*-1, 65316-*-*-1, 65317-*-*-1, 65318-*-*-1, 65319-*-*-1, 65320-*-*-1, 65321-*-*-1, 65322-*-*-1, 66818-*-*-1, 70551-*-*-1, 70552-*-*-1, 70565-*-*-1, 70566-*-*-1, 70567-*-*-1, 71803-*-*-1, 71804-*-*-1, 71805-*-*-1, 71806-*-*-1, 75717-*-*-1, 76191-*-*-1, 76516-*-*-1, 76806-*-*-1, 76807-*-*-1, 76808-*-*-1, 76852-*-*-1, 76853-*-*-1, 76854-*-*-1, 76855-*-*-1, 77374-*-*-1, 77375-*-*-1, 77501-*-*-1, 77502-*-*-1, 77503-*-*-1, 77504-*-*-1, 77505-*-*-1, 78097-*-*-1, 78098-*-*-1, 78110-*-*-1, 78111-*-*-1, 79425-*-*-1, 79426-*-*-1, 81292-*-*-1, 81293-*-*-1, 81681-*-*-1, 82172-*-*-1, 82173-*-*-1, 82174-*-*-1, 82326-*-*-1, 82702-*-*-1, 82703-*-*-1, 82704-*-*-1, 82778-*-*-1, 83543-*-*-1, 83544-*-*-1, 84535-*-*-1, 84536-*-*-1, 84537-*-*-1, 85411001, 85412001, 86024001, 86025001, 86026001, 86806001, 86807001, 87173001, 87174001, 87175001, 87390001, 87950001, 88204001, 88205001, 88552001, 88616001, 89535001, 90377001, 90378001, 90379001, 91280001, 91281001, 92631001, 92633001, 95437001, 99667001;", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2323-2026%22", "url": "https://recallledger.net/recalls/device-z-2323-2026-tdc-veloce-25g-two-dimensional-cutter-20k-cpm-article-numbers-9/"}, {"id": "fda-device-z-2322-2026", "source": "FDA", "category": "device", "recall_number": "Z-2322-2026", "title": "TDC VELOCE\" recall (D.O.R.C. Dutch Opthalmic Research Center Intl B.V.)", "product": "TDC VELOCE\", 23G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT23, 9311.23G01, 9311.23G02, 9311.23K01, 9311.23K02, 9311.23K03, 9623.G0201, 9623.G0202, 9623.K0201, 9311.23G01-00;", "reason": "An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.", "hazard_level": "Class II", "company": "D.O.R.C. Dutch Opthalmic Research Center Intl B.V.", "company_location": "Zuidland, N/A, Netherlands", "date": "2026-04-30", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "Worldwide - US Nationwide and the countries of AUSTRALIA, AUSTRIA, BELGIUM, BULGARIA, CZECHIA, FINLAND, FRANCE, GERMANY, GREAT BRITAIN, HONG KONG, IRELAND, ITALY, JAPAN, NETHERLANDS, NEW ZEALAND, POLAND, SLOVENIA, SOUTH AFRICA, SPAIN, SWEDEN, TAIWAN, TURKEY.", "states": [], "nationwide": true, "quantity": "314 boxes, totaling 1884 units", "codes": "1. Article Number: 9268.VIT23; UDI-DI: 08717872031866; 2. Article Number: 9311.23G01; UDI-DI: 08717872035109; 3. Article Number: 9311.23G02; UDI-DI: 08717872035338; 4. Article Number: 9311.23K01; UDI-DI: N/A; 5. Article Number: 9311.23K02; UDI-DI: N/A; 6. Article Number: 9311.23K03; UDI-DI: N/A; 7. Article Number: 9623.G0201; UDI-DI: N/A; 8. Article Number: 9623.G0202; UDI-DI: N/A; 9. Article Number: 9623.K0201; UDI-DI: N/A; 10. Article Number: 9311.23G01-00; UDI-DI: 08717872035307; Lot Numbers: 100637001, 57682-*-*-1, 64312-*-*-1, 69017-*-*-1, 73237-*-*-1, 74225-*-*-1, 75735-*-*-1, 79460-*-*-1, 80338-*-*-1, 80963-*-*-1, 81335-*-*-1, 81679-*-*-1, 82213-*-*-1, 82325-*-*-1, 82742-*-*-1, 82779-*-*-1, 83584-*-*-1, 84580-*-*-1, 85451001, 86069001, 86798001, 86799001, 87205001, 88231001, 91957001, 92629001, 92630001, 93336001, 94351001, 95436001, 95462001, 96097001, 96123001, 97279001, 97789001, 98643001, 99130001, 99185001, 99697001;", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2322-2026%22", "url": "https://recallledger.net/recalls/device-z-2322-2026-tdc-veloce-23g-two-dimensional-cutter-20k-cpm-article-numbers-9/"}, {"id": "fda-device-z-2320-2026", "source": "FDA", "category": "device", "recall_number": "Z-2320-2026", "title": "EXCOR Pediatric Ventricular Assist Device recall (BERLIN HEART GMBH)", "product": "EXCOR Pediatric Ventricular Assist Device (VAD) System Blood Pump PU Valves: 10 ml, REF: P10P-001; 30 ml, REF: P30P-001x01", "reason": "Blood pump inner package expiration date does not match the outer-correct expiration date, which may lead to delays in surgical procedures.", "hazard_level": "Class II", "company": "BERLIN HEART GMBH", "company_location": "Berlin, N/A, Germany", "date": "2026-04-24", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "US Nationwide distribution in the states of MA, SC.", "states": ["MA", "SC"], "nationwide": true, "quantity": "3", "codes": "REF/UDI-DI/serial number: P10P-001/04260090040102/2230714, 2230709; P30P-001x01/04260090040126/2230254", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2320-2026%22", "url": "https://recallledger.net/recalls/device-z-2320-2026-excor-pediatric-ventricular-assist-device-vad-system-blood-pump-pu-v/"}, {"id": "fda-device-z-2319-2026", "source": "FDA", "category": "device", "recall_number": "Z-2319-2026", "title": "Mahurkar Elite PASS Trays recall (Mozarc Medical US LLC)", "product": "Mahurkar Elite PASS Trays; Description (Product Number/CFN): 12 FR x 13cm Acute Dual Lumen Catheter with Straight Extensions, PASS Tray (8888221413), 12 FR x 16cm Acute Dual Lumen Catheter with Curved Extensions, PASS Tray (8888222416), 12 FR x 16cm Acute Dual Lumen Catheter with Straight Extensions, PASS Tray (8888221416), 12 FR x 20cm Acute Dual Lumen Catheter with Curved Extensions, PASS Tray (8888222420), 12 FR x 20cm Acute Dual Lumen Catheter with Straight Extensions, PASS Tray (8888221420), 12 FR x 24cm Acute Dual Lumen Catheter with Curved Extensions, PASS Tray (8888222424), 12 FR x 24cm Acute Dual Lumen Catheter with Straight Extensions, PASS Tray (8888221424), 12 FR x 30cm Acute Dual Lumen Catheter with Straight Extensions, PASS Tray (8888221430), 12.5 FR x 13 cm Acute Triple Lumen Catheter with Curved Extensions, PASS Tray (8888233413), 12.5 FR x 16 cm Acute Triple Lumen Catheter with Curved Extensions, PASS Tray (8888233416), 12.5 FR x 20 cm Acute Triple Lumen Catheter with Curved Extensions, PASS Tray (8888233420), 12.5 FR x 20 cm Acute Triple Lumen Catheter with Straight Extensions, PASS Tray (8888231420), 12.5 FR x 24 cm Acute Triple Lumen Catheter with Curved Extensions, PASS Tray (8888233424), 12.5 FR x 24 cm, Acute Triple Lumen Catheter with Straight Extensions PASS Tray (8888231424), 12.5 FR x 30 cm, Triple Lumen Catheter with Straight Extensions PASS Tray (8888231430), 12.5FR x 13cm Acute Triple Lumen Catheter with Straight Extensions, PASS Tray (8888231413), 12.5FR x 16cm Acute Triple Lumen Catheter with Straight Extensions, PASS Tray (8888231416), 13.5 FR x 16 cm High Flow Acute Dual Lumen Catheter with Curved Cannula, PASS Tray (8888213416), 13.5 Fr x 16cm High Flow Acute Dual Lumen Catheter with Straight Extensions, PASS Tray (8888211416), 13.5 FR x 20 cm High Flow Acute Dual Lumen Catheter with Curved Cannula, PASS Tray (8888213420), 13.5 Fr x 20cm High Flow Acute Dual Lumen Catheter with Straight Extensions, PASS Tray (8888211420), 13.5FR x 13cm High Flow Acute Dual Lumen Catheter with Curved Extensions, PASS Tray (8888212413), 13.5FR x 13cm High Flow Acute Dual Lumen Catheter with Straight Extensions, PASS Tray (8888211413), 13.5FR x 16cm High Flow Acute Dual Lumen Catheter with Curved Extensions, PASS Tray (8888212416), 13.5FR x 20cm High Flow Acute Dual Lumen Catheter with Curved Extensions, PASS Tray (8888212420), 13.5FR x 24cm High Flow Acute Dual Lumen Catheter with Straight Extensions, PASS Tray (8888211424); for acute hemodialysis, aphaeresis, and infusion.", "reason": "The Tegaderm CHG dressing, as specified in product labeling, was missing from certain lots of Mahurkar Elite PASS Trays.", "hazard_level": "Class II", "company": "Mozarc Medical US LLC", "company_location": "Mansfield, MA, United States", "date": "2026-04-29", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "US Nationwide distribution.", "states": [], "nationwide": true, "quantity": "25627", "codes": "1. Product Number (CFN): 8888221413; UDI-DI: 10884521788541; Lot numbers: 241620022, 252020038; 2. Product Number (CFN): 8888222416; UDI-DI: 10884521788602; Lot numbers: 241690023, 241830147; 3. Product Number (CFN): 8888221416; UDI-DI: 10884521788558; Lot numbers: 251250041, 251740190, 252020039, 252090031, 253350256; 4. Product Number (CFN): 8888222420; UDI-DI: 10884521788619; Lot numbers: 251740186, 252510026, 253280016; 5. Product Number (CFN): 8888221420; UDI-DI: 10884521788565; Lot numbers: 241620407, 251950032; 6. Product Number (CFN): 8888222424; UDI-DI: 10884521788626; Lot number: 243040007; 7. Product Number (CFN): 8888221424; UDI-DI: 10884521788572; Lot numbers: 241200034, 251250039, 252020037; 8. Product Number (CFN): 8888221430; UDI-DI: 10884521788589; Lot number: 251250042; 9. Product Number (CFN): 8888233413; UDI-DI: 10884521788718; Lot number: 250310009; 10. Product Number (CFN): 8888233416; UDI-DI: 10884521788725; Lot numbers: 250350008, 250690152, 250690153, 250870012, 251010012, 251010013, 251320332, 251320333, 251390368, 251390369, 252580023; 11. Product Number (CFN): 8888233420; UDI-DI: 10884521788732; Lot numbers: 250870013, 250970052, 251320330, 251320331; 12. Product Number (CFN): 8888231420; UDI-DI: 10884521788688; Lot numbers: 241690216, 252020046, 252230023, 252580025; 13. Product Number (CFN): 8888233424; UDI-DI: 10884521788749; Lot numbers: 251740197, 252300054; 14. Product Number (CFN): 8888231424; UDI-DI: 10884521788695; Lot numbers: 251460351, 251740196, 252020045, 252230022, 252580024; 15. Product Number (CFN): 8888231430; UDI-DI: 10884521788701; Lot number: 252730009; 16. Product Number (CFN): 8888231413; UDI-DI: 10884521788664; Lot number: 250310010; 17. Product Number (CFN): 8888231416; UDI-DI: 10884521788671; Lot numbers: 252230021, 252510030, 252650294, 253140280; 18. Product Number (CFN): 8888213416; UDI-DI: 10884521788527; Lot number: 252300325; 19. Product Number (CFN): 8888211416; UDI-DI: 10884521788435; Lot numbers: 241060237, 250830187, 250900067, 251250037, 251430012, 252870014; 20. Product Number (CFN): 8888213420; UDI-DI: 10884521788534; Lot number: 252300051; 21. Product Number (CFN): 8888211420; UDI-DI: 10884521788442; Lot numbers: 241480021, 242390056, 250070005, 250310011, 250310012, 250760180, 250900066, 251250035, 251950034; 22. Product Number (CFN): 8888212413; UDI-DI: 10884521788473; Lot number: 242950260; 23. Product Number (CFN): 8888211413; UDI-DI: 10884521788428; Lot number: 252510028; 24. Product Number (CFN): 8888212416; UDI-DI: 10884521788480; Lot numbers: 243160028, 250760159, 251250036, 251320325; 25. Product Number (CFN): 8888212420; UDI-DI: 10884521788497; Lot numbers: 241350005, 250310006, 251740192, 252160037; 26. Product Number (CFN): 8888211424; UDI-DI: 10884521788459; Lot numbers: 250830185, 250830186, 250900298, 250900299, 251740179, 251950033;", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2319-2026%22", "url": "https://recallledger.net/recalls/device-z-2319-2026-mahurkar-elite-pass-trays-description-product-number-cfn-12-fr-x/"}, {"id": "fda-device-z-2318-2026", "source": "FDA", "category": "device", "recall_number": "Z-2318-2026", "title": "Allia Moveo angiographic X-ray system recall (GE Medical Systems, LLC)", "product": "Allia Moveo angiographic X-ray system", "reason": "GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrical shock to service personnel performing installation, maintenance, or troubleshooting activities inside the C-FRT cabinet while power is ON.", "hazard_level": "Class II", "company": "GE Medical Systems, LLC", "company_location": "Waukesha, WI, United States", "date": "2026-04-20", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "Worldwide - US Nationwide distribution.", "states": [], "nationwide": true, "quantity": "3 units", "codes": "UDI-DI: 00198953052488; Serial Numbers: C4-25-001, C4-25-002, C4-26-001, C4-26-002, C4-26-004, C4-26-005", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2318-2026%22", "url": "https://recallledger.net/recalls/device-z-2318-2026-allia-moveo-angiographic-x-ray-system/"}, {"id": "fda-device-z-2317-2026", "source": "FDA", "category": "device", "recall_number": "Z-2317-2026", "title": "Allia IGS Pulse angiographic X-ray system recall (GE Medical Systems, LLC)", "product": "Allia IGS Pulse angiographic X-ray system", "reason": "GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrical shock to service personnel performing installation, maintenance, or troubleshooting activities inside the C-FRT cabinet while power is ON.", "hazard_level": "Class II", "company": "GE Medical Systems, LLC", "company_location": "Waukesha, WI, United States", "date": "2026-04-20", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "Worldwide - US Nationwide distribution.", "states": [], "nationwide": true, "quantity": "5 units", "codes": "UDI-DI: 00195278827647; Serial Numbers: DVMSS2500001HL, DVMSS2500002HL, DVMSS2500003HL, DVMSS2500004HL, DVMSS2500005HL, DVMSS2500006HL, DVMSS2600001HL, DVMSS2600002HL", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2317-2026%22", "url": "https://recallledger.net/recalls/device-z-2317-2026-allia-igs-pulse-angiographic-x-ray-system/"}, {"id": "fda-device-z-2316-2026", "source": "FDA", "category": "device", "recall_number": "Z-2316-2026", "title": "Allia IGS 7 Pulse angiographic X-ray system recall (GE Medical Systems, LLC)", "product": "Allia IGS 7 Pulse angiographic X-ray system", "reason": "GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrical shock to service personnel performing installation, maintenance, or troubleshooting activities inside the C-FRT cabinet while power is ON.", "hazard_level": "Class II", "company": "GE Medical Systems, LLC", "company_location": "Waukesha, WI, United States", "date": "2026-04-20", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "Worldwide - US Nationwide distribution.", "states": [], "nationwide": true, "quantity": "35 units", "codes": "UDI-DI: 00195278719720; Serial Numbers: D3-23-024, D3-23-029, D3-24-001, D3-24-002, D3-24-005, D3-24-006, D3-24-008, D3-24-009, D3-24-010, D3-24-013, D3-24-014, D3-24-016, D3-24-019, D3-24-020, D3-24-021, D3-24-023, D3-24-025, D3-25-001, D3-25-002, D3-25-003, D3-25-005, D3-25-006, D3-25-007, D3-25-008, D3-25-009, D3-25-010, D3-25-013, D3-25-016, D3-25-017, D3-25-018, D3-25-026, D3-25-027, D3-25-029, D3-25-030, D3-25-034, D3-25-036, D3-25-037, D3-26-001, D3-26-002, D3-26-007", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2316-2026%22", "url": "https://recallledger.net/recalls/device-z-2316-2026-allia-igs-7-pulse-angiographic-x-ray-system/"}, {"id": "fda-device-z-2315-2026", "source": "FDA", "category": "device", "recall_number": "Z-2315-2026", "title": "Allia IGS 5 Pulse angiographic X-ray system recall (GE Medical Systems, LLC)", "product": "Allia IGS 5 Pulse angiographic X-ray system", "reason": "GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrical shock to service personnel performing installation, maintenance, or troubleshooting activities inside the C-FRT cabinet while power is ON.", "hazard_level": "Class II", "company": "GE Medical Systems, LLC", "company_location": "Waukesha, WI, United States", "date": "2026-04-20", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "Worldwide - US Nationwide distribution.", "states": [], "nationwide": true, "quantity": "121 units", "codes": "UDI-DI: 00195278719263; Serial Numbers: M2-23-039, M2-23-056, M2-24-004, M2-24-019, M2-24-020, M2-24-025, M2-24-030, M2-24-031, M2-24-032, M2-24-033, M2-24-034, M2-24-037, M2-24-038, M2-24-039, M2-24-040, M2-24-046, M2-24-057, M2-24-062, M2-24-064, M2-24-066, M2-24-069, M2-24-071, M2-24-077, M2-24-078, M2-24-080, M2-24-083, M2-25-003, M2-25-004, M2-25-005, M2-25-011, M2-25-013, M2-25-015, M2-25-017, M2-25-019, M2-25-023, M2-25-024, M2-25-025, M2-25-026, M2-25-028, M2-25-032, M2-25-036, M2-25-037, M2-25-039, M2-25-040, M2-25-041, M2-25-042, M2-25-043, M2-25-046, M2-25-048, M2-25-049, M2-25-056, M2-25-057, M2-25-058, M2-25-062, M2-25-065, M2-25-067, M2-25-072, M2-25-074, M2-25-077, M2-25-078, M2-25-080, M2-25-250, M2-25-300, M2-26-002, M2-26-004, M2-26-006, M2-26-007, M2-UP2502, M3-22-012, M3-23-117, M3-24-019, M3-24-021, M3-24-023, M3-24-034, M3-24-052, M3-24-061, M3-24-074, M3-24-079, M3-24-086, M3-24-090, M3-24-094, M3-24-095, M3-24-097, M3-24-099, M3-24-101, M3-24-104, M3-24-111, M3-24-120, M3-24-128, M3-24-136, M3-24-137, M3-24-141, M3-24-143, M3-24-149, M3-24-151, M3-24-156, M3-24-159, M3-24-161, M3-24-163, M3-24-165, M3-24-168, M3-24-169, M3-24-172, M3-24-175, M3-25-003, M3-25-012, M3-25-017, M3-25-020, M3-25-027, M3-25-036, M3-25-061, M3-25-063, M3-25-069, M3-25-074, M3-25-076, M3-25-079, M3-25-080, M3-25-084, M3-25-085, M3-25-088, M3-25-089, M3-25-094, M3-25-104, M3-25-106, M3-25-107, M3-25-115, M3-25-118, M3-25-119, M3-25-120, M3-25-128, M3-25-130, M3-25-132, M3-25-145, M3-25-147, M3-25-148, M3-25-149, M3-25-150, M3-25-151, M3-26-002, M3-26-003, M3-26-005, M3-26-007, M3-26-021, M3-26-024, M3-26-027, M3-26-028, M3-26-033, M3-26-034, M3-UP2501, M3-UP2503", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2315-2026%22", "url": "https://recallledger.net/recalls/device-z-2315-2026-allia-igs-5-pulse-angiographic-x-ray-system/"}, {"id": "fda-device-z-2314-2026", "source": "FDA", "category": "device", "recall_number": "Z-2314-2026", "title": "Allia IGS 3 Pulse angiographic X-ray system recall (GE Medical Systems, LLC)", "product": "Allia IGS 3 Pulse angiographic X-ray system", "reason": "GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrical shock to service personnel performing installation, maintenance, or troubleshooting activities inside the C-FRT cabinet while power is ON.", "hazard_level": "Class II", "company": "GE Medical Systems, LLC", "company_location": "Waukesha, WI, United States", "date": "2026-04-20", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "Worldwide - US Nationwide distribution.", "states": [], "nationwide": true, "quantity": "9 units", "codes": "UDI-DI: 00195278719577; Serial Numbers: M3-24-053, M3-24-124, M3-25-029, M3-25-051, M3-25-053, M3-25-091, M3-25-098, M3-25-124, M3-26-010, M3-26-030", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2314-2026%22", "url": "https://recallledger.net/recalls/device-z-2314-2026-allia-igs-3-pulse-angiographic-x-ray-system/"}, {"id": "fda-device-z-2313-2026", "source": "FDA", "category": "device", "recall_number": "Z-2313-2026", "title": "Plum Duo Precision IV Pump recall (ICU Medical, Inc.)", "product": "Plum Duo Precision IV Pump, 40002-0403", "reason": "Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and starting delivery. This may potentially lead to under- or over-delivery.", "hazard_level": "Class II", "company": "ICU Medical, Inc.", "company_location": "Lake Forest, IL, United States", "date": "2026-04-29", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "Worldwide - US Nationwide distribution in the states of ID, IL, IN, KS, MA, MD, NM, NY, PA, TN, TX and the country of Canada.", "states": ["ID", "IL", "IN", "KS", "MA", "MD", "NM", "NY", "PA", "TN", "TX"], "nationwide": true, "quantity": "13,613", "codes": "UDI-DI M335400031 Plum Duo Precision IV Pump v1.2.3", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2313-2026%22", "url": "https://recallledger.net/recalls/device-z-2313-2026-plum-duo-precision-iv-pump-40002-0403/"}, {"id": "fda-device-z-2312-2026", "source": "FDA", "category": "device", "recall_number": "Z-2312-2026", "title": "Plum Duo Infusion Pump recall (ICU Medical, Inc.)", "product": "Plum Duo Infusion Pump, 40002-0401", "reason": "Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and starting delivery. This may potentially lead to under- or over-delivery.", "hazard_level": "Class II", "company": "ICU Medical, Inc.", "company_location": "Lake Forest, IL, United States", "date": "2026-04-29", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "Worldwide - US Nationwide distribution in the states of ID, IL, IN, KS, MA, MD, NM, NY, PA, TN, TX and the country of Canada.", "states": ["ID", "IL", "IN", "KS", "MA", "MD", "NM", "NY", "PA", "TN", "TX"], "nationwide": true, "quantity": "13,613", "codes": "UDI-DI M335400021 Plum Duo Infusion Pump v1.2.3", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2312-2026%22", "url": "https://recallledger.net/recalls/device-z-2312-2026-plum-duo-infusion-pump-40002-0401/"}, {"id": "fda-device-z-2311-2026", "source": "FDA", "category": "device", "recall_number": "Z-2311-2026", "title": "Plum Solo Precision IV Pump recall (ICU Medical, Inc.)", "product": "Plum Solo Precision IV Pump, 40001-0401", "reason": "Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and starting delivery. This may potentially lead to under- or over-delivery.", "hazard_level": "Class II", "company": "ICU Medical, Inc.", "company_location": "Lake Forest, IL, United States", "date": "2026-04-29", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "Worldwide - US Nationwide distribution in the states of ID, IL, IN, KS, MA, MD, NM, NY, PA, TN, TX and the country of Canada.", "states": ["ID", "IL", "IN", "KS", "MA", "MD", "NM", "NY", "PA", "TN", "TX"], "nationwide": true, "quantity": "13,613", "codes": "UDI-DI M335400011 Plum Solo Precision IV Pump v1.0.3", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2311-2026%22", "url": "https://recallledger.net/recalls/device-z-2311-2026-plum-solo-precision-iv-pump-40001-0401/"}, {"id": "fda-device-z-2280-2026", "source": "FDA", "category": "device", "recall_number": "Z-2280-2026", "title": "Fresh Roast Systems ColorTrack. Model Name: ColorTrack. Model Number: BENCH R-100 recall (Fresh Roast Systems Inc)", "product": "Fresh Roast Systems ColorTrack. Model Name: ColorTrack. Model Number: BENCH R-100", "reason": "A defect has been identified in the manufacture of the Fresh Roast Systems ColorTrack instrument model number BENCH R-100 which could under very rare specific misuse circumstances potentially allow human access to infrared laser light levels in excess of the safety Classification of the product.", "hazard_level": "Class II", "company": "Fresh Roast Systems Inc", "company_location": "Key Biscayne, FL, United States", "date": "2026-04-15", "report_date": "2026-06-17", "status": "Ongoing", "distribution": "U.S.", "states": [], "nationwide": false, "quantity": "38", "codes": "Only Model Number provide. Model Number: BENCH R-100", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2280-2026%22", "url": "https://recallledger.net/recalls/device-z-2280-2026-fresh-roast-systems-colortrack-model-name-colortrack-model-number/"}, {"id": "fda-food-h-0860-2026", "source": "FDA", "category": "food", "recall_number": "H-0860-2026", "title": "Malazi 100% PURE SUDANESE SESAME Tahina G.W.: 1K.g recall (Nassar Investment Company LLC)", "product": "Malazi 100% PURE SUDANESE SESAME Tahina G.W.: 1K.g UPC 6 224011 088244 Produced by: AL-MALAZ COMPANY FOR TRADE AND INDUSTRY Piece No. 110-250 acres area Badr City - Egypt", "reason": "Salmonella. The firm was notified by the North Carolina Department of Agriculture that the product test positive for Salmonella.", "hazard_level": "Class I", "company": "Nassar Investment Company LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-30", "report_date": "2026-06-10", "status": "Ongoing", "distribution": "Product was shipped to MI & NC.", "states": ["MI", "NC"], "nationwide": false, "quantity": "11cs/6/ 2lb bottles", "codes": "PROD: 31/12/2024 EXP: 30/12/2026", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0860-2026%22", "url": "https://recallledger.net/recalls/food-h-0860-2026-malazi-100-pure-sudanese-sesame-tahina-g-w-1k-g-upc-6-224011-088244/"}, {"id": "fda-food-h-0859-2026", "source": "FDA", "category": "food", "recall_number": "H-0859-2026", "title": "cafe nouria blueberry muffin recall (The Brownie Baker Inc.)", "product": "cafe nouria blueberry muffin NET WT. 6 OZ (170g) UPC: 811070033986", "reason": "Undeclared walnuts", "hazard_level": "Class II", "company": "The Brownie Baker Inc.", "company_location": "Fresno, CA, United States", "date": "2026-04-27", "report_date": "2026-06-10", "status": "Ongoing", "distribution": "U.S. Distribution: IL Foreign Distribution: Not Applicable", "states": ["IL"], "nationwide": false, "quantity": "432 cases (9 units/case); 3,888 units", "codes": "Lot: 6082", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0859-2026%22", "url": "https://recallledger.net/recalls/food-h-0859-2026-cafe-nouria-blueberry-muffin-net-wt-6-oz-170g-upc-811070033986/"}, {"id": "fda-device-z-2310-2026", "source": "FDA", "category": "device", "recall_number": "Z-2310-2026", "title": "Brand Name: Da Vinci 5 Product Name: ASSY recall (Intuitive Surgical, Inc.)", "product": "Brand Name: Da Vinci 5 Product Name: ASSY,DV5 TOWER,IS5000 Model/Catalog Number: 380746 Software Version: N/A Product Description: Preface: This report under 21 CFR 806.10 is being submitted for the dV5 system tower, as the NIR Handheld Camera or SOCK is developed and integrated as part of the dV5 system. The affected component of the dV5 system tower is the NIR handheld camera, and is supplied by Schoelly as the manufacturer. Therefore, the product description in this report references the NIR handheld camera system. Product Description: The NIR handheld camera system is compatible for use with the da Vinci¿ 5 system to aid in surgery. The components of the NIR handheld camera system include a camera control unit and a light source, NIR handheld camera, and additional components that together, connect to the Tower of the da Vinci 5 system. When setting up the da Vinci 5 system, the image from the NIR handheld camera system is displayed on the Tower monitor. Component: Yes, the SOCK is the component and integrated into the dV5 system", "reason": "Due to unintentionally activated near infrared handheld camera when attempting to turn off illumination during normal clinical workflow transitions, particularly when switching from the handheld camera to the robotic endoscope.", "hazard_level": "Class II", "company": "Intuitive Surgical, Inc.", "company_location": "Sunnyvale, CA, United States", "date": "2026-04-24", "report_date": "2026-06-10", "status": "Ongoing", "distribution": "U.S.: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NE, NH, NJ, NM, NV, NY, NC, ND, OH, OK, OR, PA, PR, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, and WY. O.U.S.: Australia, Belgium, France, Germany, Italy, Japan, Netherlands, New Zealand, Poland, Romania, Saudi Arabia, South Korea, Spain, Switzerland, and United Kingdom", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": false, "quantity": "1357 systems", "codes": "Lot Code: Part Number: 380746 UDI: 00886874119662 FDA Medical Device Listing Number: D531324 (U.S.) Part Number: 470653-01 Serial Numbers: 1008007 1008008 1008009 1008010 1008011 1008012 1008013 1008015 1008016 1008017 1008020 1008021 1008022 1008024 1008100 1008101 1008102 1008104 1008105 1008107 1008108 1008109 1008112 1008113 1008114 1008115 1008116 1008117 1008997 1008998 1009902 1010029 1010033 1010034 1010036 1010272 1010296 1010297 1010318 1010319 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1153867 1153869 1156018 1156020 1156021 1156022 1156023 1157113 1157114 1157115 1157116 1157117 1157118 1157119 1157121 1157122 1157615 1157636 1157647 1157678 1157689 1157700 1157701 1157703 1157707 1157718 1157719 1157720 1157722 1157723 1157725 1157726 1157727 1157739 1157741 1157743 1157747 1157749 1157755 1186377 Part Number: 470653-03 Serial Numbers: 1186136 1186139 1157705 1157706 1157721 1161015 1161017 1161028 1161029 1161030 1161056 1161064 1161066 1161067 1161068 1161069 1161070 1161071 1161073 1161074 1161075 1161076 1161077 1161078 1161080 1161081 1161082 1161149 1161150 1164405 1164407 1164428 1164449 1164450 1164455 1164456 1164464 1164465 1164466 1164519 1164520 1164522 1164523 1164524 1164525 1164526 1164527 1164528 1164530 1164531 1164532 1164533 1164537 1164541 1164545 1164549 1164550 1166267 1166268 1166269 1166272 1166273 1166275 1166276 1166280 1166281 1166285 1166312 1166313 1166314 1166316 1166323 1166325 1166328 1166329 1166330 1166331 1166333 1166334 1166336 1168930 1168932 1168933 1168934 1168938 1168939 1168941 1168942 1168943 1168944 1168945 1168946 1168947 1168950 1168953 1168954 1168955 1168956 1168962 1168968 1171019 1171036 1171038 1171039 1171040 1171041 1171043 1171045 1171059 1171060 1171062 1171063 1171069 1171072 1171073 1176677 1176698 1176741 1176742 1176743 1176744 1176745 1176746 1176748 1176749 1176750 1176751 1176752 1178538 1178543 1178555 1178567 1179195 1179201 1179203 1179224 1179225 1179226 1179228 1179229 1179231 1179232 1179254 1179255 1179276 1179277 1179298 1179299 1179300 1179301 1179312 1179313 1179333 1179338 1179340 1179343 1181818 1181819 1181820 1181822 1181823 1181824 1181825 1181827 1181828 1181830 1181832 1181833 1181855 1181857 1181861 1184449 1186134 1186135 1186145 1186168 1186374 1186385 1187866 1188191 1188194 1188195 1188206 1188207 1188208 1188209 1188210 1188211 1188212 1188213 1188219 1188220 1188222 1190015 1190016 1190017 1190018 1190019 1190021 1190022 1190023 1190025 1190029 (O.U.S.) Part Number: 470653-01 Serial Numbers: 1014033 1014035 1014142 1014157 1014161 1014162 1026777 1026778 1026785 1028055 1028081 1028084 1043799 1043800 1043801 1043821 1043895 1043898 1045998 1046052 1047715 1047717 1137738 1137745 1140562 1140569 1140584 1140589 1140591 1140592 Part Number: 470653-03 Serial Numbers: 1179196 1161059 1168931 1171068 1159334 1157750 1157748 1166282 1157753 1171021 1168936 1161053 1157758 1164454 1164467 1159327 1159259 1159329 1157702 1157757 1159331 1164548 1157759 1161060 1186384 1171066 1161079 1157756 1159330 1164457 1159328 1168966 1159335 1164406 1157751 1168969 1166266 1161054 1168951 1159326 1159332 1159324 1157120 1166283", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2310-2026%22", "url": "https://recallledger.net/recalls/device-z-2310-2026-brand-name-da-vinci-5-product-name-assy-dv5-tower-is5000-model-cat/"}, {"id": "fda-device-z-2309-2026", "source": "FDA", "category": "device", "recall_number": "Z-2309-2026", "title": "Sharpoint 2.2MM recall (SSC- Surgical Specialties Corporation)", "product": "Sharpoint 2.2MM, ANGLED, DOUBLE- BEVEL Model/Catalog Number: 72-2231 Microsurgical Knife", "reason": "3.0mm surgical knives labeled and packaged as 2.2mm surgical knives.", "hazard_level": "Class II", "company": "SSC- Surgical Specialties Corporation", "company_location": "Chula Vista, CA, United States", "date": "2026-04-23", "report_date": "2026-06-10", "status": "Ongoing", "distribution": "Worldwide - US Nationwide distribution in the states of Texas, Utah, Michigan and the countries of Turkey, Germany, Romania, Poland, United Kingdom.", "states": ["MI", "TX", "UT"], "nationwide": true, "quantity": "1818 units", "codes": "UDI-DI 00848782027514; Lot Number FA22CHQ", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2309-2026%22", "url": "https://recallledger.net/recalls/device-z-2309-2026-sharpoint-2-2mm-angled-double-bevel-model-catalog-number-72-2231/"}, {"id": "fda-device-z-2308-2026", "source": "FDA", "category": "device", "recall_number": "Z-2308-2026", "title": "TITANIUM/FLUOROPLASTIC PISTON 0.6MM DIA X 3.75MM L Model/Catalog Number: 409-375 ... recall (Grace Medical, Inc.)", "product": "TITANIUM/FLUOROPLASTIC PISTON 0.6MM DIA X 3.75MM L Model/Catalog Number: 409-375 Product Description: Stapes Prosthesis", "reason": "Due to incorrect functional length on device labeling.", "hazard_level": "Class II", "company": "Grace Medical, Inc.", "company_location": "Bartlett, TN, United States", "date": "2026-04-03", "report_date": "2026-06-10", "status": "Ongoing", "distribution": "U.S Nationwide distribution in the state of MD.", "states": ["MD"], "nationwide": true, "quantity": "7", "codes": "Model/Catalog Number: 409-375 UDI code: (01)00844505000772(10)122927(17)310301 Lot Number: 122927", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2308-2026%22", "url": "https://recallledger.net/recalls/device-z-2308-2026-titanium-fluoroplastic-piston-0-6mm-dia-x-3-75mm-l-model-catalog-nu/"}, {"id": "fda-device-z-2307-2026", "source": "FDA", "category": "device", "recall_number": "Z-2307-2026", "title": "Aligned Medical AMS16835 Fluids Kit RX recall (Windstone Medical Packaging, Inc.)", "product": "Aligned Medical AMS16835 Fluids Kit RX", "reason": "Lidocaine Hydrochloride Injection, USP, which was recalled by a supplier for quality issues, was included in custom convenience kits.", "hazard_level": "Class II", "company": "Windstone Medical Packaging, Inc.", "company_location": "Billings, MT, United States", "date": "2026-04-27", "report_date": "2026-06-10", "status": "Ongoing", "distribution": "US Nationwide distribution in the states of IL, VA.", "states": ["IL", "VA"], "nationwide": true, "quantity": "875 kits", "codes": "UDI-DI: B098AMS168350; Lot Numbers: 233828, 236048, 236359, 236662, 238580, 239934, 239935", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2307-2026%22", "url": "https://recallledger.net/recalls/device-z-2307-2026-aligned-medical-ams16835-fluids-kit-rx/"}, {"id": "fda-device-z-2306-2026", "source": "FDA", "category": "device", "recall_number": "Z-2306-2026", "title": "MAC 5 A4 Resting ECG Analysis System 855001-001 recall (GE Medical Systems China Co., Ltd.)", "product": "MAC 5 A4 Resting ECG Analysis System 855001-001; MAC 5 A5 Resting ECG Analysis System 8855002-001. Electrocardiograph", "reason": "Software in development inadvertently made available for customer use. Use of this software version can result in clinical information being associated with the incorrect patient. This could impact clinical decision-making.", "hazard_level": "Class II", "company": "GE Medical Systems China Co., Ltd.", "company_location": "Wuxi, China", "date": "2026-04-21", "report_date": "2026-06-10", "status": "Ongoing", "distribution": "Worldwide - US Nationwide distribution in the states of Florida and Georgia. The countries of India, Italy, Republic of Korea, and United Kingdom.", "states": ["FL", "GA"], "nationwide": true, "quantity": "16", "codes": "Software version 3.00 855001-001, UDI-DI 00195278276070 8855002-001, UDI-DI 00195278276124", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2306-2026%22", "url": "https://recallledger.net/recalls/device-z-2306-2026-mac-5-a4-resting-ecg-analysis-system-855001-001-mac-5-a5-resting-ecg/"}, {"id": "fda-device-z-2304-2026", "source": "FDA", "category": "device", "recall_number": "Z-2304-2026", "title": "BD Pyxis MedBank Mini REF: 1147-00 Medication cabinet recall (CareFusion 303, Inc.)", "product": "BD Pyxis MedBank Mini REF: 1147-00 Medication cabinet", "reason": "Fingerprint scanner may overheat to a temperature to cause 1st degree burn.", "hazard_level": "Class II", "company": "CareFusion 303, Inc.", "company_location": "San Diego, CA, United States", "date": "2026-04-30", "report_date": "2026-06-10", "status": "Ongoing", "distribution": "US: Nationwide OUS: AE, AU, BE, BH, BR, CA, CL, ES, GB, IT, KW, MA, MX, NZ, PT, QA, SA, SG, TH, TW", "states": ["CA"], "nationwide": true, "quantity": "114 units", "codes": "All Serial Numbers/UDI:10885403517181", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2304-2026%22", "url": "https://recallledger.net/recalls/device-z-2304-2026-bd-pyxis-medbank-mini-ref-1147-00-medication-cabinet/"}, {"id": "fda-device-z-2303-2026", "source": "FDA", "category": "device", "recall_number": "Z-2303-2026", "title": "BD Pyxis MedBank Tower REF: 1145-00 Medication cabinet recall (CareFusion 303, Inc.)", "product": "BD Pyxis MedBank Tower REF: 1145-00 Medication cabinet", "reason": "Fingerprint scanner may overheat to a temperature to cause 1st degree burn.", "hazard_level": "Class II", "company": "CareFusion 303, Inc.", "company_location": "San Diego, CA, United States", "date": "2026-04-30", "report_date": "2026-06-10", "status": "Ongoing", "distribution": "US: Nationwide OUS: AE, AU, BE, BH, BR, CA, CL, ES, GB, IT, KW, MA, MX, NZ, PT, QA, SA, SG, TH, TW", "states": ["CA"], "nationwide": true, "quantity": "607 units", "codes": "All Serial Numbers/UDI:10885403517167", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2303-2026%22", "url": "https://recallledger.net/recalls/device-z-2303-2026-bd-pyxis-medbank-tower-ref-1145-00-medication-cabinet/"}, {"id": "fda-device-z-2302-2026", "source": "FDA", "category": "device", "recall_number": "Z-2302-2026", "title": "BD Pyxis MedStation ES Tower REF: 352 Medication cabinet recall (CareFusion 303, Inc.)", "product": "BD Pyxis MedStation ES Tower REF: 352 Medication cabinet", "reason": "Fingerprint scanner may overheat to a temperature to cause 1st degree burn.", "hazard_level": "Class II", "company": "CareFusion 303, Inc.", "company_location": "San Diego, CA, United States", "date": "2026-04-30", "report_date": "2026-06-10", "status": "Ongoing", "distribution": "US: Nationwide OUS: AE, AU, BE, BH, BR, CA, CL, ES, GB, IT, KW, MA, MX, NZ, PT, QA, SA, SG, TH, TW", "states": ["CA"], "nationwide": true, "quantity": "465 units", "codes": "All Serial Numbers/UDI:10885403512674", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2302-2026%22", "url": "https://recallledger.net/recalls/device-z-2302-2026-bd-pyxis-medstation-es-tower-ref-352-medication-cabinet/"}, {"id": "fda-device-z-2301-2026", "source": "FDA", "category": "device", "recall_number": "Z-2301-2026", "title": "BD Pyxis Mini Main REF: 349 Medication cabinet recall (CareFusion 303, Inc.)", "product": "BD Pyxis Mini Main REF: 349 Medication cabinet", "reason": "Fingerprint scanner may overheat to a temperature to cause 1st degree burn.", "hazard_level": "Class II", "company": "CareFusion 303, Inc.", "company_location": "San Diego, CA, United States", "date": "2026-04-30", "report_date": "2026-06-10", "status": "Ongoing", "distribution": "US: Nationwide OUS: AE, AU, BE, BH, BR, CA, CL, ES, GB, IT, KW, MA, MX, NZ, PT, QA, SA, SG, TH, TW", "states": ["CA"], "nationwide": true, "quantity": "709 units", "codes": "All Serial Numbers/UDI:10885403512582", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2301-2026%22", "url": "https://recallledger.net/recalls/device-z-2301-2026-bd-pyxis-mini-main-ref-349-medication-cabinet/"}, {"id": "fda-device-z-2300-2026", "source": "FDA", "category": "device", "recall_number": "Z-2300-2026", "title": "BD Pyxis Anesthesia Station 4000 REF: 338 Medication cabinet recall (CareFusion 303, Inc.)", "product": "BD Pyxis Anesthesia Station 4000 REF: 338 Medication cabinet", "reason": "Fingerprint scanner may overheat to a temperature to cause 1st degree burn.", "hazard_level": "Class II", "company": "CareFusion 303, Inc.", "company_location": "San Diego, CA, United States", "date": "2026-04-30", "report_date": "2026-06-10", "status": "Ongoing", "distribution": "US: Nationwide OUS: AE, AU, BE, BH, BR, CA, CL, ES, GB, IT, KW, MA, MX, NZ, PT, QA, SA, SG, TH, TW", "states": ["CA"], "nationwide": true, "quantity": "1 unit", "codes": "All Serial Numbers/UDI:10885403477829", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2300-2026%22", "url": "https://recallledger.net/recalls/device-z-2300-2026-bd-pyxis-anesthesia-station-4000-ref-338-medication-cabinet/"}, {"id": "fda-device-z-2299-2026", "source": "FDA", "category": "device", "recall_number": "Z-2299-2026", "title": "BD Pyxis Anesthesia Station ES REF: 327 Medication cabinet recall (CareFusion 303, Inc.)", "product": "BD Pyxis Anesthesia Station ES REF: 327 Medication cabinet", "reason": "Fingerprint scanner may overheat to a temperature to cause 1st degree burn.", "hazard_level": "Class II", "company": "CareFusion 303, Inc.", "company_location": "San Diego, CA, United States", "date": "2026-04-30", "report_date": "2026-06-10", "status": "Ongoing", "distribution": "US: Nationwide OUS: AE, AU, BE, BH, BR, CA, CL, ES, GB, IT, KW, MA, MX, NZ, PT, QA, SA, SG, TH, TW", "states": ["CA"], "nationwide": true, "quantity": "4,579 units", "codes": "All Serial Numbers/UDI:10885403477836", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2299-2026%22", "url": "https://recallledger.net/recalls/device-z-2299-2026-bd-pyxis-anesthesia-station-es-ref-327-medication-cabinet/"}, {"id": "fda-device-z-2298-2026", "source": "FDA", "category": "device", "recall_number": "Z-2298-2026", "title": "BD Pyxis MedStation ES REF: 323 Medication cabinet recall (CareFusion 303, Inc.)", "product": "BD Pyxis MedStation ES REF: 323 Medication cabinet", "reason": "Fingerprint scanner may overheat to a temperature to cause 1st degree burn.", "hazard_level": "Class II", "company": "CareFusion 303, Inc.", "company_location": "San Diego, CA, United States", "date": "2026-04-30", "report_date": "2026-06-10", "status": "Ongoing", "distribution": "US: Nationwide OUS: AE, AU, BE, BH, BR, CA, CL, ES, GB, IT, KW, MA, MX, NZ, PT, QA, SA, SG, TH, TW", "states": ["CA"], "nationwide": true, "quantity": "15,933", "codes": "All Serial Numbers/UDI:10885403512667", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2298-2026%22", "url": "https://recallledger.net/recalls/device-z-2298-2026-bd-pyxis-medstation-es-ref-323-medication-cabinet/"}, {"id": "fda-device-z-2297-2026", "source": "FDA", "category": "device", "recall_number": "Z-2297-2026", "title": "BD Pyxis MedStation 4000 REF: 303 Medication cabinet recall (CareFusion 303, Inc.)", "product": "BD Pyxis MedStation 4000 REF: 303 Medication cabinet", "reason": "Fingerprint scanner may overheat to a temperature to cause 1st degree burn.", "hazard_level": "Class II", "company": "CareFusion 303, Inc.", "company_location": "San Diego, CA, United States", "date": "2026-04-30", "report_date": "2026-06-10", "status": "Ongoing", "distribution": "US: Nationwide OUS: AE, AU, BE, BH, BR, CA, CL, ES, GB, IT, KW, MA, MX, NZ, PT, QA, SA, SG, TH, TW", "states": ["CA"], "nationwide": true, "quantity": "1 unit", "codes": "All Serial Numbers/UDI:10885403512629", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2297-2026%22", "url": "https://recallledger.net/recalls/device-z-2297-2026-bd-pyxis-medstation-4000-ref-303-medication-cabinet/"}, {"id": "fda-device-z-2296-2026", "source": "FDA", "category": "device", "recall_number": "Z-2296-2026", "title": "Avanta Multi-Patient Administration Tube Sets recall (Bayer Medical Care, Inc.)", "product": "Avanta Multi-Patient Administration Tube Sets (AVA 500 MPAT (Part 2 of 2)) used with the Medrad¿ Avanta Injection System; Catalog number: AVA 500 MPAT (Part 2 of 2); Affected material numbers: 87629007, 60729458, 86566648;", "reason": "Supplier changes resulted in a fit issue with the Contrast Flow Control Valve (CFCV) interface on the Avanta Injector System. Multiple customer reports indicate that the stopcock cannot be reliably engaged with the CFCV snap interface. In instances where engagement is achieved through applied force, the connection is unstable, and the stopcock may disengage before or during contrast injection, leading to procedure interruption.", "hazard_level": "Class II", "company": "Bayer Medical Care, Inc.", "company_location": "Indianola, PA, United States", "date": "2026-04-24", "report_date": "2026-06-10", "status": "Ongoing", "distribution": "Worldwide - US Nationwide distribution including in the states of AL, AR, AZ, CA, CO, DE, FL, IA, IL, IN, KS, KY, LA, MA, MD, ME, MO, NC, NY, OH, OK, PA, SC, TN, TX, VA, WI and the countries of AE, BA, BE, CA, CH, CN, DE, DK, ES, FR, GB, HK, HR, IL, KW, MT, MX, NL, RO, RU, SE, ZA.", "states": ["AL", "AR", "AZ", "CA", "CO", "DE", "FL", "IA", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MO", "MT", "NC", "NY", "OH", "OK", "PA", "SC", "TN", "TX", "VA", "WI"], "nationwide": true, "quantity": "11,300 units (1650 US, 9650 OUS)", "codes": "Catalog number: AVA 500 MPAT (Part 2 of 2) Affected material numbers: 87629007, 60729458, 86566648; Affected batch numbers: 251702, 252302, 252502, 252602, 252702, 252802, 253304, 253702, 253704, 253804, 254202, 254304, 254704, 254802;", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2296-2026%22", "url": "https://recallledger.net/recalls/device-z-2296-2026-avanta-multi-patient-administration-tube-sets-ava-500-mpat-part-2-of/"}, {"id": "fda-device-z-2294-2026", "source": "FDA", "category": "device", "recall_number": "Z-2294-2026", "title": "Digital Angiography System Trinias:UD150G-40 / D150GC-40 recall (Shimadzu Medical Systems)", "product": "Digital Angiography System Trinias:UD150G-40 / D150GC-40; Digital Angiography System BRANSIST safire:UD150G-40 / D150GC-40; Digital Angiography System BRANSIST alexa:UD150G-40 / D150GC-40; Digital Radiography System RADspeed Pro: UD150B-40 / UD150V-40 / UD150L-40 / UD150L-40E/D150BC-40 / D150VC-40 / D150LC-40 / D150LC-40E/D150BC-41 / D150VC-41 / D150LC-41; Digital Radiography System RADspeed safire: UD150B-40 / D150BC-40; Radiography System RADspeed fit: N/A (Integrated in the system); X-RAY R/F SYSTEM SONIALVISION safire17:UD150B-40 / D150BC-40; X-RAY R/F SYSTEM SONIALVISION safire Plus: UD150B-40 / D150BC-4;0 X-RAY R/F SYSTEM SONIALVISION safire: UD150B-40 / D150BC-40; X-RAY R/F SYSTEM SONIALVISION VERSA: UD150B-40 / UD150V-40 / UD150L-40/D150BC-40 / D150VC-40 / D150LC-40; X-RAY R/F SYSTEM FLUOROspeed 300:UD150B-40 / UD150V-40 / UD150L-40/D150BC-40 / D150VC-40 / D150LC-40; X-RAY R/F SYSTEM SONIALVISION G4:D150BC-40S; X-RAY R/F SYSTEM FLUOROspeed X1:D150BC-40S", "reason": "Electromagnetic contactors within high voltage generator may weld together, resulting in current being supplied to power supply even if power is off.", "hazard_level": "Class II", "company": "Shimadzu Medical Systems", "company_location": "Long Beach, CA, United States", "date": "2026-04-20", "report_date": "2026-06-10", "status": "Ongoing", "distribution": "Worldwide - US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NJ, NM, NV, NY, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV and the countries of Canada, The Bahamas, China, Denmark, Haiti.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "MI", "MN", "MO", "MS", "MT", "NC", "NE", "NJ", "NM", "NV", "NY", "OK", "OR", "PA", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "WA", "WI", "WV"], "nationwide": true, "quantity": "3487 units", "codes": "System Serial Numbers:SMS20080542 SMS20120038 SMS20140084 SMS20090038 SMSMA110013 SMS20090239 SMS20080581 SMS20090099 SMS20110202 SMS2010011 SMS20080609 SMS20100127 SMS20090157 SMS20080573 SMS20100230 SMSMA130031 SMS20105020 SMS20080009 SMS20080174 SMS20090316 SMS20090281 SMSMA100027 SMSHP100002 SMSHP100001 SMS20100007 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"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2294-2026%22", "url": "https://recallledger.net/recalls/device-z-2294-2026-digital-angiography-system-trinias-ud150g-40-d150gc-40-digital-angi/"}, {"id": "fda-device-z-2293-2026", "source": "FDA", "category": "device", "recall_number": "Z-2293-2026", "title": "Arvis Hip & Knee 2.0 Instrument Set recall (Kico Knee Innovation Company)", "product": "Arvis Hip & Knee 2.0 Instrument Set, REF: IN-21200 containing one of the following components: IN-10500, Impactor V-Block Assembly; IN-10600 , Tracker B; IN-16400, Tracker A; IN-16100, Tracker C", "reason": "The Impactor V-Block Assembly and Trackers A, B, C and E may exhibit signs of early wear and/or corrosion on the exposed magnet face.", "hazard_level": "Class II", "company": "Kico Knee Innovation Company", "company_location": "Pymble, Australia", "date": "2026-04-23", "report_date": "2026-06-10", "status": "Ongoing", "distribution": "Worldwide - US Nationwide distribution in the states of MS, CA, IA, IN, MI, CO, MT, FL, IL, NY, AL, WI, NE, AZ, MN, VT, NH, MD, RI, MA, NJ, PA, KS, WA, ID, OR, TN, VA, PR and the countries of Australia, France, Germany, Italy.", "states": ["AL", "AZ", "CA", "CO", "FL", "IA", "ID", "IL", "IN", "KS", "MA", "MD", "MI", "MN", "MS", "MT", "NE", "NH", "NJ", "NY", "OR", "PA", "PR", "RI", "TN", "VA", "VT", "WA", "WI"], "nationwide": true, "quantity": "124 kits", "codes": "All Lots/serial Numbers; UDI: IN-28000: 00810180350020; IN-10500: (01)00810180350686; IN-10600 (01)00810180350693; IN-16400:(01)00810180350525; IN-16100: (01)00810180350563;", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2293-2026%22", "url": "https://recallledger.net/recalls/device-z-2293-2026-arvis-hip-knee-2-0-instrument-set-ref-in-21200-containing-one-of-t/"}, {"id": "fda-device-z-2292-2026", "source": "FDA", "category": "device", "recall_number": "Z-2292-2026", "title": "Arvis Hip & Knee 3.0 Instrument Set recall (Kico Knee Innovation Company)", "product": "Arvis Hip & Knee 3.0 Instrument Set, REF: IN-28000 containing one of the following components: IN-10500, Impactor V-Block Assembly; IN-10600 , Tracker B; IN-16400, Tracker A; IN-16100, Tracker C; IN-28050, Tracker E", "reason": "The V-Block Assembly and Trackers A, B, C and E may exhibit signs of early wear and/or corrosion on the exposed magnet face.", "hazard_level": "Class II", "company": "Kico Knee Innovation Company", "company_location": "Pymble, Australia", "date": "2026-04-23", "report_date": "2026-06-10", "status": "Ongoing", "distribution": "Worldwide - US Nationwide distribution in the states of MS, CA, IA, IN, MI, CO, MT, FL, IL, NY, AL, WI, NE, AZ, MN, VT, NH, MD, RI, MA, NJ, PA, KS, WA, ID, OR, TN, VA, PR and the countries of Australia, France, Germany, Italy.", "states": ["AL", "AZ", "CA", "CO", "FL", "IA", "ID", "IL", "IN", "KS", "MA", "MD", "MI", "MN", "MS", "MT", "NE", "NH", "NJ", "NY", "OR", "PA", "PR", "RI", "TN", "VA", "VT", "WA", "WI"], "nationwide": true, "quantity": "69 units", "codes": "All Lots/serial Numbers; UDI: IN-28000: 00810180350020; IN-10500: (01)00810180350686; IN-10600 (01)00810180350693; IN-16400:(01)00810180350525; IN-16100: (01)00810180350563; IN-28050: 00810180350051", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2292-2026%22", "url": "https://recallledger.net/recalls/device-z-2292-2026-arvis-hip-knee-3-0-instrument-set-ref-in-28000-containing-one-of-t/"}, {"id": "fda-device-z-2283-2026", "source": "FDA", "category": "device", "recall_number": "Z-2283-2026", "title": "Brand Name: HiResolution\" Bionic Ear System Product Name: HiRes Ultra 3D CI HiFocus... recall (Advanced Bionics, LLC)", "product": "Brand Name: HiResolution\" Bionic Ear System Product Name: HiRes Ultra 3D CI HiFocus Mid Scala Model/Catalog Number: CI-1601-04 Software Version: N/A Product Description: The HiResolution Bionic Ear System is a cochlear implant designed to provide useful hearing to individuals with severe-to-profound hearing loss. It consists of internal and external components. The internal components include the HiRes\" Ultra 3D receiver and either the HiFocus\" SlimJ electrode or the HiFocus\" Mid-Scala (MS) electrode array that are implanted surgically under the skin behind the ear. The external components include a sound processor (body-worn or ear-level), a headpiece, and a cable. The system converts sound into electrical energy that activates the auditory nerve. The auditory nerve then sends information to the brain, where it is interpreted as sound. Component: N/A", "reason": "Due to incorrect shelf-life expiration date.", "hazard_level": "Class II", "company": "Advanced Bionics, LLC", "company_location": "Valencia, CA, United States", "date": "2026-04-30", "report_date": "2026-06-10", "status": "Ongoing", "distribution": "U.S. Nationwide distribution in the states of CA, CO, GA, IL, IN, KS, MA, MD, MI, MO, MT, NC, TN, WA and WI.", "states": ["CA", "CO", "GA", "IL", "IN", "KS", "MA", "MD", "MI", "MO", "MT", "NC", "TN", "WA", "WI"], "nationwide": true, "quantity": "36", "codes": "Model Number: CI-1601-04 UDI codes: (01)00840094455993(11)260220(17)290228(21)2225141 (01)00840094455993(11)260220(17)290228(21)2225150 (01)00840094455993(11)260220(17)290228(21)2225152 (01)00840094455993(11)260220(17)290228(21)2225155 (01)00840094455993(11)260220(17)290228(21)2225160 (01)00840094455993(11)260220(17)290228(21)2225188 (01)00840094455993(11)250929(17)280930(21)2227161 (01)00840094455993(11)260309(17)290331(21)2229827 (01)00840094455993(11)260309(17)290331(21)2229839 (01)00840094455993(11)260309(17)290331(21)2229849 (01)00840094455993(11)250918(17)280930(21)2214172 (01)00840094455993(11)260220(17)290228(21)2225146 (01)00840094455993(11)260220(17)290228(21)2225154 (01)00840094455993(11)260220(17)290228(21)2225168 (01)00840094455993(11)260220(17)290228(21)2225189 (01)00840094455993(11)250929(17)280930(21)2226476 (01)00840094455993(11)250929(17)280930(21)2227006 (01)00840094455993(11)250929(17)280930(21)2227007 (01)00840094455993(11)250929(17)280930(21)2227012 (01)00840094455993(11)250929(17)280930(21)2227038 (01)00840094455993(11)250929(17)280930(21)2227071 (01)00840094455993(11)250929(17)280930(21)2227112 (01)00840094455993(11)250929(17)280930(21)2227122 (01)00840094455993(11)250929(17)280930(21)2227129 (01)00840094455993(11)250929(17)280930(21)2227148 (01)00840094455993(11)250929(17)280930(21)2227151 (01)00840094455993(11)250929(17)280930(21)2227183 (01)00840094455993(11)250929(17)280930(21)2227196 (01)00840094455993(11)250929(17)280930(21)2227202 (01)00840094455993(11)250929(17)280930(21)2227207 (01)00840094455993(11)250929(17)280930(21)2227212 (01)00840094455993(11)250929(17)280930(21)2227215 (01)00840094455993(11)250929(17)280930(21)2227220 (01)00840094455993(11)250929(17)280930(21)2227235 (01)00840094455993(11)260309(17)290331(21)2229803 (01)00840094455993(11)260309(17)290331(21)2229836 Lot Numbers: 2225141 2225150 2225152 2225155 2225160 2225188 2227161 2229827 2229839 2229849 2214172 2225146 2225154 2225168 2225189 2226476 2227006 2227007 2227012 2227038 2227071 2227112 2227122 2227129 2227148 2227151 2227183 2227196 2227202 2227207 2227212 2227215 2227220 2227235 2229803 2229836 Lot Code: Serial Number/UDI Refer to Exhibit_0005", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2283-2026%22", "url": "https://recallledger.net/recalls/device-z-2283-2026-brand-name-hiresolution-bionic-ear-system-product-name-hires-ultra/"}, {"id": "fda-device-z-2281-2026", "source": "FDA", "category": "device", "recall_number": "Z-2281-2026", "title": "Covidien EndoStitch\" Polysorb Single Use Loading Unit recall (Covidien, LP)", "product": "Covidien EndoStitch\" Polysorb Single Use Loading Unit; Product numbers: 170053 and 170071;", "reason": "The presence of holes in the pouch may compromise the package s ability to maintain the sterile barrier and protect the product from environmental exposure.", "hazard_level": "Class II", "company": "Covidien, LP", "company_location": "North Haven, CT, United States", "date": "2026-04-15", "report_date": "2026-06-10", "status": "Ongoing", "distribution": "Domestic: Nationwide distribution; International: Austria, Canada, Denmark, France, Italy;", "states": [], "nationwide": true, "quantity": "2448 units", "codes": "1. Product Number: 170053; UDI-DI: 10884521126732; UPN: 20884521126739; Lot number: J5L2332Y; 2. Product Number: 170071; UDI-DI: 10884521126787; UPN: 20884521126784; Lot number: J5H2924Y;", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2281-2026%22", "url": "https://recallledger.net/recalls/device-z-2281-2026-covidien-endostitch-polysorb-single-use-loading-unit-product-number/"}, {"id": "fda-device-z-2279-2026", "source": "FDA", "category": "device", "recall_number": "Z-2279-2026", "title": "CASE v7.0 Cardiac Testing System Model no. 3031234-001 Product Code SU3 recall (GE Medical Systems Information Technologies Inc)", "product": "CASE v7.0 Cardiac Testing System Model no. 3031234-001 Product Code SU3", "reason": "Electrical sparking may occur at the printer head. If the Electrostatic Discharge (ESD) printer brush becomes dislodged, electrical sparking at the printer head can result in charring or discoloration of thermal printer paper. Ignition of the paper could potentially result in serious thermal injury.", "hazard_level": "Class II", "company": "GE Medical Systems Information Technologies Inc", "company_location": "Milwaukee, WI, United States", "date": "2026-04-24", "report_date": "2026-06-10", "status": "Ongoing", "distribution": "Worldwide distribution - US Nationwide and the countries of Algeria, Australia, Bangladesh, Cambodia, Canada, Croatia, Denmark, Finland, France, Germany, Greece, Hong Kong, India, Indonesia, Ireland, Italy, Japan, South Korea, Lebanon, Libya, Lithuania, Malaysia, Myanmar, Netherlands, New Zealand, Norway, Philippines, Poland, Qatar, Romania, Saudi Arabia, Senegal, Singapore, South Africa, Spain, Sri Lanka, Sweden, Taiwan, Tanzania, Thailand, Tunisia, Turkey, United Arab Emirates, United Kingdom.", "states": [], "nationwide": true, "quantity": "1835", "codes": "UDI-DI 00195278617644 Serial numbers SU325232838SA SU325032272SA SU325293027SA SU325222794SA SU325122553SA SU325363223SA 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"https://recallledger.net/recalls/device-z-2279-2026-case-v7-0-cardiac-testing-system-model-no-3031234-001-product-code/"}, {"id": "fda-device-z-2275-2026", "source": "FDA", "category": "device", "recall_number": "Z-2275-2026", "title": "PhaseOne Antimicrobial Solution recall (Oculus Technologies of Mexico, S.A. de C.V.)", "product": "PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050", "reason": "The recall is being conducted due to corrosion of the internal metallic spring within the sprayer component. This condition is caused by material incompatibility between the product solution and the stainless steel spring and may result in visible discoloration and the presence of trace levels of metallic elements (including iron, chromium, and nickel) in the solution during use.", "hazard_level": "Class II", "company": "Oculus Technologies of Mexico, S.A. de C.V.", "company_location": "Zapopan, Mexico", "date": "2026-04-27", "report_date": "2026-06-10", "status": "Ongoing", "distribution": "US Nationwide distribution in the states of AZ, CA, CO, FL, GA, IL, IN, KY, MI, MS, NC, NJ, NY, TN, TX, UT, VA.", "states": ["AZ", "CA", "CO", "FL", "GA", "IL", "IN", "KY", "MI", "MS", "NC", "NJ", "NY", "TN", "TX", "UT", "VA"], "nationwide": true, "quantity": "5904 units", "codes": "UDI:00860009268616 Lot: 25G263", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2275-2026%22", "url": "https://recallledger.net/recalls/device-z-2275-2026-phaseone-antimicrobial-solution-model-catalog-number-15050/"}, {"id": "fda-device-z-2273-2026", "source": "FDA", "category": "device", "recall_number": "Z-2273-2026", "title": "Covidien Mon-a-Therm general purpose temperature probe size: 9 Fr REF: 90050 recall (Covidien LLC)", "product": "Covidien Mon-a-Therm general purpose temperature probe size: 9 Fr REF: 90050", "reason": "Temperature probe devices lack FDA clearance.", "hazard_level": "Class II", "company": "Covidien LLC", "company_location": "Boulder, CO, United States", "date": "2026-04-23", "report_date": "2026-06-10", "status": "Ongoing", "distribution": "US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, FL, GA, HI, IL, LA, MA, MD, MI, MN, MO, MS, NC, NE, NJ, NY, OH, OK, OR, PA, PR, TN, TX, UT, VA, WA, WV.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "FL", "GA", "HI", "IL", "LA", "MA", "MD", "MI", "MN", "MO", "MS", "NC", "NE", "NJ", "NY", "OH", "OK", "OR", "PA", "PR", "TN", "TX", "UT", "VA", "WA", "WV"], "nationwide": true, "quantity": "128,900 units", "codes": "UDI: 10884521828391, 30884521828395/ Lot: 24D1130JZX 25A1086JZX 25E1332JZX 25I1054JZX 24D1133JZX 25A1087JZX 25F0946JZX 25I1055JZX 24E1015JZX 25A1088JZX 25F0947JZX 25I1056JZX 24E1017JZX 25D0379JZX 25F0948JZX 25I1057JZX 24E1018JZX 25D0380JZX 25F0949JZX 25I1058JZX 24L0848JZX 25D0381JZX 25F0950JZX 25I1059JZX 24L0850JZX 25D1271JZX 25F0953JZX 25I1061JZX 25A1069JZX 25D1272JZX 25F0954JZX 25K1129JZX 25A1070JZX 25D1273JZX 25G1163JZX 25K1130JZX 25A1072JZX 25E1263JZX 25H0935JZX 25K1131JZX 25A1075JZX 25E1264JZX 25H0936JZX 25L0542JZX 25A1076JZX 25E1265JZX 25H0938JZX 25L0545JZX 25A1077JZX 25E1326JZX 25H0939JZX 25L0899JZX 25A1082JZX 25E1329JZX 25H0940JZX 25L0901JZX 25A1084JZX 25E1331JZX 25H0942JZX 25L0903JZX 25A1085JZX", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2273-2026%22", "url": "https://recallledger.net/recalls/device-z-2273-2026-covidien-mon-a-therm-general-purpose-temperature-probe-size-9-fr-r/"}, {"id": "fda-device-z-2272-2026", "source": "FDA", "category": "device", "recall_number": "Z-2272-2026", "title": "Covidien Mon-a-Therm General Purpose Temperature Probe REF: 90044 recall (Covidien LLC)", "product": "Covidien Mon-a-Therm General Purpose Temperature Probe REF: 90044", "reason": "Temperature probe devices lack FDA clearance.", "hazard_level": "Class II", "company": "Covidien LLC", "company_location": "Boulder, CO, United States", "date": "2026-04-23", "report_date": "2026-06-10", "status": "Ongoing", "distribution": "US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, FL, GA, HI, IL, LA, MA, MD, MI, MN, MO, MS, NC, NE, NJ, NY, OH, OK, OR, PA, PR, TN, TX, UT, VA, WA, WV.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "FL", "GA", "HI", "IL", "LA", "MA", "MD", "MI", "MN", "MO", "MS", "NC", "NE", "NJ", "NY", "OH", "OK", "OR", "PA", "PR", "TN", "TX", "UT", "VA", "WA", "WV"], "nationwide": true, "quantity": "1775 units", "codes": "UDI: 30884521828388/ Lot: 25F0945JZX 25H0949JZX, 25I1065JZX, 25I1066JZX", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2272-2026%22", "url": "https://recallledger.net/recalls/device-z-2272-2026-covidien-mon-a-therm-general-purpose-temperature-probe-ref-90044/"}, {"id": "fda-device-z-2271-2026", "source": "FDA", "category": "device", "recall_number": "Z-2271-2026", "title": "Covidien Mon-a-Therm Esophageal Stethoscope with Temperature Sensor 400TM REF: 90042 recall (Covidien LLC)", "product": "Covidien Mon-a-Therm Esophageal Stethoscope with Temperature Sensor 400TM REF: 90042", "reason": "Temperature probe devices lack FDA clearance.", "hazard_level": "Class II", "company": "Covidien LLC", "company_location": "Boulder, CO, United States", "date": "2026-04-23", "report_date": "2026-06-10", "status": "Ongoing", "distribution": "US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, FL, GA, HI, IL, LA, MA, MD, MI, MN, MO, MS, NC, NE, NJ, NY, OH, OK, OR, PA, PR, TN, TX, UT, VA, WA, WV.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "FL", "GA", "HI", "IL", "LA", "MA", "MD", "MI", "MN", "MO", "MS", "NC", "NE", "NJ", "NY", "OH", "OK", "OR", "PA", "PR", "TN", "TX", "UT", "VA", "WA", "WV"], "nationwide": true, "quantity": "23,000 units", "codes": "UDI: 30884521820900/ Lot: 25D1267JZX 25E1322JZX, 25E1324JZX, 25H0920JZX,", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2271-2026%22", "url": "https://recallledger.net/recalls/device-z-2271-2026-covidien-mon-a-therm-esophageal-stethoscope-with-temperature-sensor-40/"}, {"id": "fda-device-z-2262-2026", "source": "FDA", "category": "device", "recall_number": "Z-2262-2026", "title": "Brand Name: Exacta Mix Product Name: Vented Micro-Volume Inlet Model/Catalog Number:... recall (Baxter Healthcare Corporation)", "product": "Brand Name: Exacta Mix Product Name: Vented Micro-Volume Inlet Model/Catalog Number: H938175 Product Description: Tubing sets with push-on connector on one end (to attach to the Fluid Selector Valve) and a spike or other appropriate connector on the opposite end to attach the source container.", "reason": "Affected lots may contain incorrect 0.8-micron filters. Use of a 0.8-micron filter in place of the validated 3-micron filter may lead to reduced flow efficiency, incomplete or slower transfers of ingredients, or system alarms. This issue may lead to clinical effects such as electrolyte imbalance, metabolic instability, delayed recovery, etc.", "hazard_level": "Class II", "company": "Baxter Healthcare Corporation", "company_location": "Deerfield, IL, United States", "date": "2026-04-22", "report_date": "2026-06-10", "status": "Ongoing", "distribution": "Worldwide - US Nationwide distribution including in the states of Alabama, Arkansas, Arizona, California, Colorado, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maine, Maryland, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, and West Virginia. The countries of Taiwan and Uruguay.", "states": ["AL", "AR", "AZ", "CA", "CO", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "SD", "TN", "TX", "UT", "VA", "WA", "WI", "WV"], "nationwide": true, "quantity": "105675", "codes": "Lot Code: Lot numbers: 804084, 804088, and 804089 UDI Number: 00085412475806", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2262-2026%22", "url": "https://recallledger.net/recalls/device-z-2262-2026-brand-name-exacta-mix-product-name-vented-micro-volume-inlet-model/"}, {"id": "fda-device-z-2261-2026", "source": "FDA", "category": "device", "recall_number": "Z-2261-2026", "title": "COVIDIEN Shiley Tracheostomy Tube Cuffed with Inner Cannula REF 6FEN UDI-DI code:... recall (Covidien LLC)", "product": "COVIDIEN Shiley Tracheostomy Tube Cuffed with Inner Cannula REF 6FEN UDI-DI code: 60884522007028 The devices are intended for use in providing tracheal access for airway management. Shiley Tracheostomy Tubes are double cannula tracheostomy tubes with reusable inner cannulae (LPC, FEN, CFS, CFN, LGT) and twist-lock connectors. These Shiley Tracheostomy Tubes have a radiopaque, biocompatible outer cannula constructed of polyvinyl chloride.", "reason": "Due to customer complaint regarding incorrect display box labeling.", "hazard_level": "Class II", "company": "Covidien LLC", "company_location": "Boulder, CO, United States", "date": "2026-04-15", "report_date": "2026-06-10", "status": "Ongoing", "distribution": "Worldwide - U.S.: Nationwide distribution in the state of TX and the countries of France, French, Polynesia, Italy, Pakistan, Poland, Portugal, Spain, and Taiwan.", "states": ["TX"], "nationwide": true, "quantity": "1,002", "codes": "Product Number: 6FEN UDI-DI code: 60884522007028 Lot Number: 25H0868JZX", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2261-2026%22", "url": "https://recallledger.net/recalls/device-z-2261-2026-covidien-shiley-tracheostomy-tube-cuffed-with-inner-cannula-ref-6fen/"}, {"id": "fda-device-z-2257-2026", "source": "FDA", "category": "device", "recall_number": "Z-2257-2026", "title": "BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in. recall (Becton Dickinson & Company)", "product": "BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 405637, 405707.", "reason": "This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.", "hazard_level": "Class I", "company": "Becton Dickinson & Company", "company_location": "Franklin Lakes, NJ, United States", "date": "2026-04-27", "report_date": "2026-06-10", "status": "Ongoing", "distribution": "Nationwide distribution to AK, AL, AR, AZ, CA, CO, CT, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MO, MS, NC, NE, NH, NJ, NV, NY, OH, OR, PA, PR, SD, TN, TX, UT, VA, WA, WI, WV, WY.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "FL", "GA", "IA", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "MI", "MO", "MS", "NC", "NE", "NH", "NJ", "NV", "NY", "OH", "OR", "PA", "PR", "SD", "TN", "TX", "UT", "VA", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "5,940 units", "codes": "1. Catalog Number: 405637. UDI Numbers: (01)00382904056377(17)260628(10)B01V160D, (01)00382904056377(17)270101(10)B01V241D, (01)00382904056377(17)270101(10)B01V265D, (01)00382904056377(17)261001(10)B02V183D. Lot Numbers (Expiration Date): B01V160D (2026-06-28), B01V241D (2027-01-01), B01V265D (2027-01-01), B02V183D (2026-10-01). 2. Catalog Number: 405707. UDI Number: (01)00382904057077(17)270101(10)B02V230D. Lot Number (Expiration Date): B02V230D (2027-01-01).", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2257-2026%22", "url": "https://recallledger.net/recalls/device-z-2257-2026-bdspinal-tray-with-bdwhitacre-needle-25-g-x-3-5-in-lidocaine-hcl/"}, {"id": "fda-device-z-2256-2026", "source": "FDA", "category": "device", "recall_number": "Z-2256-2026", "title": "BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in. recall (Becton Dickinson & Company)", "product": "BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405671.", "reason": "This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.", "hazard_level": "Class I", "company": "Becton Dickinson & Company", "company_location": "Franklin Lakes, NJ, United States", "date": "2026-04-27", "report_date": "2026-06-10", "status": "Ongoing", "distribution": "Nationwide distribution to AK, AL, AR, AZ, CA, CO, CT, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MO, MS, NC, NE, NH, NJ, NV, NY, OH, OR, PA, PR, SD, TN, TX, UT, VA, WA, WI, WV, WY.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "FL", "GA", "IA", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "MI", "MO", "MS", "NC", "NE", "NH", "NJ", "NV", "NY", "OH", "OR", "PA", "PR", "SD", "TN", "TX", "UT", "VA", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "0 units", "codes": "Catalog Number: 405671. UDI Number: (01)00382904056711(17)270101(10)B01V275D. Lot Number (Expiration Date): B01V275D (2027-01-01). ***Expansion 07/08/2026 UDI Number: (01)00382904056711(17)270101(10)B01V294D; Lot Number (Expiration Date): B01V294D (2027-01-01).", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2256-2026%22", "url": "https://recallledger.net/recalls/device-z-2256-2026-bdspinal-tray-with-bdwhitacre-needle-25-g-x-3-5-in-lidocaine-hcl/"}, {"id": "fda-device-z-2255-2026", "source": "FDA", "category": "device", "recall_number": "Z-2255-2026", "title": "BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in. recall (Becton Dickinson & Company)", "product": "BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 400866, 405672, 405673, 405674, 405675, 405709, 405721, 405723, 406704.", "reason": "This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.", "hazard_level": "Class I", "company": "Becton Dickinson & Company", "company_location": "Franklin Lakes, NJ, United States", "date": "2026-04-27", "report_date": "2026-06-10", "status": "Ongoing", "distribution": "Nationwide distribution to AK, AL, AR, AZ, CA, CO, CT, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MO, MS, NC, NE, NH, NJ, NV, NY, OH, OR, PA, PR, SD, TN, TX, UT, VA, WA, WI, WV, WY.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "FL", "GA", "IA", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "MI", "MO", "MS", "NC", "NE", "NH", "NJ", "NV", "NY", "OH", "OR", "PA", "PR", "SD", "TN", "TX", "UT", "VA", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "13,320 units", "codes": "1. Catalog Number: 400866. UDI Number: (01)10885403469497(17)270101(10)B01V232D. Lot Number (Expiration Date): B01V232D (2027-01-01). 2. Catalog Number: 405672. UDI Number: (01)00382904056728(17)270101(10)B03V267D. Lot Number (Expiration Date): B03V267D (2027-01-01). 3. Catalog Number: 405673. UDI Numbers: (01)00382904056735(17)261001(10)B01V225D, (01)00382904056735(17)270101(10)B01V281D, (01)00382904056735(17)261001(10)B02V211D, (01)00382904056735(17)261001(10)B02V217D. Lot Numbers (Expiration Date): B01V225D (2026-10-01), B01V281D (2027-01-01), B02V211D (2026-10-01), B02V217D (2026-10-01). 4. Catalog Number: 405674. UDI Number: (01)00382904056742(17)261001(10)B01V218D. Lot Number (Expiration Date): B01V218D (2026-10-01). 5. Catalog Number: 405675. UDI Numbers: (01)00382904056759(17)261001(10)B01V183D, (01)00382904056759(17)260901(10)B01V198D. Lot Numbers (Expiration Date): B01V183D (2026-10-01), B01V198D (2026-09-01). 6. Catalog Number: 405709. UDI Numbers: (01)00382904057091(17)261001(10)B02V202D, (01)00382904057091(17)260628(10)B02V174D. Lot Numbers (Expiration Date): B02V202D (2026-10-01), B02V174D (2026-06-28). 7. Catalog Number: 405721. UDI Number: (01)00382904057213(17)270101(10)B02V227D. Lot Number (Expiration Date): B02V227D (2027-01-01). 8. Catalog Number: 405723. UDI Number: (01)00382904057237(17)260628(10)B01V174D, (01)00382904057237(17)270101(10)B02V254D, (01)00382904057237(17)261001(10)B01V189D. Lot Numbers (Expiration Date): B01V174D (2026-06-28), B02V254D (2027-01-01), B01V189D (2026-10-01). 9. Catalog Number: 406704. UDI Number: (01)00382904067045(17)270101(10)B02V246D. Lot Number (Expiration Date): B02V246D (2027-01-01).", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2255-2026%22", "url": "https://recallledger.net/recalls/device-z-2255-2026-bdspinal-tray-with-bdwhitacre-needle-25-g-x-3-5-in-lidocaine-hcl/"}, {"id": "fda-device-z-2254-2026", "source": "FDA", "category": "device", "recall_number": "Z-2254-2026", "title": "BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in. recall (Becton Dickinson & Company)", "product": "BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 2 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405658.", "reason": "This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.", "hazard_level": "Class I", "company": "Becton Dickinson & Company", "company_location": "Franklin Lakes, NJ, United States", "date": "2026-04-27", "report_date": "2026-06-10", "status": "Ongoing", "distribution": "Nationwide distribution to AK, AL, AR, AZ, CA, CO, CT, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MO, MS, NC, NE, NH, NJ, NV, NY, OH, OR, PA, PR, SD, TN, TX, UT, VA, WA, WI, WV, WY.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "FL", "GA", "IA", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "MI", "MO", "MS", "NC", "NE", "NH", "NJ", "NV", "NY", "OH", "OR", "PA", "PR", "SD", "TN", "TX", "UT", "VA", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "150 units", "codes": "Catalog Number: 405658. UDI Number: (01)00382904056582(17)261001(10)B01V217D. Lot Number (Expiration Date): B01V217D (2026-10-01).", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2254-2026%22", "url": "https://recallledger.net/recalls/device-z-2254-2026-bdspinal-tray-with-bdwhitacre-needle-25-g-x-3-5-in-lidocaine-hcl/"}, {"id": "fda-device-z-2253-2026", "source": "FDA", "category": "device", "recall_number": "Z-2253-2026", "title": "BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in. recall (Becton Dickinson & Company)", "product": "BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in., BD¿Quincke Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405741.", "reason": "This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.", "hazard_level": "Class I", "company": "Becton Dickinson & Company", "company_location": "Franklin Lakes, NJ, United States", "date": "2026-04-27", "report_date": "2026-06-10", "status": "Ongoing", "distribution": "Nationwide distribution to AK, AL, AR, AZ, CA, CO, CT, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MO, MS, NC, NE, NH, NJ, NV, NY, OH, OR, PA, PR, SD, TN, TX, UT, VA, WA, WI, WV, WY.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "FL", "GA", "IA", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "MI", "MO", "MS", "NC", "NE", "NH", "NJ", "NV", "NY", "OH", "OR", "PA", "PR", "SD", "TN", "TX", "UT", "VA", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "290 units", "codes": "Catalog Number: 405741. UDI Number: (01)00382904057411(17)261001(10)B02V204D. Lot Number (Expiration Date): B02V204D (2026-10-01).", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2253-2026%22", "url": "https://recallledger.net/recalls/device-z-2253-2026-bdspinal-tray-with-bdwhitacre-needle-25-g-x-3-5-in-bdquincke-need/"}, {"id": "fda-device-z-2252-2026", "source": "FDA", "category": "device", "recall_number": "Z-2252-2026", "title": "BD¿Spinal Tray with BD¿Whitacre Needle 24 G x 3.5 in. recall (Becton Dickinson & Company)", "product": "BD¿Spinal Tray with BD¿Whitacre Needle 24 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 400868, 405652.", "reason": "This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.", "hazard_level": "Class I", "company": "Becton Dickinson & Company", "company_location": "Franklin Lakes, NJ, United States", "date": "2026-04-27", "report_date": "2026-06-10", "status": "Ongoing", "distribution": "Nationwide distribution to AK, AL, AR, AZ, CA, CO, CT, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MO, MS, NC, NE, NH, NJ, NV, NY, OH, OR, PA, PR, SD, TN, TX, UT, VA, WA, WI, WV, WY.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "FL", "GA", "IA", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "MI", "MO", "MS", "NC", "NE", "NH", "NJ", "NV", "NY", "OH", "OR", "PA", "PR", "SD", "TN", "TX", "UT", "VA", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "3,550 units", "codes": "1. Catalog Numbers: 400868. UDI Numbers: (01)10885403469510(17)261001(10)B01V206D, (01)10885403469510(17)261001(10)B01V220D, (01)10885403469510(17)270101(10)B02V266D. Lot Number (Expiration Date): B01V206D (2026-10-01), B01V220D (2026-10-01), B02V266D (2027-01-01). 2. Catalog Number: 405652. UDI Numbers: (01)00382904056520(17)270130(10)B01V353D, (01)00382904056520(17)270101(10)B02V267D. Lot Numbers (Expiration Date): B01V353D (2027-01-30), B02V267D (2027-01-01).", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2252-2026%22", "url": "https://recallledger.net/recalls/device-z-2252-2026-bdspinal-tray-with-bdwhitacre-needle-24-g-x-3-5-in-lidocaine-hcl/"}, {"id": "fda-device-z-2251-2026", "source": "FDA", "category": "device", "recall_number": "Z-2251-2026", "title": "BD¿Spinal Tray with BD¿Whitacre Needle 22 G x 3.5 in. recall (Becton Dickinson & Company)", "product": "BD¿Spinal Tray with BD¿Whitacre Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405645.", "reason": "This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.", "hazard_level": "Class I", "company": "Becton Dickinson & Company", "company_location": "Franklin Lakes, NJ, United States", "date": "2026-04-27", "report_date": "2026-06-10", "status": "Ongoing", "distribution": "Nationwide distribution to AK, AL, AR, AZ, CA, CO, CT, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MO, MS, NC, NE, NH, NJ, NV, NY, OH, OR, PA, PR, SD, TN, TX, UT, VA, WA, WI, WV, WY.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "FL", "GA", "IA", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "MI", "MO", "MS", "NC", "NE", "NH", "NJ", "NV", "NY", "OH", "OR", "PA", "PR", "SD", "TN", "TX", "UT", "VA", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "330 units", "codes": "Catalog Number: 405645. UDI Numbers: (01)00382904056452(17)261001(10)B01V223D. Lot Number (Expiration Date): B01V223D (2026-10-01).", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2251-2026%22", "url": "https://recallledger.net/recalls/device-z-2251-2026-bdspinal-tray-with-bdwhitacre-needle-22-g-x-3-5-in-lidocaine-hcl/"}, {"id": "fda-device-z-2250-2026", "source": "FDA", "category": "device", "recall_number": "Z-2250-2026", "title": "BD¿Spinal Tray with BD¿Quincke Needle 26 G x 3.5 in. recall (Becton Dickinson & Company)", "product": "BD¿Spinal Tray with BD¿Quincke Needle 26 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405632.", "reason": "This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.", "hazard_level": "Class I", "company": "Becton Dickinson & Company", "company_location": "Franklin Lakes, NJ, United States", "date": "2026-04-27", "report_date": "2026-06-10", "status": "Ongoing", "distribution": "Nationwide distribution to AK, AL, AR, AZ, CA, CO, CT, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MO, MS, NC, NE, NH, NJ, NV, NY, OH, OR, PA, PR, SD, TN, TX, UT, VA, WA, WI, WV, WY.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "FL", "GA", "IA", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "MI", "MO", "MS", "NC", "NE", "NH", "NJ", "NV", "NY", "OH", "OR", "PA", "PR", "SD", "TN", "TX", "UT", "VA", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "890 units", "codes": "Catalog Number: 405632. UDI Number: (01)00382904056322(17)270101(10)B01V231D; Lot Number (Expiration Date): B01V231D (2027-01-01). ***Expansion 07/08/2026 UDI Number: (01)00382904056322(17)270101(10)B02V248D; Lot Number (Expiration Date): B02V248D (2027-01-01).", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2250-2026%22", "url": "https://recallledger.net/recalls/device-z-2250-2026-bdspinal-tray-with-bdquincke-needle-26-g-x-3-5-in-lidocaine-hcl-1/"}, {"id": "fda-device-z-2249-2026", "source": "FDA", "category": "device", "recall_number": "Z-2249-2026", "title": "BD¿Spinal Tray with BD¿Quincke Needle 25 G x 3.5 in. recall (Becton Dickinson & Company)", "product": "BD¿Spinal Tray with BD¿Quincke Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 405621, 405735.", "reason": "This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.", "hazard_level": "Class I", "company": "Becton Dickinson & Company", "company_location": "Franklin Lakes, NJ, United States", "date": "2026-04-27", "report_date": "2026-06-10", "status": "Ongoing", "distribution": "Nationwide distribution to AK, AL, AR, AZ, CA, CO, CT, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MO, MS, NC, NE, NH, NJ, NV, NY, OH, OR, PA, PR, SD, TN, TX, UT, VA, WA, WI, WV, WY.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "FL", "GA", "IA", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "MI", "MO", "MS", "NC", "NE", "NH", "NJ", "NV", "NY", "OH", "OR", "PA", "PR", "SD", "TN", "TX", "UT", "VA", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "3,130 units", "codes": "1. Catalog Number: 405621. UDI Numbers: (01)00382904056216(17)260601(10)B01V142D, (01)00382904056216(17)260628(10)B01V176D. Lot Numbers (Expiration Date): B01V142D (2026-06-01), B01V176D (2026-06-28). 2. Catalog Number: 405735. UDI Numbers: (01)00382904057350(17)260601(10)B01V149D, (01)00382904057350(17)261001(10)B01V190D. Lot Numbers (Expiration Date): B01V149D (2026-06-01), B01V190D (2026-10-01).", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2249-2026%22", "url": "https://recallledger.net/recalls/device-z-2249-2026-bdspinal-tray-with-bdquincke-needle-25-g-x-3-5-in-lidocaine-hcl-1/"}, {"id": "fda-device-z-2248-2026", "source": "FDA", "category": "device", "recall_number": "Z-2248-2026", "title": "BD¿Spinal Tray with BD¿Quincke Needle 22 G x 3.5 in. recall (Becton Dickinson & Company)", "product": "BD¿Spinal Tray with BD¿Quincke Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405609.", "reason": "This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.", "hazard_level": "Class I", "company": "Becton Dickinson & Company", "company_location": "Franklin Lakes, NJ, United States", "date": "2026-04-27", "report_date": "2026-06-10", "status": "Ongoing", "distribution": "Nationwide distribution to AK, AL, AR, AZ, CA, CO, CT, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MO, MS, NC, NE, NH, NJ, NV, NY, OH, OR, PA, PR, SD, TN, TX, UT, VA, WA, WI, WV, WY.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "FL", "GA", "IA", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "MI", "MO", "MS", "NC", "NE", "NH", "NJ", "NV", "NY", "OH", "OR", "PA", "PR", "SD", "TN", "TX", "UT", "VA", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "990 units", "codes": "Catalog Number: 405609. UDI Numbers: (10)00382904056094(17)261001(10)B01V212D, (10)00382904056094(17)270101(10)B01V238D. Lot Numbers (Expiration Date): B01V212D (2026-10-01), B01V238D (2027-01-01).", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2248-2026%22", "url": "https://recallledger.net/recalls/device-z-2248-2026-bdspinal-tray-with-bdquincke-needle-22-g-x-3-5-in-lidocaine-hcl-1/"}, {"id": "fda-food-h-0858-2026", "source": "FDA", "category": "food", "recall_number": "H-0858-2026", "title": "Wawa Fruit Punch Pint recall (Wawa Beverage Company)", "product": "Wawa Fruit Punch Pint (16oz), Plastic bottle", "reason": "Undeclared Milk Allergen,", "hazard_level": "Class I", "company": "Wawa Beverage Company", "company_location": "Media, PA, United States", "date": "2026-04-02", "report_date": "2026-06-03", "status": "Completed", "distribution": "The product has been distributed to the following states: DE, MD, NJ, PA, VA", "states": ["DE", "MD", "NJ", "PA", "VA"], "nationwide": false, "quantity": "Wawa Fruit Punch Pint (16oz) - 1,694", "codes": "UPC: 726191018432", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0858-2026%22", "url": "https://recallledger.net/recalls/food-h-0858-2026-wawa-fruit-punch-pint-16oz-plastic-bottle/"}, {"id": "fda-food-h-0857-2026", "source": "FDA", "category": "food", "recall_number": "H-0857-2026", "title": "Wawa Diet Lemonade Pint recall (Wawa Beverage Company)", "product": "Wawa Diet Lemonade Pint (16oz), Plastic bottle", "reason": "Undeclared Milk Allergen,", "hazard_level": "Class I", "company": "Wawa Beverage Company", "company_location": "Media, PA, United States", "date": "2026-04-02", "report_date": "2026-06-03", "status": "Completed", "distribution": "The product has been distributed to the following states: DE, MD, NJ, PA, VA", "states": ["DE", "MD", "NJ", "PA", "VA"], "nationwide": false, "quantity": "Wawa Diet Lemonade Pint (16oz) - 374", "codes": "UPC: 726191055901", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0857-2026%22", "url": "https://recallledger.net/recalls/food-h-0857-2026-wawa-diet-lemonade-pint-16oz-plastic-bottle/"}, {"id": "fda-food-h-0856-2026", "source": "FDA", "category": "food", "recall_number": "H-0856-2026", "title": "Wawa Diet Iced Tea Lemon Pint recall (Wawa Beverage Company)", "product": "Wawa Diet Iced Tea Lemon Pint (16oz),Plastic bottle", "reason": "Undeclared Milk Allergen,", "hazard_level": "Class I", "company": "Wawa Beverage Company", "company_location": "Media, PA, United States", "date": "2026-04-02", "report_date": "2026-06-03", "status": "Completed", "distribution": "The product has been distributed to the following states: DE, MD, NJ, PA, VA", "states": ["DE", "MD", "NJ", "PA", "VA"], "nationwide": false, "quantity": "Wawa Diet Iced Tea Lemon Pint (16oz) \u0013 616", "codes": "UPC: 726191018548", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0856-2026%22", "url": "https://recallledger.net/recalls/food-h-0856-2026-wawa-diet-iced-tea-lemon-pint-16oz-plastic-bottle/"}, {"id": "fda-food-h-0855-2026", "source": "FDA", "category": "food", "recall_number": "H-0855-2026", "title": "Wawa Iced Tea Lemon 16 oz Pint recall (Wawa Beverage Company)", "product": "Wawa Iced Tea Lemon 16 oz Pint, Plastic bottle", "reason": "Undeclared Milk Allergen,", "hazard_level": "Class I", "company": "Wawa Beverage Company", "company_location": "Media, PA, United States", "date": "2026-04-02", "report_date": "2026-06-03", "status": "Completed", "distribution": "The product has been distributed to the following states: DE, MD, NJ, PA, VA", "states": ["DE", "MD", "NJ", "PA", "VA"], "nationwide": false, "quantity": "Wawa Iced Tea Lemon Pint (16oz) - 15,510", "codes": "UPC: 726191018425", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0855-2026%22", "url": "https://recallledger.net/recalls/food-h-0855-2026-wawa-iced-tea-lemon-16-oz-pint-plastic-bottle/"}, {"id": "fda-food-h-0849-2026", "source": "FDA", "category": "food", "recall_number": "H-0849-2026", "title": "(BULK) SPL-BEV Banana CWT (Banana Smoothie); Super Sack Tote Item# 355-0099 recall (Honeyville, Inc)", "product": "(BULK) SPL-BEV Banana CWT (Banana Smoothie); Super Sack Tote Item# 355-0099", "reason": "Firm received and used potentially contaminated (Salmonella) ingredient to manufacture various products.", "hazard_level": "Class I", "company": "Honeyville, Inc", "company_location": "Ogden, UT, United States", "date": "2026-04-21", "report_date": "2026-06-03", "status": "Ongoing", "distribution": "Distribution is to California and Utah consignees.", "states": ["CA", "UT"], "nationwide": false, "quantity": "4980 pounds (all on hold at customer location)", "codes": "Lot number# 0325357B201", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0849-2026%22", "url": "https://recallledger.net/recalls/food-h-0849-2026-bulk-spl-bev-banana-cwt-banana-smoothie-super-sack-tote-item-355/"}, {"id": "fda-device-z-2260-2026", "source": "FDA", "category": "device", "recall_number": "Z-2260-2026", "title": "Medline medical convenience kit labeled as EYE TRAY-LF recall (Medline Industries, LP)", "product": "Medline medical convenience kit labeled as EYE TRAY-LF, Medline Kit SKU DYNJ21627P", "reason": "Specific Medline Kits contain Cardinal Health Monoject 1mL Luer Lock Syringes, Tuberculin Print, Sterile. Cardinal Health has recalled these syringes because the outer carton and blister pack are labeled as a 1 mL Luer Lock Tuberculin Syringe (Product Code 1180100777), but the syringes inside are U-100 insulin syringes.", "hazard_level": "Class II", "company": "Medline Industries, LP", "company_location": "Northfield, IL, United States", "date": "2026-04-10", "report_date": "2026-06-03", "status": "Ongoing", "distribution": "US Nationwide distribution in the states of California.", "states": ["CA"], "nationwide": true, "quantity": "8 kits", "codes": "UDI/DI 10198459151569 (each), 40198459151560 (case), Lot Numbers: 26BMC538", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2260-2026%22", "url": "https://recallledger.net/recalls/device-z-2260-2026-medline-medical-convenience-kit-labeled-as-eye-tray-lf-medline-kit-sk/"}, {"id": "fda-device-z-2259-2026", "source": "FDA", "category": "device", "recall_number": "Z-2259-2026", "title": "Allura system recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)", "product": "Allura system; System Code Description (Model Numbers): Allura Xper FD10 (722003, 722010, 722026), Allura Xper FD10 OR Table (722022, 722033), Allura Xper FD10/10 (722005, 722011, 722027), Allura Xper FD20 (722006, 722012, 722028), Allura Xper FD20 Biplane (722008, 722013), Allura Xper FD20 OR Table (722015, 722023, 722035), Allura Xper FD20 Biplane OR Table (722025), Allura Xper FD20/10 (722029), Allura Xper FD20/15 (722058), Allura Xper FD20/15 OR Table (722059), Allura Xper FD20/20 (722038), Allura Xper FD20/20 OR Table (722039);", "reason": "It was identified that HDDs used in the PCs of Azurion and Allura systems may show a decrease in performance as they age, particularly beyond six years of service. Issues with an HDD may, depending on the specific system PC in which the affected HDD is installed, result in loss of imaging functionality. Additionally, in Allura systems, this may lead to loss of motorized movement, or loss of data. In some cases, a system restart may temporarily restore functionality.", "hazard_level": "Class II", "company": "PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.", "company_location": "Best, Netherlands", "date": "2026-04-30", "report_date": "2026-06-03", "status": "Ongoing", "distribution": "Worldwide distribution - US Nationwide and the countries of Canada, Afghanistan, Albania, Algeria, Argentina, Australia, Austria, Bahrain, Bangladesh, Belarus, Belgium, Bolivia, Bosnia and Herzegovina, Brazil, Brunei Darussal, Bulgaria, Chile, China, Colombia, Costa Rica, Croatia, Cuba, Cyprus, Czech Republic, Denmark, Dominican Republic, Ecuador, Egypt, Estonia, Fiji, Finland, France, French Polynesia, Georgia, Germany, Greece, Guinea, Honduras, Hong Kong, Hungary, India, Indonesia, Iran, Iraq, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan, Kenya, Korea, South, Kosovo, Kuwait, Kyrgyzstan, Lao, Latvia, Lebanon, Libya, Lithuania, Macedonia, Malaysia, Maldives, Malta, Martinique, Mauritius, Mexico, Moldova, Mongolia, Morocco, Myanmar, Nepal, Netherlands, New Caledonia, New Zealand, Nicaragua, Nigeria, Norway, Oman, Pakistan, Palestine, Panama, Papua New Guinea, Paraguay, Peru, Philippines, Poland, Portugal, Qatar, R¿union, Romania, Russian Fed., Russian Federation, Saudi Arabia, Serbia, Singapore, Slovakia, Slovenia, South Africa, South Korea, Spain, Sri Lanka, Sudan, Sweden, Switzerland, Syrian Arab Republic, Taiwan, Tanzania, Thailand, Trinidad and Tobago, Tunisia, Turkey, Turkmenistan, Ukraine, United Arab Emirates, United Kingdom, Uruguay, Uzbekistan, Vietnam, Yemen.", "states": ["GA"], "nationwide": true, "quantity": "", "codes": "1. Allura Xper FD10; Model: 722003; UDI-DI: N/A; Serial Numbers: 445, 1555, 1114, 1529, 472, 1349, 1594, 1311, 1472, 1187, 1700, 1031, 912, 913, 940, 285, 1637, 5, 797, 639, 452, 1585, 535, 1338, 1641, 1916, 614, 605, 492, 1612, 505, 239, 1216, 1169, 1118, 115, 519, 356, 715, 423, 1399, 789, 1509, 1016, 875, 1923, 313, 314, 1919, 1458, 369, 1176, 1230, 1925, 339, 1325, 1633, 596, 1784, 464, 796, 1928, 1025, 292, 1669, 1697, 708, 1, 1760, 1452, 346, 961, 1172, 354, 416, 363, 582, 161, 569, 922; 2. Allura Xper FD10; Model: 722010; UDI: (01)00884838059030(21)1123, (01)00884838059030(21)932, (01)00884838059030(21)239, (01)00884838059030(21)360, (01)00884838059030(21)500, (01)00884838059030(21)794, (01)00884838059030(21)939, (01)00884838059030(21)921, (01)00884838059030(21)286, (01)00884838059030(21)1440, (01)00884838059030(21)1144, (01)00884838059030(21)521, (01)00884838059030(21)33, (01)00884838059030(21)107, (01)00884838059030(21)1025, (01)00884838059030(21)668, (01)00884838059030(21)656, (01)00884838059030(21)1261, (01)00884838059030(21)1170, (01)00884838059030(21)585, (01)00884838059030(21)1128, (01)00884838059030(21)882, (01)00884838059030(21)1230, (01)00884838059030(21)280, (01)00884838059030(21)488, (01)00884838059030(21)787, (01)00884838059030(21)968, (01)00884838059030(21)890, (01)00884838059030(21)780, (01)00884838059030(21)190, (01)00884838059030(21)1181, (01)00884838059030(21)694, (01)00884838059030(21)1279, (01)00884838059030(21)344, (01)00884838059030(21)1149, (01)00884838059030(21)423, (01)00884838059030(21)1176, (01)00884838059030(21)1173, (01)00884838059030(21)1040, (01)00884838059030(21)1309, (01)00884838059030(21)763, (01)00884838059030(21)931, (01)00884838059030(21)478, (01)00884838059030(21)1298, (01)00884838059030(21)970, (01)00884838059030(21)1226, (01)00884838059030(21)290, (01)00884838059030(21)365, (01)00884838059030(21)651, (01)00884838059030(21)1292, (01)00884838059030(21)1275, (01)00884838059030(21)755, (01)00884838059030(21)671, (01)00884838059030(21)677, (01)00884838059030(21)1336, (01)00884838059030(21)477, (01)00884838059030(21)1078, (01)00884838059030(21)467, (01)00884838059030(21)1369, (01)00884838059030(21)792, (01)00884838059030(21)679, (01)00884838059030(21)485, (01)00884838059030(21)395, (01)00884838059030(21)592, (01)00884838059030(21)1312, (01)00884838059030(21)1302, (01)00884838059030(21)505, (01)00884838059030(21)714, (01)00884838059030(21)414, (01)00884838059030(21)785, (01)00884838059030(21)1283, (01)00884838059030(21)119, (01)00884838059030(21)662, (01)00884838059030(21)698, (01)00884838059030(21)690, (01)00884838059030(21)1235, (01)00884838059030(21)1233, (01)00884838059030(21)1236, (01)00884838059030(21)1234, (01)00884838059030(21)158, (01)00884838059030(21)1009, (01)00884838059030(21)992, (01)00884838059030(21)1214, (01)00884838059030(21)1064, (01)00884838059030(21)979, (01)00884838059030(21)764, (01)00884838059030(21)920, (01)00884838059030(21)788, (01)00884838059030(21)1396, (01)00884838059030(21)902, (01)00884838059030(21)1344, (01)00884838059030(21)1183, (01)00884838059030(21)453, (01)00884838059030(21)1118, (01)00884838059030(21)411, (01)00884838059030(21)1210, (01)00884838059030(21)1209, (01)00884838059030(21)1041, (01)00884838059030(21)1042, (01)00884838059030(21)1432, (01)00884838059030(21)308, (01)00884838059030(21)833, (01)00884838059030(21)1310, (01)00884838059030(21)728, (01)00884838059030(21)791, (01)00884838059030(21)480, (01)00884838059030(21)1263, (01)00884838059030(21)987, (01)00884838059030(21)986, (01)00884838059030(21)422, (01)00884838059030(21)905, (01)00884838059030(21)218, (01)00884838059030(21)1005, (01)00884838059030(21)1425, (01)00884838059030(21)1397, (01)00884838059030(21)1398, (01)00884838059030(21)1132, (01)00884838059030(21)468, (01)00884838059030(21)1442, (01)00884838059030(21)1048, (01)00884838059030(21)648, (01)00884838059030(21)646, (01)00884838059030(21)1126, (01)00884838059030(21)873, (01)00884838059030(21)252, (01)00884838059030(21)343, (01)00884838059030(21)1011, (01)00884838059030(21)1370, (01)00884838059030(21)838, (01)00884838059030(21)1391, (01)00884838059030(21)999, (01)00884838059030(21)285, (01)00884838059030(21)636, (01)00884838059030(21)624, (01)00884838059030(21)241, (01)00884838059030(21)1084, (01)00884838059030(21)896, (01)00884838059030(21)673, (01)00884838059030(21)683, (01)00884838059030(21)1441, (01)00884838059030(21)914, (01)00884838059030(21)531, (01)00884838059030(21)818, (01)00884838059030(21)1395, (01)00884838059030(21)637, (01)00884838059030(21)917, (01)00884838059030(21)214, (01)00884838059030(21)1043, (01)00884838059030(21)1365, (01)00884838059030(21)1109, (01)00884838059030(21)1297, (01)00884838059030(21)572, (01)00884838059030(21)1436, (01)00884838059030(21)638, (01)00884838059030(21)1112, (01)00884838059030(21)1373, (01)00884838059030(21)946, (01)00884838059030(21)878, (01)00884838059030(21)1108, (01)00884838059030(21)809, (01)00884838059030(21)830, (01)00884838059030(21)839, (01)00884838059030(21)1069, (01)00884838059030(21)1287, (01)00884838059030(21)1308, (01)00884838059030(21)1424, (01)00884838059030(21)604, (01)00884838059030(21)605, (01)00884838059030(21)777, (01)00884838059030(21)666, (01)00884838059030(21)654, (01)00884838059030(21)1122, (01)00884838059030(21)601, (01)00884838059030(21)301, (01)00884838059030(21)426, (01)00884838059030(21)924, (01)00884838059030(21)1198, (01)00884838059030(21)577, (01)00884838059030(21)1047, 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Allura Xper FD10; Model: 722026; UDI: (01)00884838054189(21)683, (01)00884838054189(21)155, (01)00884838054189(21)618, (01)00884838054189(21)1051, (01)00884838054189(21)1052, (01)00884838054189(21)786, (01)00884838054189(21)654, (01)00884838054189(21)1132, (01)00884838054189(21)458, (01)00884838054189(21)1100, (01)00884838054189(21)770, (01)00884838054189(21)436, (01)00884838054189(21)1338, (01)00884838054189(21)1068, (01)00884838054189(21)233, (01)00884838054189(21)78, (01)00884838054189(21)432, (01)00884838054189(21)224, (01)00884838054189(21)1072, (01)00884838054189(21)93, (01)00884838054189(21)796, (01)00884838054189(21)543, (01)00884838054189(21)1248, (01)00884838054189(21)561, (01)00884838054189(21)1129, (01)00884838054189(21)781, (01)00884838054189(21)344, (01)00884838054189(21)374, (01)00884838054189(21)634, (01)00884838054189(21)908, (01)00884838054189(21)130, (01)00884838054189(21)370, (01)00884838054189(21)235, (01)00884838054189(21)190, (01)00884838054189(21)259, 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(01)00884838054189(21)1090, (01)00884838054189(21)305, (01)00884838054189(21)163, (01)00884838054189(21)466, (01)00884838054189(21)105, (01)00884838054189(21)1273, (01)00884838054189(21)788, (01)00884838054189(21)419, (01)00884838054189(21)170, (01)00884838054189(21)384, (01)00884838054189(21)1344, (01)00884838054189(21)1345, (01)00884838054189(21)247, (01)00884838054189(21)481, (01)00884838054189(21)827, (01)00884838054189(21)212, (01)00884838054189(21)318, (01)00884838054189(21)316, (01)00884838054189(21)317, (01)00884838054189(21)1030, (01)00884838054189(21)1178, (01)00884838054189(21)1131, (01)00884838054189(21)675, (01)00884838054189(21)256, (01)00884838054189(21)336, (01)00884838054189(21)1322, (01)00884838054189(21)623, (01)00884838054189(21)1130, (01)00884838054189(21)1172, (01)00884838054189(21)892, (01)00884838054189(21)588, (01)00884838054189(21)291, (01)00884838054189(21)1257, (01)00884838054189(21)743, (01)00884838054189(21)408, (01)00884838054189(21)286, (01)00884838054189(21)1H071046, (01)00884838054189(21)1162, (01)00884838054189(21)70, (01)00884838054189(21)1323, (01)00884838054189(21)1325, (01)00884838054189(21)260, (01)00884838054189(21)106, (01)00884838054189(21)83, (01)00884838054189(21)876, (01)00884838054189(21)211, (01)00884838054189(21)655, (01)00884838054189(21)568, (01)00884838054189(21)198, (01)00884838054189(21)268, (01)00884838054189(21)495, (01)00884838054189(21)974, (01)00884838054189(21)793, (01)00884838054189(21)160, (01)00884838054189(21)907, (01)00884838054189(21)486, (01)00884838054189(21)1251, (01)00884838054189(21)469, (01)00884838054189(21)669; 4. Allura Xper FD10 OR Table; Model: 722022; UDI: (01)00884838059078(21)6; 5. Allura Xper FD10 OR Table; Model: 722033; UDI: (01)00884838054233(21)1; 6. Allura Xper FD10/10; Model: 722005; UDI-DI: N/A: Serial Numbers: 329, 456, 474, 261, 270, 343, 399, 212, 392, 234, 53, 58, 229, 25, 54, 403, 55, 351, 85, 26, 561, 428, 416, 72, 125, 76; 7. Allura Xper FD10/10; Model: 722011; UDI: (01)00884838059047(21)49, (01)00884838059047(21)137, (01)00884838059047(21)375, (01)00884838059047(21)332, (01)00884838059047(21)102, (01)00884838059047(21)103, (01)00884838059047(21)95, (01)00884838059047(21)107, (01)00884838059047(21)380, (01)00884838059047(21)268, (01)00884838059047(21)132, (01)00884838059047(21)171, (01)00884838059047(21)157, (01)00884838059047(21)270, (01)00884838059047(21)362, (01)00884838059047(21)76, (01)00884838059047(21)79, (01)00884838059047(21)234, (01)00884838059047(21)308, (01)00884838059047(21)324, (01)00884838059047(21)177, (01)00884838059047(21)84, (01)00884838059047(21)82, (01)00884838059047(21)319, (01)00884838059047(21)17, (01)00884838059047(21)133, (01)00884838059047(21)168, (01)00884838059047(21)345, (01)00884838059047(21)344, (01)00884838059047(21)83, (01)00884838059047(21)59, (01)00884838059047(21)170, (01)00884838059047(21)163, (01)00884838059047(21)101, (01)00884838059047(21)255, (01)00884838059047(21)173, (01)00884838059047(21)325, (01)00884838059047(21)87, (01)00884838059047(21)155, (01)00884838059047(21)40, (01)00884838059047(21)154, (01)00884838059047(21)215, (01)00884838059047(21)273, (01)00884838059047(21)222, (01)00884838059047(21)203, (01)00884838059047(21)214, (01)00884838059047(21)242, (01)00884838059047(21)220, (01)00884838059047(21)166, (01)00884838059047(21)71, (01)00884838059047(21)156, (01)00884838059047(21)36, (01)00884838059047(21)300, (01)00884838059047(21)213, (01)00884838059047(21)372, (01)00884838059047(21)41, (01)00884838059047(21)100, (01)00884838059047(21)190, (01)00884838059047(21)278, (01)00884838059047(21)299, (01)00884838059047(21)260, (01)00884838059047(21)280, (01)00884838059047(21)199, (01)00884838059047(21)194, (01)00884838059047(21)75, (01)00884838059047(21)307, (01)00884838059047(21)301, (01)00884838059047(21)303, (01)00884838059047(21)302, (01)00884838059047(21)306, (01)00884838059047(21)304, (01)00884838059047(21)305, (01)00884838059047(21)294, (01)00884838059047(21)293, (01)00884838059047(21)184, (01)00884838059047(21)266, (01)00884838059047(21)146, (01)00884838059047(21)310, (01)00884838059047(21)272, (01)00884838059047(21)238, (01)00884838059047(21)152, (01)00884838059047(21)286, (01)00884838059047(21)309, (01)00884838059047(21)43, (01)00884838059047(21)334, (01)00884838059047(21)338, (01)00884838059047(21)165, (01)00884838059047(21)80, (01)00884838059047(21)112, (01)00884838059047(21)233, (01)00884838059047(21)188, (01)00884838059047(21)139, (01)00884838059047(21)99, (01)00884838059047(21)313, (01)00884838059047(21)277, (01)00884838059047(21)223, (01)00884838059047(21)108, (01)00884838059047(21)26, (01)00884838059047(21)340, (01)00884838059047(21)32, (01)00884838059047(21)69, (01)00884838059047(21)367, (01)00884838059047(21)374, (01)00884838059047(21)328, (01)00884838059047(21)228, (01)00884838059047(21)251, (01)00884838059047(21)231, (01)00884838059047(21)323, (01)00884838059047(21)224, (01)00884838059047(21)81, (01)00884838059047(21)145, (01)00884838059047(21)117, (01)00884838059047(21)153, (01)00884838059047(21)6, (01)00884838059047(21)129, (01)00884838059047(21)355, (01)00884838059047(21)91, (01)00884838059047(21)227, (01)00884838059047(21)202, (01)00884838059047(21)114, (01)00884838059047(21)274, (01)00884838059047(21)21, (01)00884838059047(21)378, (01)00884838059047(21)376, (01)00884838059047(21)377, (01)00884838059047(21)127, (01)00884838059047(21)180, (01)00884838059047(21)259, (01)00884838059047(21)211, (01)00884838059047(21)206, (01)00884838059047(21)217, (01)00884838059047(21)314, (01)00884838059047(21)98, (01)00884838059047(21)201, (01)00884838059047(21)341, (01)00884838059047(21)347, (01)00884838059047(21)261, (01)00884838059047(21)178, (01)00884838059047(21)183, (01)00884838059047(21)271, (01)00884838059047(21)230, (01)00884838059047(21)198, (01)00884838059047(21)321, (01)00884838059047(21)204, (01)00884838059047(21)94, (01)00884838059047(21)244, (01)00884838059047(21)287, (01)00884838059047(21)38, (01)00884838059047(21)176, (01)00884838059047(21)39, (01)00884838059047(21)282, (01)00884838059047(21)329, (01)00884838059047(21)246, (01)00884838059047(21)295, (01)00884838059047(21)337, (01)00884838059047(21)292, (01)00884838059047(21)125; 8. Allura Xper FD10/10; Model: 722027; UDI: (01)00884838054196(21)351, (01)00884838054196(21)332, (01)00884838054196(21)1, (01)00884838054196(21)71, (01)00884838054196(21)319, (01)00884838054196(21)43, (01)00884838054196(21)101, (01)00884838054196(21)29, (01)00884838054196(21)50, (01)00884838054196(21)112, (01)00884838054196(21)240, (01)00884838054196(21)241, (01)00884838054196(21)298, (01)00884838054196(21)175, (01)00884838054196(21)280, (01)00884838054196(21)107, (01)00884838054196(21)183, (01)00884838054196(21)202, (01)00884838054196(21)164, (01)00884838054196(21)153, (01)00884838054196(21)335, (01)00884838054196(21)288, (01)00884838054196(21)342, (01)00884838054196(21)134, (01)00884838054196(21)156, (01)00884838054196(21)307, (01)00884838054196(21)265, (01)00884838054196(21)306, (01)00884838054196(21)152, (01)00884838054196(21)169, (01)00884838054196(21)106, (01)00884838054196(21)203, (01)00884838054196(21)234, (01)00884838054196(21)267, (01)00884838054196(21)209, (01)00884838054196(21)284, (01)00884838054196(21)263, (01)00884838054196(21)127, (01)00884838054196(21)116, (01)00884838054196(21)174, (01)00884838054196(21)56, (01)00884838054196(21)39, (01)00884838054196(21)49, (01)00884838054196(21)120, (01)00884838054196(21)123, (01)00884838054196(21)133, (01)00884838054196(21)305, (01)00884838054196(21)246, (01)00884838054196(21)255, (01)00884838054196(21)40, (01)00884838054196(21)178, (01)00884838054196(21)104, (01)00884838054196(21)42, (01)00884838054196(21)266, (01)00884838054196(21)187, (01)00884838054196(21)321, (01)00884838054196(21)328, (01)00884838054196(21)282, (01)00884838054196(21)184, (01)00884838054196(21)53, (01)00884838054196(21)146, (01)00884838054196(21)35, (01)00884838054196(21)337, (01)00884838054196(21)357, (01)00884838054196(21)213, (01)00884838054196(21)293, (01)00884838054196(21)292, (01)00884838054196(21)170, (01)00884838054196(21)346, (01)00884838054196(21)211, (01)00884838054196(21)95, (01)00884838054196(21)144, (01)00884838054196(21)238, (01)00884838054196(21)247, (01)00884838054196(21)154, (01)00884838054196(21)188, (01)00884838054196(21)347, (01)00884838054196(21)196, (01)00884838054196(21)159, (01)00884838054196(21)339, (01)00884838054196(21)343, (01)00884838054196(21)256, (01)00884838054196(21)167, (01)00884838054196(21)334, (01)00884838054196(21)338, (01)00884838054196(21)162, (01)00884838054196(21)5, (01)00884838054196(21)160, (01)00884838054196(21)61, (01)00884838054196(21)36, (01)00884838054196(21)294, (01)00884838054196(21)345, (01)00884838054196(21)76, (01)00884838054196(21)94, (01)00884838054196(21)172, (01)00884838054196(21)323, (01)00884838054196(21)324, (01)00884838054196(21)151, (01)00884838054196(21)7, (01)00884838054196(21)44, (01)00884838054196(21)99, (01)00884838054196(21)189, (01)00884838054196(21)85, (01)00884838054196(21)102, (01)00884838054196(21)78, (01)00884838054196(21)212, (01)00884838054196(21)165, (01)00884838054196(21)268, (01)00884838054196(21)356, (01)00884838054196(21)244, (01)00884838054196(21)55, (01)00884838054196(21)86, (01)00884838054196(21)254, (01)00884838054196(21)6, (01)00884838054196(21)117, (01)00884838054196(21)362, (01)00884838054196(21)271, (01)00884838054196(21)186, (01)00884838054196(21)259, (01)00884838054196(21)236, (01)00884838054196(21)201, (01)00884838054196(21)275, (01)00884838054196(21)135, (01)00884838054196(21)277, (01)00884838054196(21)350, (01)00884838054196(21)349, (01)00884838054196(21)348, (01)00884838054196(21)273, (01)00884838054196(21)58, (01)00884838054196(21)249, (01)00884838054196(21)149, (01)00884838054196(21)148, (01)00884838054196(21)38, (01)00884838054196(21)47, (01)00884838054196(21)316, (01)00884838054196(21)27, (01)00884838054196(21)274, (01)00884838054196(21)80, (01)00884838054196(21)64, (01)00884838054196(21)205, (01)00884838054196(21)270, (01)00884838054196(21)223, (01)00884838054196(21)181, (01)00884838054196(21)221, (01)00884838054196(21)245, (01)00884838054196(21)46, (01)00884838054196(21)352, (01)00884838054196(21)358, (01)00884838054196(21)361, (01)00884838054196(21)60, (01)00884838054196(21)228, (01)00884838054196(21)142, (01)00884838054196(21)57, (01)00884838054196(21)100, (01)00884838054196(21)214, (01)00884838054196(21)145, (01)00884838054196(21)299, (01)00884838054196(21)30, (01)00884838054196(21)114, (01)00884838054196(21)115, (01)00884838054196(21)204, (01)00884838054196(21)225, (01)00884838054196(21)297, (01)00884838054196(21)182, (01)00884838054196(21)48, (01)00884838054196(21)110, (01)00884838054196(21)84, (01)00884838054196(21)132, (01)00884838054196(21)177, (01)00884838054196(21)300, (01)00884838054196(21)79, (01)00884838054196(21)130, (01)00884838054196(21)210, (01)00884838054196(21)82, (01)00884838054196(21)260, (01)00884838054196(21)261, (01)00884838054196(21)103, (01)00884838054196(21)322, (01)00884838054196(21)128, (01)00884838054196(21)360, (01)00884838054196(21)310, (01)00884838054196(21)125, (01)00884838054196(21)68, (01)00884838054196(21)291, (01)00884838054196(21)180, (01)00884838054196(21)287, (01)00884838054196(21)264, (01)00884838054196(21)272, (01)00884838054196(21)59, (01)00884838054196(21)155, (01)00884838054196(21)207, (01)00884838054196(21)122, (01)00884838054196(21)45, (01)00884838054196(21)166, (01)00884838054196(21)158, (01)00884838054196(21)239, (01)00884838054196(21)33, (01)00884838054196(21)31, (01)00884838054196(21)137, (01)00884838054196(21)308, (01)00884838054196(21)243, (01)00884838054196(21)242, (01)00884838054196(21)131, (01)00884838054196(21)218, (01)00884838054196(21)66, (01)00884838054196(21)147, (01)00884838054196(21)197, (01)00884838054196(21)168, (01)00884838054196(21)118, (01)00884838054196(21)73, (01)00884838054196(21)235, (01)00884838054196(21)278, (01)00884838054196(21)250, (01)00884838054196(21)227, (01)00884838054196(21)96, (01)00884838054196(21)119, (01)00884838054196(21)233, (01)00884838054196(21)329, (01)00884838054196(21)296, (01)00884838054196(21)193, (01)00884838054196(21)143, (01)00884838054196(21)219, (01)00884838054196(21)276, (01)00884838054196(21)326, (01)00884838054196(21)312, (01)00884838054196(21)304, (01)00884838054196(21)311, (01)00884838054196(21)199, (01)00884838054196(21)75, (01)00884838054196(21)121, (01)00884838054196(21)87, (01)00884838054196(21)91, (01)00884838054196(21)192, (01)00884838054196(21)289, (01)00884838054196(21)217, (01)00884838054196(21)355, (01)00884838054196(21)232, (01)00884838054196(21)67, (01)00884838054196(21)315, (01)00884838054196(21)69, (01)00884838054196(21)19, (01)00884838054196(21)34, (01)00884838054196(21)141, (01)00884838054196(21)18, (01)00884838054196(21)138, (01)00884838054196(21)309, (01)00884838054196(21)51, (01)00884838054196(21)171, (01)00884838054196(21)136, (01)00884838054196(21)191, (01)00884838054196(21)269, (01)00884838054196(21)62, (01)00884838054196(21)206, (01)00884838054196(21)330, (01)00884838054196(21)90, (01)00884838054196(21)195, (01)00884838054196(21)215, (01)00884838054196(21)88, (01)00884838054196(21)139, (01)00884838054196(21)220, (01)00884838054196(21)198, (01)00884838054196(21)150, (01)00884838054196(21)208, (01)00884838054196(21)28, (01)00884838054196(21)163, (01)00884838054196(21)286, (01)00884838054196(21)23, (01)00884838054196(21)24, (01)00884838054196(21)21, (01)00884838054196(21)65; 9. Allura Xper FD20; Model: 722006; UDI-DI: N/A; Serial Numbers: 518, 2274, 2183, 1407, 1913, 1259, 674, 2126, 2140, 683, 1942, 1752, 1341, 1922, 2122, 1439, 1093, 878, 1888, 886, 587, 2200, 2323, 1174, 1589, 2199, 638, 723, 1364, 774, 1588, 2002, 2058, 2042, 1872, 680, 1627, 1338, 1807, 1476, 468, 1661, 2143, 1000, 1480, 2203, 2283, 1507, 2195, 810, 722, 2135, 1446, 2425, 1921, 1007, 1845, 641, 1387, 1276, 1373, 1983, 1270, 1591, 1022, 1712, 1198, 812, 1454, 1349, 1751, 1455, 1456, 2053, 1819, 492, 1552, 1999, 1117, 1424, 717, 1253, 609, 1791, 8, 1524, 1468, 1075, 1851, 578, 589, 1180, 687, 1652, 1557, 1884, 1580, 491, 1602, 971, 1824, 2103, 1533, 63, 2465, 1246, 1598, 689, 2171, 585, 1823, 1991, 1617, 2144, 1787, 952, 1650, 1538, 1880, 1530, 1568, 2248, 2552, 1397, 636, 724, 2231, 1149, 940, 1658, 963, 1749, 1408, 617, 1056, 1540, 1330, 602, 640; 10. Allura Xper FD20; Model: 722012; UDI: (01)00884838059054(21)423, (01)00884838059054(21)1506, (01)00884838059054(21)1713, (01)00884838059054(21)1396, (01)00884838059054(21)2821, (01)00884838059054(21)828, (01)00884838059054(21)383, (01)00884838059054(21)2942, (01)00884838059054(21)2308, (01)00884838059054(21)613, (01)00884838059054(21)1271, (01)00884838059054(21)1281, (01)00884838059054(21)1945, (01)00884838059054(21)1188, (01)00884838059054(21)2323, (01)00884838059054(21)369, (01)00884838059054(21)124, (01)00884838059054(21)848, (01)00884838059054(21)2265, (01)00884838059054(21)814, (01)00884838059054(21)1120, (01)00884838059054(21)815, (01)00884838059054(21)2610, (01)00884838059054(21)278, (01)00884838059054(21)352, (01)00884838059054(21)511, (01)00884838059054(21)856, (01)00884838059054(21)560, (01)00884838059054(21)1645, (01)00884838059054(21)2522, (01)00884838059054(21)2735, (01)00884838059054(21)1407, (01)00884838059054(21)2924, (01)00884838059054(21)1608, (01)00884838059054(21)2707, (01)00884838059054(21)1696, (01)00884838059054(21)570, (01)00884838059054(21)1293, (01)00884838059054(21)424, (01)00884838059054(21)1047, (01)00884838059054(21)274, (01)00884838059054(21)2933, (01)00884838059054(21)150, (01)00884838059054(21)2740, (01)00884838059054(21)336, (01)00884838059054(21)741, (01)00884838059054(21)1649, (01)00884838059054(21)655, (01)00884838059054(21)1192, (01)00884838059054(21)577, (01)00884838059054(21)578, (01)00884838059054(21)2203, (01)00884838059054(21)1036, (01)00884838059054(21)1063, (01)00884838059054(21)1209, (01)00884838059054(21)2254, (01)00884838059054(21)1357, (01)00884838059054(21)2835, (01)00884838059054(21)2843, (01)00884838059054(21)1854, (01)00884838059054(21)1084, (01)00884838059054(21)1027, (01)00884838059054(21)888, (01)00884838059054(21)518, (01)00884838059054(21)1672, (01)00884838059054(21)760, (01)00884838059054(21)859, (01)00884838059054(21)187, (01)00884838059054(21)1908, (01)00884838059054(21)1848, (01)00884838059054(21)735, (01)00884838059054(21)2149, (01)00884838059054(21)277, (01)00884838059054(21)1923, (01)00884838059054(21)1743, (01)00884838059054(21)1961, (01)00884838059054(21)731, (01)00884838059054(21)1724, (01)00884838059054(21)174, (01)00884838059054(21)1306, (01)00884838059054(21)1210, (01)00884838059054(21)1545, (01)00884838059054(21)1692, (01)00884838059054(21)1117, (01)00884838059054(21)651, (01)00884838059054(21)192, (01)00884838059054(21)923, (01)00884838059054(21)925, (01)00884838059054(21)2150, (01)00884838059054(21)2937, (01)00884838059054(21)1277, (01)00884838059054(21)2856, (01)00884838059054(21)2855, (01)00884838059054(21)2712, (01)00884838059054(21)1478, (01)00884838059054(21)1561, (01)00884838059054(21)2696, (01)00884838059054(21)1430, (01)00884838059054(21)1519, (01)00884838059054(21)2068, (01)00884838059054(21)2138, (01)00884838059054(21)2234, (01)00884838059054(21)1326, (01)00884838059054(21)1943, (01)00884838059054(21)1549, (01)00884838059054(21)2006, (01)00884838059054(21)1613, (01)00884838059054(21)2454, (01)00884838059054(21)1126, (01)00884838059054(21)2721, (01)00884838059054(21)758, (01)00884838059054(21)1868, (01)00884838059054(21)2313, (01)00884838059054(21)2658, (01)00884838059054(21)1335, (01)00884838059054(21)959, (01)00884838059054(21)1461, (01)00884838059054(21)1455, (01)00884838059054(21)2085, (01)00884838059054(21)1477, (01)00884838059054(21)695, (01)00884838059054(21)1336, (01)00884838059054(21)2171, (01)00884838059054(21)1542, (01)00884838059054(21)430, (01)00884838059054(21)89, (01)00884838059054(21)1119, (01)00884838059054(21)2161, (01)00884838059054(21)1723, (01)00884838059054(21)865, (01)00884838059054(21)531, (01)00884838059054(21)2202, (01)00884838059054(21)2828, (01)00884838059054(21)1515, (01)00884838059054(21)1285, (01)00884838059054(21)2219, (01)00884838059054(21)1118, (01)00884838059054(21)2269, (01)00884838059054(21)767, (01)00884838059054(21)601, (01)00884838059054(21)1014, (01)00884838059054(21)1035, (01)00884838059054(21)2293, (01)00884838059054(21)2286, (01)00884838059054(21)1034, (01)00884838059054(21)768, (01)00884838059054(21)1948, (01)00884838059054(21)670, (01)00884838059054(21)1207, (01)00884838059054(21)2898, (01)00884838059054(21)990, (01)00884838059054(21)893, (01)00884838059054(21)243, (01)00884838059054(21)974, (01)00884838059054(21)1656, (01)00884838059054(21)1108, (01)00884838059054(21)2607, (01)00884838059054(21)1166, (01)00884838059054(21)2134, (01)00884838059054(21)1599, (01)00884838059054(21)2929, (01)00884838059054(21)1141, (01)00884838059054(21)132, (01)00884838059054(21)1218, (01)00884838059054(21)1683, (01)00884838059054(21)2288, (01)00884838059054(21)2920, (01)00884838059054(21)1002, (01)00884838059054(21)1975, (01)00884838059054(21)1735, (01)00884838059054(21)1408, (01)00884838059054(21)615, (01)00884838059054(21)484, (01)00884838059054(21)483, (01)00884838059054(21)1686, (01)00884838059054(21)505, (01)00884838059054(21)1583, (01)00884838059054(21)2305, (01)00884838059054(21)590, (01)00884838059054(21)2302, (01)00884838059054(21)756, (01)00884838059054(21)691, (01)00884838059054(21)1508, (01)00884838059054(21)616, (01)00884838059054(21)2896, (01)00884838059054(21)1305, (01)00884838059054(21)1406, (01)00884838059054(21)733, (01)00884838059054(21)2722, (01)00884838059054(21)2726, (01)00884838059054(21)2086, (01)00884838059054(21)451, (01)00884838059054(21)625, (01)00884838059054(21)2930, (01)00884838059054(21)2883, (01)00884838059054(21)1032, (01)00884838059054(21)976, (01)00884838059054(21)1746, (01)00884838059054(21)2518, (01)00884838059054(21)1919, (01)00884838059054(21)2755, (01)00884838059054(21)1714, (01)00884838059054(21)1798, (01)00884838059054(21)2741, (01)00884838059054(21)1104, (01)00884838059054(21)1560, (01)00884838059054(21)1327, (01)00884838059054(21)1003, (01)00884838059054(21)1610, (01)00884838059054(21)490, (01)00884838059054(21)1083, (01)00884838059054(21)1195, (01)00884838059054(21)943, (01)00884838059054(21)208, (01)00884838059054(21)1630, (01)00884838059054(21)1733, (01)00884838059054(21)1734, (01)00884838059054(21)2201, (01)00884838059054(21)1189, (01)00884838059054(21)1054, (01)00884838059054(21)2736, (01)00884838059054(21)2147, (01)00884838059054(21)790, (01)00884838059054(21)782, (01)00884838059054(21)562, (01)00884838059054(21)104, (01)00884838059054(21)971, (01)00884838059054(21)1594, (01)00884838059054(21)476, (01)00884838059054(21)1871, (01)00884838059054(21)2506, (01)00884838059054(21)1726, (01)00884838059054(21)2890, (01)00884838059054(21)579, (01)00884838059054(21)1249, (01)00884838059054(21)498, (01)00884838059054(21)2057, (01)00884838059054(21)2829, (01)00884838059054(21)2512, (01)00884838059054(21)1586, (01)00884838059054(21)1265, (01)00884838059054(21)1446, (01)00884838059054(21)1344, (01)00884838059054(21)513, (01)00884838059054(21)1625, (01)00884838059054(21)1675, (01)00884838059054(21)1307, (01)00884838059054(21)2307, (01)00884838059054(21)1316, (01)00884838059054(21)70, 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(01)00884838059054(21)1639, (01)00884838059054(21)657, (01)00884838059054(21)2499, (01)00884838059054(21)2141, (01)00884838059054(21)1619, (01)00884838059054(21)143, (01)00884838059054(21)1368, (01)00884838059054(21)1149, (01)00884838059054(21)292, (01)00884838059054(21)113, (01)00884838059054(21)2458, (01)00884838059054(21)105, (01)00884838059054(21)1742, (01)00884838059054(21)1949, (01)00884838059054(21)1850, (01)00884838059054(21)1901, (01)00884838059054(21)845, (01)00884838059054(21)2100, (01)00884838059054(21)273; 11. Allura Xper FD20; Model: 722028; UDI: (01)00884838054202(21)1756, (01)00884838054202(21)1569, (01)00884838054202(21)1956, (01)00884838054202(21)129, (01)00884838054202(21)1233, (01)00884838054202(21)2206, (01)00884838054202(21)1690, (01)00884838054202(21)928, (01)00884838054202(21)1774, (01)00884838054202(21)317, (01)00884838054202(21)2502, (01)00884838054202(21)869, (01)00884838054202(21)668, (01)00884838054202(21)1017, (01)00884838054202(21)540, (01)00884838054202(21)548, (01)00884838054202(21)406, (01)00884838054202(21)590, (01)00884838054202(21)596, (01)00884838054202(21)1957, (01)00884838054202(21)2261, (01)00884838054202(21)110, (01)00884838054202(21)173, (01)00884838054202(21)866, (01)00884838054202(21)1310, (01)00884838054202(21)1043, (01)00884838054202(21)466, (01)00884838054202(21)1077, (01)00884838054202(21)896, (01)00884838054202(21)995, (01)00884838054202(21)987, (01)00884838054202(21)877, (01)00884838054202(21)1343, (01)00884838054202(21)1439, (01)00884838054202(21)895, 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(01)00884838054202(21)1788, (01)00884838054202(21)2073, (01)00884838054202(21)704, (01)00884838054202(21)429, (01)00884838054202(21)707, (01)00884838054202(21)1685, (01)00884838054202(21)1731, (01)00884838054202(21)1799, (01)00884838054202(21)458, (01)00884838054202(21)311, (01)00884838054202(21)2170, (01)00884838054202(21)291, (01)00884838054202(21)1102, (01)00884838054202(21)1557, (01)00884838054202(21)974, (01)00884838054202(21)2171, (01)00884838054202(21)1170, (01)00884838054202(21)2026, (01)00884838054202(21)1740, (01)00884838054202(21)597, (01)00884838054202(21)1241, (01)00884838054202(21)2190, (01)00884838054202(21)1297, (01)00884838054202(21)103, (01)00884838054202(21)120, (01)00884838054202(21)512, (01)00884838054202(21)482, (01)00884838054202(21)693, (01)00884838054202(21)599, (01)00884838054202(21)947, (01)00884838054202(21)1996, (01)00884838054202(21)673, (01)00884838054202(21)2065, (01)00884838054202(21)74, (01)00884838054202(21)2949, (01)00884838054202(21)633, (01)00884838054202(21)648, (01)00884838054202(21)657, (01)00884838054202(21)2199, (01)00884838054202(21)1550, (01)00884838054202(21)1453, (01)00884838054202(21)276, (01)00884838054202(21)403, (01)00884838054202(21)517, (01)00884838054202(21)1975, (01)00884838054202(21)1714, (01)00884838054202(21)245, (01)00884838054202(21)649, (01)00884838054202(21)334, (01)00884838054202(21)898, (01)00884838054202(21)285, (01)00884838054202(21)605, (01)00884838054202(21)427, (01)00884838054202(21)752, (01)00884838054202(21)622, (01)00884838054202(21)1257, (01)00884838054202(21)354, (01)00884838054202(21)653, (01)00884838054202(21)366; 12. Allura Xper FD20 Biplane; Model: 722008; UDI-DI: N/A; Serial Numbers: 445, 487, 306, 267, 491, 349, 197, 264, 19, 124, 521, 472, 231, 246, 115, 319, 465, 142, 419, 312, 37, 167, 435, 480, 169, 121, 259, 253, 359, 391, 283, 410, 93, 87, 46, 542, 122, 8, 468, 250, 482, 63, 213, 398, 31; 13. Allura Xper FD20 Biplane; Model: 722013; UDI: (01)00884838059061(21)293, (01)00884838059061(21)424, (01)00884838059061(21)100, (01)00884838059061(21)174, (01)00884838059061(21)86, (01)00884838059061(21)46, (01)00884838059061(21)170, (01)00884838059061(21)218, (01)00884838059061(21)441, (01)00884838059061(21)249, (01)00884838059061(21)639, (01)00884838059061(21)290, (01)00884838059061(21)153, (01)00884838059061(21)410, (01)00884838059061(21)289, (01)00884838059061(21)519, (01)00884838059061(21)518, (01)00884838059061(21)626, (01)00884838059061(21)126, (01)00884838059061(21)141, (01)00884838059061(21)496, (01)00884838059061(21)379, (01)00884838059061(21)115, (01)00884838059061(21)601, (01)00884838059061(21)214, (01)00884838059061(21)637, (01)00884838059061(21)360, (01)00884838059061(21)389, (01)00884838059061(21)303, (01)00884838059061(21)268, (01)00884838059061(21)264, (01)00884838059061(21)631, (01)00884838059061(21)254, (01)00884838059061(21)255, (01)00884838059061(21)515, (01)00884838059061(21)129, (01)00884838059061(21)603, (01)00884838059061(21)278, (01)00884838059061(21)347, (01)00884838059061(21)426, (01)00884838059061(21)505, (01)00884838059061(21)109, (01)00884838059061(21)462, (01)00884838059061(21)149, (01)00884838059061(21)124, (01)00884838059061(21)216, (01)00884838059061(21)246, (01)00884838059061(21)84, (01)00884838059061(21)479, (01)00884838059061(21)69, (01)00884838059061(21)105, (01)00884838059061(21)638, (01)00884838059061(21)375, (01)00884838059061(21)531, (01)00884838059061(21)404, (01)00884838059061(21)575, (01)00884838059061(21)147, (01)00884838059061(21)475, (01)00884838059061(21)262, (01)00884838059061(21)125, (01)00884838059061(21)316, (01)00884838059061(21)497, (01)00884838059061(21)357, (01)00884838059061(21)495, (01)00884838059061(21)573, (01)00884838059061(21)342, (01)00884838059061(21)564, (01)00884838059061(21)164, (01)00884838059061(21)178, (01)00884838059061(21)556, (01)00884838059061(21)297, (01)00884838059061(21)253, (01)00884838059061(21)511, (01)00884838059061(21)492, (01)00884838059061(21)550, (01)00884838059061(21)96, (01)00884838059061(21)179, (01)00884838059061(21)228, (01)00884838059061(21)194, (01)00884838059061(21)151, (01)00884838059061(21)106, (01)00884838059061(21)330, (01)00884838059061(21)461, (01)00884838059061(21)304, (01)00884838059061(21)72, (01)00884838059061(21)241, (01)00884838059061(21)422, (01)00884838059061(21)267, (01)00884838059061(21)150, (01)00884838059061(21)428, (01)00884838059061(21)634, (01)00884838059061(21)327, (01)00884838059061(21)442, (01)00884838059061(21)175, (01)00884838059061(21)217, (01)00884838059061(21)383, (01)00884838059061(21)346, (01)00884838059061(21)308, (01)00884838059061(21)562, (01)00884838059061(21)309, (01)00884838059061(21)152, (01)00884838059061(21)561, (01)00884838059061(21)205, (01)00884838059061(21)61, (01)00884838059061(21)435, (01)00884838059061(21)266, (01)00884838059061(21)567, (01)00884838059061(21)168, (01)00884838059061(21)607, (01)00884838059061(21)283, (01)00884838059061(21)171, (01)00884838059061(21)66, (01)00884838059061(21)36, (01)00884838059061(21)585, (01)00884838059061(21)271, (01)00884838059061(21)117, (01)00884838059061(21)443, (01)00884838059061(21)107, (01)00884838059061(21)343, (01)00884838059061(21)223, (01)00884838059061(21)165, (01)00884838059061(21)453, (01)00884838059061(21)370, (01)00884838059061(21)108, (01)00884838059061(21)291, (01)00884838059061(21)259, (01)00884838059061(21)455, (01)00884838059061(21)368, (01)00884838059061(21)315, (01)00884838059061(21)325, (01)00884838059061(21)532, (01)00884838059061(21)598, (01)00884838059061(21)440, (01)00884838059061(21)172, (01)00884838059061(21)301, (01)00884838059061(21)415, (01)00884838059061(21)540, (01)00884838059061(21)184, (01)00884838059061(21)185, (01)00884838059061(21)188, (01)00884838059061(21)187, (01)00884838059061(21)437, (01)00884838059061(21)189, (01)00884838059061(21)186, (01)00884838059061(21)183, (01)00884838059061(21)190, (01)00884838059061(21)413, (01)00884838059061(21)560, (01)00884838059061(21)400, (01)00884838059061(21)300, (01)00884838059061(21)295, (01)00884838059061(21)448, (01)00884838059061(21)444, (01)00884838059061(21)110, (01)00884838059061(21)624, (01)00884838059061(21)65, (01)00884838059061(21)633, (01)00884838059061(21)630, (01)00884838059061(21)361, (01)00884838059061(21)549, (01)00884838059061(21)417, (01)00884838059061(21)449, (01)00884838059061(21)506, (01)00884838059061(21)177, (01)00884838059061(21)629, (01)00884838059061(21)476, (01)00884838059061(21)527, (01)00884838059061(21)276, (01)00884838059061(21)247, (01)00884838059061(21)156, (01)00884838059061(21)499, (01)00884838059061(21)302, (01)00884838059061(21)62, (01)00884838059061(21)618, (01)00884838059061(21)608, (01)00884838059061(21)133, (01)00884838059061(21)70, (01)00884838059061(21)352, (01)00884838059061(21)457, (01)00884838059061(21)547, (01)00884838059061(21)312, (01)00884838059061(21)366, (01)00884838059061(21)390, (01)00884838059061(21)544, (01)00884838059061(21)236, (01)00884838059061(21)157, (01)00884838059061(21)243, (01)00884838059061(21)144, (01)00884838059061(21)525, (01)00884838059061(21)238, (01)00884838059061(21)570, (01)00884838059061(21)349, (01)00884838059061(21)359, (01)00884838059061(21)454, (01)00884838059061(21)613, (01)00884838059061(21)623, (01)00884838059061(21)222, (01)00884838059061(21)335, (01)00884838059061(21)445, (01)00884838059061(21)538, (01)00884838059061(21)416, (01)00884838059061(21)628, (01)00884838059061(21)619, (01)00884838059061(21)47, (01)00884838059061(21)206, (01)00884838059061(21)620, (01)00884838059061(21)384, (01)00884838059061(21)526, (01)00884838059061(21)332, (01)00884838059061(21)358, (01)00884838059061(21)470, (01)00884838059061(21)378, (01)00884838059061(21)296, (01)00884838059061(21)227, (01)00884838059061(21)31, (01)00884838059061(21)58, (01)00884838059061(21)589, (01)00884838059061(21)367, (01)00884838059061(21)299, (01)00884838059061(21)616, (01)00884838059061(21)447, (01)00884838059061(21)530, (01)00884838059061(21)232, (01)00884838059061(21)324, (01)00884838059061(21)311, (01)00884838059061(21)176, (01)00884838059061(21)554, (01)00884838059061(21)134, (01)00884838059061(21)163, (01)00884838059061(21)104, (01)00884838059061(21)403, (01)00884838059061(21)478, (01)00884838059061(21)459, (01)00884838059061(21)17, (01)00884838059061(21)528, (01)00884838059061(21)318, (01)00884838059061(21)28, (01)00884838059061(21)237, (01)00884838059061(21)559, (01)00884838059061(21)372, (01)00884838059061(21)256, (01)00884838059061(21)374, (01)00884838059061(21)487, (01)00884838059061(21)405, (01)00884838059061(21)380, (01)00884838059061(21)434, (01)00884838059061(21)130, (01)00884838059061(21)473, (01)00884838059061(21)551, (01)00884838059061(21)557, (01)00884838059061(21)294, (01)00884838059061(21)412, (01)00884838059061(21)128, (01)00884838059061(21)388, (01)00884838059061(21)207, (01)00884838059061(21)258, (01)00884838059061(21)429, (01)00884838059061(21)95, (01)00884838059061(21)411, (01)00884838059061(21)353, (01)00884838059061(21)542, (01)00884838059061(21)533, (01)00884838059061(21)622, (01)00884838059061(21)182, (01)00884838059061(21)574, (01)00884838059061(21)139, (01)00884838059061(21)137, (01)00884838059061(21)250, (01)00884838059061(21)563, (01)00884838059061(21)502, (01)00884838059061(21)450, (01)00884838059061(21)436, (01)00884838059061(21)406, (01)00884838059061(21)510, (01)00884838059061(21)458, (01)00884838059061(21)261, (01)00884838059061(21)503, (01)00884838059061(21)348, (01)00884838059061(21)595, (01)00884838059061(21)586, (01)00884838059061(21)535, (01)00884838059061(21)569, (01)00884838059061(21)425, (01)00884838059061(21)334, (01)00884838059061(21)344, (01)00884838059061(21)355, (01)00884838059061(21)465, (01)00884838059061(21)345, (01)00884838059061(21)522, (01)00884838059061(21)64, (01)00884838059061(21)408, (01)00884838059061(21)208, (01)00884838059061(21)555, (01)00884838059061(21)394, (01)00884838059061(21)57, (01)00884838059061(21)493; 14. Allura Xper FD20 OR Table; Model: 722015; UDI-DI: N/A; Serial Numbers: 3, 13; 15. Allura Xper FD20 OR Table; Model: 722023; UDI: (01)00884838059085(21)49, (01)00884838059085(21)41, (01)00884838059085(21)142, (01)00884838059085(21)110, (01)00884838059085(21)12, (01)00884838059085(21)179, (01)00884838059085(21)124, (01)00884838059085(21)27, (01)00884838059085(21)98, (01)00884838059085(21)66, (01)00884838059085(21)118, (01)00884838059085(21)117, (01)00884838059085(21)138, (01)00884838059085(21)42, (01)00884838059085(21)64, (01)00884838059085(21)116, (01)00884838059085(21)127, (01)00884838059085(21)175, (01)00884838059085(21)75, (01)00884838059085(21)83, (01)00884838059085(21)82, (01)00884838059085(21)46, (01)00884838059085(21)35, (01)00884838059085(21)109, (01)00884838059085(21)33, (01)00884838059085(21)146, (01)00884838059085(21)165, (01)00884838059085(21)169, (01)00884838059085(21)101, (01)00884838059085(21)103, (01)00884838059085(21)129, (01)00884838059085(21)10, (01)00884838059085(21)105, (01)00884838059085(21)90, (01)00884838059085(21)107, (01)00884838059085(21)100, (01)00884838059085(21)47, (01)00884838059085(21)159, (01)00884838059085(21)137, (01)00884838059085(21)119, (01)00884838059085(21)164, (01)00884838059085(21)70, (01)00884838059085(21)95, (01)00884838059085(21)177, (01)00884838059085(21)158, (01)00884838059085(21)5, (01)00884838059085(21)86, (01)00884838059085(21)34, (01)00884838059085(21)132, (01)00884838059085(21)9, (01)00884838059085(21)108, (01)00884838059085(21)121, (01)00884838059085(21)31, (01)00884838059085(21)112, (01)00884838059085(21)173, (01)00884838059085(21)114, (01)00884838059085(21)170, (01)00884838059085(21)172, (01)00884838059085(21)4, (01)00884838059085(21)14, (01)00884838059085(21)85, (01)00884838059085(21)13, (01)00884838059085(21)88, (01)00884838059085(21)25, (01)00884838059085(21)87, (01)00884838059085(21)94, (01)00884838059085(21)57, (01)00884838059085(21)125, (01)00884838059085(21)73, (01)00884838059085(21)106, (01)00884838059085(21)67, (01)00884838059085(21)16, (01)00884838059085(21)96, (01)00884838059085(21)58, (01)00884838059085(21)38, (01)00884838059085(21)141, (01)00884838059085(21)32, (01)00884838059085(21)84, (01)00884838059085(21)68, (01)00884838059085(21)134, (01)00884838059085(21)79, (01)00884838059085(21)52, (01)00884838059085(21)56, (01)00884838059085(21)69, (01)00884838059085(21)37, (01)00884838059085(21)21, (01)00884838059085(21)123, (01)00884838059085(21)157, (01)00884838059085(21)102, (01)00884838059085(21)126, (01)00884838059085(21)145, (01)00884838059085(21)144, (01)00884838059085(21)15, (01)00884838059085(21)135, (01)00884838059085(21)152, (01)00884838059085(21)149, (01)00884838059085(21)60, (01)00884838059085(21)150; 16. Allura Xper FD20 OR Table; Model: 722035; UDI: (01)00884838054240(21)119, (01)00884838054240(21)126, (01)00884838054240(21)169, (01)00884838054240(21)72, (01)00884838054240(21)124, (01)00884838054240(21)161, (01)00884838054240(21)183, (01)00884838054240(21)245, (01)00884838054240(21)246, (01)00884838054240(21)242, (01)00884838054240(21)46, (01)00884838054240(21)196, (01)00884838054240(21)52, (01)00884838054240(21)236, (01)00884838054240(21)147, (01)00884838054240(21)172, (01)00884838054240(21)123, (01)00884838054240(21)74, (01)00884838054240(21)60, (01)00884838054240(21)59, (01)00884838054240(21)88, (01)00884838054240(21)30, (01)00884838054240(21)216, (01)00884838054240(21)212, (01)00884838054240(21)85, (01)00884838054240(21)21, (01)00884838054240(21)47, (01)00884838054240(21)222, (01)00884838054240(21)121, (01)00884838054240(21)131, (01)00884838054240(21)145, (01)00884838054240(21)127, (01)00884838054240(21)38, (01)00884838054240(21)187, (01)00884838054240(21)243, (01)00884838054240(21)143, (01)00884838054240(21)244, (01)00884838054240(21)125, (01)00884838054240(21)117, (01)00884838054240(21)100, (01)00884838054240(21)57, (01)00884838054240(21)247, (01)00884838054240(21)34, (01)00884838054240(21)165, (01)00884838054240(21)252, (01)00884838054240(21)101, (01)00884838054240(21)89, (01)00884838054240(21)192, (01)00884838054240(21)111, (01)00884838054240(21)128, (01)00884838054240(21)227, (01)00884838054240(21)174, (01)00884838054240(21)144, (01)00884838054240(21)28, (01)00884838054240(21)84, (01)00884838054240(21)130, (01)00884838054240(21)263, (01)00884838054240(21)132, (01)00884838054240(21)25, (01)00884838054240(21)98, (01)00884838054240(21)134, (01)00884838054240(21)35, (01)00884838054240(21)226, (01)00884838054240(21)190, (01)00884838054240(21)3, (01)00884838054240(21)6, (01)00884838054240(21)1, (01)00884838054240(21)249, (01)00884838054240(21)109, (01)00884838054240(21)251, (01)00884838054240(21)207, (01)00884838054240(21)158, (01)00884838054240(21)160, (01)00884838054240(21)237, (01)00884838054240(21)163, (01)00884838054240(21)79, (01)00884838054240(21)248, (01)00884838054240(21)253, (01)00884838054240(21)94, (01)00884838054240(21)80, (01)00884838054240(21)250, (01)00884838054240(21)154, (01)00884838054240(21)69, (01)00884838054240(21)97, (01)00884838054240(21)148, (01)00884838054240(21)170, (01)00884838054240(21)195, (01)00884838054240(21)26, (01)00884838054240(21)122, (01)00884838054240(21)96, (01)00884838054240(21)107, (01)00884838054240(21)142, (01)00884838054240(21)58, (01)00884838054240(21)166, (01)00884838054240(21)235, (01)00884838054240(21)230, (01)00884838054240(21)83, (01)00884838054240(21)53, (01)00884838054240(21)32, (01)00884838054240(21)164, (01)00884838054240(21)56, (01)00884838054240(21)40, (01)00884838054240(21)11, (01)00884838054240(21)10, (01)00884838054240(21)62, (01)00884838054240(21)265, (01)00884838054240(21)221, (01)00884838054240(21)257, (01)00884838054240(21)255, (01)00884838054240(21)229, (01)00884838054240(21)256, (01)00884838054240(21)254, (01)00884838054240(21)261, (01)00884838054240(21)260, (01)00884838054240(21)238, (01)00884838054240(21)113, (01)00884838054240(21)258, (01)00884838054240(21)241, (01)00884838054240(21)188, (01)00884838054240(21)259, (01)00884838054240(21)267, (01)00884838054240(21)167, (01)00884838054240(21)204, (01)00884838054240(21)43, (01)00884838054240(21)33, (01)00884838054240(21)37, (01)00884838054240(21)104, (01)00884838054240(21)233, (01)00884838054240(21)114, (01)00884838054240(21)108, (01)00884838054240(21)153, (01)00884838054240(21)70, (01)00884838054240(21)65, (01)00884838054240(21)191, (01)00884838054240(21)77, (01)00884838054240(21)110, (01)00884838054240(21)225, (01)00884838054240(21)75, (01)00884838054240(21)76, (01)00884838054240(21)193, (01)00884838054240(21)185, (01)00884838054240(21)186, (01)00884838054240(21)129, (01)00884838054240(21)103, (01)00884838054240(21)71, (01)00884838054240(21)92, (01)00884838054240(21)151, (01)00884838054240(21)201, (01)00884838054240(21)208, (01)00884838054240(21)149, (01)00884838054240(21)205, (01)00884838054240(21)19, (01)00884838054240(21)50, (01)00884838054240(21)51, (01)00884838054240(21)61, (01)00884838054240(21)211, (01)00884838054240(21)99, (01)00884838054240(21)12, (01)00884838054240(21)15, (01)00884838054240(21)198, (01)00884838054240(21)82, (01)00884838054240(21)105, (01)00884838054240(21)136, (01)00884838054240(21)194, (01)00884838054240(21)23, (01)00884838054240(21)200, (01)00884838054240(21)116, (01)00884838054240(21)13, (01)00884838054240(21)106, (01)00884838054240(21)206, (01)00884838054240(21)168, (01)00884838054240(21)203, (01)00884838054240(21)146, (01)00884838054240(21)81, (01)00884838054240(21)156, (01)00884838054240(21)45, (01)00884838054240(21)173, (01)00884838054240(21)49, (01)00884838054240(21)64, (01)00884838054240(21)171, (01)00884838054240(21)184, (01)00884838054240(21)102, (01)00884838054240(21)17, (01)00884838054240(21)215, (01)00884838054240(21)29, (01)00884838054240(21)231, (01)00884838054240(21)16, (01)00884838054240(21)202; 17. Allura Xper FD20 Biplane OR Table; Model: 722025; UDI: (01)00884838059108(21)2, (01)00884838059108(21)3, (01)00884838059108(21)6; 18. Allura Xper FD20/10; Model: 722029; UDI: (01)00884838054219(21)57, (01)00884838054219(21)7, (01)00884838054219(21)88, (01)00884838054219(21)56, (01)00884838054219(21)126, (01)00884838054219(21)94, (01)00884838054219(21)30, (01)00884838054219(21)31, (01)00884838054219(21)21, (01)00884838054219(21)97, (01)00884838054219(21)91, (01)00884838054219(21)110, (01)00884838054219(21)63, (01)00884838054219(21)100, (01)00884838054219(21)60, (01)00884838054219(21)55, (01)00884838054219(21)62, (01)00884838054219(21)129, (01)00884838054219(21)71, (01)00884838054219(21)36, (01)00884838054219(21)26, (01)00884838054219(21)49, (01)00884838054219(21)114, (01)00884838054219(21)128, (01)00884838054219(21)108, (01)00884838054219(21)103, (01)00884838054219(21)107, (01)00884838054219(21)81, (01)00884838054219(21)43, (01)00884838054219(21)52, (01)00884838054219(21)119, (01)00884838054219(21)118, (01)00884838054219(21)80, (01)00884838054219(21)78, (01)00884838054219(21)47, (01)00884838054219(21)106, (01)00884838054219(21)123, (01)00884838054219(21)122, (01)00884838054219(21)127, (01)00884838054219(21)14, (01)00884838054219(21)101, (01)00884838054219(21)116, (01)00884838054219(21)102, (01)00884838054219(21)115, (01)00884838054219(21)19, (01)00884838054219(21)109, (01)00884838054219(21)120, (01)00884838054219(21)92, (01)00884838054219(21)69, (01)00884838054219(21)27, (01)00884838054219(21)46, (01)00884838054219(21)93, (01)00884838054219(21)51, (01)00884838054219(21)50, (01)00884838054219(21)124, (01)00884838054219(21)87, (01)00884838054219(21)20, (01)00884838054219(21)32, (01)00884838054219(21)104, (01)00884838054219(21)34, (01)00884838054219(21)45, (01)00884838054219(21)59, (01)00884838054219(21)79, (01)00884838054219(21)24, (01)00884838054219(21)96, (01)00884838054219(21)70, (01)00884838054219(21)39, (01)00884838054219(21)66, (01)00884838054219(21)82, (01)00884838054219(21)75, (01)00884838054219(21)40, (01)00884838054219(21)33, (01)00884838054219(21)23, (01)00884838054219(21)25, (01)00884838054219(21)85, (01)00884838054219(21)37, (01)00884838054219(21)44, (01)00884838054219(21)58, (01)00884838054219(21)38, (01)00884838054219(21)61, (01)00884838054219(21)98, (01)00884838054219(21)53, (01)00884838054219(21)89, (01)00884838054219(21)35, (01)00884838054219(21)48; 19. Allura Xper FD20/15; Model: 722058; UDI: (01)00884838059115(21)100, (01)00884838059115(21)239, (01)00884838059115(21)305, (01)00884838059115(21)259, (01)00884838059115(21)203, (01)00884838059115(21)373, (01)00884838059115(21)111, (01)00884838059115(21)38, (01)00884838059115(21)23, (01)00884838059115(21)290, (01)00884838059115(21)124, (01)00884838059115(21)274, (01)00884838059115(21)366, (01)00884838059115(21)340, (01)00884838059115(21)162, (01)00884838059115(21)186, (01)00884838059115(21)4, (01)00884838059115(21)405, (01)00884838059115(21)196, (01)00884838059115(21)156, (01)00884838059115(21)285, (01)00884838059115(21)277, (01)00884838059115(21)65, (01)00884838059115(21)168, (01)00884838059115(21)56, (01)00884838059115(21)178, (01)00884838059115(21)138, (01)00884838059115(21)212, (01)00884838059115(21)249, (01)00884838059115(21)257, (01)00884838059115(21)337, (01)00884838059115(21)265, (01)00884838059115(21)109, (01)00884838059115(21)134, (01)00884838059115(21)71, (01)00884838059115(21)238, (01)00884838059115(21)190, (01)00884838059115(21)219, (01)00884838059115(21)197, (01)00884838059115(21)325, (01)00884838059115(21)24, (01)00884838059115(21)123, (01)00884838059115(21)319, (01)00884838059115(21)378, (01)00884838059115(21)61, (01)00884838059115(21)205, (01)00884838059115(21)149, (01)00884838059115(21)264, (01)00884838059115(21)167, (01)00884838059115(21)365, (01)00884838059115(21)199, (01)00884838059115(21)278, (01)00884838059115(21)215, (01)00884838059115(21)288, (01)00884838059115(21)254, (01)00884838059115(21)94, (01)00884838059115(21)304, (01)00884838059115(21)279, (01)0088483805 9115(21)171, (01)00884838059115(21)82, (01)00884838059115(21)85, (01)00884838059115(21)202, (01)00884838059115(21)99, (01)00884838059115(21)182, (01)00884838059115(21)22, (01)00884838059115(21)200, (01)00884838059115(21)129, (01)00884838059115(21)59, (01)00884838059115(21)172, (01)00884838059115(21)110, (01)00884838059115(21)399, (01)00884838059115(21)72, (01)00884838059115(21)332, (01)00884838059115(21)92, (01)00884838059115(21)142, (01)00884838059115(21)67, (01)00884838059115(21)106, (01)00884838059115(21)335, (01)00884838059115(21)415, (01)00884838059115(21)11, (01)00884838059115(21)114, (01)00884838059115(21)151, (01)00884838059115(21)232, (01)00884838059115(21)395, (01)00884838059115(21)292, (01)00884838059115(21)380, (01)00884838059115(21)183, (01)00884838059115(21)349, (01)00884838059115(21)261, (01)00884838059115(21)15, (01)00884838059115(21)375, (01)00884838059115(21)161, (01)00884838059115(21)78, (01)00884838059115(21)368, (01)00884838059115(21)9, (01)00884838059115(21)372, (01)00884838059115(21)252, (01)00884838059115(21)320, (01)00884838059115(21)213, (01)00884838059115(21)293, (01)00884838059115(21)389, (01)00884838059115(21)169, (01)00884838059115(21)97, (01)00884838059115(21)336, (01)00884838059115(21)25, (01)00884838059115(21)143, (01)00884838059115(21)133, (01)00884838059115(21)192, (01)00884838059115(21)49, (01)00884838059115(21)412, (01)00884838059115(21)201, (01)00884838059115(21)101, (01)00884838059115(21)89, (01)00884838059115(21)66, (01)00884838059115(21)163, (01)00884838059115(21)170, (01)00884838059115(21)77, (01)00884838059115(21)273, (01)00884838059115(21)35, (01)00884838059115(21)222, (01)00884838059115(21)229, (01)00884838059115(21)248, (01)00884838059115(21)334, (01)00884838059115(21)384, (01)00884838059115(21)40, (01)00884838059115(21)268, (01)00884838059115(21)240, (01)00884838059115(21)258, (01)00884838059115(21)289, (01)00884838059115(21)269, (01)00884838059115(21)226, (01)00884838059115(21)244, (01)00884838059115(21)141, (01)00884838059115(21)391, (01)00884838059115(21)241, (01)00884838059115(21)164, (01)00884838059115(21)381, (01)00884838059115(21)281, (01)00884838059115(21)154, (01)00884838059115(21)246, (01)00884838059115(21)127, (01)00884838059115(21)315, (01)00884838059115(21)256, (01)00884838059115(21)93, (01)00884838059115(21)233, (01)00884838059115(21)348, (01)00884838059115(21)204, (01)00884838059115(21)396, (01)00884838059115(21)7, (01)00884838059115(21)185, (01)00884838059115(21)95, (01)00884838059115(21)131, (01)00884838059115(21)377, (01)00884838059115(21)60, (01)00884838059115(21)68, (01)00884838059115(21)206, (01)00884838059115(21)150, (01)00884838059115(21)333, (01)00884838059115(21)84, (01)00884838059115(21)398, (01)00884838059115(21)313, (01)00884838059115(21)3, (01)00884838059115(21)39, (01)00884838059115(21)344, (01)00884838059115(21)376, (01)00884838059115(21)382, (01)00884838059115(21)408, (01)00884838059115(21)360, (01)00884838059115(21)370, (01)00884838059115(21)400, (01)00884838059115(21)387, (01)00884838059115(21)356, (01)00884838059115(21)419, (01)00884838059115(21)394, (01)00884838059115(21)407, (01)00884838059115(21)413, (01)00884838059115(21)392, (01)00884838059115(21)411, (01)00884838059115(21)358, (01)00884838059115(21)409, (01)00884838059115(21)385, (01)00884838059115(21)416, (01)00884838059115(21)367, (01)00884838059115(21)331, (01)00884838059115(21)379, (01)00884838059115(21)418, (01)00884838059115(21)421, (01)00884838059115(21)369, (01)00884838059115(21)420, (01)00884838059115(21)397, (01)00884838059115(21)357, (01)00884838059115(21)393, (01)00884838059115(21)388, (01)00884838059115(21)108, (01)00884838059115(21)211, (01)00884838059115(21)126, (01)00884838059115(21)125, (01)00884838059115(21)301, (01)00884838059115(21)12, (01)00884838059115(21)30, (01)00884838059115(21)355, (01)00884838059115(21)354, (01)00884838059115(21)159, (01)00884838059115(21)139, (01)00884838059115(21)128, (01)00884838059115(21)81, (01)00884838059115(21)58, (01)00884838059115(21)96, (01)00884838059115(21)343, (01)00884838059115(21)177, (01)00884838059115(21)115, (01)00884838059115(21)19, (01)00884838059115(21)18, (01)00884838059115(21)311, (01)00884838059115(21)386, (01)00884838059115(21)291, (01)00884838059115(21)327, (01)00884838059115(21)220, (01)00884838059115(21)214, (01)00884838059115(21)145, (01)00884838059115(21)223, (01)00884838059115(21)137, (01)00884838059115(21)136, (01)00884838059115(21)119, (01)00884838059115(21)103, (01)00884838059115(21)404, (01)00884838059115(21)27, (01)00884838059115(21)32, (01)00884838059115(21)350, (01)00884838059115(21)422, (01)00884838059115(21)423, (01)00884838059115(21)347, (01)00884838059115(21)73, (01)00884838059115(21)43, (01)00884838059115(21)55, (01)00884838059115(21)194, (01)00884838059115(21)189, (01)00884838059115(21)237, (01)00884838059115(21)230, (01)00884838059115(21)221, (01)00884838059115(21)247, (01)00884838059115(21)116, (01)00884838059115(21)242, (01)00884838059115(21)29, (01)00884838059115(21)37, (01)00884838059115(21)276, (01)00884838059115(21)345, (01)00884838059115(21)166, (01)00884838059115(21)179, (01)00884838059115(21)53, (01)00884838059115(21)87, (01)00884838059115(21)303, (01)00884838059115(21)90, (01)00884838059115(21)112, (01)00884838059115(21)245, (01)00884838059115(21)148, (01)00884838059115(21)41, (01)00884838059115(21)234, (01)00884838059115(21)208, (01)00884838059115(21)117, (01)00884838059115(21)193, (01)00884838059115(21)76, (01)00884838059115(21)236, (01)00884838059115(21)266, (01)00884838059115(21)130, (01)00884838059115(21)235, (01)00884838059115(21)251, (01)00884838059115(21)86, (01)00884838059115(21)31, (01)00884838059115(21)195, (01)00884838059115(21)144, (01)00884838059115(21)330, (01)00884838059115(21)63, (01)00884838059115(21)295, (01)00884838059115(21)70, (01)00884838059115(21)187, (01)00884838059115(21)79, (01)00884838059115(21)10, (01)00884838059115(21)33, (01)00884838059115(21)75, (01)00884838059115(21)361, (01)00884838059115(21)153, (01)00884838059115(21)284, (01)00884838059115(21)102, (01)00884838059115(21)21, (01)00884838059115(21)64, (01)00884838059115(21)45, (01)00884838059115(21)36, (01)00884838059115(21)181, (01)00884838059115(21)351, (01)00884838059115(21)272, (01)00884838059115(21)210, (01)00884838059115(21)243, (01)00884838059115(21)20, (01)00884838059115(21)98, (01)00884838059115(21)34, (01)00884838059115(21)16, (01)00884838059115(21)218; 20. Allura Xper FD20/15 OR Table; Model: 722059; UDI: (01)00884838059122(21)33, (01)00884838059122(21)7, (01)00884838059122(21)35, (01)00884838059122(21)40, (01)00884838059122(21)38, (01)00884838059122(21)41, (01)00884838059122(21)37, (01)00884838059122(21)2; 21. Allura Xper FD20/20; Model: 722038; UDI: (01)00884838054226(21)71, (01)00884838054226(21)115, (01)00884838054226(21)42, (01)00884838054226(21)108, (01)00884838054226(21)173, (01)00884838054226(21)119, (01)00884838054226(21)60, (01)00884838054226(21)38, (01)00884838054226(21)37, (01)00884838054226(21)99, (01)00884838054226(21)130, (01)00884838054226(21)48, (01)00884838054226(21)157, (01)00884838054226(21)131, (01)00884838054226(21)41, (01)00884838054226(21)141, (01)00884838054226(21)137, (01)00884838054226(21)49, (01)00884838054226(21)63, (01)00884838054226(21)35, (01)00884838054226(21)167, (01)00884838054226(21)55, (01)00884838054226(21)70, (01)00884838054226(21)39, (01)00884838054226(21)62, (01)00884838054226(21)46, (01)00884838054226(21)118, (01)00884838054226(21)67, (01)00884838054226(21)78, (01)00884838054226(21)120, (01)00884838054226(21)7, (01)00884838054226(21)106, (01)00884838054226(21)102, (01)00884838054226(21)169, (01)00884838054226(21)11, (01)00884838054226(21)89, (01)00884838054226(21)117, (01)00884838054226(21)40, (01)00884838054226(21)105, (01)00884838054226(21)113, (01)00884838054226(21)110, (01)00884838054226(21)5, (01)00884838054226(21)134, (01)00884838054226(21)88, (01)00884838054226(21)64, (01)00884838054226(21)112, (01)00884838054226(21)143, (01)00884838054226(21)94, (01)00884838054226(21)109, (01)00884838054226(21)73, (01)00884838054226(21)166, (01)00884838054226(21)147, (01)00884838054226(21)31, (01)00884838054226(21)3, (01)00884838054226(21)127, (01)00884838054226(21)92, (01)00884838054226(21)135, (01)00884838054226(21)32, (01)00884838054226(21)69, (01)00884838054226(21)121, (01)00884838054226(21)123, (01)00884838054226(21)98, (01)00884838054226(21)129, (01)00884838054226(21)79, (01)00884838054226(21)14, (01)00884838054226(21)148, (01)00884838054226(21)153, (01)00884838054226(21)122, (01)00884838054226(21)164, (01)00884838054226(21)111, (01)00884838054226(21)160, (01)00884838054226(21)172, (01)00884838054226(21)171, (01)00884838054226(21)159, (01)00884838054226(21)155, (01)00884838054226(21)144, (01)00884838054226(21)163, (01)00884838054226(21)152, (01)00884838054226(21)168, (01)00884838054226(21)161, (01)00884838054226(21)158, (01)00884838054226(21)156, (01)00884838054226(21)138, (01)00884838054226(21)162, (01)00884838054226(21)132, (01)00884838054226(21)95, (01)00884838054226(21)116, (01)00884838054226(21)45, (01)00884838054226(21)9, (01)00884838054226(21)150, (01)00884838054226(21)146, (01)00884838054226(21)90, (01)00884838054226(21)27, (01)00884838054226(21)91, (01)00884838054226(21)154, (01)00884838054226(21)104, (01)00884838054226(21)124, (01)00884838054226(21)30, (01)00884838054226(21)136, (01)00884838054226(21)93, (01)00884838054226(21)66, (01)00884838054226(21)140, (01)00884838054226(21)75, (01)00884838054226(21)50, (01)00884838054226(21)68, (01)00884838054226(21)58, (01)00884838054226(21)54, (01)00884838054226(21)47, (01)00884838054226(21)36, (01)00884838054226(21)170, (01)00884838054226(21)29; 22. Allura Xper FD20/20 OR Table; Model: 722039; UDI: (01)00884838054271(21)4, (01)00884838054271(21)2, (01)00884838054271(21)5, (01)00884838054271(21)8, (01)00884838054271(21)6;", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2259-2026%22", "url": "https://recallledger.net/recalls/device-z-2259-2026-allura-system-system-code-description-model-numbers-allura-xper-fd/"}, {"id": "fda-device-z-2258-2026", "source": "FDA", "category": "device", "recall_number": "Z-2258-2026", "title": "Azurion system recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)", "product": "Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063, 722221), Azurion 3 M15 (722064, 722222), Azurion 5 M12 (722227), Azurion 5 M20 (722228), Azurion 7 B12 (722067, 722225), Azurion 7 B20 (722068, 722226), Azurion 7 M12 (722078, 722223), Azurion 7 M20 (722079, 722224).", "reason": "It was identified that HDDs used in the PCs of Azurion and Allura systems may show a decrease in performance as they age, particularly beyond six years of service. Issues with an HDD may, depending on the specific system PC in which the affected HDD is installed, result in loss of imaging functionality. Additionally, in Allura systems, this may lead to loss of motorized movement, or loss of data. In some cases, a system restart may temporarily restore functionality.", "hazard_level": "Class II", "company": "PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.", "company_location": "Best, Netherlands", "date": "2026-04-30", "report_date": "2026-06-03", "status": "Ongoing", "distribution": "Worldwide distribution - US Nationwide and the countries of Canada, Afghanistan, Albania, Algeria, Argentina, Australia, Austria, Bahrain, Bangladesh, Belarus, Belgium, Bolivia, Bosnia and Herzegovina, Brazil, Brunei Darussal, Bulgaria, Chile, China, Colombia, Costa Rica, Croatia, Cuba, Cyprus, Czech Republic, Denmark, Dominican Republic, Ecuador, Egypt, Estonia, Fiji, Finland, France, French Polynesia, Georgia, Germany, Greece, Guinea, Honduras, Hong Kong, Hungary, India, Indonesia, Iran, Iraq, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan, Kenya, Korea, South, Kosovo, Kuwait, Kyrgyzstan, Lao, Latvia, Lebanon, Libya, Lithuania, Macedonia, Malaysia, Maldives, Malta, Martinique, Mauritius, Mexico, Moldova, Mongolia, Morocco, Myanmar, Nepal, Netherlands, New Caledonia, New Zealand, Nicaragua, Nigeria, Norway, Oman, Pakistan, Palestine, Panama, Papua New Guinea, Paraguay, Peru, Philippines, Poland, Portugal, Qatar, R¿union, Romania, Russian Fed., Russian Federation, Saudi Arabia, Serbia, Singapore, Slovakia, Slovenia, South Africa, South Korea, Spain, Sri Lanka, Sudan, Sweden, Switzerland, Syrian Arab Republic, Taiwan, Tanzania, Thailand, Trinidad and Tobago, Tunisia, Turkey, Turkmenistan, Ukraine, United Arab Emirates, United Kingdom, Uruguay, Uzbekistan, Vietnam, Yemen.", "states": ["GA"], "nationwide": true, "quantity": "3069 units (872 US, 2224 OUS)", "codes": "1. Azurion 3 M12; Model: 722063; UDI: (01)00884838085275(21)122, (01)00884838085275(21)64, (01)00884838085275(21)56, (01)00884838085275(21)131, (01)00884838085275(21)84, (01)00884838085275(21)132, (01)00884838085275(21)98, (01)00884838085275(21)108, (01)00884838085275(21)77, (01)00884838085275(21)82, (01)00884838085275(21)47, (01)00884838085275(21)80, (01)00884838085275(21)146, (01)00884838085275(21)102, (01)00884838085275(21)117, (01)00884838085275(21)2, (01)00884838085275(21)149, (01)00884838085275(21)99, (01)00884838085275(21)44, (01)00884838085275(21)3, (01)00884838085275(21)28, (01)00884838085275(21)144, (01)00884838085275(21)62, (01)00884838085275(21)119, (01)00884838085275(21)61, (01)00884838085275(21)22, (01)00884838085275(21)29, (01)00884838085275(21)40, (01)00884838085275(21)70, (01)00884838085275(21)30, (01)00884838085275(21)25, (01)00884838085275(21)19, (01)00884838085275(21)120, (01)00884838085275(21)121, (01)00884838085275(21)110, (01)00884838085275(21)16, (01)00884838085275(21)14, (01)00884838085275(21)17, (01)00884838085275(21)53, (01)00884838085275(21)103, (01)00884838085275(21)101, (01)00884838085275(21)143, (01)00884838085275(21)41, (01)00884838085275(21)104, (01)00884838085275(21)116, (01)00884838085275(21)151, (01)00884838085275(21)93, (01)00884838085275(21)141, (01)00884838085275(21)115, (01)00884838085275(21)73, (01)00884838085275(21)150, (01)00884838085275(21)128, (01)00884838085275(21)105, (01)00884838085275(21)4, (01)00884838085275(21)50, (01)00884838085275(21)129, (01)00884838085275(21)72, (01)00884838085275(21)38, (01)00884838085275(21)21, (01)00884838085275(21)78, (01)00884838085275(21)23, (01)00884838085275(21)76, (01)00884838085275(21)63, (01)00884838085275(21)69, (01)00884838085275(21)59, (01)00884838085275(21)51, (01)00884838085275(21)92, (01)00884838085275(21)139, (01)00884838085275(21)130, (01)00884838085275(21)75, (01)00884838085275(21)24, (01)00884838085275(21)94, (01)00884838085275(21)100, (01)00884838085275(21)54, (01)00884838085275(21)46, (01)00884838085275(21)26, (01)00884838085275(21)71, (01)00884838085275(21)106, (01)00884838085275(21)83, (01)00884838085275(21)37, (01)00884838085275(21)36, (01)00884838085275(21)27, (01)00884838085275(21)15, (01)00884838085275(21)135, (01)00884838085275(21)123, (01)00884838085275(21)107, (01)00884838085275(21)85, (01)00884838085275(21)89, (01)00884838085275(21)88, (01)00884838085275(21)86, (01)00884838085275(21)90, (01)00884838085275(21)91, (01)00884838085275(21)79, (01)00884838085275(21)133, (01)00884838085275(21)81, (01)00884838085275(21)140, (01)00884838085275(21)52, (01)00884838085275(21)48, (01)00884838085275(21)55, (01)00884838085275(21)113; 2. Azurion 3 M12; Model: 722221; UDI: (01)00884838099203(21)3, (01)00884838099203(21)7, (01)00884838099203(21)6, (01)00884838099203(21)9, (01)00884838099203(21)4, (01)00884838099203(21)23, (01)00884838099203(21)26, (01)00884838099203(21)15, (01)00884838099203(21)2, (01)00884838099203(21)5, (01)00884838099203(21)1, (01)00884838099203(21)11; 3. Azurion 3 M15; Model: 722064; UDI: (01)00884838085282(21)209, (01)00884838085282(21)238, (01)00884838085282(21)201, (01)00884838085282(21)258, (01)00884838085282(21)260, (01)00884838085282(21)261, (01)00884838085282(21)314, (01)00884838085282(21)229, (01)00884838085282(21)291, (01)00884838085282(21)270, (01)00884838085282(21)267, (01)00884838085282(21)218, (01)00884838085282(21)61, (01)00884838085282(21)162, (01)00884838085282(21)161, (01)00884838085282(21)297, (01)00884838085282(21)169, (01)00884838085282(21)131, (01)00884838085282(21)190, (01)00884838085282(21)268, (01)00884838085282(21)220, (01)00884838085282(21)173, (01)00884838085282(21)256, (01)00884838085282(21)290, (01)00884838085282(21)89, (01)00884838085282(21)303, (01)00884838085282(21)157, (01)00884838085282(21)130, (01)00884838085282(21)263, (01)00884838085282(21)60, (01)00884838085282(21)264, (01)00884838085282(21)253, (01)00884838085282(21)254, (01)00884838085282(21)257, (01)00884838085282(21)280, (01)00884838085282(21)9, (01)00884838085282(21)277, (01)00884838085282(21)102, (01)00884838085282(21)137, (01)00884838085282(21)84, (01)00884838085282(21)78, (01)00884838085282(21)49, (01)00884838085282(21)193, (01)00884838085282(21)271, (01)00884838085282(21)185, (01)00884838085282(21)214, (01)00884838085282(21)212, (01)00884838085282(21)266, (01)00884838085282(21)213, (01)00884838085282(21)180, (01)00884838085282(21)250, (01)00884838085282(21)186, (01)00884838085282(21)246, (01)00884838085282(21)282, (01)00884838085282(21)354, (01)00884838085282(21)274, (01)00884838085282(21)127, (01)00884838085282(21)106, (01)00884838085282(21)276, (01)00884838085282(21)58, (01)00884838085282(21)81, (01)00884838085282(21)200, (01)00884838085282(21)179, (01)00884838085282(21)156, (01)00884838085282(21)149, (01)00884838085282(21)288, (01)00884838085282(21)287, (01)00884838085282(21)231, (01)00884838085282(21)150, (01)00884838085282(21)230, (01)00884838085282(21)233, (01)00884838085282(21)197, (01)00884838085282(21)44, (01)00884838085282(21)289, (01)00884838085282(21)176, (01)00884838085282(21)184, (01)00884838085282(21)6, (01)00884838085282(21)10, (01)00884838085282(21)82, (01)00884838085282(21)35, (01)00884838085282(21)69, (01)00884838085282(21)39, (01)00884838085282(21)45, (01)00884838085282(21)66, (01)00884838085282(21)40, (01)00884838085282(21)55, (01)00884838085282(21)36, (01)00884838085282(21)94, (01)00884838085282(21)104, (01)00884838085282(21)132, (01)00884838085282(21)67, (01)00884838085282(21)183, (01)00884838085282(21)70, (01)00884838085282(21)50, (01)00884838085282(21)138, (01)00884838085282(21)293, (01)00884838085282(21)292, (01)00884838085282(21)321, (01)00884838085282(21)237, (01)00884838085282(21)5, (01)00884838085282(21)208, (01)00884838085282(21)342, (01)00884838085282(21)57, (01)00884838085282(21)222, (01)00884838085282(21)391, (01)00884838085282(21)98, (01)00884838085282(21)320, (01)00884838085282(21)79, (01)00884838085282(21)65, (01)00884838085282(21)87, (01)00884838085282(21)109, (01)00884838085282(21)75, (01)00884838085282(21)46, (01)00884838085282(21)101, (01)00884838085282(21)311, (01)00884838085282(21)121, (01)00884838085282(21)68, (01)00884838085282(21)228, (01)00884838085282(21)252, (01)00884838085282(21)91, (01)00884838085282(21)73, (01)00884838085282(21)74, (01)00884838085282(21)124, (01)00884838085282(21)191, (01)00884838085282(21)122, (01)00884838085282(21)119, (01)00884838085282(21)309, (01)00884838085282(21)251, (01)00884838085282(21)387, (01)00884838085282(21)269, (01)00884838085282(21)11, (01)00884838085282(21)147, (01)00884838085282(21)262, (01)00884838085282(21)133, (01)00884838085282(21)337, (01)00884838085282(21)275, (01)00884838085282(21)412, (01)00884838085282(21)405, (01)00884838085282(21)396, (01)00884838085282(21)247, (01)00884838085282(21)406, (01)00884838085282(21)340, (01)00884838085282(21)393, (01)00884838085282(21)322, (01)00884838085282(21)385, (01)00884838085282(21)333, (01)00884838085282(21)236, (01)00884838085282(21)234, (01)00884838085282(21)413, (01)00884838085282(21)7, (01)00884838085282(21)308, (01)00884838085282(21)225, (01)00884838085282(21)344, (01)00884838085282(21)389, (01)00884838085282(21)265, (01)00884838085282(21)235, (01)00884838085282(21)120, (01)00884838085282(21)341, (01)00884838085282(21)100, (01)00884838085282(21)51, (01)00884838085282(21)118, (01)00884838085282(21)62, (01)00884838085282(21)123, (01)00884838085282(21)177, (01)00884838085282(21)47, (01)00884838085282(21)272, (01)00884838085282(21)110, (01)00884838085282(21)59, (01)00884838085282(21)167, (01)00884838085282(21)174, (01)00884838085282(21)165, (01)00884838085282(21)41, (01)00884838085282(21)168, (01)00884838085282(21)148, (01)00884838085282(21)182, (01)00884838085282(21)112, (01)00884838085282(21)302, (01)00884838085282(21)86, (01)00884838085282(21)317, (01)00884838085282(21)198, (01)00884838085282(21)206, (01)00884838085282(21)136, (01)00884838085282(21)312, (01)00884838085282(21)143, (01)00884838085282(21)403, (01)00884838085282(21)386, (01)00884838085282(21)226, (01)00884838085282(21)43, (01)00884838085282(21)80, (01)00884838085282(21)12, (01)00884838085282(21)285, (01)00884838085282(21)338, (01)00884838085282(21)215, (01)00884838085282(21)164, (01)00884838085282(21)114, (01)00884838085282(21)327, (01)00884838085282(21)144, (01)00884838085282(21)227, (01)00884838085282(21)295, (01)00884838085282(21)294, (01)00884838085282(21)319, (01)00884838085282(21)241, (01)00884838085282(21)126, (01)00884838085282(21)92, (01)00884838085282(21)284, (01)00884838085282(21)175, (01)00884838085282(21)199, (01)00884838085282(21)188, (01)00884838085282(21)296, (01)00884838085282(21)172, (01)00884838085282(21)283, (01)00884838085282(21)306, (01)00884838085282(21)210, (01)00884838085282(21)134, (01)00884838085282(21)255, (01)00884838085282(21)207, (01)00884838085282(21)192, (01)00884838085282(21)116, (01)00884838085282(21)221, (01)00884838085282(21)189, (01)00884838085282(21)117, (01)00884838085282(21)313, (01)00884838085282(21)187, (01)00884838085282(21)96, (01)00884838085282(21)135, (01)00884838085282(21)108, (01)00884838085282(21)37, (01)00884838085282(21)72; 4. Azurion 3 M15; Model: 722222; UDI: (01)00884838099210(21)12, (01)00884838099210(21)15, (01)00884838099210(21)19, (01)00884838099210(21)23, (01)00884838099210(21)17, (01)00884838099210(21)35, (01)00884838099210(21)21, (01)00884838099210(21)18, (01)00884838099210(21)24, (01)00884838099210(21)9, (01)00884838099210(21)5, (01)00884838099210(21)14, (01)00884838099210(21)10, (01)00884838099210(21)13; 5. Azurion 5 M12; Model: 722227; UDI: (01)00884838099227(21)23, (01)00884838099227(21)19, (01)00884838099227(21)5, (01)00884838099227(21)6, (01)00884838099227(21)7, (01)00884838099227(21)36, (01)00884838099227(21)18, (01)00884838099227(21)15, (01)00884838099227(21)14, (01)00884838099227(21)17, (01)00884838099227(21)2, (01)00884838099227(21)1, (01)00884838099227(21)12, (01)00884838099227(21)3, (01)00884838099227(21)11, (01)00884838099227(21)13, (01)00884838099227(21)4; 6. Azurion 5 M20; Model: 722228; UDI: (01)00884838099234(21)10, (01)00884838099234(21)18, (01)00884838099234(21)23, (01)00884838099234(21)3, (01)00884838099234(21)16, (01)00884838099234(21)22, (01)00884838099234(21)4, (01)00884838099234(21)12, (01)00884838099234(21)14, (01)00884838099234(21)7, (01)00884838099234(21)5; 7. Azurion 7 B12; Model: 722067; UDI: (01)00884838085350(21)42, (01)00884838085350(21)172, (01)00884838085350(21)173, (01)00884838085350(21)109, (01)00884838085350(21)250, (01)00884838085350(21)103, (01)00884838085350(21)192, (01)00884838085350(21)92, (01)00884838085350(21)114, (01)00884838085350(21)225, (01)00884838085350(21)69, (01)00884838085350(21)214, (01)00884838085350(21)41, (01)00884838085350(21)221, (01)00884838085350(21)98, (01)00884838085350(21)81, (01)00884838085350(21)123, (01)00884838085350(21)46, (01)00884838085350(21)115, (01)00884838085350(21)150, (01)00884838085350(21)163, (01)00884838085350(21)131, (01)00884838085350(21)71, (01)00884838085350(21)75, (01)00884838085350(21)147, (01)00884838085350(21)132, (01)00884838085350(21)244, (01)00884838085350(21)104, (01)00884838085350(21)208, (01)00884838085350(21)36, (01)00884838085350(21)234, (01)00884838085350(21)141, (01)00884838085350(21)70, (01)00884838085350(21)26, (01)00884838085350(21)148, (01)00884838085350(21)133, (01)00884838085350(21)57, (01)00884838085350(21)128, (01)00884838085350(21)188, (01)00884838085350(21)151, (01)00884838085350(21)68, (01)00884838085350(21)233, (01)00884838085350(21)111, (01)00884838085350(21)255, (01)00884838085350(21)43, (01)00884838085350(21)33, (01)00884838085350(21)22, (01)00884838085350(21)146, (01)00884838085350(21)270, (01)00884838085350(21)238, (01)00884838085350(21)187, (01)00884838085350(21)74, (01)00884838085350(21)154, (01)00884838085350(21)157, (01)00884838085350(21)251, (01)00884838085350(21)237, (01)00884838085350(21)222, (01)00884838085350(21)262, (01)00884838085350(21)29, (01)00884838085350(21)59, (01)00884838085350(21)209, (01)00884838085350(21)260, (01)00884838085350(21)191, (01)00884838085350(21)95, (01)00884838085350(21)218, (01)00884838085350(21)231, (01)00884838085350(21)169, (01)00884838085350(21)127, (01)00884838085350(21)211, (01)00884838085350(21)212, (01)00884838085350(21)210, (01)00884838085350(21)213, (01)00884838085350(21)30, (01)00884838085350(21)206, (01)00884838085350(21)23, (01)00884838085350(21)203, (01)00884838085350(21)138, (01)00884838085350(21)34, (01)00884838085350(21)53, (01)00884838085350(21)113, (01)00884838085350(21)254, (01)00884838085350(21)140, (01)00884838085350(21)143, (01)00884838085350(21)144, (01)00884838085350(21)142, (01)00884838085350(21)266, (01)00884838085350(21)60, (01)00884838085350(21)97, (01)00884838085350(21)45, (01)00884838085350(21)107, (01)00884838085350(21)112, (01)00884838085350(21)101, (01)00884838085350(21)100, (01)00884838085350(21)168, (01)00884838085350(21)235, (01)00884838085350(21)272, (01)00884838085350(21)58, (01)00884838085350(21)47, (01)00884838085350(21)176, (01)00884838085350(21)64, (01)00884838085350(21)156, (01)00884838085350(21)52, (01)00884838085350(21)232, (01)00884838085350(21)55, (01)00884838085350(21)54, (01)00884838085350(21)165, (01)00884838085350(21)25, (01)00884838085350(21)35, (01)00884838085350(21)202, (01)00884838085350(21)149, (01)00884838085350(21)243, (01)00884838085350(21)32, (01)00884838085350(21)207, (01)00884838085350(21)76, (01)00884838085350(21)108, (01)00884838085350(21)226, (01)00884838085350(21)48, (01)00884838085350(21)264, (01)00884838085350(21)102, (01)00884838085350(21)84, (01)00884838085350(21)105, (01)00884838085350(21)99, (01)00884838085350(21)21, (01)00884838085350(21)159, (01)00884838085350(21)49, (01)00884838085350(21)185, (01)00884838085350(21)51, (01)00884838085350(21)239, (01)00884838085350(21)40, (01)00884838085350(21)94, (01)00884838085350(21)63, (01)00884838085350(21)96, (01)00884838085350(21)129, (01)00884838085350(21)245, (01)00884838085350(21)186, (01)00884838085350(21)130, (01)00884838085350(21)252, (01)00884838085350(21)161, (01)00884838085350(21)120, (01)00884838085350(21)170, (01)00884838085350(21)197, (01)00884838085350(21)195, (01)00884838085350(21)196, (01)00884838085350(21)171, (01)00884838085350(21)193, (01)00884838085350(21)80, (01)00884838085350(21)28, (01)00884838085350(21)229, (01)00884838085350(21)145, (01)00884838085350(21)79, (01)00884838085350(21)93, (01)00884838085350(21)137, (01)00884838085350(21)50, (01)00884838085350(21)44, (01)00884838085350(21)38, (01)00884838085350(21)175, (01)00884838085350(21)227, (01)00884838085350(21)167, (01)00884838085350(21)78, (01)00884838085350(21)86, (01)00884838085350(21)91, (01)00884838085350(21)189, (01)00884838085350(21)198, (01)00884838085350(21)37, (01)00884838085350(21)72, (01)00884838085350(21)199, (01)00884838085350(21)88, (01)00884838085350(21)27, (01)00884838085350(21)121, (01)00884838085350(21)179, (01)00884838085350(21)183, (01)00884838085350(21)118, (01)00884838085350(21)117, (01)00884838085350(21)85, (01)00884838085350(21)90, (01)00884838085350(21)89, (01)00884838085350(21)119, (01)00884838085350(21)87, (01)00884838085350(21)31, (01)00884838085350(21)110, (01)00884838085350(21)178, (01)00884838085350(21)73, (01)00884838085350(21)194, (01)00884838085350(21)39, (01)00884838085350(21)56, (01)00884838085350(21)139, (01)00884838085350(21)61, 8. Azurion 7 B12; Model: 722225; UDI: (01)00884838099265(21)29, (01)00884838099265(21)8, (01)00884838099265(21)38, (01)00884838099265(21)14, (01)00884838099265(21)243, (01)00884838099265(21)4, (01)00884838099265(21)30, (01)00884838099265(21)7, (01)00884838099265(21)17, (01)00884838099265(21)31, (01)00884838099265(21)32, (01)00884838099265(21)18, (01)00884838099265(21)19, (01)00884838099265(21)10, (01)00884838099265(21)35, (01)00884838099265(21)36, (01)00884838099265(21)15, (01)00884838099265(21)11, (01)00884838099265(21)21, (01)00884838099265(21)16, (01)00884838099265(21)27, (01)00884838099265(21)12, (01)00884838099265(21)9; 9. Azurion 7 B20; Model: 722068; UDI: (01)00884838085367(21)467, (01)00884838085367(21)178, (01)00884838085367(21)335, (01)00884838085367(21)147, (01)00884838085367(21)205, (01)00884838085367(21)170, (01)00884838085367(21)494, (01)00884838085367(21)95, (01)00884838085367(21)440, (01)00884838085367(21)247, (01)00884838085367(21)225, (01)00884838085367(21)64, (01)00884838085367(21)149, (01)00884838085367(21)153, (01)00884838085367(21)324, (01)00884838085367(21)323, (01)00884838085367(21)320, (01)00884838085367(21)85, (01)00884838085367(21)89, (01)00884838085367(21)109, (01)00884838085367(21)407, (01)00884838085367(21)239, (01)00884838085367(21)505, (01)00884838085367(21)271, (01)00884838085367(21)443, (01)00884838085367(21)104, (01)00884838085367(21)370, (01)00884838085367(21)322, (01)00884838085367(21)136, (01)00884838085367(21)373, (01)00884838085367(21)442, (01)00884838085367(21)308, (01)00884838085367(21)354, (01)00884838085367(21)75, (01)00884838085367(21)279, (01)00884838085367(21)196, (01)00884838085367(21)510, (01)00884838085367(21)110, (01)00884838085367(21)446, (01)00884838085367(21)78, (01)00884838085367(21)330, (01)00884838085367(21)73, (01)00884838085367(21)288, (01)00884838085367(21)285, (01)00884838085367(21)295, (01)00884838085367(21)528, (01)00884838085367(21)329, (01)00884838085367(21)184, (01)00884838085367(21)350, (01)00884838085367(21)304, (01)00884838085367(21)470, (01)00884838085367(21)457, (01)00884838085367(21)472, (01)00884838085367(21)319, (01)00884838085367(21)520, (01)00884838085367(21)490, (01)00884838085367(21)243, (01)00884838085367(21)103, (01)00884838085367(21)261, (01)00884838085367(21)262, (01)00884838085367(21)277, (01)00884838085367(21)150, (01)00884838085367(21)172, (01)00884838085367(21)117, (01)00884838085367(21)130, (01)00884838085367(21)356, (01)00884838085367(21)143, (01)00884838085367(21)146, (01)00884838085367(21)84, (01)00884838085367(21)251, (01)00884838085367(21)469, (01)00884838085367(21)431, (01)00884838085367(21)361, (01)00884838085367(21)76, (01)00884838085367(21)374, (01)00884838085367(21)270, (01)00884838085367(21)114, (01)00884838085367(21)477, (01)00884838085367(21)232, (01)00884838085367(21)137, (01)00884838085367(21)282, (01)00884838085367(21)487, (01)00884838085367(21)413, (01)00884838085367(21)337, (01)00884838085367(21)101, (01)00884838085367(21)213, (01)00884838085367(21)82, (01)00884838085367(21)265, (01)00884838085367(21)275, (01)00884838085367(21)459, (01)00884838085367(21)276, (01)00884838085367(21)62, (01)00884838085367(21)506, (01)00884838085367(21)473, (01)00884838085367(21)417, (01)00884838085367(21)302, (01)00884838085367(21)314, (01)00884838085367(21)88, (01)00884838085367(21)468, (01)00884838085367(21)126, (01)00884838085367(21)211, (01)00884838085367(21)422, (01)00884838085367(21)454, (01)00884838085367(21)410, (01)00884838085367(21)283, (01)00884838085367(21)231, (01)00884838085367(21)466, (01)00884838085367(21)495, (01)00884838085367(21)207, (01)00884838085367(21)167, (01)00884838085367(21)445, (01)00884838085367(21)438, (01)00884838085367(21)289, (01)00884838085367(21)233, (01)00884838085367(21)173, (01)00884838085367(21)536, (01)00884838085367(21)204, (01)00884838085367(21)77, (01)00884838085367(21)313, (01)00884838085367(21)236, (01)00884838085367(21)133, (01)00884838085367(21)481, (01)00884838085367(21)280, (01)00884838085367(21)307, (01)00884838085367(21)210, (01)00884838085367(21)258, (01)00884838085367(21)328, (01)00884838085367(21)199, (01)00884838085367(21)480, (01)00884838085367(21)53, (01)00884838085367(21)72, (01)00884838085367(21)364, (01)00884838085367(21)491, (01)00884838085367(21)423, (01)00884838085367(21)509, (01)00884838085367(21)246, (01)00884838085367(21)142, (01)00884838085367(21)376, (01)00884838085367(21)257, (01)00884838085367(21)140, (01)00884838085367(21)369, (01)00884838085367(21)508, (01)00884838085367(21)97, (01)00884838085367(21)87, (01)00884838085367(21)303, (01)00884838085367(21)48, (01)00884838085367(21)301, (01)00884838085367(21)460, (01)00884838085367(21)478, (01)00884838085367(21)522, (01)00884838085367(21)448, (01)00884838085367(21)242, (01)00884838085367(21)238, (01)00884838085367(21)160, (01)00884838085367(21)83, (01)00884838085367(21)68, (01)00884838085367(21)544, (01)00884838085367(21)230, (01)00884838085367(21)360, (01)00884838085367(21)93, (01)00884838085367(21)36, (01)00884838085367(21)372, (01)00884838085367(21)179, (01)00884838085367(21)306, (01)00884838085367(21)182, (01)00884838085367(21)327, (01)00884838085367(21)244, (01)00884838085367(21)382, (01)00884838085367(21)192, (01)00884838085367(21)428, (01)00884838085367(21)432, (01)00884838085367(21)215, (01)00884838085367(21)338, (01)00884838085367(21)399, (01)00884838085367(21)339, (01)00884838085367(21)316, (01)00884838085367(21)555, (01)00884838085367(21)347, (01)00884838085367(21)148, (01)00884838085367(21)134, (01)00884838085367(21)38, (01)00884838085367(21)158, (01)00884838085367(21)318, (01)00884838085367(21)518, (01)00884838085367(21)250, (01)00884838085367(21)118, (01)00884838085367(21)336, (01)00884838085367(21)185, (01)00884838085367(21)206, (01)00884838085367(21)50, (01)00884838085367(21)489, (01)00884838085367(21)521, (01)00884838085367(21)37, (01)00884838085367(21)79, (01)00884838085367(21)529, (01)00884838085367(21)254, (01)00884838085367(21)427, (01)00884838085367(21)394, (01)00884838085367(21)71, (01)00884838085367(21)47, (01)00884838085367(21)534, (01)00884838085367(21)292, (01)00884838085367(21)497, (01)00884838085367(21)35, (01)00884838085367(21)293, (01)00884838085367(21)227, (01)00884838085367(21)359, (01)00884838085367(21)527, (01)00884838085367(21)387, (01)00884838085367(21)168, (01)00884838085367(21)128, (01)00884838085367(21)129, (01)00884838085367(21)396, (01)00884838085367(21)486, (01)00884838085367(21)69, (01)00884838085367(21)453, (01)00884838085367(21)174, (01)00884838085367(21)484, (01)00884838085367(21)483, (01)00884838085367(21)334, (01)00884838085367(21)425, (01)00884838085367(21)181, (01)00884838085367(21)166, (01)00884838085367(21)408, (01)00884838085367(21)415, (01)00884838085367(21)141, (01)00884838085367(21)365, (01)00884838085367(21)471, (01)00884838085367(21)240, (01)00884838085367(21)450, (01)00884838085367(21)516, (01)00884838085367(21)198, (01)00884838085367(21)228, (01)00884838085367(21)380, (01)00884838085367(21)420, (01)00884838085367(21)397, (01)00884838085367(21)212, (01)00884838085367(21)475, (01)00884838085367(21)269, (01)00884838085367(21)414, (01)00884838085367(21)268, (01)00884838085367(21)74, (01)00884838085367(21)115, (01)00884838085367(21)349, (01)00884838085367(21)291, (01)00884838085367(21)519, (01)00884838085367(21)234, (01)00884838085367(21)219, (01)00884838085367(21)195, (01)00884838085367(21)60, (01)00884838085367(21)549, (01)00884838085367(21)46, (01)00884838085367(21)96, (01)00884838085367(21)416, (01)00884838085367(21)249, (01)00884838085367(21)426, (01)00884838085367(21)162, 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(01)00884838085367(21)300, (01)00884838085367(21)224, (01)00884838085367(21)67, (01)00884838085367(21)61, (01)00884838085367(21)157, (01)00884838085367(21)154, (01)00884838085367(21)100, (01)00884838085367(21)217, (01)00884838085367(21)253, (01)00884838085367(21)391, (01)00884838085367(21)144, (01)00884838085367(21)379, (01)00884838085367(21)202, (01)00884838085367(21)105, (01)00884838085367(21)226, (01)00884838085367(21)315, (01)00884838085367(21)464, (01)00884838085367(21)197, (01)00884838085367(21)63, (01)00884838085367(21)252, (01)00884838085367(21)175, (01)00884838085367(21)274, (01)00884838085367(21)163, (01)00884838085367(21)186, (01)00884838085367(21)260, (01)00884838085367(21)502, (01)00884838085367(21)152, (01)00884838085367(21)498, (01)00884838085367(21)156, (01)00884838085367(21)296, (01)00884838085367(21)208, (01)00884838085367(21)430, (01)00884838085367(21)161, (01)00884838085367(21)436, (01)00884838085367(21)409, (01)00884838085367(21)155, (01)00884838085367(21)298, (01)00884838085367(21)191, (01)00884838085367(21)278, (01)00884838085367(21)368, (01)00884838085367(21)94, (01)00884838085367(21)66, (01)00884838085367(21)108, (01)00884838085367(21)200, (01)00884838085367(21)201, (01)00884838085367(21)98, (01)00884838085367(21)189, (01)00884838085367(21)311, (01)00884838085367(21)367, (01)00884838085367(21)297, (01)00884838085367(21)132, (01)00884838085367(21)507, (01)00884838085367(21)451, 10. Azurion 7 B20; Model: 722226; UDI: (01)00884838099272(21)108, (01)00884838099272(21)117, (01)00884838099272(21)78, (01)00884838099272(21)11, (01)00884838099272(21)59, (01)00884838099272(21)75, (01)00884838099272(21)19, (01)00884838099272(21)141, (01)00884838099272(21)21, (01)00884838099272(21)60, (01)00884838099272(21)61, (01)00884838099272(21)10, (01)00884838099272(21)142, (01)00884838099272(21)99, (01)00884838099272(21)36, (01)00884838099272(21)5, (01)00884838099272(21)14, (01)00884838099272(21)45, (01)00884838099272(21)97, (01)00884838099272(21)18, (01)00884838099272(21)47, (01)00884838099272(21)1, (01)00884838099272(21)194, (01)00884838099272(21)29, (01)00884838099272(21)50, (01)00884838099272(21)16, (01)00884838099272(21)82, (01)00884838099272(21)55, (01)00884838099272(21)6, (01)00884838099272(21)7, (01)00884838099272(21)53, (01)00884838099272(21)52, (01)00884838099272(21)63, (01)00884838099272(21)26, (01)00884838099272(21)69, (01)00884838099272(21)42, (01)00884838099272(21)115, (01)00884838099272(21)43, (01)00884838099272(21)73, (01)00884838099272(21)70, (01)00884838099272(21)128, (01)00884838099272(21)40, (01)00884838099272(21)137, (01)00884838099272(21)110, (01)00884838099272(21)68, (01)00884838099272(21)64, (01)00884838099272(21)49, (01)00884838099272(21)38, (01)00884838099272(21)33, (01)00884838099272(21)30, (01)00884838099272(21)92, (01)00884838099272(21)62, (01)00884838099272(21)34, (01)00884838099272(21)71, (01)00884838099272(21)91, (01)00884838099272(21)35, (01)00884838099272(21)31, (01)00884838099272(21)56, (01)00884838099272(21)28, (01)00884838099272(21)79, (01)00884838099272(21)77; 11. Azurion 7 M12; Model: 722078; UDI: (01)00884838085251(21)302, (01)00884838085251(21)585, (01)00884838085251(21)410, (01)00884838085251(21)753, (01)00884838085251(21)523, (01)00884838085251(21)293, (01)00884838085251(21)840, (01)00884838085251(21)291, (01)00884838085251(21)536, (01)00884838085251(21)537, (01)00884838085251(21)870, (01)00884838085251(21)613, (01)00884838085251(21)598, (01)00884838085251(21)679, (01)00884838085251(21)224, (01)00884838085251(21)829, (01)00884838085251(21)249, (01)00884838085251(21)546, (01)00884838085251(21)478, (01)00884838085251(21)479, (01)00884838085251(21)513, (01)00884838085251(21)278, (01)00884838085251(21)437, (01)00884838085251(21)438, (01)00884838085251(21)456, (01)00884838085251(21)833, (01)00884838085251(21)566, (01)00884838085251(21)488, (01)00884838085251(21)550, (01)00884838085251(21)327, (01)00884838085251(21)571, (01)00884838085251(21)545, (01)00884838085251(21)544, (01)00884838085251(21)465, (01)00884838085251(21)376, 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(01)00884838085251(21)617, (01)00884838085251(21)336, (01)00884838085251(21)226, (01)00884838085251(21)761, (01)00884838085251(21)221, (01)00884838085251(21)220, (01)00884838085251(21)799, (01)00884838085251(21)839, (01)00884838085251(21)354, (01)00884838085251(21)154, (01)00884838085251(21)153, (01)00884838085251(21)957, (01)00884838085251(21)471, (01)00884838085251(21)357, (01)00884838085251(21)133, (01)00884838085251(21)132, (01)00884838085251(21)130, (01)00884838085251(21)261, (01)00884838085251(21)158, (01)00884838085251(21)507, (01)00884838085251(21)854, (01)00884838085251(21)477, (01)00884838085251(21)785, (01)00884838085251(21)789, (01)00884838085251(21)404, (01)00884838085251(21)877, (01)00884838085251(21)422, (01)00884838085251(21)194, (01)00884838085251(21)802, (01)00884838085251(21)801, (01)00884838085251(21)140, (01)00884838085251(21)878, (01)00884838085251(21)608, (01)00884838085251(21)952, (01)00884838085251(21)10, (01)00884838085251(21)123, (01)00884838085251(21)319, (01)00884838085251(21)805, (01)00884838085251(21)686, (01)00884838085251(21)397, (01)00884838085251(21)127, (01)00884838085251(21)128, (01)00884838085251(21)253, (01)00884838085251(21)594, (01)00884838085251(21)301, (01)00884838085251(21)300, (01)00884838085251(21)332, (01)00884838085251(21)35, (01)00884838085251(21)321, (01)00884838085251(21)341, (01)00884838085251(21)563, (01)00884838085251(21)316, (01)00884838085251(21)314, (01)00884838085251(21)496, (01)00884838085251(21)641, (01)00884838085251(21)30, (01)00884838085251(21)950, (01)00884838085251(21)331, (01)00884838085251(21)652, (01)00884838085251(21)349, (01)00884838085251(21)236, (01)00884838085251(21)979, (01)00884838085251(21)831, (01)00884838085251(21)501, (01)00884838085251(21)841, (01)00884838085251(21)682, (01)00884838085251(21)843, (01)00884838085251(21)830, (01)00884838085251(21)323, (01)00884838085251(21)315, (01)00884838085251(21)680, (01)00884838085251(21)365, (01)00884838085251(21)311, (01)00884838085251(21)312, (01)00884838085251(21)283, (01)00884838085251(21)282, (01)00884838085251(21)602, (01)00884838085251(21)203, (01)00884838085251(21)202, (01)00884838085251(21)674, (01)00884838085251(21)675, (01)00884838085251(21)673, (01)00884838085251(21)676, (01)00884838085251(21)609, (01)00884838085251(21)295, (01)00884838085251(21)368, (01)00884838085251(21)369, (01)00884838085251(21)615, (01)00884838085251(21)618, (01)00884838085251(21)310, (01)00884838085251(21)199, (01)00884838085251(21)455, (01)00884838085251(21)668, (01)00884838085251(21)352, (01)00884838085251(21)193, (01)00884838085251(21)280, (01)00884838085251(21)667, (01)00884838085251(21)567, (01)00884838085251(21)884, (01)00884838085251(21)183, (01)00884838085251(21)749, (01)00884838085251(21)692, (01)00884838085251(21)32, (01)00884838085251(21)241, (01)00884838085251(21)935, (01)00884838085251(21)407, (01)00884838085251(21)505, (01)00884838085251(21)408, (01)00884838085251(21)157, (01)00884838085251(21)752, (01)00884838085251(21)138, (01)00884838085251(21)463, (01)00884838085251(21)461, (01)00884838085251(21)554, (01)00884838085251(21)423, (01)00884838085251(21)252, (01)00884838085251(21)426, (01)00884838085251(21)169, (01)00884838085251(21)650, (01)00884838085251(21)351, (01)00884838085251(21)442, (01)00884838085251(21)968, (01)00884838085251(21)210, (01)00884838085251(21)207, (01)00884838085251(21)208, (01)00884838085251(21)209, (01)00884838085251(21)211, (01)00884838085251(21)623, (01)00884838085251(21)622, (01)00884838085251(21)629, (01)00884838085251(21)129, (01)00884838085251(21)529, (01)00884838085251(21)144, (01)00884838085251(21)750, (01)00884838085251(21)400, (01)00884838085251(21)401, (01)00884838085251(21)411, (01)00884838085251(21)259, (01)00884838085251(21)457, (01)00884838085251(21)926, (01)00884838085251(21)597, (01)00884838085251(21)899, (01)00884838085251(21)322, (01)00884838085251(21)173, (01)00884838085251(21)418, (01)00884838085251(21)637, (01)00884838085251(21)670, (01)00884838085251(21)909, (01)00884838085251(21)601, (01)00884838085251(21)37, (01)00884838085251(21)227, (01)00884838085251(21)984, (01)00884838085251(21)907, (01)00884838085251(21)875, (01)00884838085251(21)717, (01)00884838085251(21)716, (01)00884838085251(21)947, (01)00884838085251(21)945, (01)00884838085251(21)942, (01)00884838085251(21)948, (01)00884838085251(21)940, (01)00884838085251(21)946, (01)00884838085251(21)701, (01)00884838085251(21)620, (01)00884838085251(21)798, (01)00884838085251(21)856, (01)00884838085251(21)710, (01)00884838085251(21)1000, (01)00884838085251(21)663, (01)00884838085251(21)965, (01)00884838085251(21)964, (01)00884838085251(21)736, (01)00884838085251(21)735, (01)00884838085251(21)820, (01)00884838085251(21)819, (01)00884838085251(21)272, (01)00884838085251(21)712, (01)00884838085251(21)714, (01)00884838085251(21)732, (01)00884838085251(21)774, (01)00884838085251(21)381, (01)00884838085251(21)233, (01)00884838085251(21)638, (01)00884838085251(21)318, (01)00884838085251(21)593, (01)00884838085251(21)624, (01)00884838085251(21)776, (01)00884838085251(21)775, (01)00884838085251(21)21, (01)00884838085251(21)267, (01)00884838085251(21)268, (01)00884838085251(21)487, (01)00884838085251(21)421, (01)00884838085251(21)760, (01)00884838085251(21)542, (01)00884838085251(21)614, (01)00884838085251(21)864, (01)00884838085251(21)148, (01)00884838085251(21)837, (01)00884838085251(21)458, (01)00884838085251(21)596, (01)00884838085251(21)377, (01)00884838085251(21)281, (01)00884838085251(21)659, (01)00884838085251(21)784, (01)00884838085251(21)528, (01)00884838085251(21)44, (01)00884838085251(21)42, (01)00884838085251(21)45, (01)00884838085251(21)43, (01)00884838085251(21)41, (01)00884838085251(21)466, (01)00884838085251(21)704, (01)00884838085251(21)219, (01)00884838085251(21)28, (01)00884838085251(21)29, (01)00884838085251(21)217, (01)00884838085251(21)260, (01)00884838085251(21)103, (01)00884838085251(21)430, (01)00884838085251(21)342, (01)00884838085251(21)126, (01)00884838085251(21)184, (01)00884838085251(21)778, (01)00884838085251(21)547, (01)00884838085251(21)586, (01)00884838085251(21)879, (01)00884838085251(21)159, (01)00884838085251(21)363, (01)00884838085251(21)896, (01)00884838085251(21)642, (01)00884838085251(21)472, (01)00884838085251(21)39, (01)00884838085251(21)172, (01)00884838085251(21)961, (01)00884838085251(21)33, (01)00884838085251(21)643, (01)00884838085251(21)581, (01)00884838085251(21)552, (01)00884838085251(21)525, (01)00884838085251(21)857, (01)00884838085251(21)731, (01)00884838085251(21)433, (01)00884838085251(21)432, (01)00884838085251(21)636, (01)00884838085251(21)954, (01)00884838085251(21)447, (01)00884838085251(21)333, (01)00884838085251(21)358, (01)00884838085251(21)540, (01)00884838085251(21)619, (01)00884838085251(21)492, (01)00884838085251(21)527, (01)00884838085251(21)600, (01)00884838085251(21)816, (01)00884838085251(21)434, (01)00884838085251(21)892, (01)00884838085251(21)124, (01)00884838085251(21)122, (01)00884838085251(21)146, (01)00884838085251(21)201, (01)00884838085251(21)509, (01)00884838085251(21)495, (01)00884838085251(21)515, (01)00884838085251(21)353, (01)00884838085251(21)303, (01)00884838085251(21)304, (01)00884838085251(21)186, (01)00884838085251(21)286, (01)00884838085251(21)548, (01)00884838085251(21)518, (01)00884838085251(21)486, (01)00884838085251(21)474, (01)00884838085251(21)475, (01)00884838085251(21)853, (01)00884838085251(21)180, (01)00884838085251(21)243, (01)00884838085251(21)244, (01)00884838085251(21)335, (01)00884838085251(21)549, (01)00884838085251(21)46, (01)00884838085251(21)616, (01)00884838085251(21)972, (01)00884838085251(21)533, (01)00884838085251(21)182, (01)00884838085251(21)850, (01)00884838085251(21)696, (01)00884838085251(21)345, (01)00884838085251(21)939, (01)00884838085251(21)869, (01)00884838085251(21)874, (01)00884838085251(21)871, (01)00884838085251(21)18, (01)00884838085251(21)551, (01)00884838085251(21)917, (01)00884838085251(21)543, (01)00884838085251(21)516, (01)00884838085251(21)12, (01)00884838085251(21)416, (01)00884838085251(21)155, (01)00884838085251(21)446, (01)00884838085251(21)685, (01)00884838085251(21)715, (01)00884838085251(21)225, (01)00884838085251(21)913, (01)00884838085251(21)582, (01)00884838085251(21)908, (01)00884838085251(21)19, (01)00884838085251(21)435, (01)00884838085251(21)16, (01)00884838085251(21)11, (01)00884838085251(21)664, (01)00884838085251(21)901, (01)00884838085251(21)508, (01)00884838085251(21)530, (01)00884838085251(21)198; 12. Azurion 7 M12; Model: 722223; UDI: (01)00884838099241(21)189, (01)00884838099241(21)47, (01)00884838099241(21)77, (01)00884838099241(21)36, (01)00884838099241(21)37, (01)00884838099241(21)87, (01)00884838099241(21)69, (01)00884838099241(21)67, (01)00884838099241(21)52, (01)00884838099241(21)127, (01)00884838099241(21)104, (01)00884838099241(21)96, (01)00884838099241(21)130, (01)00884838099241(21)89, (01)00884838099241(21)119, (01)00884838099241(21)99, (01)00884838099241(21)100, (01)00884838099241(21)155, (01)00884838099241(21)18, (01)00884838099241(21)17, (01)00884838099241(21)46, (01)00884838099241(21)132, (01)00884838099241(21)10, (01)00884838099241(21)134, (01)00884838099241(21)7, (01)00884838099241(21)25, (01)00884838099241(21)106, (01)00884838099241(21)78, (01)00884838099241(21)40, (01)00884838099241(21)9, (01)00884838099241(21)8, (01)00884838099241(21)157, (01)00884838099241(21)64, (01)00884838099241(21)28, (01)00884838099241(21)111, (01)00884838099241(21)35, (01)00884838099241(21)65, (01)00884838099241(21)68, (01)00884838099241(21)61, (01)00884838099241(21)43, (01)00884838099241(21)21, (01)00884838099241(21)76, (01)00884838099241(21)48, (01)00884838099241(21)12, (01)00884838099241(21)30, (01)00884838099241(21)22, (01)00884838099241(21)26, (01)00884838099241(21)176, (01)00884838099241(21)91, (01)00884838099241(21)115, (01)00884838099241(21)170, (01)00884838099241(21)92, (01)00884838099241(21)41, (01)00884838099241(21)80, (01)00884838099241(21)74, (01)00884838099241(21)72, (01)00884838099241(21)24, (01)00884838099241(21)38, (01)00884838099241(21)34, (01)00884838099241(21)27, (01)00884838099241(21)83, (01)00884838099241(21)86, (01)00884838099241(21)33, (01)00884838099241(21)13, (01)00884838099241(21)107; 13. Azurion 7 M20; Model: 722079; UDI: (01)00884838085268(21)1023, (01)00884838085268(21)646, (01)00884838085268(21)645, (01)00884838085268(21)1013, (01)00884838085268(21)1387, (01)00884838085268(21)460, (01)00884838085268(21)35, (01)00884838085268(21)40, (01)00884838085268(21)43, (01)00884838085268(21)703307, (01)00884838085268(21)1048, (01)00884838085268(21)1137, (01)00884838085268(21)401, (01)00884838085268(21)1010, (01)00884838085268(21)266, (01)00884838085268(21)534, (01)00884838085268(21)535, (01)00884838085268(21)1054, (01)00884838085268(21)536, (01)00884838085268(21)818, (01)00884838085268(21)412, (01)00884838085268(21)617, (01)00884838085268(21)488, (01)00884838085268(21)53, (01)00884838085268(21)57, (01)00884838085268(21)905, (01)00884838085268(21)55, (01)00884838085268(21)992, (01)00884838085268(21)691, (01)00884838085268(21)848, (01)00884838085268(21)809, (01)00884838085268(21)1033, (01)00884838085268(21)836, (01)00884838085268(21)891, (01)00884838085268(21)1155, 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"https://recallledger.net/recalls/device-z-2258-2026-azurion-system-system-code-description-model-numbers-azurion-3-m12/"}, {"id": "fda-device-z-2247-2026", "source": "FDA", "category": "device", "recall_number": "Z-2247-2026", "title": "GE HealthCare ApexPro v6.0 eDelivery Software recall (GE Medical Systems Information Technologies Inc)", "product": "GE HealthCare ApexPro v6.0 eDelivery Software, REF #5700026, Product Code SUV; used in conjunction wtih ApexPro CARESCAPE Telemetry Server (CTS) v6.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)", "reason": "GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a persistent NO COMM or OFF NETWORK condition at the CARESCAPE Central Station or CIC Pro Clinical Information Center (Central Station).", "hazard_level": "Class II", "company": "GE Medical Systems Information Technologies Inc", "company_location": "Waukesha, WI, United States", "date": "2026-04-24", "report_date": "2026-06-03", "status": "Ongoing", "distribution": "Worldwide distribution.", "states": [], "nationwide": false, "quantity": "2187 units", "codes": "UDI (01)00195278512390(10)APv6.0.0.5, Serial Number or Sales Order Number: SUV25423440TA, SUV25423443TA, SUV25423444TA, SUV25423445TA, SUV25423446TA, SUV25423447TA, SUV25493641TA, SUV26093921TA, SUV26093922TA, SUV26093923TA, SUV26093924TA, SUV26093925TA, SUV26093926TA, SUV26093927TA, SUV26093928TA, SUV26093929TA, SUV26093930TA, SUV26093931TA, SUV26093932TA, SUV26033814TA, SUV26033815TA, SUV26033816TA, SUV26033817TA, SUV26033818TA, SUV26033819TA, SUV26033820TA, SUV25112833TA, SUV25112834TA, SUV25202954TA, SUV24251609SA, SUV24251610SA, SUV24251611SA, SUV24251612SA, SUV24251613SA, SUV24251614SA, SUV24251615SA, SUV24251616SA, SUV24141336SA, SUV23260213SA, SUV23260214SA, SUV23260215SA, SUV23260216SA, SUV23260217SA, SUV24241569SA, SUV24241570SA, 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HealthCare TRADE IN CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA, REF #5697603-902, Product Code KSA; used in conjunction wtih ApexPro CARESCAPE Telemetry Server (CTS) v6.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)", "reason": "GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a persistent NO COMM or OFF NETWORK condition at the CARESCAPE Central Station or CIC Pro Clinical Information Center (Central Station).", "hazard_level": "Class II", "company": "GE Medical Systems Information Technologies Inc", "company_location": "Waukesha, WI, United States", "date": "2026-04-24", "report_date": "2026-06-03", "status": "Ongoing", "distribution": "Worldwide distribution.", "states": [], "nationwide": false, "quantity": "2366 units", "codes": "No UDI, Serial Number or Sales Order Number: KSA7536146, KSA7536158, KSA7536159, 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KSA6945208, KSA6945219, KSA6945223, KSA6945230, KSA6945236, KSA6945296, KSA6945314, KSA6945321, KSA6945340, KSA6945350, KSA6945353, KSA6945382, KSA6945387, KSA6899004, KSA6664048, KSA6664049, KSA6664054, KSA6664059, KSA6664075, KSA6664037, KSA6664045, KSA6664065, KSA6664069, KSA6623192, KSA6626641, KSA6626649, KSA6626687, KSA6626691, KSA6626701, KSA6626706, KSA6626707, KSA6626715, KSA6626718, KSA7120720, KSA7162574, KSA7162580, KSA7162632, KSA7162655, KSA6419987, KSA6419993, KSA6420030, KSA6420053, KSA6420080, KSA6420081, KSA6420082, KSA6420102, KSA6664002, KSA6664005, KSA6664036, KSA6664052, KSA6664057, KSA6664078, KSA6664090, KSA6664091, KSA6664006, KSA6866903, KSA6866924, KSA6866928, KSA6866933, KSA6866942, KSA6866977, KSA6866981, KSA6866987, KSA6866992, KSA6866996, KSA6899000, KSA6899060, KSA6945146, KSA6945185, KSA6945190, KSA6945191, KSA6945224, KSA6945250, KSA6945278, KSA6945294, KSA6945311, KSA6945391, KSA6945199, KSA6945204, KSA6945226, KSA6945244, KSA6945258, KSA6945302, KSA6945303, KSA6945319, KSA6945355, KSA6945358, KSA6945359, KSA6945384, KSA7013899, KSA7013902, KSA7013903, KSA7013905, KSA7013912, KSA7013914, KSA7013918, KSA7013921, KSA7013932, KSA7013940, KSA7013955, KSA7013956, KSA7013957, KSA7013963, KSA7013964, KSA7013973, KSA7013975, KSA7013986, KSA6569809, KSA6569821, KSA6569833, KSA6569840, KSA6569867, KSA6569890, KSA6569898, KSA6623189, KSA6623195, KSA6626637, KSA6626651, KSA6626690, KSA6626699, KSA6626713, KSA6626719, KSA6898999, KSA6899011, KSA6899013, KSA6899018, KSA6899021, KSA6899028, KSA6899029, KSA6899033, KSA6899034, KSA6899037, KSA6899051, KSA6899054, KSA6899059, KSA6899067, KSA6899070, KSA6899072, KSA6899074, KSA6899078, KSA6899080, KSA6899084, KSA6899085, KSA6899086, KSA6899092, KSA6899093, KSA6899097, KSA6945099, KSA6945100, KSA6945108, KSA6945113, KSA6945130, KSA6945140, KSA6945171, KSA6945175, KSA6945177, KSA6945183, KSA6945187, KSA6945189, KSA6945254, KSA6945262, KSA6945283, KSA6945288, KSA6945298, KSA6945310, KSA6945328, KSA6945331, KSA6945370, KSA6945377, KSA6945213, KSA6649214, KSA6649226, KSA6649261, KSA6649267, KSA6649272, KSA7120679, KSA7120683, KSA7120693, KSA7120725, KSA7120750, KSA7120754, KSA6689288, KSA6689302, KSA6689309, KSA6689313, KSA6689322, KSA6689364, KSA6689373, KSA6689375, KSA6689382, KSA7442815, KSA7676896, KSA7754382, KSA7754398, KSA7754402, KSA7769599, KSA7769600, KSA7769603, KSA7773423, KSA7773430, KSA7773436, KSA7773442, KSA7744947, KSA7744960, KSA7754384, KSA7754387, KSA7754395, KSA7769605, KSA7769607, KSA7769618, KSA7769622, KSA7773422, KSA7773428, KSA7773444, KSA7239656, KSA7239665, KSA7239668, KSA7239676, KSA7239677, KSA7239678, KSA7239683, KSA7239684, KSA7239686, KSA7239688, KSA7239694, KSA7239696, KSA7239697, KSA7239703, KSA7239704, KSA7239707, KSA7239708, KSA7239711, KSA7239712, KSA7239725, KSA7239728, KSA7239729, KSA7239736, KSA7239737, KSA7239741, KSA7239742, KSA7239743, KSA7239748, KSA6808841, KSA6808859, KSA6808902, KSA6808935, KSA6808936, KSA6623190, KSA6623209, KSA6623225, KSA6808870, KSA6808880, KSA7120744, KSA7120755, KSA6623204, KSA6623268, KSA6899005, KSA6899045, KSA6899050, KSA6899055, KSA6899089, KSA6623199, KSA6623214, KSA6626624, KSA6590128, KSA6590137, KSA6590143, KSA6590163, KSA6590170, KSA6590184, KSA6590210, KSA6590221, KSA6626663, KSA6626676, KSA6420092, KSA6420117, KSA6536467, KSA6536501, KSA6536510, KSA6536515, KSA6569806, KSA6569864, KSA6569903, KSA7724020, KSA7724027, KSA7724037, KSA7724040, KSA7727679, KSA7727686, KSA7727699, KSA7732509, KSA7732526, KSA7754383, KSA7773427, KSA6649211, KSA6649233, KSA6649263, KSA6569808, KSA6569839, KSA6569863, KSA6569871, KSA6569876, KSA6569888, KSA6808839, KSA6808853, KSA6808860, KSA6808893, KSA6808905, KSA6808919, KSA6808921, KSA6808924, KSA6808926, KSA6808938, KSA6409191, KSA6409209, KSA6409245, KSA6420002, KSA6420011, KSA6420108, KSA6477136, KSA6477153, KSA6477164, KSA6477184, KSA6477193, KSA6477196, KSA6477212, KSA6477225, KSA7550168, KSA7676876, KSA7724025, KSA7724045, KSA7727682, KSA7120701, KSA7120751, KSA7120713, KSA7120721, KSA7120731, KSA7120738, KSA7120741, KSA7120776, KSA7120777, KSA7013919, KSA7013934, KSA7013987, KSA6664013, KSA6664014, KSA6664016, KSA6664021, KSA6664083, KSA6664085, KSA6689285, KSA6689330, KSA6689353, KSA7391451, KSA7391479, KSA7442788, KSA7442812, KSA7442857, KSA7442859, KSA7442877, KSA7442879, KSA7442888, KSA7442895, KSA6866906, KSA6866919, KSA6866950, KSA6866970, KSA6866975, KSA6866976, KSA6866980, KSA6808847, KSA6808848, KSA6808849, KSA6808869, KSA6808888, KSA6808895, KSA6808914, KSA6808915, KSA6808918, KSA6808925, KSA7520462, KSA7520480, KSA6945229, KSA6623203, KSA6623229, KSA6623247, KSA6623264, KSA6626633, KSA6626634, KSA6626695, KSA6626717, KSA6623210, KSA6664055, KSA6664064, KSA7724021, KSA7724030, KSA7724033, KSA7732497, KSA7536149, KSA7120761, KSA7162595, KSA6945157, KSA6945235, KSA6945249, KSA6945275, KSA6945247, KSA6945290, KSA6945291, KSA6945327, KSA6945365, KSA7754377, KSA7769601, KSA7773419, KSA7773421, KSA7773429, KSA7773435, KSA6664003, KSA6866989, KSA7162566, KSA7162571, KSA7162585, KSA7162591, KSA7162594, KSA7162597, KSA7162607, KSA7162611, KSA7162615, KSA7162617, KSA7162620, KSA7162627, KSA7162633, KSA7162642, KSA7162643, KSA7162644, KSA7162647, KSA7162658, KSA7391429, KSA7391469, KSA7391472, KSA7096912, KSA7096925, KSA7096926, KSA7096929, KSA7096934, KSA7096936, KSA7096937, KSA7096938, KSA7096944, KSA7096948, KSA7096962, KSA7096973, KSA7096984, KSA7120708, KSA6945097, KSA6945109, KSA6945118, KSA6945128, KSA6945129, KSA6945132, KSA6945141, KSA6945181, KSA6017431, KSA6017433, KSA6017477, KSA6017495, KSA6017393, KSA6945394, KSA6899002, KSA6899019, KSA6899020, KSA6899030, KSA6899091, KSA6899048, KSA6899082, KSA6623185, KSA6623238, KSA6623261, KSA6649178, KSA6649227, KSA6649269, KSA6945147, KSA6945173, KSA6945277, KSA6945336, KSA6945120, KSA6945127, KSA6945148, KSA6945149, KSA6945156, KSA6945163, KSA6945168, KSA6945178, KSA6945179, KSA6945193, KSA6945260, KSA6945312, KSA6945341, KSA6945361, KSA6945395, KSA6964884, KSA6964914, KSA6964918, KSA6964930, KSA6964931, KSA6964941, KSA6626689, KSA7013890, KSA7013891, KSA7013893, KSA7013913, KSA7013923, KSA7013924, KSA7013942, KSA7013948, KSA7013954, KSA6945154, KSA6945215, KSA6945273, KSA6945300, KSA6945333, KSA6945352, KSA6945381, KSA6626630, KSA6626631, KSA6626657, KSA6626660, KSA6626665, KSA6626667, KSA6626672, KSA6626694, KSA6626697, KSA6626700, KSA6626709, KSA6964900, KSA6964911, KSA6964912, KSA6964922, KSA6964924, KSA6899044, KSA7239669, KSA7239670, KSA7239687, KSA7239698, KSA7239705, KSA7239714, KSA7239727, KSA7239730, KSA7239733, KSA7239746, KSA6569873, KSA6623228, KSA6623243, KSA6623266, KSA6623276, KSA6626640, KSA6626642, KSA6626643, KSA6626650, KSA6626653, KSA6626673, KSA6626675, KSA6626678, KSA6626711, KSA7096993, KSA7120702, KSA7120703, KSA7120705, KSA7120710, KSA7120759, KSA7120769, KSA7162573, KSA7162599, KSA7162601, KSA7162635, KSA7162651, KSA7162657, KSA6945165, KSA6945315, KSA6477102, KSA6477115, KSA6477145, KSA6477150, KSA6945209, KSA6945212, KSA6945232, KSA6945271, KSA6945276, KSA6409175, KSA6409178, KSA6409192, KSA6409193, KSA6409204, KSA6409207, KSA6409210, KSA6409212, KSA6409226, KSA6409232, KSA6409236, KSA7162604, KSA7162645, KSA7744936, KSA7744945, KSA7744948, KSA7744954, KSA7744962, KSA7744963, KSA7754380, KSA7754388, KSA7754394, KSA7754403, KSA7754406, KSA7769595, KSA7769604, KSA7769616, KSA7769620, KSA7773418, KSA7773426, KSA7773437, KSA7773441, KSA7442825, KSA7442839, KSA7676899, KSA7727681, KSA7744940, KSA7744942, KSA7744949, KSA7744950, KSA7754378, KSA7754379, KSA7754381, KSA7754392, KSA7754393, KSA7754397, KSA7754399, KSA7754404, KSA7769594, KSA7769611, KSA7769615, KSA7769619, KSA7773425, KSA7773432, KSA7773438, KSA6623255, KSA6626621, KSA6626629, KSA6626664, KSA6626714, KSA7442808, KSA6899036, KSA7724028, KSA7239735, KSA7013974, KSA6623222, KSA6626644, KSA6626692, KSA7120717, KSA7120745, KSA7162629, KSA7162648, KSA7120687, KSA7162567, KSA7162598, KSA7239659, KSA7239660, KSA7239671, KSA7239680, KSA7239715, KSA7239717, KSA7239720, KSA7239731, KSA7239732, KSA7304420, KSA6945182, KSA6945211, KSA7120718, KSA7013941, KSA7574789, KSA6477112, KSA6477120, KSA6477152, KSA6477179, KSA6477194, KSA6866946, KSA6866969, KSA6477157, KSA6477176, KSA6477185, KSA6477192, KSA6477228, KSA6899008, KSA6899056, KSA6945266, KSA6945323, KSA7013889, KSA7013898, KSA7013904, KSA7013908, KSA7013909, KSA7013911, KSA7013920, KSA7013922, KSA7013927, KSA7013929, KSA7013930, KSA7013931, KSA7013936, KSA7013945, KSA7013951, KSA7013960, KSA7013961, KSA7013965, KSA7013966, KSA7013970, KSA7013981, KSA7013988, KSA6477127, KSA6477174, KSA6477226, KSA6477245, KSA6477252, KSA6569835, KSA6664030, KSA6664033, KSA6664086, KSA6866930, KSA6866949, KSA6866982, KSA6477200, KSA6477117, KSA6477146, KSA6477190, KSA6477229, KSA6536456, KSA6945124, KSA6945139, KSA6945180, KSA6945216, KSA6945263, KSA6945284, KSA6017386, KSA6017421, KSA6017437, KSA6017510, KSA6945227, KSA6945242, KSA6945256, KSA6945264, KSA6945299, KSA6945308, KSA6945338, KSA6536461, KSA6536464, KSA6536468, KSA6536475, KSA6536477, KSA6536483, KSA6536491, KSA7162564, KSA7162578, KSA7162636, KSA7162652, KSA6664017, KSA6664018, KSA6866905, KSA6945119, KSA6945143, KSA6945150, KSA6945164, KSA6945239, KSA6945243, KSA6945282, KSA6945316, KSA6945354, KSA6945373, KSA6623193, KSA6623196, KSA6623211, KSA6623213, KSA6623215, KSA6623217, KSA6623224, KSA6623227, KSA6623252, KSA6623254, KSA6623257, KSA6623271, KSA6626620, KSA6626647, KSA6626669, KSA5646290, KSA6477220, KSA6649208, KSA6866960, KSA6808916, KSA6536519, KSA6409201, KSA6945162, KSA6649220, KSA6866902, KSA6866916, KSA6866937, KSA6649202, KSA6649249, KSA6649262, KSA6623283, KSA6590123, KSA6590124, KSA6590126, KSA6590138, KSA6590139, KSA6590140, KSA6590141, KSA6590161, KSA6590172, KSA6590174, KSA6590177, KSA6590188, KSA6590191, KSA6590197, KSA6590199, KSA6590208, KSA6590211, KSA6623207, KSA6623233, KSA6623256, KSA6623260, KSA6623263, KSA6623277, KSA6623279, KSA6623281, KSA6623284, KSA6664092, KSA6808871, KSA6808890, KSA6808894, KSA6808903, KSA6808907, KSA6808917, KSA6409157, KSA6409237, KSA6409247, KSA6477109, KSA6477114, KSA6477144, KSA6477151, KSA6477181, KSA6477197, KSA6477231, KSA6477240, KSA6477250, KSA6536529, KSA7550151, KSA7550173, KSA7574767, KSA7574784, KSA7590252, KSA7590258, KSA7590260, KSA7590263, KSA7590266, KSA7667307, KSA7667318, KSA7667321, KSA7667323, KSA7667332, KSA6664088, KSA7590242, KSA7590264, KSA7667311, KSA7667325, KSA7667326, KSA7667328, KSA7667333, KSA7667334, KSA7667306, KSA7667314, KSA7667315, KSA7667319, KSA7667327, KSA7667335, KSA6945159, KSA6808899, KSA7442791, KSA7442841, KSA7667309, KSA7667313, KSA7667329, KSA7676872, KSA7676873, KSA7676880, KSA7676891, KSA7676892, KSA7676894, KSA7676897, KSA7676898, KSA7676900, KSA7702195, KSA7702197, KSA7702202, KSA7702204, KSA7702205, KSA7702206, KSA7702207, KSA7702209, KSA7702211, KSA7702212, KSA7702213, KSA7702215, KSA7702216, KSA7702217, KSA7702218, KSA7702221, KSA6536441, KSA7574786, KSA7590241, KSA7590269, KSA7590246, KSA7590247, KSA7590267, KSA7667308, KSA7667312, KSA7667316, KSA7667322, KSA7676875, KSA7676877, KSA7676879, KSA7676881, KSA7676882, KSA7676884, KSA7676885, KSA7676887, KSA7676890, KSA7676895, KSA7702194, KSA7702200, KSA7702201, KSA7702203, KSA7702210, KSA7702214, KSA7702219, KSA7702220, KSA7702223, KSA7590249, KSA7590251, KSA7590257, KSA7590262, KSA7667310, KSA7667324, KSA7667330, KSA6623231, KSA6626671, KSA6626684, KSA6626703, KSA6664038, KSA6866912, KSA7120682, KSA7120732, KSA7120733, KSA7120749, KSA7120756, KSA7120774, KSA7162628, KSA7550171, KSA7574788, KSA6945255, KSA7520488, KSA6964960, KSA6899039, KSA6954214, KSA6954225, KSA6954228, KSA6954231, KSA6954233, KSA6954238, KSA6954239, KSA6954248, KSA6954258, KSA6954259, KSA6954262, KSA6954264, KSA6954266, KSA6954285, KSA6954289, KSA6954300, KSA6954304, KSA6954309, KSA6945362, KSA6649242, KSA6536463, KSA7727680, KSA7732508, KSA7732519, KSA6689341, KSA6689348, KSA6689362, KSA6689367, KSA6649189, KSA6649222, KSA6649224, KSA6649236, KSA6649237, KSA6649243, KSA6649253, KSA6649259, KSA6649264, KSA6649265, KSA7442807, KSA7727685, KSA7732514, KSA6689298, KSA6689308, KSA6689336, KSA6689340, KSA6689345, KSA6689357, KSA7520470, KSA7520472, KSA7536139, KSA7536145, KSA7536152, KSA7536154, KSA7536163, KSA7536165, KSA7536166, KSA7536168, KSA7442783, KSA7442795, KSA7442803, KSA7442806, KSA7442809, KSA7442820, KSA7442824, KSA7442826, KSA7442831, KSA7442832, KSA7442833, KSA7442835, KSA7442842, KSA7442860, KSA7442864, KSA7442875, KSA7442890, KSA6649229, KSA6569831, KSA6569893, KSA6569895, KSA6569899, KSA6536447, KSA6536451, KSA6536455, KSA6536462, KSA6536476, KSA6536478, KSA6536489, KSA6536498, KSA6536506, KSA6536508, KSA6536509, KSA6536513, KSA6536518, KSA6536533, KSA6536540, KSA6623186, KSA6623240, KSA6623269, KSA6649201, KSA6649215, KSA6649235, KSA6649260, KSA6649270, KSA6866901, KSA6664023, KSA7120689, KSA7120757, KSA6626627, KSA5646249, KSA5646255, KSA5646273, KSA5646279, KSA7391402, KSA7391434, KSA7391441, KSA7391457, KSA7391465, KSA7391474, KSA7391484, KSA7391488, KSA7391494, KSA7391497, KSA7391500, KSA7442776, KSA7442785, KSA7442793, KSA7442794, KSA7442796, KSA7442802, KSA7442805, KSA7442811, KSA7442823, KSA7442834, KSA7442844, KSA7442846, KSA7442855, KSA7442868, KSA7442869, KSA7442872, KSA7442884, KSA7442885, KSA7442889, KSA7442893, KSA7509842, KSA6945152, KSA7485765, KSA6649176, KSA6649180, KSA6649192, KSA6649194, KSA6649199, KSA6649200, KSA6649207, KSA6649248, KSA6866953, KSA6866958, KSA7120685, KSA7120697, KSA7120709, KSA7120711, KSA7120714, KSA7120726, KSA7120753, KSA7120765, KSA7120775, KSA6649174, KSA6649181, KSA6649187, KSA6649188, KSA6649190, KSA6649209, KSA6649210, KSA6649213, KSA6649231, KSA6649238, KSA6649239, KSA6649240, KSA6649245, KSA6649254, KSA6649271, KSA6623206, KSA6623219, KSA6623235, KSA6623245, KSA6945111, KSA6945135, KSA6945155, KSA6945186, KSA6945198, KSA6945339, KSA6945369, KSA6945380, KSA6899035, KSA7391416, KSA7391476, KSA7485740, KSA7590243, KSA6664015, KSA6664020, KSA6664027, KSA7239662, KSA7239666, KSA7239692, KSA7239719, KSA7239723, KSA7239724, KSA7239726, KSA7304375, KSA7304382, KSA7304401, KSA7304412, KSA7304419, KSA7304423, KSA7304429, KSA7304433, KSA7304436, KSA7304439, KSA7304446, KSA7304458, KSA7667320, KSA7676888, KSA7724022, KSA7724024, KSA7727684, KSA7727689, KSA7727690, KSA7727692, KSA7727695, KSA7727696, KSA7727700, KSA7727702, KSA7732506, KSA7732515, KSA7732520, KSA7732521, KSA7732522, KSA6954220, KSA6954230, KSA6954241, KSA6954274, KSA6954281, KSA6954287, KSA6954302, KSA7120680, KSA7120681, KSA7120686, KSA7120690, KSA7120706, KSA7120712, KSA7120722, KSA7120727, KSA7120729, KSA7120746, KSA7120760, KSA7120763, KSA7120772, KSA7096906, KSA7096913, KSA7096954, KSA7096991, KSA7096992, KSA6954270, KSA7162606, KSA7162646, KSA7162649, KSA7239650, KSA7239651, KSA7239658, KSA7239661, KSA7239663, KSA7239664, KSA7239681, KSA7239685, KSA7239745, KSA7304362, KSA7304399, KSA7304402, KSA7304408, KSA7304428, KSA7304445, KSA7485736, KSA7485739, KSA7485747, KSA7485764, KSA7495810, KSA7495818, KSA7495822, KSA7509828, KSA7509829, KSA7509832, KSA7509833, KSA7509835, KSA7509838, KSA7509840, KSA7509844, KSA7509847, KSA7509849, KSA7509854, KSA6569828, KSA6569855, KSA6569859, KSA6569878, KSA6569885, KSA6569902, KSA6409160, KSA6409166, KSA6409168, KSA6409182, KSA6409184, KSA6409185, KSA6409189, KSA6409190, KSA6409199, KSA6409200, KSA6409214, KSA6409218, KSA6409224, KSA6409229, KSA6409243, KSA6409250, KSA6409252, KSA6409254, KSA6569827, KSA6569832, KSA6569858, KSA6569869, KSA6409158, KSA6477103, KSA6477106, KSA6477107, KSA6477108, KSA6477119, KSA6477122, KSA6477125, KSA6477129, KSA6477133, KSA6477137, KSA6477140, KSA6477147, KSA6477149, KSA6477156, KSA6477167, KSA6477172, KSA6477180, KSA6477188, KSA6477189, KSA6477195, KSA6477202, KSA6477204, KSA6477211, KSA6477213, KSA6477215, KSA6477216, KSA6477217, KSA6477218, KSA6477230, KSA6477232, KSA6477233, KSA6477236, KSA6477238, KSA6477239, 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KSA6945376, KSA6945378, KSA6945383, KSA6945392, KSA6945396, KSA7727674, KSA7769598, KSA7676883, KSA6689289, KSA6689294, KSA6689301, KSA6689303, KSA6689319, KSA6689320, KSA6689324, KSA6689325, KSA6689334, KSA6689335, KSA6689337, KSA6689376, KSA7520483, KSA6663994, KSA6663997, KSA6663998, KSA6664019, KSA6664022, KSA7096907, KSA7096917, KSA7096921, KSA7096951, KSA7096952, KSA7096967, KSA7096978, KSA7096988, KSA7096996, KSA6569805, KSA6569810, KSA6569818, KSA6569829, KSA6569837, KSA6569847, KSA6569850, KSA6569851, KSA6569861, KSA6569881, KSA6689286, KSA7096914, KSA7096919, KSA7096920, KSA7096930, KSA7096949, KSA7096956, KSA7096969, KSA7096982, KSA7096987, KSA7096990, KSA7096997, KSA6964913, KSA6964920, KSA6964938, KSA7391427, KSA7442849, KSA7536144, KSA7096902, KSA7096909, KSA7096911, KSA7096915, KSA7096916, KSA7096923, KSA7096933, KSA7096939, KSA7096960, KSA7096965, KSA7096966, KSA7096974, KSA7096975, KSA7096981, KSA7096983, KSA7096989, KSA7096995, KSA6964890, KSA6945133, KSA6964878, 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KSA6899032, KSA6899046, KSA6899047, KSA6899052, KSA6899053, KSA6899057, KSA6899058, KSA6899061, KSA6899062, KSA6899064, KSA6899066, KSA6899071, KSA6899075, KSA6899077, KSA6899079, KSA6899081, KSA6899087, KSA6899090, KSA6899094, KSA6899095, KSA6899096, KSA7120692, KSA7120716, KSA7120739, KSA7120748, KSA7120691, KSA7120730, KSA7120734, KSA7120736, KSA7120742, KSA7120747, KSA7162568, KSA7162569, KSA7162579, KSA6964883, KSA6689379, KSA7120684, KSA7120698, KSA7162613, KSA7162654, KSA7162659, KSA6590127, KSA6590129, KSA6590130, KSA6590149, KSA6590151, KSA6590155, KSA6590173, KSA6590181, KSA6590185, KSA6590201, KSA6590202, KSA6590212, KSA6590214, KSA6590215, KSA6590222, KSA6536449, KSA7013928, KSA7013944, KSA7013958, KSA7013979, KSA7724018, KSA7727683, KSA7727693, KSA7727694, KSA7727697, KSA7727698, KSA7732498, KSA7732502, KSA7732504, KSA7732505, KSA7732511, KSA7732517, KSA7732518, KSA7732523, KSA7732524, KSA6689290, KSA6689304, KSA6689318, KSA6689354, KSA6689361, KSA6689368, KSA6689372, KSA6689377, KSA6623234, KSA6626628, KSA6626638, KSA6626683, KSA6626688, KSA6590132, KSA6590134, KSA6590135, KSA6590144, KSA6590146, KSA6590147, KSA6590156, KSA6590157, KSA6590158, KSA6590159, KSA6590160, KSA6590166, KSA6590169, KSA6590175, KSA6590176, KSA6590187, KSA6590192, KSA6590194, KSA6590198, KSA6590200, KSA6590203, KSA6590204, KSA6590205, KSA6590207, KSA6590213, KSA6590218, KSA6590219, KSA6420058, KSA6569807, KSA6569815, KSA6569819, KSA6569854, KSA6569872, KSA6569874, KSA6569877, KSA6569897, KSA6536470, KSA6536480, KSA6536482, KSA6536531, KSA6536536, KSA6623200, KSA6623201, KSA6623218, KSA6626652, KSA6626656, KSA6626662, KSA6626674, KSA6626677, KSA6626680, KSA6626693, KSA6420000, KSA6420006, KSA6420027, KSA6420049, KSA6420054, KSA6420066, KSA6420094, KSA6420100, KSA6866910, KSA6623242, KSA6945101, KSA6945196, KSA7485742, KSA7485746, KSA7485751, KSA7509836, KSA7520461, KSA7520464, KSA7520465, KSA7520479, KSA7520484, KSA7536140, KSA7536141, KSA7536148, KSA7536155, KSA7536156, 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KSA6954305, KSA7120719, KSA7391405, KSA7391417, KSA7391421, KSA7391423, KSA7391425, KSA7391426, KSA7391448, KSA7391471, KSA7391487, KSA7391499, KSA6664050, KSA6664068, KSA7013971, KSA7013982, KSA7013983, KSA7724034, KSA6409162, KSA6409170, KSA6409174, KSA6409194, KSA6409196, KSA6409239, KSA6409246, KSA6409248, KSA7485741, KSA7442798, KSA7442840, KSA7442865, KSA7442894, KSA6477101, KSA6477105, KSA6477110, KSA6477121, KSA6477131, KSA6477158, KSA6477162, KSA6477165, KSA6477169, KSA6477170, KSA6477178, KSA6477182, KSA6477186, KSA6477187, KSA6477203, KSA6477207, KSA6477214, KSA6477227, KSA6477244, KSA6477246, KSA6477251, KSA6477253, KSA6569862, KSA6569883, KSA6569884, KSA6649186, KSA6649217, KSA6945318, KSA6590153, KSA6945112, KSA6945151, KSA6945222, KSA6945252, KSA6945274, KSA6945279, KSA6945335, KSA6945389, KSA6017323, KSA6017357, KSA6017436, KSA6017457, KSA6017464, KSA6017466, KSA6017472, KSA6017473, KSA6017476, KSA6017480, KSA6017486, KSA6017488, KSA6017489, KSA6017492, KSA6017501, KSA6017506, KSA6945106, KSA6945269, KSA6945287, KSA7744935, KSA7744937, KSA7744938, KSA7744941, KSA7744943, KSA7744946, KSA7744951, KSA7744952, KSA7744959, KSA7744964, KSA7239657, KSA7239653, KSA7239689, KSA6945248, KSA7727677, KSA6945202, KSA6945210, KSA6945231, KSA6945241, KSA6945245, KSA6945281, KSA6945306, KSA6663996, KSA6664004, KSA6664009, KSA6664010, KSA6664012, KSA6664028, KSA6664032, KSA6664035, KSA6664056, KSA6664061, KSA6664080, KSA6664011, KSA6664034.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2246-2026%22", "url": "https://recallledger.net/recalls/device-z-2246-2026-ge-healthcare-trade-in-carescape-telemetry-server-ark-2250l-north-am/"}, {"id": "fda-device-z-2245-2026", "source": "FDA", "category": "device", "recall_number": "Z-2245-2026", "title": "GE HealthCare CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA recall (GE Medical Systems Information Technologies Inc)", "product": "GE HealthCare CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA, REF #5697603, Product Code KSA; used in conjunction wtih ApexPro CARESCAPE Telemetry Server (CTS) v6.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)", "reason": "GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a persistent NO COMM or OFF NETWORK condition at the CARESCAPE Central Station or CIC Pro Clinical Information Center (Central Station).", "hazard_level": "Class II", "company": "GE Medical Systems Information Technologies Inc", "company_location": "Waukesha, WI, United States", "date": "2026-04-24", "report_date": "2026-06-03", "status": "Ongoing", "distribution": "Worldwide distribution.", "states": [], "nationwide": false, "quantity": "1249 units", "codes": "no UDI, Serial Number or Sales Order Number: KSA7013962, KSA5646256, KSA5646267, 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KSA6420019, KSA6420115, KSA6536502, KSA6945144, KSA5646260, KSA5646309, KSA6409227, KSA6409235, KSA7391443, KSA7391446, KSA7391463, KSA7391468, KSA6964949, KSA6689349, KSA7013968, KSA7509830, KSA7520489, KSA6964903, KSA6964919, KSA6964968, KSA7304444, KSA7304459, KSA6866954, KSA6866986, KSA6689291, KSA6689356, KSA6689365, KSA6866904, KSA6866917, KSA6866938, KSA6866952, KSA6866961, KSA6866968, KSA6017366, KSA6017412, KSA6017423, KSA6017485, KSA7716936, KSA6017456, KSA6626646, KSA6626698, KSA6626704, KSA7391475, KSA6477104, KSA6477111, KSA6477124, KSA6409163, KSA6409223, KSA6409228, KSA6569804, KSA6569812, KSA6569846, KSA6017372, KSA6017392, KSA6017422, KSA6017429, KSA6017490, KSA5646286, KSA5646326, KSA6017483, KSA6017509, KSA6409172, KSA6590178, KSA6590190, KSA6649183, KSA6954218, KSA6954235, KSA6954288, KSA6964908, KSA6964954, KSA6964957, KSA6689299, KSA6689329, KSA6689338, KSA6689343, KSA6689370, KSA7120770, KSA7120778, KSA7162565, KSA7162565, KSA7162572, KSA7162572, KSA6689284, KSA6689316, KSA6689366, KSA7495813, KSA7769596, KSA6945206, KSA6945261, KSA6945342, KSA6954240, KSA6954243, KSA6954255, KSA6954278, KSA6954283, KSA6954286, KSA6954297, KSA6954301, KSA6954303, KSA6954307, KSA6954310, KSA6954313, KSA7716929, KSA6409161, KSA6409195, KSA7304366, KSA7013895, KSA7013939, KSA7013949, KSA7013953, KSA7013967, KSA7013976, KSA7013980, KSA7013984, KSA7096905, KSA7096918, KSA7096931, KSA7096943, KSA7096945, KSA7096958, KSA7096963, KSA7096977, KSA7096998, KSA7096999, KSA7097000, KSA5646241, KSA7239655, KSA6626654, KSA6626681, KSA6626696, KSA7162637, KSA6017317, KSA6017396, KSA6017402, KSA6626623, KSA6964891, KSA6964942, KSA6964947, KSA6420078, KSA6664000, KSA6420039, KSA6663995, KSA6866966, KSA6649244, KSA6649247, KSA5646317, KSA5646327, KSA6017440, KSA7304368, KSA7304371, KSA7304381, KSA7442843, KSA6954254, KSA6954263, KSA6954267, KSA6954290, KSA6954296, KSA6954311, KSA6536459, KSA6536459, KSA6663993, KSA6420024, KSA5646266, KSA6409169, KSA6409171, KSA6409215, KSA6477116, KSA6477183, KSA6945356, KSA6866909, KSA6866922, KSA6866932, KSA6866943, KSA6866947, KSA6866965, KSA6866988, KSA6866998, KSA6954217, KSA6954236, KSA6954265, KSA6954272, KSA6954292, KSA6954306, KSA6954308, KSA6954312, KSA7727687, KSA7304443, KSA7754385, KSA7754396, KSA7754401, KSA7769593, KSA7769606, KSA7769621, KSA7773433, KSA7773439, KSA7773443, KSA6964876, KSA6964877, KSA7120723, KSA6664024, KSA6664026, KSA6664043, KSA6664070, KSA6664074, KSA6808850, KSA6808904, KSA6626668, KSA6626668, KSA6626679, KSA6626679, KSA6626705, KSA6626705, KSA6626708, KSA6626708, KSA6964951, KSA7013952, KSA7495835, KSA6017470, KSA6808851, KSA6808923, KSA7442782, KSA7442887, KSA5646245, KSA5646262, KSA5646277, KSA5646303, KSA5646308, KSA5646318, KSA6017313, KSA6017320, KSA6017328, KSA6017339, KSA6017355, KSA6017356, KSA6017426, KSA6017444, KSA6017462, KSA6017467, KSA6017474, KSA6017475, KSA6017491, KSA6017494, KSA6017498, KSA6017499, KSA6017511, KSA6649266, KSA6649257, KSA6808909, KSA7096903, KSA7096903, KSA7096904, KSA7096904, KSA7162618, KSA7162661, KSA7239673, KSA7239738, KSA7162602, KSA7162616, KSA7162625, KSA7162634, KSA7239709, KSA7239740, KSA7239747, KSA7727703, KSA7732507, KSA7162577, KSA6017428, KSA6866934, KSA6964872, KSA6866994, KSA6945334, KSA7162582, KSA7162587, KSA7716920, KSA7716924, KSA7716927, KSA7304386, KSA7304388, KSA7304391, KSA7304392, KSA7304394, KSA7304409, KSA7304432, KSA7304434, KSA7304448, KSA6866923, KSA7391415, KSA7391436, KSA7391439, KSA7391440, KSA7391452, KSA7391461, KSA7495826, KSA6409187, KSA7304387, KSA7304455, KSA7304457, KSA5646288, KSA5646315, KSA6866907, KSA6866955, KSA6964897, KSA6590162, KSA6664076, KSA6477142, KSA6477177, KSA6477205, KSA6477248, KSA6808896, KSA6808920, KSA7304378, KSA7304383, KSA7304390, KSA7304393, KSA7304398, KSA7304403, KSA7304415, KSA7304447, KSA7304453, KSA7442790, KSA7120735, KSA7550162, KSA7120694, KSA6536503, KSA6536516, KSA5646282, KSA6649241, KSA6017447, KSA6689295, KSA7013917, KSA7013935, KSA7442883, KSA7162630, KSA6689287, KSA6689374, KSA5646258, KSA5646294, KSA5646323, KSA6017451, KSA6964873, KSA6964888, KSA6964904, KSA6964905, KSA6964944, KSA6964946, KSA6964961, KSA6964965, KSA7013896, KSA7013969, KSA6017342, KSA6017460, KSA6017468, KSA6899012, KSA6899065, KSA7520476, KSA6808931, KSA6808846, KSA6808898, KSA6945367, KSA6964902, KSA6623246, KSA6623253, KSA6623258, KSA6626685, KSA6626702, KSA6964870, KSA7574765, KSA7550160, KSA7574768, KSA7391419, KSA7391422, KSA7391498, KSA7550166, KSA6649221, KSA7304422, KSA6017322, KSA6017358, KSA6017397, KSA6017439, KSA6626710, KSA7391489, KSA7442873, KSA7391407, KSA7391462, KSA7391482, KSA7442778, KSA7442871, KSA7442880, KSA6590125, KSA7162624, KSA6409180, KSA7162596, KSA7754391, KSA6409198, KSA6899023, KSA6899024, KSA6899038, KSA6899049, KSA6899068, KSA6899069, KSA6899083, KSA6899088, KSA6017338, KSA6409188, KSA6808892, KSA6808892, KSA6808933, KSA6808933, KSA6017344, KSA6017415, KSA6017420, KSA6017430, KSA6689339, KSA7391501, KSA7391481, KSA6664040, KSA6664067, KSA7509837, KSA7509845, KSA7509851, KSA7509855, KSA7509856, KSA7509857, KSA7304441, KSA7391456, KSA7391477, KSA7442874, KSA7485743, KSA7485745, KSA7485750, KSA7485752, KSA5646261, KSA7716913, KSA7716923, KSA7716925, KSA7716928, KSA7716933, KSA7716934, KSA7716938, KSA7304365, KSA7391496, KSA7442786, KSA7442801, KSA7442878, KSA6017479, KSA6017497, KSA7495808, KSA7495809, KSA7495814, KSA7495815, KSA7495819, KSA7495821, KSA7495823, KSA7495827, KSA7495830, KSA7495831, KSA7495834, KSA7495836, KSA7509843, KSA7509850, KSA7509853, KSA7520468, KSA7520471, KSA7520475, KSA7442787, KSA7442828, KSA7442854, KSA7442892, KSA7120688, KSA6664025, KSA6945104, KSA6569900, KSA6945110, KSA6945325, KSA6945330, KSA7724023, KSA7732503, KSA6409234, KSA6536514, KSA6945153, KSA7013892, KSA7013894, KSA7013900, KSA7013915, KSA7013933, KSA7013937, KSA7013938, KSA7013943, KSA6689292, KSA6689296, KSA6689297, KSA6689315, KSA6689332, KSA6689359, KSA6689369, KSA6945158, KSA6945293, KSA6945207, KSA6945259, KSA6945364, KSA7442816, KSA7442851, KSA6477098, KSA6477113, KSA6477126, KSA6477163, KSA6477191, KSA6945098, KSA6945172, KSA7120696, KSA5646254, KSA6626682, KSA6964871, KSA6964874, KSA6964889, KSA6964892, KSA6964899, KSA6964935, KSA6964943, KSA6964959, KSA6945103, KSA6945105, KSA6945115, KSA6945122, KSA6945137, KSA6945138, KSA6945161, KSA6945169, KSA6945170, KSA6945174, KSA6945184, KSA6945195, KSA6945197, KSA6945200, KSA6945218, KSA6945221, KSA6945233, KSA6945237, KSA6945240, KSA6945267, KSA6945272, KSA6945280, KSA6945285, KSA6945286, KSA6945292, KSA6945309, KSA6945313, KSA6945324, KSA6945337, KSA6945345, KSA6945347, KSA6945348, KSA6945371, KSA6945386, KSA6964909, KSA6964915, KSA6964917, KSA6964939, KSA6964952, KSA6017326, KSA6017340, KSA6017353, KSA6017363, KSA6017379, KSA6017389, KSA6017425, KSA6017432, KSA6017438, KSA6945136, KSA6945320, KSA6964967, KSA6945268, KSA6945289, KSA6945301, KSA6945393, KSA6409216, KSA7120740, KSA7442810, KSA6569823, KSA6945117, KSA6945253, KSA6409251, KSA7120700, KSA6569813, KSA6945220, KSA6945234, KSA6409222, KSA6945176, KSA7442866, KSA5646324, KSA5646324, KSA6017496, KSA7013978, KSA6623212, KSA6623230, KSA6420033, KSA6649179, KSA6649182, KSA6649184, KSA6649212, KSA6649246, KSA6649251, KSA6649258, KSA6664008, KSA7727691, KSA7727701, KSA7732501, KSA7744955, KSA7744958, KSA7391403, KSA7391455, KSA7391492, KSA7304372, KSA7304414, KSA7732510, KSA7520478, KSA7391432, KSA7550176, KSA7716918, KSA7304379, KSA7162641, KSA7239672, KSA7239718, KSA7162590, KSA7442882, KSA7304395, KSA7304460, KSA6945374, KSA7013972, KSA6964879, KSA6964916, KSA6964948, KSA6866967, KSA7485749, KSA7391473, KSA6964893, KSA6623272, KSA6536527, KSA6536505, KSA6536521, KSA6536522, KSA6536523, KSA7509831, KSA7520485, KSA7550172, KSA7574778, KSA6536487, KSA6536492, KSA6536500, KSA7304456, KSA6536452, KSA6536458, KSA6664047, KSA7520469, KSA7520487, KSA7162576, KSA6536538, KSA6945390, KSA6664063, KSA6536444, KSA6536471, KSA6536474, KSA6536493, KSA7391437, KSA7096910.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2245-2026%22", "url": "https://recallledger.net/recalls/device-z-2245-2026-ge-healthcare-carescape-telemetry-server-ark-2250l-north-america-re/"}, {"id": "fda-device-z-2244-2026", "source": "FDA", "category": "device", "recall_number": "Z-2244-2026", "title": "GE HealthCare IOU ASSY ARK2250 CARESCAPE TELEMETRY SERVER recall (GE Medical Systems Information Technologies Inc)", "product": "GE HealthCare IOU ASSY ARK2250 CARESCAPE TELEMETRY SERVER, REF #2108729-901, Product Code SS9; ApexPro CARESCAPE Telemetry Server (CTS) v5.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)", "reason": "GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a persistent NO COMM or OFF NETWORK condition at the CARESCAPE Central Station or CIC Pro Clinical Information Center (Central Station).", "hazard_level": "Class II", "company": "GE Medical Systems Information Technologies Inc", "company_location": "Waukesha, WI, United States", "date": "2026-04-24", "report_date": "2026-06-03", "status": "Ongoing", "distribution": "Worldwide distribution.", "states": [], "nationwide": false, "quantity": "7 units", "codes": "Serial #/Sales Order #: SS920500004SA, SS920500005SA, SS920500003SA, SS920500006SA, SS921120011SA, SS921120019SA, SS921120015SA.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2244-2026%22", "url": "https://recallledger.net/recalls/device-z-2244-2026-ge-healthcare-iou-assy-ark2250-carescape-telemetry-server-ref-210872/"}, {"id": "fda-device-z-2243-2026", "source": "FDA", "category": "device", "recall_number": "Z-2243-2026", "title": "GE HealthCare APEXPRO v5.0 - ARK2250 - Software Disaster Recovery USB Kit - Orderable... recall (GE Medical Systems Information Technologies Inc)", "product": "GE HealthCare APEXPRO v5.0 - ARK2250 - Software Disaster Recovery USB Kit - Orderable by GE Service only, REF #2108523-01; ApexPro CARESCAPE Telemetry Server (CTS) v5.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)", "reason": "GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a persistent NO COMM or OFF NETWORK condition at the CARESCAPE Central Station or CIC Pro Clinical Information Center (Central Station).", "hazard_level": "Class II", "company": "GE Medical Systems Information Technologies Inc", "company_location": "Waukesha, WI, United States", "date": "2026-04-24", "report_date": "2026-06-03", "status": "Ongoing", "distribution": "Worldwide distribution.", "states": [], "nationwide": false, "quantity": "14 units", "codes": "UDI none, Serial number or Sales Order number SS921120014SA, SS921120017SA, SS921120021SA, SS921120018SA, SS921120020SA, SS920390001SA, SS921120007SA, SS921120008SA, SS921120012SA, SS921120016SA, SS920500001SA, SS920500002SA, SS921120009SA, SS921120010SA.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2243-2026%22", "url": "https://recallledger.net/recalls/device-z-2243-2026-ge-healthcare-apexpro-v5-0-ark2250-software-disaster-recovery-usb/"}, {"id": "fda-device-z-2242-2026", "source": "FDA", "category": "device", "recall_number": "Z-2242-2026", "title": "GE HealthCare CARESCAPE TELEMETRY SERVER V5 ATO MODEL recall (GE Medical Systems Information Technologies Inc)", "product": "GE HealthCare CARESCAPE TELEMETRY SERVER V5 ATO MODEL, REF #2063702-101, Product Code SS9; used in conjunction with ApexPro CARESCAPE Telemetry Server (CTS) v5.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)", "reason": "GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a persistent NO COMM or OFF NETWORK condition at the CARESCAPE Central Station or CIC Pro Clinical Information Center (Central Station).", "hazard_level": "Class II", "company": "GE Medical Systems Information Technologies Inc", "company_location": "Waukesha, WI, United States", "date": "2026-04-24", "report_date": "2026-06-03", "status": "Ongoing", "distribution": "Worldwide distribution.", "states": [], "nationwide": false, "quantity": "476 units", "codes": "UDI (01)00840682144773(10)v5.0.2R1C1, Serial Number or Sales Order Number: SS924160026SA, SS921080002SA, SS923080001SA, SS923080006SA, SS922460008SA, SS921320004SA, SS921320010SA, SS921320012SA, SS922120001SA, SS921210005SA, SS921060024SA, SS921060026SA, SS924290077SA, SS923290011SA, SS923290012SA, SS923290013SA, SS923290014SA, SS921520004SA, SS922080001SA, SS922080002SA, SS922120002SA, SS922120003SA, SS924200022SA, SS924450085SA, SS924220065SA, SS921210002SA, SS921210003SA, SS924220066SA, SS924050001SA, SS922170005SA, SS924160027SA, SS924160028SA, SS924160029SA, SS924160031SA, SS924160032SA, SS924160033SA, SS921300003SA, SS921420015SA, SS921420016SA, SS921520002SA, SS920520004SA, SS922250001SA, SS923510002SA, SS923510003SA, SS924160023SA, SS924170017SA, SS924200031SA, SS924200032SA, SS924090011SA, SS924090016SA, SS924090018SA, SS924090020SA, SS924090021SA, SS924090024SA, SS924140003SA, SS924140006SA, SS924140011SA, SS924140012SA, SS924140014SA, SS924170006SA, SS924170007SA, SS924170008SA, SS924170009SA, SS924170010SA, SS924170011SA, SS924170012SA, SS924170013SA, SS924170014SA, SS924170015SA, SS924170016SA, SS921110009SA, SS921420013SA, SS922170004SA, SS922340005SA, SS922290002SA, SS923220003SA, SS923290008SA, SS924020004SA, SS921040002SA, SS921050002SA, SS921060023SA, SS921060025SA, SS921060020SA, SS921060022SA, SS921060016SA, SS921060017SA, SS921060018SA, SS921060021SA, SS921110004SA, SS921110001SA, SS921240007SA, SS920490011SA, SS924430083SA, SS924050023SA, SS924060001SA, SS922080004SA, SS922080005SA, SS922080006SA, SS923240002SA, SS923520001SA, SS922120004SA, SS922390002SA, SS923400001SA, SS922340008SA, SS922340009SA, SS922340010SA, SS922020001SA, SS923230004SA, SS923230005SA, SS923230006SA, SS923470001SA, SS923470002SA, SS923470003SA, SS923470006SA, SS923470007SA, SS923480001SA, SS924060011SA, SS922240002SA, SS924060012SA, SS924070006SA, SS924070010SA, SS921110005SA, SS921180006SA, SS921420001SA, SS921470002SA, SS921470004SA, SS922250003SA, SS922340004SA, SS922460004SA, SS922460007SA, SS924060008SA, SS924060009SA, SS924060010SA, SS922130001SA, SS921300001SA, SS922410002SA, SS920500009SA, SS920500008SA, SS921240009SA, SS923430002SA, SS922010003SA, SS923370001SA, SS924050013SA, SS924050025SA, SS924050009SA, SS924050010SA, SS924050017SA, SS924290078SA, SS920430005SA, SS920430006SA, SS920460004SA, SS921140001SA, SS924040005SA, SS920450002SA, SS920450003SA, SS923230017SA, SS924070007SA, SS924070005SA, SS924090013SA, SS924090014SA, SS923250002SA, SS923250003SA, SS920520001SA, SS921180010SA, SS922340011SA, SS920490001SA, SS923030004SA, SS923240001SA, SS924140001SA, SS923110002SA, SS924040006SA, SS922310001SA, SS921080001SA, SS924050007SA, SS921180008SA, SS923520002SA, SS922340006SA, SS924050016SA, SS924050012SA, SS924150001SA, SS924150002SA, SS921320001SA, SS921320002SA, SS921320003SA, SS921320006SA, SS921320007SA, SS921320008SA, SS921320009SA, SS921320011SA, SS921300005SA, SS921240001SA, SS920450001SA, SS921300006SA, SS923450001SA, SS921520003SA, SS924130001SA, SS924130003SA, SS922410003SA, SS922460003SA, SS921520008SA, SS924130004SA, SS920430001SA, SS920510003SA, SS920510007SA, SS920510010SA, SS923070001SA, SS921300002SA, SS924070009SA, SS922040008SA, SS920510009SA, SS924050003SA, SS922090001SA, SS923290007SA, SS923300001SA, SS923300002SA, SS924050006SA, SS924050011SA, SS924050008SA, SS922080003SA, SS923030003SA, SS921130001SA, SS921150001SA, SS921150002SA, SS921460009SA, SS921320005SA, SS922180001SA, SS920490002SA, SS921460007SA, SS924050005SA, SS925270092SA, SS925270093SA, SS925270095SA, SS925270094SA, SS924160022SA, SS924050015SA, SS925330096SA, SS920430002SA, SS920430004SA, SS924070015SA, SS925260090SA, SS925260091SA, SS921460005SA, SS922250002SA, SS923030002SA, SS923030006SA, SS924050014SA, SS924430084SA, SS921470005SA, SS921210001SA, SS921210007SA, SS921210008SA, SS921210009SA, SS921210010SA, SS924050004SA, SS923230026SA, SS921420017SA, SS921150003SA, SS921050001SA, SS924070003SA, SS924070004SA, SS922120005SA, SS922250004SA, SS924200024SA, SS924200025SA, SS924200026SA, SS924200027SA, SS924200028SA, SS924200029SA, SS924200030SA, SS921110003SA, SS923110003SA, SS922390001SA, SS922290001SA, SS924140004SA, SS923200001SA, SS921150005SA, SS924090017SA, SS923290006SA, SS921240004SA, SS921240005SA, SS921240006SA, SS921240010SA, SS921460003SA, SS921420018SA, SS921420019SA, SS924170004SA, SS924170005SA, SS924170003SA, SS924090015SA, SS924140016SA, SS924090027SA, SS924090026SA, SS924090023SA, SS924090006SA, SS922040001SA, SS924090012SA, SS921110006SA, SS924170001SA, SS924170002SA, SS924090025SA, SS924090019SA, SS923070002SA, SS923070003SA, SS922040006SA, SS923400003SA, SS921300007SA, SS922380001SA, SS921460001SA, SS921460004SA, SS920430003SA, SS921250001SA, SS923220001SA, SS922050001SA, SS922050002SA, SS922050003SA, SS922050004SA, SS924200023SA, SS924010001SA, SS924070011SA, SS920500007SA, SS920500010SA, SS922010001SA, SS923320001SA, SS923230011SA, SS923230012SA, SS923230013SA, SS923230015SA, SS923230016SA, SS923230014SA, SS923230007SA, SS923230008SA, SS923230009SA, SS923230010SA, SS922290003SA, SS921460006SA, SS922300001SA, SS923230021SA, SS923230023SA, SS923230022SA, SS923230020SA, SS923230019SA, SS923230018SA, SS924220059SA, SS924220060SA, SS920490010SA, SS923080003SA, SS923080002SA, SS922460006SA, SS922460005SA, SS924040001SA, SS921040001SA, SS922210001SA, SS924150006SA, SS924470086SA, SS924070012SA, SS924070014SA, SS924150004SA, SS924070013SA, SS921520001SA, SS924160015SA, SS924160016SA, SS924160001SA, SS924160002SA, SS924160003SA, SS924160004SA, SS924160005SA, SS924160006SA, SS924160007SA, SS924160008SA, SS924160009SA, SS924160010SA, SS924160011SA, SS924160012SA, SS924160013SA, SS924160014SA, SS921460010SA, SS924160024SA, SS923290002SA, SS923290003SA, SS922220001SA, SS922220002SA, SS922220003SA, SS921130003SA, SS921130004SA, SS925140088SA, SS924130002SA, SS923290004SA, SS923290005SA, SS922110001SA, SS922110002SA, SS921520007SA, SS921520009SA, SS921520005SA, SS924420082SA, SS924420081SA, SS922010002SA, SS924090022SA, SS925120087SA, SS922040002SA, SS922040004SA, SS922040005SA, SS921180009SA, SS922040003SA, SS922040007SA, SS920490006SA, SS920490009SA, SS924040011SA, SS922460002SA, SS922050005SA, SS921490002SA, SS923080005SA, SS924070001SA, SS924040002SA, SS921470003SA, SS920490004SA, SS920510005SA, SS921210006SA, SS920520003SA, SS920510008SA, SS920490005SA, SS921240008SA, SS924040009SA, SS921150004SA, SS922300002SA, SS921420011SA, SS920490007SA, SS920490008SA, SS921420002SA, SS920490003SA, SS920510012SA, SS920510011SA, SS923250001SA, SS924040007SA, SS922390003SA, SS922420001SA, SS921130002SA, SS921350001SA, SS923110004SA, SS924050018SA, SS924050019SA, SS924050020SA, SS924050021SA, SS924050022SA, SS924050024SA, SS923210002SA, SS923210003SA, SS924050002SA, SS921300004SA, SS922340007SA, SS923400002SA, SS923420001SA, SS924020002SA, SS920510004SA, SS924060002SA, SS921520006SA, SS923080004SA, SS922240001SA, SS923030005SA, SS921460011SA, SS920510002SA, SS924020001SA, SS924020003SA, SS923030001SA, SS921210004SA, SS924150003SA, SS921060027SA, SS921030011SA, SS923170001SA, SS922170001SA, SS922170002SA, SS922170003SA, SS923230024SA, SS920510001SA, SS922310002SA, SS923290001SA, SS922300003SA.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2242-2026%22", "url": "https://recallledger.net/recalls/device-z-2242-2026-ge-healthcare-carescape-telemetry-server-v5-ato-model-ref-2063702-10/"}, {"id": "fda-device-z-2239-2026", "source": "FDA", "category": "device", "recall_number": "Z-2239-2026", "title": "HydroMARK Breast Biopsy Site Marker recall (Devicor Medical Products Inc)", "product": "HydroMARK Breast Biopsy Site Marker, Model Number: 4010-02-15-T3", "reason": "Incorrect inner package labeling. Boxes labeled 4010-02-15-T3 markers may contain individual packages labeled as T4 Markers.", "hazard_level": "Class II", "company": "Devicor Medical Products Inc", "company_location": "Cincinnati, OH, United States", "date": "2026-04-24", "report_date": "2026-06-03", "status": "Ongoing", "distribution": "Worldwide distribution - US Nationwide and the countries of Canada, Singapore.", "states": [], "nationwide": true, "quantity": "1910 units", "codes": "Lot Number: F12607207D", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2239-2026%22", "url": "https://recallledger.net/recalls/device-z-2239-2026-hydromark-breast-biopsy-site-marker-model-number-4010-02-15-t3/"}, {"id": "fda-device-z-2237-2026", "source": "FDA", "category": "device", "recall_number": "Z-2237-2026", "title": "Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection recall (Medline Industries, LP)", "product": "Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) SPINAL ANESTHESIA TRAY-LF, Medline Kit SKU DYNJRA0102A; 2) SPINAL TRAY-LF, Medline Kit SKU DYNJRA0143B; 3) SPINAL PREP TRAY-LF, Medline Kit SKU DYNJRA0205B; 4) SPINAL TRAY, Medline Kit SKU DYNJRA0255B; 5) SPINAL TRAY, Medline Kit SKU DYNJRA0320; 6) SPINAL TRAY, Medline Kit SKU DYNJRA0320A; 7) SPINAL BLOCK TRAY- LF, Medline Kit SKU DYNJRA0413C; 8) SPINAL TRAY, Medline Kit SKU DYNJRA0461D; 9) 25G SPINAL BLOCK TRAY, Medline Kit SKU DYNJRA0945; 10) SPINAL TRAY, Medline Kit SKU DYNJRA1140B; 11) SPINAL TRAY, Medline Kit SKU DYNJRA1192; 12) SPINAL TRAY 25G, Medline Kit SKU DYNJRA1240; 13) TRAY, SPINAL PENCIL POINT 25G, Medline Kit SKU DYNJRA1288; 14) SPINAL 25G WHITACRE, Medline Kit SKU DYNJRA1301; 15) SPINAL BLOCK TRAY WHITACRE 24G, Medline Kit SKU DYNJRA1304; 16) AHN SPINAL TRAY, Medline Kit SKU DYNJRA1376; 17) SPINAL TRAY, Medline Kit SKU DYNJRA1477A; 18) ADULT SPINAL KIT, Medline Kit SKU DYNJRA1538; 19) SPINAL TRAY, Medline Kit SKU DYNJRA1558A; 20) SPINAL TRAY, Medline Kit SKU DYNJRA1560A; 21) SPINAL TRAY, Medline Kit SKU DYNJRA1565; 22) SPINAL ANESTHESIA TRAY, Medline Kit SKU DYNJRA1577C; 23) SPINAL NEEDLE TRAY, Medline Kit SKU DYNJRA1584; 24) 25G WHITACRE SPINAL TRAY, Medline Kit SKU DYNJRA1740A; 25) SPINAL TRAY, Medline Kit SKU DYNJRA1744A; 26) SPINAL TRAY, Medline Kit SKU DYNJRA1750A; 27) SPINAL TRAY, Medline Kit SKU DYNJRA1784; 28) SPINAL TRAY, Medline Kit SKU DYNJRA1790; 29) SPINAL TRAY, Medline Kit SKU DYNJRA1796; 30) MSSC SPINAL TRAY, Medline Kit SKU DYNJRA1802B; 31) SPINAL TRAY, Medline Kit SKU DYNJRA1818; 32) SPINAL TRAY, Medline Kit SKU DYNJRA1839; 33) SPINAL TRAY, Medline Kit SKU DYNJRA1884; 34) SPINAL TRAY, Medline Kit SKU DYNJRA1884A; 35) 24G SPINAL KIT, Medline Kit SKU DYNJRA1889; 36) SPINAL TRAY, Medline Kit SKU DYNJRA1929; 37) SPINAL TRAY, Medline Kit SKU DYNJRA1969; 38) SPINAL TRAY, Medline Kit SKU DYNJRA1982; 39) SPINAL TRAY/PENCAN, Medline Kit SKU DYNJRA1983A; 40) SPINAL NEEDLE TRAY, Medline Kit SKU DYNJRA1987; 41) SPINAL TRAY - 3 ML CHLORAPREP, Medline Kit SKU DYNJRA2005; 42) SPINAL TRAY, Medline Kit SKU DYNJRA2023; 43) SPINAL TRAY, Medline Kit SKU DYNJRA2068A; 44) SPINAL BLOCK TRAY, Medline Kit SKU DYNJRA2088; 45) 25G WHITACRE SPINAL TRAY, Medline Kit SKU DYNJRA2115; 46) SPINAL BLOCK 25G WHTCRE 5S BU, Medline Kit SKU DYNJRA2117; 47) SPINAL TRAY, Medline Kit SKU DYNJRA2140; 48) SPINAL TRAY, Medline Kit SKU DYNJRA2153; 49) SPINAL BLOCK TRAY WHITACRE 24G, Medline Kit SKU DYNJRA2213; 50) SPINAL TRAY, Medline Kit SKU DYNJRA2225; 51) OR SPINAL BLOCK KIT, Medline Kit SKU DYNJRA2349; 52) SPINAL TRAY, Medline Kit SKU DYNJRA2360; 53) L&D SPINAL TRAY, Medline Kit SKU DYNJRA2371; 54) TRAY, 25G WHIT SPINAL W/PHARM, Medline Kit SKU DYNJRA2381; 55) SPINAL TRAY, Medline Kit SKU DYNJRA2432A; 56) OB SPINAL TRAY, Medline Kit SKU DYNJRA2532; 57) SPINAL TRAY, Medline Kit SKU DYNJRA2534; 58) SPINAL TRAY, Medline Kit SKU DYNJRA2556; 59) SPINAL TRAY, Medline Kit SKU DYNJRA2566A; 60) SPINAL TRAY BRAUN, Medline Kit SKU DYNJRA2575; 61) SPINAL TRAY, Medline Kit SKU DYNJRA2592; 62) SPINAL TRAY, Medline Kit SKU DYNJRA2597; 63) SPINAL BLOCK, Medline Kit SKU DYNJRA2605; 64) SPINAL TRAY, Medline Kit SKU DYNJRA2606; 65) SPINAL TRAY, Medline Kit SKU DYNJRA2607; 66) SPINAL TRAY, Medline Kit SKU DYNJRA2607A; 67) SPINAL TRAY, Medline Kit SKU DYNJRA2611; 68) SPINAL BLOCK TRAY, Medline Kit SKU DYNJRA2613; 69) SPINAL TRAY, Medline Kit SKU DYNJRA2618A; 70) SPINAL TRAY, Medline Kit SKU DYNJRA2634; 71) SPINAL TRAY, Medline Kit SKU DYNJRA2638; 72) SPINAL TRAY, Medline Kit SKU DYNJRA2639; 73) JOI SPINAL BLOCK TRAY, Medline Kit SKU DYNJRA2641; 74) SPINAL TRAY, Medline Kit SKU DYNJRA2653; 75) SPINAL BLOCK 25G WHTCRE 5S BU, Medline Kit SKU DYNJRA2669; 76) SPINAL TRAY, Medline Kit SKU DYNJRA2670; 77) SPINAL BLOCK TRAY 18G INTRO, Medline Kit SKU DYNJRA2672; 78) SPINAL TRAY 24G, Medline Kit", "reason": "Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.", "hazard_level": "Class I", "company": "Medline Industries, LP", "company_location": "Northfield, IL, United States", "date": "2026-04-10", "report_date": "2026-06-03", "status": "Ongoing", "distribution": "Worldwide - US Nationwide distribution in the US Territory of Virgin Islands and the countries of Bahamas, Panama, Barbados.", "states": [], "nationwide": true, "quantity": "200702 kits", "codes": "Medline Kit SKU DYNJRA0102A: UDI/DI 10884389459003 each, 40884389459004 case, Lot Number 26ABG838; Medline Kit SKU DYNJRA0102A: UDI/DI 10884389459003 each, 40884389459004 case, Lot Number 25JBR222; Medline Kit SKU DYNJRA0102A: UDI/DI 10884389459003 each, 40884389459004 case, Lot Number 25IBJ307; Medline Kit SKU DYNJRA0102A: UDI/DI 10884389459003 each, 40884389459004 case, Lot Number 25EBR346; Medline Kit SKU DYNJRA0102A: UDI/DI 10884389459003 each, 40884389459004 case, Lot Number 24LDB145; Medline Kit SKU DYNJRA0102A: UDI/DI 10884389459003 each, 40884389459004 case, Lot Number 24FDB896; Medline Kit SKU DYNJRA0143B: UDI/DI 10195327125820 each, 40195327125821 case, Lot Number 24ABQ670; Medline Kit SKU DYNJRA0205B: UDI/DI 10195327472344 each, 40195327472345 case, Lot Number 24KMD212; Medline Kit SKU DYNJRA0255B: UDI/DI 10195327282042 each, 40195327282043 case, Lot Number 26CMG585; Medline Kit SKU DYNJRA0255B: UDI/DI 10195327282042 each, 40195327282043 case, Lot Number 26BMK211; Medline Kit SKU DYNJRA0255B: UDI/DI 10195327282042 each, 40195327282043 case, Lot Number 25JMC385; Medline Kit SKU DYNJRA0255B: UDI/DI 10195327282042 each, 40195327282043 case, Lot Number 25IMB105; Medline Kit SKU DYNJRA0255B: UDI/DI 10195327282042 each, 40195327282043 case, Lot Number 25EMC687; Medline Kit SKU DYNJRA0255B: UDI/DI 10195327282042 each, 40195327282043 case, Lot Number 24HMD675; Medline Kit SKU DYNJRA0255B: UDI/DI 10195327282042 each, 40195327282043 case, Lot Number 24HMB249; Medline Kit SKU DYNJRA0255B: UDI/DI 10195327282042 each, 40195327282043 case, Lot Number 24GMH436; Medline Kit SKU DYNJRA0320: UDI/DI 10884389656778 each, 40884389656779 case, Lot Number 24EDB314; Medline Kit SKU DYNJRA0320: UDI/DI 10884389656778 each, 40884389656779 case, Lot Number 24BDA550; Medline Kit SKU DYNJRA0320A: UDI/DI 10198459027796 each, 40198459027797 case, Lot Number 26ABJ309; Medline Kit SKU DYNJRA0320A: UDI/DI 10198459027796 each, 40198459027797 case, Lot Number 25HBT750; Medline Kit SKU DYNJRA0320A: UDI/DI 10198459027796 each, 40198459027797 case, Lot Number 25GBW261; Medline Kit SKU DYNJRA0320A: UDI/DI 10198459027796 each, 40198459027797 case, Lot Number 25FBP025; Medline Kit SKU DYNJRA0413C: UDI/DI 10195327253363 each, 40195327253364 case, Lot Number 26AMK323; Medline Kit SKU DYNJRA0413C: UDI/DI 10195327253363 each, 40195327253364 case, Lot Number 25HMB655; Medline Kit SKU DYNJRA0413C: UDI/DI 10195327253363 each, 40195327253364 case, Lot Number 25FMF763; Medline Kit SKU DYNJRA0413C: UDI/DI 10195327253363 each, 40195327253364 case, Lot Number 24KMF380; Medline Kit SKU DYNJRA0413C: UDI/DI 10195327253363 each, 40195327253364 case, Lot Number 24KMA760; Medline Kit SKU DYNJRA0413C: UDI/DI 10195327253363 each, 40195327253364 case, Lot Number 23IBH412; Medline Kit SKU DYNJRA0461D: UDI/DI 10195327120689 each, 40195327120680 case, Lot Number 24KME483; Medline Kit SKU DYNJRA0461D: UDI/DI 10195327120689 each, 40195327120680 case, Lot Number 23KMD757; Medline Kit SKU DYNJRA0945: UDI/DI 10889942598267 each, 40889942598268 case, Lot Number 26BBP431; Medline Kit SKU DYNJRA0945: UDI/DI 10889942598267 each, 40889942598268 case, Lot Number 25KBN750; Medline Kit SKU DYNJRA0945: UDI/DI 10889942598267 each, 40889942598268 case, Lot Number 25IBK141; Medline Kit SKU DYNJRA0945: UDI/DI 10889942598267 each, 40889942598268 case, Lot Number 25EBG343; Medline Kit SKU DYNJRA0945: UDI/DI 10889942598267 each, 40889942598268 case, Lot Number 25ADA288; Medline Kit SKU DYNJRA0945: UDI/DI 10889942598267 each, 40889942598268 case, Lot Number 24FDA636; Medline Kit SKU DYNJRA1140B: UDI/DI 10193489432015 each, 40193489432016 case, Lot Number 26BMI341; Medline Kit SKU DYNJRA1140B: UDI/DI 10193489432015 each, 40193489432016 case, Lot Number 25LMF246; Medline Kit SKU DYNJRA1140B: UDI/DI 10193489432015 each, 40193489432016 case, Lot Number 25JMA359; Medline Kit SKU DYNJRA1140B: UDI/DI 10193489432015 each, 40193489432016 case, Lot Number 25GMB242; Medline Kit SKU DYNJRA1140B: UDI/DI 10193489432015 each, 40193489432016 case, Lot Number 25DMI678; Medline Kit SKU DYNJRA1140B: UDI/DI 10193489432015 each, 40193489432016 case, Lot Number 24JMA139; Medline Kit SKU DYNJRA1140B: UDI/DI 10193489432015 each, 40193489432016 case, Lot Number 24BME491; Medline Kit SKU DYNJRA1140B: UDI/DI 10193489432015 each, 40193489432016 case, Lot Number 23KMB687; Medline Kit SKU DYNJRA1140B: UDI/DI 10193489432015 each, 40193489432016 case, Lot Number 23HMD531; Medline Kit SKU DYNJRA1192: UDI/DI 10888277762947 each, 40888277762948 case, Lot Number 24JDA083; Medline Kit SKU DYNJRA1192: UDI/DI 10888277762947 each, 40888277762948 case, Lot Number 24FDA375; Medline Kit SKU DYNJRA1192: UDI/DI 10888277762947 each, 40888277762948 case, Lot Number 24CDA048; Medline Kit SKU DYNJRA1192: UDI/DI 10888277762947 each, 40888277762948 case, Lot Number 23KDC201; Medline Kit SKU DYNJRA1192: UDI/DI 10888277762947 each, 40888277762948 case, Lot Number 23JDA946; Medline Kit SKU DYNJRA1240: UDI/DI 10889942965144 each, 40889942965145 case, Lot Number 26AMG752; Medline Kit SKU DYNJRA1240: UDI/DI 10889942965144 each, 40889942965145 case, Lot Number 25LME370; Medline Kit SKU DYNJRA1240: UDI/DI 10889942965144 each, 40889942965145 case, Lot Number 25HMC381; Medline Kit SKU DYNJRA1240: UDI/DI 10889942965144 each, 40889942965145 case, Lot Number 25GMG557; Medline Kit SKU DYNJRA1240: UDI/DI 10889942965144 each, 40889942965145 case, Lot Number 25FMD116; Medline Kit SKU DYNJRA1240: UDI/DI 10889942965144 each, 40889942965145 case, Lot Number 24JMA140; Medline Kit SKU DYNJRA1240: UDI/DI 10889942965144 each, 40889942965145 case, Lot Number 24IMH937; Medline Kit SKU DYNJRA1240: UDI/DI 10889942965144 each, 40889942965145 case, Lot Number 24BMH596; Medline Kit SKU DYNJRA1240: UDI/DI 10889942965144 each, 40889942965145 case, Lot Number 23JMF215; Medline Kit SKU DYNJRA1240: UDI/DI 10889942965144 each, 40889942965145 case, Lot Number 23HMI647; Medline Kit SKU DYNJRA1288: UDI/DI 10193489566291 each, 40193489566292 case, Lot Number 25IMI489; Medline Kit SKU DYNJRA1288: UDI/DI 10193489566291 each, 40193489566292 case, Lot Number 25HMB361; Medline Kit SKU DYNJRA1288: UDI/DI 10193489566291 each, 40193489566292 case, Lot Number 25DMG334; Medline Kit SKU DYNJRA1288: UDI/DI 10193489566291 each, 40193489566292 case, Lot Number 25DMD623; Medline Kit SKU DYNJRA1288: UDI/DI 10193489566291 each, 40193489566292 case, Lot Number 25DMC001; Medline Kit SKU DYNJRA1288: UDI/DI 10193489566291 each, 40193489566292 case, Lot Number 24JMA144; Medline Kit SKU DYNJRA1288: UDI/DI 10193489566291 each, 40193489566292 case, Lot Number 24GMI472; Medline Kit SKU DYNJRA1288: UDI/DI 10193489566291 each, 40193489566292 case, Lot Number 24GMG962; Medline Kit SKU DYNJRA1288: UDI/DI 10193489566291 each, 40193489566292 case, Lot Number 24GMA452; Medline Kit SKU DYNJRA1288: UDI/DI 10193489566291 each, 40193489566292 case, Lot Number 24DMF012; Medline Kit SKU DYNJRA1288: UDI/DI 10193489566291 each, 40193489566292 case, Lot Number 23IBL331; Medline Kit SKU DYNJRA1301: UDI/DI 10193489586732 each, 40193489586733 case, Lot Number 26BBQ480; Medline Kit SKU DYNJRA1301: UDI/DI 10193489586732 each, 40193489586733 case, Lot Number 25IBR270; Medline Kit SKU DYNJRA1301: UDI/DI 10193489586732 each, 40193489586733 case, Lot Number 25GBE596; Medline Kit SKU DYNJRA1301: UDI/DI 10193489586732 each, 40193489586733 case, Lot Number 24KDB789; Medline Kit SKU DYNJRA1301: UDI/DI 10193489586732 each, 40193489586733 case, Lot Number 24FDA635; Medline Kit SKU DYNJRA1304: UDI/DI 10193489590135 each, 40193489590136 case, Lot Number 25JMA655; Medline Kit SKU DYNJRA1304: UDI/DI 10193489590135 each, 40193489590136 case, Lot Number 25IMF958; Medline Kit SKU DYNJRA1304: UDI/DI 10193489590135 each, 40193489590136 case, Lot Number 24JMB108; Medline Kit SKU DYNJRA1304: UDI/DI 10193489590135 each, 40193489590136 case, Lot Number 24DMG675; Medline Kit SKU DYNJRA1304: UDI/DI 10193489590135 each, 40193489590136 case, Lot Number 23IBM788; Medline Kit SKU DYNJRA1376: UDI/DI 10193489658941 each, 40193489658942 case, Lot Number 26BBQ529; Medline Kit SKU DYNJRA1376: UDI/DI 10193489658941 each, 40193489658942 case, Lot Number 26ABT406; Medline Kit SKU DYNJRA1376: UDI/DI 10193489658941 each, 40193489658942 case, Lot Number 25LBT592; Medline Kit SKU DYNJRA1376: UDI/DI 10193489658941 each, 40193489658942 case, Lot Number 25KBR352; Medline Kit SKU DYNJRA1376: UDI/DI 10193489658941 each, 40193489658942 case, Lot Number 25JBO649; Medline Kit SKU DYNJRA1376: UDI/DI 10193489658941 each, 40193489658942 case, Lot Number 25JBB377; Medline Kit SKU DYNJRA1376: UDI/DI 10193489658941 each, 40193489658942 case, Lot Number 25HBP557; Medline Kit SKU DYNJRA1376: UDI/DI 10193489658941 each, 40193489658942 case, Lot Number 25FBU697; Medline Kit SKU DYNJRA1376: UDI/DI 10193489658941 each, 40193489658942 case, Lot Number 25DBT832; Medline Kit SKU DYNJRA1376: UDI/DI 10193489658941 each, 40193489658942 case, Lot Number 25CBC755; Medline Kit SKU DYNJRA1376: UDI/DI 10193489658941 each, 40193489658942 case, Lot Number 23JBI433; Medline Kit SKU DYNJRA1376: UDI/DI 10193489658941 each, 40193489658942 case, Lot Number 23IBL601; Medline Kit SKU DYNJRA1376: UDI/DI 10193489658941 each, 40193489658942 case, Lot Number 23GBW707; Medline Kit SKU DYNJRA1376: UDI/DI 10193489658941 each, 40193489658942 case, Lot Number 23GBE466; Medline Kit SKU DYNJRA1477A: UDI/DI 10195327298692 each, 40195327298693 case, Lot Number 23JBC917; Medline Kit SKU DYNJRA1538: UDI/DI 10193489215366 each, 40193489215367 case, Lot Number 26ABT377; Medline Kit SKU DYNJRA1538: UDI/DI 10193489215366 each, 40193489215367 case, Lot Number 26ABD865; Medline Kit SKU DYNJRA1538: UDI/DI 10193489215366 each, 40193489215367 case, Lot Number 25KBB315; Medline Kit SKU DYNJRA1538: UDI/DI 10193489215366 each, 40193489215367 case, Lot Number 25HBT787; Medline Kit SKU DYNJRA1538: UDI/DI 10193489215366 each, 40193489215367 case, Lot Number 25HBJ292; Medline Kit SKU DYNJRA1538: UDI/DI 10193489215366 each, 40193489215367 case, Lot Number 25FBN804; Medline Kit SKU DYNJRA1538: UDI/DI 10193489215366 each, 40193489215367 case, Lot Number 25EBM784; Medline Kit SKU DYNJRA1538: UDI/DI 10193489215366 each, 40193489215367 case, Lot Number 25ALA898; Medline Kit SKU DYNJRA1538: UDI/DI 10193489215366 each, 40193489215367 case, Lot Number 24FLA415; Medline Kit SKU DYNJRA1538: UDI/DI 10193489215366 each, 40193489215367 case, Lot Number 24DLB151; Medline Kit SKU DYNJRA1538: UDI/DI 10193489215366 each, 40193489215367 case, Lot Number 24BLA472; Medline Kit SKU DYNJRA1538: UDI/DI 10193489215366 each, 40193489215367 case, Lot Number 23JLB282; Medline Kit SKU DYNJRA1538: UDI/DI 10193489215366 each, 40193489215367 case, Lot Number 23ILA430; Medline Kit SKU DYNJRA1558A: UDI/DI 10193489422450 each, 40193489422451 case, Lot Number 26ABM540; Medline Kit SKU DYNJRA1558A: UDI/DI 10193489422450 each, 40193489422451 case, Lot Number 25IBO446; Medline Kit SKU DYNJRA1558A: UDI/DI 10193489422450 each, 40193489422451 case, Lot Number 25GBR046; Medline Kit SKU DYNJRA1558A: UDI/DI 10193489422450 each, 40193489422451 case, Lot Number 25GBP595; Medline Kit SKU DYNJRA1558A: UDI/DI 10193489422450 each, 40193489422451 case, Lot Number 25DBM632; Medline Kit SKU DYNJRA1558A: UDI/DI 10193489422450 each, 40193489422451 case, Lot Number 23ILA580; Medline Kit SKU DYNJRA1560A: UDI/DI 10193489992427 each, 40193489992428 case, Lot Number 26CLA918; Medline Kit SKU DYNJRA1560A: UDI/DI 10193489992427 each, 40193489992428 case, Lot Number 25LLA085; Medline Kit SKU DYNJRA1560A: UDI/DI 10193489992427 each, 40193489992428 case, Lot Number 25HLA940; Medline Kit SKU DYNJRA1560A: UDI/DI 10193489992427 each, 40193489992428 case, Lot Number 25DLA809; Medline Kit SKU DYNJRA1560A: UDI/DI 10193489992427 each, 40193489992428 case, Lot Number 25ALA743; Medline Kit SKU DYNJRA1560A: UDI/DI 10193489992427 each, 40193489992428 case, Lot Number 24ALA606; Medline Kit SKU DYNJRA1565: UDI/DI 10193489251654 each, 40193489251655 case, Lot Number 26BBJ338; Medline Kit SKU DYNJRA1565: UDI/DI 10193489251654 each, 40193489251655 case, Lot Number 25LBJ822; Medline Kit SKU DYNJRA1565: UDI/DI 10193489251654 each, 40193489251655 case, Lot Number 25HBT749; Medline Kit SKU DYNJRA1565: UDI/DI 10193489251654 each, 40193489251655 case, Lot Number 25FBB360; Medline Kit SKU DYNJRA1565: UDI/DI 10193489251654 each, 40193489251655 case, Lot Number 25ALA674; Medline Kit SKU DYNJRA1577C: UDI/DI 10198459030956 each, 40198459030957 case, Lot Number 26CBF846; Medline Kit SKU DYNJRA1577C: UDI/DI 10198459030956 each, 40198459030957 case, Lot Number 26ABC756; Medline Kit SKU DYNJRA1584: UDI/DI 10193489278408 each, 40193489278409 case, Lot Number 24LLA814; Medline Kit SKU DYNJRA1584: UDI/DI 10193489278408 each, 40193489278409 case, Lot Number 23KLA590; Medline Kit SKU DYNJRA1740A: UDI/DI 10195327088934 each, 40195327088935 case, Lot Number 26BMI370; Medline Kit SKU DYNJRA1740A: UDI/DI 10195327088934 each, 40195327088935 case, Lot Number 26AMD201; Medline Kit SKU DYNJRA1740A: UDI/DI 10195327088934 each, 40195327088935 case, Lot Number 25JMJ116; Medline Kit SKU DYNJRA1740A: UDI/DI 10195327088934 each, 40195327088935 case, Lot Number 25IMI411; Medline Kit SKU DYNJRA1740A: UDI/DI 10195327088934 each, 40195327088935 case, Lot Number 25GMB253; Medline Kit SKU DYNJRA1740A: UDI/DI 10195327088934 each, 40195327088935 case, Lot Number 25DMI661; Medline Kit SKU DYNJRA1740A: UDI/DI 10195327088934 each, 40195327088935 case, Lot Number 25DMD627; Medline Kit SKU DYNJRA1740A: UDI/DI 10195327088934 each, 40195327088935 case, Lot Number 25CMJ576; Medline Kit SKU DYNJRA1740A: UDI/DI 10195327088934 each, 40195327088935 case, Lot Number 25AMI062; Medline Kit SKU DYNJRA1740A: UDI/DI 10195327088934 each, 40195327088935 case, Lot Number 24JMI045; Medline Kit SKU DYNJRA1740A: UDI/DI 10195327088934 each, 40195327088935 case, Lot Number 24JMA122; Medline Kit SKU DYNJRA1740A: UDI/DI 10195327088934 each, 40195327088935 case, Lot Number 24GMJ821; Medline Kit SKU DYNJRA1740A: UDI/DI 10195327088934 each, 40195327088935 case, Lot Number 24CMF337; Medline Kit SKU DYNJRA1740A: UDI/DI 10195327088934 each, 40195327088935 case, Lot Number 24BBP807; Medline Kit SKU DYNJRA1740A: UDI/DI 10195327088934 each, 40195327088935 case, Lot Number 23JBA530; Medline Kit SKU DYNJRA1740A: UDI/DI 10195327088934 each, 40195327088935 case, Lot Number 23HBJ527; Medline Kit SKU DYNJRA1744A: UDI/DI 10195327297749 each, 40195327297740 case, Lot Number 26BBH656; Medline Kit SKU DYNJRA1750A: UDI/DI 10198459270192 each, 40198459270193 case, Lot Number 25CBF201; Medline Kit SKU DYNJRA1784: UDI/DI 10193489875126 each, 40193489875127 case, Lot Number 24CMA243; Medline Kit SKU DYNJRA1784: UDI/DI 10193489875126 each, 40193489875127 case, Lot Number 23KMD775; Medline Kit SKU DYNJRA1790: UDI/DI 10193489880441 each, 40193489880442 case, Lot Number 24GLA034; Medline Kit SKU DYNJRA1790: UDI/DI 10193489880441 each, 40193489880442 case, Lot Number 24ALA809; Medline Kit SKU DYNJRA1796: UDI/DI 10193489898477 each, 40193489898478 case, Lot Number 25GMB228; Medline Kit SKU DYNJRA1796: UDI/DI 10193489898477 each, 40193489898478 case, Lot Number 25BMC173; Medline Kit SKU DYNJRA1796: UDI/DI 10193489898477 each, 40193489898478 case, Lot Number 24KME293; Medline Kit SKU DYNJRA1796: UDI/DI 10193489898477 each, 40193489898478 case, Lot Number 24KMC186; Medline Kit SKU DYNJRA1796: UDI/DI 10193489898477 each, 40193489898478 case, Lot Number 24JMI040; Medline Kit SKU DYNJRA1796: UDI/DI 10193489898477 each, 40193489898478 case, Lot Number 23IBC188; Medline Kit SKU DYNJRA1796: UDI/DI 10193489898477 each, 40193489898478 case, Lot Number 23HBH576; Medline Kit SKU DYNJRA1802B: UDI/DI 10195327343897 each, 40195327343898 case, Lot Number 24BBA726; Medline Kit SKU DYNJRA1818: UDI/DI 10193489946888 each, 40193489946889 case, Lot Number 26BBT339; Medline Kit SKU DYNJRA1818: UDI/DI 10193489946888 each, 40193489946889 case, Lot Number 26ABW298; Medline Kit SKU DYNJRA1818: UDI/DI 10193489946888 each, 40193489946889 case, Lot Number 25LBJ837; Medline Kit SKU DYNJRA1818: UDI/DI 10193489946888 each, 40193489946889 case, Lot Number 25JBO685; Medline Kit SKU DYNJRA1818: UDI/DI 10193489946888 each, 40193489946889 case, Lot Number 25IBA272; Medline Kit SKU DYNJRA1818: UDI/DI 10193489946888 each, 40193489946889 case, Lot Number 25GBK749; Medline Kit SKU DYNJRA1818: UDI/DI 10193489946888 each, 40193489946889 case, Lot Number 25FBH676; Medline Kit SKU DYNJRA1818: UDI/DI 10193489946888 each, 40193489946889 case, Lot Number 25CBD837; Medline Kit SKU DYNJRA1818: UDI/DI 10193489946888 each, 40193489946889 case, Lot Number 25ALA358; Medline Kit SKU DYNJRA1818: UDI/DI 10193489946888 each, 40193489946889 case, Lot Number 25ALA119; Medline Kit SKU DYNJRA1818: UDI/DI 10193489946888 each, 40193489946889 case, Lot Number 24KLA542; Medline Kit SKU DYNJRA1818: UDI/DI 10193489946888 each, 40193489946889 case, Lot Number 24FLA929; Medline Kit SKU DYNJRA1818: UDI/DI 10193489946888 each, 40193489946889 case, Lot Number 24DLA123; Medline Kit SKU DYNJRA1818: UDI/DI 10193489946888 each, 40193489946889 case, Lot Number 24ALA052; Medline Kit SKU DYNJRA1818: UDI/DI 10193489946888 each, 40193489946889 case, Lot Number 23KLA873; Medline Kit SKU DYNJRA1818: UDI/DI 10193489946888 each, 40193489946889 case, Lot Number 23JLA294; Medline Kit SKU DYNJRA1818: UDI/DI 10193489946888 each, 40193489946889 case, Lot Number 23ILA293; Medline Kit SKU DYNJRA1839: UDI/DI 10193489981605 each, 40193489981606 case, Lot Number 26BBS481; Medline Kit SKU DYNJRA1839: UDI/DI 10193489981605 each, 40193489981606 case, Lot Number 26BBB042; Medline Kit SKU DYNJRA1839: UDI/DI 10193489981605 each, 40193489981606 case, Lot Number 26ABQ774; Medline Kit SKU DYNJRA1839: UDI/DI 10193489981605 each, 40193489981606 case, Lot Number 25HBB827; Medline Kit SKU DYNJRA1839: UDI/DI 10193489981605 each, 40193489981606 case, Lot Number 25GBF892; Medline Kit SKU DYNJRA1839: UDI/DI 10193489981605 each, 40193489981606 case, Lot Number 24FBT400; Medline Kit SKU DYNJRA1839: UDI/DI 10193489981605 each, 40193489981606 case, Lot Number 23HBG227; Medline Kit SKU DYNJRA1884: UDI/DI 10195327044442 each, 40195327044443 case, Lot Number 24ALA860; Medline Kit SKU DYNJRA1884: UDI/DI 10195327044442 each, 40195327044443 case, Lot Number 23LLA854; Medline Kit SKU DYNJRA1884: UDI/DI 10195327044442 each, 40195327044443 case, Lot Number 23JLA222; Medline Kit SKU DYNJRA1884: UDI/DI 10195327044442 each, 40195327044443 case, Lot Number 23ILA091; Medline Kit SKU DYNJRA1884A: UDI/DI 10195327630461 each, 40195327630462 case, Lot Number 26BBQ460; Medline Kit SKU DYNJRA1884A: UDI/DI 10195327630461 each, 40195327630462 case, Lot Number 26ABS301; Medline Kit SKU DYNJRA1884A: UDI/DI 10195327630461 each, 40195327630462 case, Lot Number 25JBT564; Medline Kit SKU DYNJRA1884A: UDI/DI 10195327630461 each, 40195327630462 case, Lot Number 25JBD791; Medline Kit SKU DYNJRA1884A: UDI/DI 10195327630461 each, 40195327630462 case, Lot Number 25IBJ312; Medline Kit SKU DYNJRA1884A: UDI/DI 10195327630461 each, 40195327630462 case, Lot Number 25GBA592; Medline Kit SKU DYNJRA1884A: UDI/DI 10195327630461 each, 40195327630462 case, Lot Number 25EBO914; Medline Kit SKU DYNJRA1884A: UDI/DI 10195327630461 each, 40195327630462 case, Lot Number 24GBI534; Medline Kit SKU DYNJRA1889: UDI/DI 10195327052409 each, 40195327052400 case, Lot Number 25LBL251; Medline Kit SKU DYNJRA1889: UDI/DI 10195327052409 each, 40195327052400 case, Lot Number 25LBG746; Medline Kit SKU DYNJRA1889: UDI/DI 10195327052409 each, 40195327052400 case, Lot Number 25KBN759; Medline Kit SKU DYNJRA1889: UDI/DI 10195327052409 each, 40195327052400 case, Lot Number 25HBG277; Medline Kit SKU DYNJRA1889: UDI/DI 10195327052409 each, 40195327052400 case, Lot Number 25FBL050; Medline Kit SKU DYNJRA1889: UDI/DI 10195327052409 each, 40195327052400 case, Lot Number 24BBR617; Medline Kit SKU DYNJRA1889: UDI/DI 10195327052409 each, 40195327052400 case, Lot Number 23JBE887; Medline Kit SKU DYNJRA1889: UDI/DI 10195327052409 each, 40195327052400 case, Lot Number 23GBP040; Medline Kit SKU DYNJRA1929: UDI/DI 10195327117436 each, 40195327117437 case, Lot Number 25JMH654; Medline Kit SKU DYNJRA1929: UDI/DI 10195327117436 each, 40195327117437 case, Lot Number 25GMB229; Medline Kit SKU DYNJRA1929: UDI/DI 10195327117436 each, 40195327117437 case, Lot Number 25DMF106; Medline Kit SKU DYNJRA1929: UDI/DI 10195327117436 each, 40195327117437 case, Lot Number 24FMI985; Medline Kit SKU DYNJRA1969: UDI/DI 10195327155759 each, 40195327155750 case, Lot Number 26BBJ366; Medline Kit SKU DYNJRA1969: UDI/DI 10195327155759 each, 40195327155750 case, Lot Number 26ABJ212; Medline Kit SKU DYNJRA1969: UDI/DI 10195327155759 each, 40195327155750 case, Lot Number 25KBR357; Medline Kit SKU DYNJRA1969: UDI/DI 10195327155759 each, 40195327155750 case, Lot Number 25IBI578; Medline Kit SKU DYNJRA1969: UDI/DI 10195327155759 each, 40195327155750 case, Lot Number 25GBS433; Medline Kit SKU DYNJRA1969: UDI/DI 10195327155759 each, 40195327155750 case, Lot Number 25DBS842; Medline Kit SKU DYNJRA1969: UDI/DI 10195327155759 each, 40195327155750 case, Lot Number 25BBJ513; Medline Kit SKU DYNJRA1969: UDI/DI 10195327155759 each, 40195327155750 case, Lot Number 24BBR619; Medline Kit SKU DYNJRA1969: UDI/DI 10195327155759 each, 40195327155750 case, Lot Number 23JBI474; Medline Kit SKU DYNJRA1969: UDI/DI 10195327155759 each, 40195327155750 case, Lot Number 23IBG943; Medline Kit SKU DYNJRA1969: UDI/DI 10195327155759 each, 40195327155750 case, Lot Number 23GBW701; Medline Kit SKU DYNJRA1969: UDI/DI 10195327155759 each, 40195327155750 case, Lot Number 23GBG665; Medline Kit SKU DYNJRA1982: UDI/DI 10195327172220 each, 40195327172221 case, Lot Number 25KBH337; Medline Kit SKU DYNJRA1982: UDI/DI 10195327172220 each, 40195327172221 case, Lot Number 25FBJ700; Medline Kit SKU DYNJRA1982: UDI/DI 10195327172220 each, 40195327172221 case, Lot Number 25DBP048; Medline Kit SKU DYNJRA1982: UDI/DI 10195327172220 each, 40195327172221 case, Lot Number 23IBU749; Medline Kit SKU DYNJRA1982: UDI/DI 10195327172220 each, 40195327172221 case, Lot Number 23HBN821; Medline Kit SKU DYNJRA1983A: UDI/DI 10195327328559 each, 40195327328550 case, Lot Number 24HMA882; Medline Kit SKU DYNJRA1983A: UDI/DI 10195327328559 each, 40195327328550 case, Lot Number 24FMI986; Medline Kit SKU DYNJRA1983A: UDI/DI 10195327328559 each, 40195327328550 case, Lot Number 24DMB103; Medline Kit SKU DYNJRA1983A: UDI/DI 10195327328559 each, 40195327328550 case, Lot Number 24CMH742; Medline Kit SKU DYNJRA1983A: UDI/DI 10195327328559 each, 40195327328550 case, Lot Number 24BBP805; Medline Kit SKU DYNJRA1983A: UDI/DI 10195327328559 each, 40195327328550 case, Lot Number 23JBI335; Medline Kit SKU DYNJRA1983A: UDI/DI 10195327328559 each, 40195327328550 case, Lot Number 23JBB539; Medline Kit SKU DYNJRA1983A: UDI/DI 10195327328559 each, 40195327328550 case, Lot Number 23IBM793; Medline Kit SKU DYNJRA1983A: UDI/DI 10195327328559 each, 40195327328550 case, Lot Number 23HBX589; Medline Kit SKU DYNJRA1983A: UDI/DI 10195327328559 each, 40195327328550 case, Lot Number 23GBO102; Medline Kit SKU DYNJRA1987: UDI/DI 10195327178055 each, 40195327178056 case, Lot Number 25DMI991; Medline Kit SKU DYNJRA1987: UDI/DI 10195327178055 each, 40195327178056 case, Lot Number 24IMG184; Medline Kit SKU DYNJRA1987: UDI/DI 10195327178055 each, 40195327178056 case, Lot Number 24CMJ744; Medline Kit SKU DYNJRA1987: UDI/DI 10195327178055 each, 40195327178056 case, Lot Number 24CME769; Medline Kit SKU DYNJRA2005: UDI/DI 10195327211134 each, 40195327211135 case, Lot Number 26BMI302; Medline Kit SKU DYNJRA2005: UDI/DI 10195327211134 each, 40195327211135 case, Lot Number 25HME970; Medline Kit SKU DYNJRA2005: UDI/DI 10195327211134 each, 40195327211135 case, Lot Number 25EMI731; Medline Kit SKU DYNJRA2005: UDI/DI 10195327211134 each, 40195327211135 case, Lot Number 24KME368; Medline Kit SKU DYNJRA2005: UDI/DI 10195327211134 each, 40195327211135 case, Lot Number 24KMD667; Medline Kit SKU DYNJRA2005: UDI/DI 10195327211134 each, 40195327211135 case, Lot Number 24GMI469; Medline Kit SKU DYNJRA2023: UDI/DI 10195327218140 each, 40195327218141 case, Lot Number 26BMH421; Medline Kit SKU DYNJRA2023: UDI/DI 10195327218140 each, 40195327218141 case, Lot Number 25IMI450; Medline Kit SKU DYNJRA2023: UDI/DI 10195327218140 each, 40195327218141 case, Lot Number 25HMC853; Medline Kit SKU DYNJRA2023: UDI/DI 10195327218140 each, 40195327218141 case, Lot Number 25CMI825; Medline Kit SKU DYNJRA2023: UDI/DI 10195327218140 each, 40195327218141 case, Lot Number 25BMH953; Medline Kit SKU DYNJRA2023: UDI/DI 10195327218140 each, 40195327218141 case, Lot Number 24HMD118; Medline Kit SKU DYNJRA2023: UDI/DI 10195327218140 each, 40195327218141 case, Lot Number 24BBO065; Medline Kit SKU DYNJRA2023: UDI/DI 10195327218140 each, 40195327218141 case, Lot Number 23IBL654; Medline Kit SKU DYNJRA2023: UDI/DI 10195327218140 each, 40195327218141 case, Lot Number 23HBR220; Medline Kit SKU DYNJRA2068A: UDI/DI 10195327427870 each, 40195327427871 case, Lot Number 26AMK410; Medline Kit SKU DYNJRA2068A: UDI/DI 10195327427870 each, 40195327427871 case, Lot Number 26AMH169; Medline Kit SKU DYNJRA2068A: UDI/DI 10195327427870 each, 40195327427871 case, Lot Number 25KMJ048; Medline Kit SKU DYNJRA2068A: UDI/DI 10195327427870 each, 40195327427871 case, Lot Number 25IMA352; Medline Kit SKU DYNJRA2068A: UDI/DI 10195327427870 each, 40195327427871 case, Lot Number 25DMH258; Medline Kit SKU DYNJRA2068A: UDI/DI 10195327427870 each, 40195327427871 case, Lot Number 25CMA052; Medline Kit SKU DYNJRA2068A: UDI/DI 10195327427870 each, 40195327427871 case, Lot Number 24JMA141; Medline Kit SKU DYNJRA2068A: UDI/DI 10195327427870 each, 40195327427871 case, Lot Number 24CMH183; Medline Kit SKU DYNJRA2068A: UDI/DI 10195327427870 each, 40195327427871 case, Lot Number 24BMJ537; Medline Kit SKU DYNJRA2068A: UDI/DI 10195327427870 each, 40195327427871 case, Lot Number 23JBB546; Medline Kit SKU DYNJRA2088: UDI/DI 10195327288495 each, 40195327288496 case, Lot Number 25LBO166; Medline Kit SKU DYNJRA2088: UDI/DI 10195327288495 each, 40195327288496 case, Lot Number 25IBP107; Medline Kit SKU DYNJRA2088: UDI/DI 10195327288495 each, 40195327288496 case, Lot Number 25DBI023; Medline Kit SKU DYNJRA2115: UDI/DI 10195327327101 each, 40195327327102 case, Lot Number 26BBR460; Medline Kit SKU DYNJRA2115: UDI/DI 10195327327101 each, 40195327327102 case, Lot Number 26ABL341; Medline Kit SKU DYNJRA2115: UDI/DI 10195327327101 each, 40195327327102 case, Lot Number 25KBT165; Medline Kit SKU DYNJRA2115: UDI/DI 10195327327101 each, 40195327327102 case, Lot Number 25FBJ911; Medline Kit SKU DYNJRA2115: UDI/DI 10195327327101 each, 40195327327102 case, Lot Number 25EBM786; Medline Kit SKU DYNJRA2115: UDI/DI 10195327327101 each, 40195327327102 case, Lot Number 24BBQ039; Medline Kit SKU DYNJRA2115: UDI/DI 10195327327101 each, 40195327327102 case, Lot Number 23IBK437; Medline Kit SKU DYNJRA2115: UDI/DI 10195327327101 each, 40195327327102 case, Lot Number 23GBE482; Medline Kit SKU DYNJRA2117: UDI/DI 10195327328801 each, 40195327328802 case, Lot Number 23HBB082; Medline Kit SKU DYNJRA2140: UDI/DI 10195327351816 each, 40195327351817 case, Lot Number 26BBB083; Medline Kit SKU DYNJRA2140: UDI/DI 10195327351816 each, 40195327351817 case, Lot Number 25KBT830; Medline Kit SKU DYNJRA2140: UDI/DI 10195327351816 each, 40195327351817 case, Lot Number 25JBJ002; Medline Kit SKU DYNJRA2140: UDI/DI 10195327351816 each, 40195327351817 case, Lot Number 25FBR550; Medline Kit SKU DYNJRA2140: UDI/DI 10195327351816 each, 40195327351817 case, Lot Number 25DBM220; Medline Kit SKU DYNJRA2140: UDI/DI 10195327351816 each, 40195327351817 case, Lot Number 24GBD223; Medline Kit SKU DYNJRA2140: UDI/DI 10195327351816 each, 40195327351817 case, Lot Number 23IBP024; Medline Kit SKU DYNJRA2153: UDI/DI 10195327366391 each, 40195327366392 case, Lot Number 26BBJ361; Medline Kit SKU DYNJRA2153: UDI/DI 10195327366391 each, 40195327366392 case, Lot Number 26ABL239; Medline Kit SKU DYNJRA2153: UDI/DI 10195327366391 each, 40195327366392 case, Lot Number 25LBC432; Medline Kit SKU DYNJRA2153: UDI/DI 10195327366391 each, 40195327366392 case, Lot Number 25JBO638; Medline Kit SKU DYNJRA2153: UDI/DI 10195327366391 each, 40195327366392 case, Lot Number 25HBK428; Medline Kit SKU DYNJRA2153: UDI/DI 10195327366391 each, 40195327366392 case, Lot Number 25EBR104; Medline Kit SKU DYNJRA2153: UDI/DI 10195327366391 each, 40195327366392 case, Lot Number 25DBU420; Medline Kit SKU DYNJRA2153: UDI/DI 10195327366391 each, 40195327366392 case, Lot Number 24GBI551; Medline Kit SKU DYNJRA2153: UDI/DI 10195327366391 each, 40195327366392 case, Lot Number 23GBH424; Medline Kit SKU DYNJRA2213: UDI/DI 10195327425876 each, 40195327425877 case, Lot Number 26CBA281; Medline Kit SKU DYNJRA2213: UDI/DI 10195327425876 each, 40195327425877 case, Lot Number 26ABL340; Medline Kit SKU DYNJRA2213: UDI/DI 10195327425876 each, 40195327425877 case, Lot Number 25KBI543; Medline Kit SKU DYNJRA2213: UDI/DI 10195327425876 each, 40195327425877 case, Lot Number 25IBR271; Medline Kit SKU DYNJRA2213: UDI/DI 10195327425876 each, 40195327425877 case, Lot Number 25FBN745; Medline Kit SKU DYNJRA2213: UDI/DI 10195327425876 each, 40195327425877 case, Lot Number 25FBJ701; Medline Kit SKU DYNJRA2213: UDI/DI 10195327425876 each, 40195327425877 case, Lot Number 25DBS268; Medline Kit SKU DYNJRA2213: UDI/DI 10195327425876 each, 40195327425877 case, Lot Number 23HBV950; Medline Kit SKU DYNJRA2225: UDI/DI 10195327432683 each, 40195327432684 case, Lot Number 23HBT397; Medline Kit SKU DYNJRA2349: UDI/DI 10195327607135 each, 40195327607136 case, Lot Number 26BBI277; Medline Kit SKU DYNJRA2349: UDI/DI 10195327607135 each, 40195327607136 case, Lot Number 25JBO671; Medline Kit SKU DYNJRA2349: UDI/DI 10195327607135 each, 40195327607136 case, Lot Number 25JBG136; Medline Kit SKU DYNJRA2349: UDI/DI 10195327607135 each, 40195327607136 case, Lot Number 25FBH739; Medline Kit SKU DYNJRA2360: UDI/DI 10195327629489 each, 40195327629480 case, Lot Number 26CBD944; Medline Kit SKU DYNJRA2360: UDI/DI 10195327629489 each, 40195327629480 case, Lot Number 26BBP631; Medline Kit SKU DYNJRA2360: UDI/DI 10195327629489 each, 40195327629480 case, Lot Number 26BBK190; Medline Kit SKU DYNJRA2360: UDI/DI 10195327629489 each, 40195327629480 case, Lot Number 26ABW305; Medline Kit SKU DYNJRA2360: UDI/DI 10195327629489 each, 40195327629480 case, Lot Number 26ABG715; Medline Kit SKU DYNJRA2371: UDI/DI 10195327644895 each, 40195327644896 case, Lot Number 26CBF837; Medline Kit SKU DYNJRA2371: UDI/DI 10195327644895 each, 40195327644896 case, Lot Number 25IBB962; Medline Kit SKU DYNJRA2371: UDI/DI 10195327644895 each, 40195327644896 case, Lot Number 25IBB964; Medline Kit SKU DYNJRA2371: UDI/DI 10195327644895 each, 40195327644896 case, Lot Number 25HBK417; Medline Kit SKU DYNJRA2371: UDI/DI 10195327644895 each, 40195327644896 case, Lot Number 24GBD226; Medline Kit SKU DYNJRA2381: UDI/DI 10195327667146 each, 40195327667147 case, Lot Number 25JBW800; Medline Kit SKU DYNJRA2381: UDI/DI 10195327667146 each, 40195327667147 case, Lot Number 25JBC388; Medline Kit SKU DYNJRA2381: UDI/DI 10195327667146 each, 40195327667147 case, Lot Number 24GBD228; Medline Kit SKU DYNJRA2432A: UDI/DI 10198459382727 each, 40198459382728 case, Lot Number 26CBF847; Medline Kit SKU DYNJRA2432A: UDI/DI 10198459382727 each, 40198459382728 case, Lot Number 26BBM310; Medline Kit SKU DYNJRA2432A: UDI/DI 10198459382727 each, 40198459382728 case, Lot Number 25GBC739; Medline Kit SKU DYNJRA2532: UDI/DI 10198459188497 each, 40198459188498 case, Lot Number 25LBF411; Medline Kit SKU DYNJRA2532: UDI/DI 10198459188497 each, 40198459188498 case, Lot Number 25HBU760; Medline Kit SKU DYNJRA2534: UDI/DI 10198459191251 each, 40198459191252 case, Lot Number 25GBW196; Medline Kit SKU DYNJRA2534: UDI/DI 10198459191251 each, 40198459191252 case, Lot Number 25FBT598; Medline Kit SKU DYNJRA2556: UDI/DI 10198459247514 each, 40198459247515 case, Lot Number 26BBE200; Medline Kit SKU DYNJRA2556: UDI/DI 10198459247514 each, 40198459247515 case, Lot Number 25LBN290; Medline Kit SKU DYNJRA2556: UDI/DI 10198459247514 each, 40198459247515 case, Lot Number 25KBQ920; Medline Kit SKU DYNJRA2556: UDI/DI 10198459247514 each, 40198459247515 case, Lot Number 25JBU726; Medline Kit SKU DYNJRA2556: UDI/DI 10198459247514 each, 40198459247515 case, Lot Number 25JBC448; Medline Kit SKU DYNJRA2556: UDI/DI 10198459247514 each, 40198459247515 case, Lot Number 25HBS669; Medline Kit SKU DYNJRA2556: UDI/DI 10198459247514 each, 40198459247515 case, Lot Number 25FBR642; Medline Kit SKU DYNJRA2556: UDI/DI 10198459247514 each, 40198459247515 case, Lot Number 25DBI029; Medline Kit SKU DYNJRA2566A: UDI/DI 10198459421822 each, 40198459421823 case, Lot Number 26CBD938; Medline Kit SKU DYNJRA2566A: UDI/DI 10198459421822 each, 40198459421823 case, Lot Number 25HBP480; Medline Kit SKU DYNJRA2566A: UDI/DI 10198459421822 each, 40198459421823 case, Lot Number 25HBK616; Medline Kit SKU DYNJRA2575: UDI/DI 10198459271830 each, 40198459271831 case, Lot Number 25LBC427; Medline Kit SKU DYNJRA2575: UDI/DI 10198459271830 each, 40198459271831 case, Lot Number 25JBX992; Medline Kit SKU DYNJRA2575: UDI/DI 10198459271830 each, 40198459271831 case, Lot Number 25JBC445; Medline Kit SKU DYNJRA2575: UDI/DI 10198459271830 each, 40198459271831 case, Lot Number 25GBO568; Medline Kit SKU DYNJRA2575: UDI/DI 10198459271830 each, 40198459271831 case, Lot Number 25GBB711; Medline Kit SKU DYNJRA2575: UDI/DI 10198459271830 each, 40198459271831 case, Lot Number 25GBG218; Medline Kit SKU DYNJRA2575: UDI/DI 10198459271830 each, 40198459271831 case, Lot Number 25BBH733; Medline Kit SKU DYNJRA2592: UDI/DI 10198459300417 each, 40198459300418 case, Lot Number 26ABL364; Medline Kit SKU DYNJRA2592: UDI/DI 10198459300417 each, 40198459300418 case, Lot Number 25KBT846; Medline Kit SKU DYNJRA2592: UDI/DI 10198459300417 each, 40198459300418 case, Lot Number 25FBC729; Medline Kit SKU DYNJRA2597: UDI/DI 10198459304835 each, 40198459304836 case, Lot Number 25GBN789; Medline Kit SKU DYNJRA2597: UDI/DI 10198459304835 each, 40198459304836 case, Lot Number 25EBA564; Medline Kit SKU DYNJRA2605: UDI/DI 10198459326370 each, 40198459326371 case, Lot Number 26ABQ772; Medline Kit SKU DYNJRA2605: UDI/DI 10198459326370 each, 40198459326371 case, Lot Number 26ABK647; Medline Kit SKU DYNJRA2605: UDI/DI 10198459326370 each, 40198459326371 case, Lot Number 25KBT820; Medline Kit SKU DYNJRA2605: UDI/DI 10198459326370 each, 40198459326371 case, Lot Number 25FBG507; Medline Kit SKU DYNJRA2606: UDI/DI 10198459328657 each, 40198459328658 case, Lot Number 25LBF412; Medline Kit SKU DYNJRA2606: UDI/DI 10198459328657 each, 40198459328658 case, Lot Number 25JBM797; Medline Kit SKU DYNJRA2606: UDI/DI 10198459328657 each, 40198459328658 case, Lot Number 25FBT691; Medline Kit SKU DYNJRA2606: UDI/DI 10198459328657 each, 40198459328658 case, Lot Number 25EBC231; Medline Kit SKU DYNJRA2607: UDI/DI 10198459331657 each, 40198459331658 case, Lot Number 25EBK954; Medline Kit SKU DYNJRA2607A: UDI/DI 10198459421839 each, 40198459421830 case, Lot Number 26CBI128; Medline Kit SKU DYNJRA2607A: UDI/DI 10198459421839 each, 40198459421830 case, Lot Number 26ABV387; Medline Kit SKU DYNJRA2611: UDI/DI 10198459336256 each, 40198459336257 case, Lot Number 26BBB084; Medline Kit SKU DYNJRA2611: UDI/DI 10198459336256 each, 40198459336257 case, Lot Number 25LBN247; Medline Kit SKU DYNJRA2611: UDI/DI 10198459336256 each, 40198459336257 case, Lot Number 25IBB903; Medline Kit SKU DYNJRA2611: UDI/DI 10198459336256 each, 40198459336257 case, Lot Number 25EBF537; Medline Kit SKU DYNJRA2613: UDI/DI 10198459339356 each, 40198459339357 case, Lot Number 25EBR108; Medline Kit SKU DYNJRA2618A: UDI/DI 10198459537998 each, 40198459537999 case, Lot Number 26CBE369; Medline Kit SKU DYNJRA2618A: UDI/DI 10198459537998 each, 40198459537999 case, Lot Number 26ABJ331; Medline Kit SKU DYNJRA2634: UDI/DI 10198459349355 each, 40198459349356 case, Lot Number 26BBL356; Medline Kit SKU DYNJRA2634: UDI/DI 10198459349355 each, 40198459349356 case, Lot Number 25JBA669; Medline Kit SKU DYNJRA2634: UDI/DI 10198459349355 each, 40198459349356 case, Lot Number 25FBP070; Medline Kit SKU DYNJRA2638: UDI/DI 10198459349591 each, 40198459349592 case, Lot Number 25FBG845; Medline Kit SKU DYNJRA2639: UDI/DI 10198459352218 each, 40198459352219 case, Lot Number 25FBU637; Medline Kit SKU DYNJRA2641: UDI/DI 10198459352546 each, 40198459352547 case, Lot Number 26BBE022; Medline Kit SKU DYNJRA2641: UDI/DI 10198459352546 each, 40198459352547 case, Lot Number 25EBO148; Medline Kit SKU DYNJRA2653: UDI/DI 10198459411021 each, 40198459411022 case, Lot Number 25IBL292; Medline Kit SKU DYNJRA2669: UDI/DI 10198459466489 each, 40198459466480 case, Lot Number 26CBI134; Medline Kit SKU DYNJRA2669: UDI/DI 10198459466489 each, 40198459466480 case, Lot Number 26BBJ402; Medline Kit SKU DYNJRA2669: UDI/DI 10198459466489 each, 40198459466480 case, Lot Number 25LBF213; Medline Kit SKU DYNJRA2669: UDI/DI 10198459466489 each, 40198459466480 case, Lot Number 25IBL293; Medline Kit SKU DYNJRA2670: UDI/DI 10198459467974 each, 40198459467975 case, Lot Number 25HBQ154; Medline Kit SKU DYNJRA2672: UDI/DI 10198459475382 each, 40198459475383 case, Lot Number 26CBD940; Medline Kit SKU DYNJRA2672: UDI/DI 10198459475382 each, 40198459475383 case, Lot Number 25KBT183; Medline Kit SKU DYNJRA2672: UDI/DI 10198459475382 each, 40198459475383 case, Lot Number 25HBT583; Medline Kit SKU DYNJRA2675A: UDI/DI 10198459616471 each, 40198459616472 case, Lot Number 26ABV388; Medline Kit SKU DYNJRA2700: UDI/DI 10198459540615 each, 40198459540616 case, Lot Number 26BBC162; Medline Kit SKU DYNJRA2700: UDI/DI 10198459540615 each, 40198459540616 case, Lot Number 25LBA445; Medline Kit SKU DYNJRA2700: UDI/DI 10198459540615 each, 40198459540616 case, Lot Number 25JBO627; Medline Kit SKU DYNJRA2708: UDI/DI 10198459555756 each, 40198459555757 case, Lot Number 26BBN582; Medline Kit SKU DYNJRA2708: UDI/DI 10198459555756 each, 40198459555757 case, Lot Number 26BBL108; Medline Kit SKU DYNJRA2708: UDI/DI 10198459555756 each, 40198459555757 case, Lot Number 25KBT823; Medline Kit SKU DYNJRA2710: UDI/DI 10198459559075 each, 40198459559076 case, Lot Number 25LBL119; Medline Kit SKU DYNJRA2710: UDI/DI 10198459559075 each, 40198459559076 case, Lot Number 25KBM981; Medline Kit SKU DYNJRA2710: UDI/DI 10198459559075 each, 40198459559076 case, Lot Number 25JBD673; Medline Kit SKU DYNJRA9029: UDI/DI 10889942466436 each, 40889942466437 case, Lot Number 25KBD330; Medline Kit SKU DYNJRA9029: UDI/DI 10889942466436 each, 40889942466437 case, Lot Number 25KBB936; Medline Kit SKU DYNJRA9029: UDI/DI 10889942466436 each, 40889942466437 case, Lot Number 25JBB447; Medline Kit SKU DYNJRA9029: UDI/DI 10889942466436 each, 40889942466437 case, Lot Number 24FBJ029; Medline Kit SKU DYNJRA9029: UDI/DI 10889942466436 each, 40889942466437 case, Lot Number 24BBR611; Medline Kit SKU DYNJRA9029: UDI/DI 10889942466436 each, 40889942466437 case, Lot Number 23JBM198; Medline Kit SKU DYNJRA9034: UDI/DI 10193489467574 each, 40193489467575 case, Lot Number 26ABR020; Medline Kit SKU DYNJRA9034: UDI/DI 10193489467574 each, 40193489467575 case, Lot Number 26ABG927; Medline Kit SKU DYNJRA9034: UDI/DI 10193489467574 each, 40193489467575 case, Lot Number 25LBH190; Medline Kit SKU DYNJRA9034: UDI/DI 10193489467574 each, 40193489467575 case, Lot Number 25KBR348; Medline Kit SKU DYNJRA9034: UDI/DI 10193489467574 each, 40193489467575 case, Lot Number 25JBV917; Medline Kit SKU DYNJRA9034: UDI/DI 10193489467574 each, 40193489467575 case, Lot Number 25JBL130; Medline Kit SKU DYNJRA9034: UDI/DI 10193489467574 each, 40193489467575 case, Lot Number 25JBH184; Medline Kit SKU DYNJRA9034: UDI/DI 10193489467574 each, 40193489467575 case, Lot Number 25IBW244; Medline Kit SKU DYNJRA9034: UDI/DI 10193489467574 each, 40193489467575 case, Lot Number 25DBE496; Medline Kit SKU DYNJRA9034: UDI/DI 10193489467574 each, 40193489467575 case, Lot Number 25DBE497; Medline Kit SKU DYNJRA9034: UDI/DI 10193489467574 each, 40193489467575 case, Lot Number 25DBD657; Medline Kit SKU DYNJRA9034: UDI/DI 10193489467574 each, 40193489467575 case, Lot Number 25DBE019; Medline Kit SKU DYNJRA9034: UDI/DI 10193489467574 each, 40193489467575 case, Lot Number 25CBK276; Medline Kit SKU DYNJRA9034: UDI/DI 10193489467574 each, 40193489467575 case, Lot Number 25CBH117; Medline Kit SKU DYNJRA9034: UDI/DI 10193489467574 each, 40193489467575 case, Lot Number 25CBE763; Medline Kit SKU DYNJRA9034: UDI/DI 10193489467574 each, 40193489467575 case, Lot Number 25CBD665; Medline Kit SKU DYNJRA9034: UDI/DI 10193489467574 each, 40193489467575 case, Lot Number 24GBD232; Medline Kit SKU DYNJRA9034: UDI/DI 10193489467574 each, 40193489467575 case, Lot Number 24FBJ504; Medline Kit SKU DYNJRA9034: UDI/DI 10193489467574 each, 40193489467575 case, Lot Number 24FBJ509; Medline Kit SKU DYNJRA9034: UDI/DI 10193489467574 each, 40193489467575 case, Lot Number 24BBR622; Medline Kit SKU DYNJRA9034: UDI/DI 10193489467574 each, 40193489467575 case, Lot Number 24BBR604; Medline Kit SKU DYNJRA9034: UDI/DI 10193489467574 each, 40193489467575 case, Lot Number 23JBH420; Medline Kit SKU DYNJRA9034: UDI/DI 10193489467574 each, 40193489467575 case, Lot Number 23JBH419; Medline Kit SKU DYNJRA9034: UDI/DI 10193489467574 each, 40193489467575 case, Lot Number 23FBR086; Medline Kit SKU DYNJRA9038: UDI/DI 10193489830477 each, 40193489830478 case, Lot Number 26BBQ555; Medline Kit SKU DYNJRA9038: UDI/DI 10193489830477 each, 40193489830478 case, Lot Number 26BBM438; Medline Kit SKU DYNJRA9038: UDI/DI 10193489830477 each, 40193489830478 case, Lot Number 26ABM602; Medline Kit SKU DYNJRA9038: UDI/DI 10193489830477 each, 40193489830478 case, Lot Number 25KBS235; Medline Kit SKU DYNJRA9038: UDI/DI 10193489830477 each, 40193489830478 case, Lot Number 25GBO785; Medline Kit SKU DYNJRA9038: UDI/DI 10193489830477 each, 40193489830478 case, Lot Number 25FBM871; Medline Kit SKU DYNJRA9038: UDI/DI 10193489830477 each, 40193489830478 case, Lot Number 25ABC406; Medline Kit SKU DYNJRA9038: UDI/DI 10193489830477 each, 40193489830478 case, Lot Number 24FBJ512; Medline Kit SKU DYNJRA9038: UDI/DI 10193489830477 each, 40193489830478 case, Lot Number 24FBJ126; Medline Kit SKU DYNJRA9038: UDI/DI 10193489830477 each, 40193489830478 case, Lot Number 24BBR602; Medline Kit SKU PAIN1279A: UDI/DI 10193489302509 each, 40193489302500 case, Lot Number 26BBC168; Medline Kit SKU PAIN1279A: UDI/DI 10193489302509 each, 40193489302500 case, Lot Number 25LBF437; Medline Kit SKU PAIN1279A: UDI/DI 10193489302509 each, 40193489302500 case, Lot Number 25JBC449; Medline Kit SKU PAIN1279A: UDI/DI 10193489302509 each, 40193489302500 case, Lot Number 25HBU729; Medline Kit SKU PAIN1279A: UDI/DI 10193489302509 each, 40193489302500 case, Lot Number 25HBM736; Medline Kit SKU PAIN1279A: UDI/DI 10193489302509 each, 40193489302500 case, Lot Number 25GBW272; Medline Kit SKU PAIN1279A: UDI/DI 10193489302509 each, 40193489302500 case, Lot Number 25BBM498; Medline Kit SKU PAIN1279A: UDI/DI 10193489302509 each, 40193489302500 case, Lot Number 25ALA737; Medline Kit SKU PAIN1279A: UDI/DI 10193489302509 each, 40193489302500 case, Lot Number 25ALA309; Medline Kit SKU PAIN1279A: UDI/DI 10193489302509 each, 40193489302500 case, Lot Number 24KLA204; Medline Kit SKU PAIN1279A: UDI/DI 10193489302509 each, 40193489302500 case, Lot Number 24FLA466; Medline Kit SKU PAIN1279A: UDI/DI 10193489302509 each, 40193489302500 case, Lot Number 24ALB132; Medline Kit SKU PAIN1279A: UDI/DI 10193489302509 each, 40193489302500 case, Lot Number 23ILA681; Medline Kit SKU PAIN1279A: UDI/DI 10193489302509 each, 40193489302500 case, Lot Number 23HLA822; Medline Kit SKU PAIN1280: UDI/DI 10888277747784 each, 40888277747785 case, Lot Number 26BMJ295; Medline Kit SKU PAIN1280: UDI/DI 10888277747784 each, 40888277747785 case, Lot Number 26AMH186; Medline Kit SKU PAIN1280: UDI/DI 10888277747784 each, 40888277747785 case, Lot Number 25KMG729; Medline Kit SKU PAIN1280: UDI/DI 10888277747784 each, 40888277747785 case, Lot Number 25JMA658; Medline Kit SKU PAIN1280: UDI/DI 10888277747784 each, 40888277747785 case, Lot Number 25GMB271; Medline Kit SKU PAIN1280: UDI/DI 10888277747784 each, 40888277747785 case, Lot Number 25DMK280; Medline Kit SKU PAIN1280: UDI/DI 10888277747784 each, 40888277747785 case, Lot Number 25DMI542; Medline Kit SKU PAIN1280: UDI/DI 10888277747784 each, 40888277747785 case, Lot Number 25DMC359; Medline Kit SKU PAIN1280: UDI/DI 10888277747784 each, 40888277747785 case, Lot Number 24JMA154; Medline Kit SKU PAIN1280: UDI/DI 10888277747784 each, 40888277747785 case, Lot Number 24HMD114; Medline Kit SKU PAIN1280: UDI/DI 10888277747784 each, 40888277747785 case, Lot Number 24EMJ390; Medline Kit SKU PAIN1280: UDI/DI 10888277747784 each, 40888277747785 case, Lot Number 24DMJ999; Medline Kit SKU PAIN1280: UDI/DI 10888277747784 each, 40888277747785 case, Lot Number 24CMD645; Medline Kit SKU PAIN1280: UDI/DI 10888277747784 each, 40888277747785 case, Lot Number 24BMA231; Medline Kit SKU PAIN1280: UDI/DI 10888277747784 each, 40888277747785 case, Lot Number 23KMD774; Medline Kit SKU PAIN1280: UDI/DI 10888277747784 each, 40888277747785 case, Lot Number 23JMF327; Medline Kit SKU PAIN1280: UDI/DI 10888277747784 each, 40888277747785 case, Lot Number 23JMB758; Medline Kit SKU PAIN1280: UDI/DI 10888277747784 each, 40888277747785 case, Lot Number 23GMG995; Medline Kit SKU PAIN1280: UDI/DI 10888277747784 each, 40888277747785 case, Lot Number 24DMJ999A; Medline Kit SKU PAIN1289A: UDI/DI 10193489495478 each, 40193489495479 case, Lot Number 26AMG738; Medline Kit SKU PAIN1289A: UDI/DI 10193489495478 each, 40193489495479 case, Lot Number 24GMH190; Medline Kit SKU PAIN1393: UDI/DI 10193489629965 each, 40193489629966 case, Lot Number 25LMH336; Medline Kit SKU PAIN1393: UDI/DI 10193489629965 each, 40193489629966 case, Lot Number 25LMF024; Medline Kit SKU PAIN1393: UDI/DI 10193489629965 each, 40193489629966 case, Lot Number 25HMB657; Medline Kit SKU PAIN1393: UDI/DI 10193489629965 each, 40193489629966 case, Lot Number 25GMI070; Medline Kit SKU PAIN1393: UDI/DI 10193489629965 each, 40193489629966 case, Lot Number 25FMA572; Medline Kit SKU PAIN1393: UDI/DI 10193489629965 each, 40193489629966 case, Lot Number 24JMA110; Medline Kit SKU PAIN1393: UDI/DI 10193489629965 each, 40193489629966 case, Lot Number 23HBM570; Medline Kit SKU PAIN1393: UDI/DI 10193489629965 each, 40193489629966 case, Lot Number 23HBE099; Medline Kit SKU PAIN1393: UDI/DI 10193489629965 each, 40193489629966 case, Lot Number 25HMB657B; Medline Kit SKU PAIN1405B: UDI/DI 10193489768206 each, 40193489768207 case, Lot Number 26BBN581; Medline Kit SKU PAIN1405B: UDI/DI 10193489768206 each, 40193489768207 case, Lot Number 26ABS329; Medline Kit SKU PAIN1405B: UDI/DI 10193489768206 each, 40193489768207 case, Lot Number 25IBE918; Medline Kit SKU PAIN1405B: UDI/DI 10193489768206 each, 40193489768207 case, Lot Number 25GBT026; Medline Kit SKU PAIN1405B: UDI/DI 10193489768206 each, 40193489768207 case, Lot Number 25FBL017; Medline Kit SKU PAIN1405B: UDI/DI 10193489768206 each, 40193489768207 case, Lot Number 25EBC429; Medline Kit SKU PAIN1405B: UDI/DI 10193489768206 each, 40193489768207 case, Lot Number 25ALA031; Medline Kit SKU PAIN1405B: UDI/DI 10193489768206 each, 40193489768207 case, Lot Number 24CLA245; Medline Kit SKU PAIN1405B: UDI/DI 10193489768206 each, 40193489768207 case, Lot Number 23ILA303; Medline Kit SKU SAMPA0124: UDI/DI 10195327691691 each, 40195327691692 case, Lot Number 24GBL109; Medline Kit SKU SAMPA0128: UDI/DI 10195327691813 each, 40195327691814 case, Lot Number 24GBF551; Medline Kit SKU SAMPA0139: UDI/DI 10198459042034 each, 40198459042035 case, Lot Number 24FBT389; Medline Kit SKU SAMPA0144: UDI/DI 10198459292194 each, 40198459292195 case, Lot Number 25CBD916; Medline Kit SKU SAMPA0146: UDI/DI 10198459421815 each, 40198459421816 case, Lot Number 25GBQ852.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2237-2026%22", "url": "https://recallledger.net/recalls/device-z-2237-2026-medline-kits-containing-huons-co-bupivacaine-hcl-in-dextrose-injectio/"}, {"id": "fda-device-z-2236-2026", "source": "FDA", "category": "device", "recall_number": "Z-2236-2026", "title": "Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection recall (Medline Industries, LP)", "product": "Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) SPINAL BLOCK TRAY, Medline Kit SKU DYNJRA1097; 2) TRAY, SPINAL PENCIL POINT 25G, Medline Kit SKU DYNJRA1154; 3) SPINAL TRAY, Medline Kit SKU DYNJRA1192A; 4) BLOCK TRAY, Medline Kit SKU DYNJRA1212; 5) SPINAL NEEDLE TRAY, Medline Kit SKU DYNJRA1285; 6) SPINAL BLOCK TRAY WHITACRE 24G, Medline Kit SKU DYNJRA9031; 7) SPINAL BLOCK TRAY 25G WHITACRE, Medline Kit SKU DYNJRA9032; 8) 25G SPINAL TRAY, Medline Kit SKU PAIN1239.", "reason": "Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.", "hazard_level": "Class I", "company": "Medline Industries, LP", "company_location": "Northfield, IL, United States", "date": "2026-04-10", "report_date": "2026-06-03", "status": "Ongoing", "distribution": "Worldwide - US Nationwide distribution in the US Territory of Virgin Islands and the countries of Bahamas, Panama, Barbados.", "states": [], "nationwide": true, "quantity": "30120 kits", "codes": "Medline Kit SKU DYNJRA1097: UDI/DI 10889942879236 each, 40889942879237 case, Lot Number 26BBJ392; Medline Kit SKU DYNJRA1097: UDI/DI 10889942879236 each, 40889942879237 case, Lot Number 26ABS354; Medline Kit SKU DYNJRA1097: UDI/DI 10889942879236 each, 40889942879237 case, Lot Number 25LBC413; Medline Kit SKU DYNJRA1097: UDI/DI 10889942879236 each, 40889942879237 case, Lot Number 25IBK142; Medline Kit SKU DYNJRA1097: UDI/DI 10889942879236 each, 40889942879237 case, Lot Number 25FBD584; Medline Kit SKU DYNJRA1097: UDI/DI 10889942879236 each, 40889942879237 case, Lot Number 25BBK828; Medline Kit SKU DYNJRA1097: UDI/DI 10889942879236 each, 40889942879237 case, Lot Number 24FBT398; Medline Kit SKU DYNJRA1097: UDI/DI 10889942879236 each, 40889942879237 case, Lot Number 24BBR608; Medline Kit SKU DYNJRA1097: UDI/DI 10889942879236 each, 40889942879237 case, Lot Number 23JBB581; Medline Kit SKU DYNJRA1097: UDI/DI 10889942879236 each, 40889942879237 case, Lot Number 23IBQ010; Medline Kit SKU DYNJRA1097: UDI/DI 10889942879236 each, 40889942879237 case, Lot Number 23HBM569; Medline Kit SKU DYNJRA1154: UDI/DI 10889942935864 each, 40889942935865 case, Lot Number 26AMK346; Medline Kit SKU DYNJRA1154: UDI/DI 10889942935864 each, 40889942935865 case, Lot Number 25KMG102; Medline Kit SKU DYNJRA1154: UDI/DI 10889942935864 each, 40889942935865 case, Lot Number 25JMA641; Medline Kit SKU DYNJRA1154: UDI/DI 10889942935864 each, 40889942935865 case, Lot Number 25GMC349; Medline Kit SKU DYNJRA1154: UDI/DI 10889942935864 each, 40889942935865 case, Lot Number 25DMG474; Medline Kit SKU DYNJRA1154: UDI/DI 10889942935864 each, 40889942935865 case, Lot Number 25DMC357; Medline Kit SKU DYNJRA1154: UDI/DI 10889942935864 each, 40889942935865 case, Lot Number 25ADB659; Medline Kit SKU DYNJRA1154: UDI/DI 10889942935864 each, 40889942935865 case, Lot Number 24LDB606; Medline Kit SKU DYNJRA1154: UDI/DI 10889942935864 each, 40889942935865 case, Lot Number 24KDB682; Medline Kit SKU DYNJRA1154: UDI/DI 10889942935864 each, 40889942935865 case, Lot Number 24JDC049; Medline Kit SKU DYNJRA1154: UDI/DI 10889942935864 each, 40889942935865 case, Lot Number 24FDA638; Medline Kit SKU DYNJRA1154: UDI/DI 10889942935864 each, 40889942935865 case, Lot Number 23JDC468; Medline Kit SKU DYNJRA1192A: UDI/DI 10198459155666 each, 40198459155667 case, Lot Number 26BBJ394; Medline Kit SKU DYNJRA1192A: UDI/DI 10198459155666 each, 40198459155667 case, Lot Number 25LBR313; Medline Kit SKU DYNJRA1192A: UDI/DI 10198459155666 each, 40198459155667 case, Lot Number 25KBP760; Medline Kit SKU DYNJRA1192A: UDI/DI 10198459155666 each, 40198459155667 case, Lot Number 25JBV827; Medline Kit SKU DYNJRA1192A: UDI/DI 10198459155666 each, 40198459155667 case, Lot Number 25JBG134; Medline Kit SKU DYNJRA1192A: UDI/DI 10198459155666 each, 40198459155667 case, Lot Number 25HBK390; Medline Kit SKU DYNJRA1192A: UDI/DI 10198459155666 each, 40198459155667 case, Lot Number 25DBF619; Medline Kit SKU DYNJRA1212: UDI/DI 10888277789838 each, 40888277789839 case, Lot Number 26BBT340; Medline Kit SKU DYNJRA1212: UDI/DI 10888277789838 each, 40888277789839 case, Lot Number 26ABU446; Medline Kit SKU DYNJRA1212: UDI/DI 10888277789838 each, 40888277789839 case, Lot Number 25JBE914; Medline Kit SKU DYNJRA1212: UDI/DI 10888277789838 each, 40888277789839 case, Lot Number 25GBT022; Medline Kit SKU DYNJRA1212: UDI/DI 10888277789838 each, 40888277789839 case, Lot Number 25EBS286; Medline Kit SKU DYNJRA1212: UDI/DI 10888277789838 each, 40888277789839 case, Lot Number 25DBJ529; Medline Kit SKU DYNJRA1212: UDI/DI 10888277789838 each, 40888277789839 case, Lot Number 25ADA237; Medline Kit SKU DYNJRA1212: UDI/DI 10888277789838 each, 40888277789839 case, Lot Number 24JDB280; Medline Kit SKU DYNJRA1212: UDI/DI 10888277789838 each, 40888277789839 case, Lot Number 24FDA639; Medline Kit SKU DYNJRA1212: UDI/DI 10888277789838 each, 40888277789839 case, Lot Number 24EDB329; Medline Kit SKU DYNJRA1212: UDI/DI 10888277789838 each, 40888277789839 case, Lot Number 24DDB935; Medline Kit SKU DYNJRA1212: UDI/DI 10888277789838 each, 40888277789839 case, Lot Number 24BDA655; Medline Kit SKU DYNJRA1285: UDI/DI 10193489566123 each, 40193489566124 case, Lot Number 26ABG845; Medline Kit SKU DYNJRA1285: UDI/DI 10193489566123 each, 40193489566124 case, Lot Number 25LBI115; Medline Kit SKU DYNJRA1285: UDI/DI 10193489566123 each, 40193489566124 case, Lot Number 25IBP109; Medline Kit SKU DYNJRA1285: UDI/DI 10193489566123 each, 40193489566124 case, Lot Number 25EBE523; Medline Kit SKU DYNJRA1285: UDI/DI 10193489566123 each, 40193489566124 case, Lot Number 24LDA129; Medline Kit SKU DYNJRA1285: UDI/DI 10193489566123 each, 40193489566124 case, Lot Number 24KDB674; Medline Kit SKU DYNJRA1285: UDI/DI 10193489566123 each, 40193489566124 case, Lot Number 24FDA633; Medline Kit SKU DYNJRA1285: UDI/DI 10193489566123 each, 40193489566124 case, Lot Number 23JDC158; Medline Kit SKU DYNJRA9031: UDI/DI 10889942802289 each, 40889942802280 case, Lot Number 26ABC785; Medline Kit SKU DYNJRA9031: UDI/DI 10889942802289 each, 40889942802280 case, Lot Number 25LBH049; Medline Kit SKU DYNJRA9031: UDI/DI 10889942802289 each, 40889942802280 case, Lot Number 25KBK340; Medline Kit SKU DYNJRA9031: UDI/DI 10889942802289 each, 40889942802280 case, Lot Number 25BBH830; Medline Kit SKU DYNJRA9031: UDI/DI 10889942802289 each, 40889942802280 case, Lot Number 25BBF629; Medline Kit SKU DYNJRA9031: UDI/DI 10889942802289 each, 40889942802280 case, Lot Number 24GBD224; Medline Kit SKU DYNJRA9031: UDI/DI 10889942802289 each, 40889942802280 case, Lot Number 24FBJ060; Medline Kit SKU DYNJRA9031: UDI/DI 10889942802289 each, 40889942802280 case, Lot Number 23IBQ015; Medline Kit SKU DYNJRA9031: UDI/DI 10889942802289 each, 40889942802280 case, Lot Number 23HBR199; Medline Kit SKU DYNJRA9031: UDI/DI 10889942802289 each, 40889942802280 case, Lot Number 23GBR079; Medline Kit SKU DYNJRA9032: UDI/DI 10889942802272 each, 40889942802273 case, Lot Number 25KBJ715; Medline Kit SKU DYNJRA9032: UDI/DI 10889942802272 each, 40889942802273 case, Lot Number 25JBP382; Medline Kit SKU DYNJRA9032: UDI/DI 10889942802272 each, 40889942802273 case, Lot Number 25JBB437; Medline Kit SKU DYNJRA9032: UDI/DI 10889942802272 each, 40889942802273 case, Lot Number 25GBH340; Medline Kit SKU DYNJRA9032: UDI/DI 10889942802272 each, 40889942802273 case, Lot Number 25FBD726; Medline Kit SKU DYNJRA9032: UDI/DI 10889942802272 each, 40889942802273 case, Lot Number 25ABP028; Medline Kit SKU PAIN1239: UDI/DI 10889942873814 each, 40889942873815 case, Lot Number 26CBD939; Medline Kit SKU PAIN1239: UDI/DI 10889942873814 each, 40889942873815 case, Lot Number 26BBB061; Medline Kit SKU PAIN1239: UDI/DI 10889942873814 each, 40889942873815 case, Lot Number 25LBT244; Medline Kit SKU PAIN1239: UDI/DI 10889942873814 each, 40889942873815 case, Lot Number 25FBU644; Medline Kit SKU PAIN1239: UDI/DI 10889942873814 each, 40889942873815 case, Lot Number 24DLA279.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2236-2026%22", "url": "https://recallledger.net/recalls/device-z-2236-2026-medline-kits-containing-huons-co-bupivacaine-hcl-in-dextrose-injectio/"}, {"id": "fda-device-z-2235-2026", "source": "FDA", "category": "device", "recall_number": "Z-2235-2026", "title": "Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection recall (Medline Industries, LP)", "product": "Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: SPINAL BLOCK 22G QUINCKE 5S BU, Medline Kit SKU DYNJRA9026", "reason": "Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.", "hazard_level": "Class I", "company": "Medline Industries, LP", "company_location": "Northfield, IL, United States", "date": "2026-04-10", "report_date": "2026-06-03", "status": "Ongoing", "distribution": "Worldwide - US Nationwide distribution in the US Territory of Virgin Islands and the countries of Bahamas, Panama, Barbados.", "states": [], "nationwide": true, "quantity": "4370 kits", "codes": "Medline Kit SKU DYNJRA9026: UDI/DI 10884389285688 each, 40884389285689, case, Lot Numbers: 26BBD235, 26ABB534, 25DBT837, 25CBH118, 24FBT403, 24FBJ505.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2235-2026%22", "url": "https://recallledger.net/recalls/device-z-2235-2026-medline-kits-containing-huons-co-bupivacaine-hcl-in-dextrose-injectio/"}, {"id": "fda-device-z-2234-2026", "source": "FDA", "category": "device", "recall_number": "Z-2234-2026", "title": "Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection recall (Medline Industries, LP)", "product": "Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) BLOCK TRAY, Medline Kit SKU DYNJRA1181C; 2) SPINAL BLOCK 25G WHTCRE 5S BU, Medline Kit SKu DYNJRA1860.", "reason": "Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.", "hazard_level": "Class I", "company": "Medline Industries, LP", "company_location": "Northfield, IL, United States", "date": "2026-04-10", "report_date": "2026-06-03", "status": "Ongoing", "distribution": "Worldwide - US Nationwide distribution in the US Territory of Virgin Islands and the countries of Bahamas, Panama, Barbados.", "states": [], "nationwide": true, "quantity": "270 kits", "codes": "Medline Kit SKU DYNJRA1181C: UDI/DI 10193489457605 each, 40193489457606 case, Lot Number 25DMF105; Medline Kit SKU DYNJRA1181C: UDI/DI 10193489457605 each, 40193489457606 case, Lot Number 25CMB575; Medline Kit SKU DYNJRA1860: UDI/DI 10195327008413 each, 40195327008414 case, Lot Number 24DMB099.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2234-2026%22", "url": "https://recallledger.net/recalls/device-z-2234-2026-medline-kits-containing-huons-co-bupivacaine-hcl-in-dextrose-injectio/"}, {"id": "fda-device-z-2233-2026", "source": "FDA", "category": "device", "recall_number": "Z-2233-2026", "title": "Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection recall (Medline Industries, LP)", "product": "Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) SPINAL TRAY W/PENCIL POINT NDL, Medline Kit SKU DYNJRA0245; 2) SPINAL TRAY W/PENCIL POINT NDL, Medline Kit SKU DYNJRA0555; 3) SPINAL TRAY, Medline Kit SKU DYNJRA0836A; 4) SPINAL TRAY, Medline Kit SKU DYNJRA0978A; 5) TRAY, SPINAL, WHIT 24GX4, Medline Kit SKU DYNJRA1034; 6) SPINAL BLOCK 25G WHTCRE 5S BU, Medline Kit SKU DYNJRA9028; 7) TRAY, SPINAL PENCIL POINT 25G, Medline Kit SKU DYNJRA9030.", "reason": "Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.", "hazard_level": "Class I", "company": "Medline Industries, LP", "company_location": "Northfield, IL, United States", "date": "2026-04-10", "report_date": "2026-06-03", "status": "Ongoing", "distribution": "Worldwide - US Nationwide distribution in the US Territory of Virgin Islands and the countries of Bahamas, Panama, Barbados.", "states": [], "nationwide": true, "quantity": "41720 kits", "codes": "Medline SKU DYNJRA0245: UDI/DI 10884389573488 each, 40884389573489 case, Lot Number 26AMH714; Medline SKU DYNJRA0245: UDI/DI 10884389573488 each, 40884389573489 case, Lot Number 26AMF179; Medline SKU DYNJRA0245: UDI/DI 10884389573488 each, 40884389573489 case, Lot Number 25IMI476; Medline SKU DYNJRA0245: UDI/DI 10884389573488 each, 40884389573489 case, Lot Number 25GME934; Medline SKU DYNJRA0245: UDI/DI 10884389573488 each, 40884389573489 case, Lot Number 24JMA156; Medline SKU DYNJRA0245: UDI/DI 10884389573488 each, 40884389573489 case, Lot Number 24IMG162; Medline SKU DYNJRA0245: UDI/DI 10884389573488 each, 40884389573489 case, Lot Number 23IBG784; Medline SKU DYNJRA0245: UDI/DI 10884389573488 each, 40884389573489 case, Lot Number 23HBG512; Medline SKU DYNJRA0245: UDI/DI 10884389573488 each, 40884389573489 case, Lot Number 23HBA325; Medline SKU DYNJRA0555: UDI/DI 10888277270923 each, 40888277270924 case, Lot Number 26AMK307; Medline SKU DYNJRA0555: UDI/DI 10888277270923 each, 40888277270924 case, Lot Number 25LME383; Medline SKU DYNJRA0555: UDI/DI 10888277270923 each, 40888277270924 case, Lot Number 25JMJ632; Medline SKU DYNJRA0555: UDI/DI 10888277270923 each, 40888277270924 case, Lot Number 25IMI508; Medline SKU DYNJRA0555: UDI/DI 10888277270923 each, 40888277270924 case, Lot Number 25IMB093; Medline SKU DYNJRA0555: UDI/DI 10888277270923 each, 40888277270924 case, Lot Number 25GMB270; Medline SKU DYNJRA0555: UDI/DI 10888277270923 each, 40888277270924 case, Lot Number 25EMD040; Medline SKU DYNJRA0555: UDI/DI 10888277270923 each, 40888277270924 case, Lot Number 25EMB958; Medline SKU DYNJRA0555: UDI/DI 10888277270923 each, 40888277270924 case, Lot Number 24HMD548; Medline SKU DYNJRA0555: UDI/DI 10888277270923 each, 40888277270924 case, Lot Number 24HMA551; Medline SKU DYNJRA0555: UDI/DI 10888277270923 each, 40888277270924 case, Lot Number 24GMI471; Medline SKU DYNJRA0555: UDI/DI 10888277270923 each, 40888277270924 case, Lot Number 24DBA515; Medline SKU DYNJRA0555: UDI/DI 10888277270923 each, 40888277270924 case, Lot Number 24BBQ043; Medline SKU DYNJRA0555: UDI/DI 10888277270923 each, 40888277270924 case, Lot Number 23IBH382; Medline SKU DYNJRA0555: UDI/DI 10888277270923 each, 40888277270924 case, Lot Number 23GBD403; Medline SKU DYNJRA0836A: UDI/DI 10889942833795 each, 40889942833796 case, Lot Number 26BMH362; Medline SKU DYNJRA0836A: UDI/DI 10889942833795 each, 40889942833796 case, Lot Number 25LMC760; Medline SKU DYNJRA0836A: UDI/DI 10889942833795 each, 40889942833796 case, Lot Number 25JME361; Medline SKU DYNJRA0836A: UDI/DI 10889942833795 each, 40889942833796 case, Lot Number 25IMI413; Medline SKU DYNJRA0836A: UDI/DI 10889942833795 each, 40889942833796 case, Lot Number 25HMH140; Medline SKU DYNJRA0836A: UDI/DI 10889942833795 each, 40889942833796 case, Lot Number 25HMA304; Medline SKU DYNJRA0836A: UDI/DI 10889942833795 each, 40889942833796 case, Lot Number 25GMB268; Medline SKU DYNJRA0836A: UDI/DI 10889942833795 each, 40889942833796 case, Lot Number 25FMF696; Medline SKU DYNJRA0836A: UDI/DI 10889942833795 each, 40889942833796 case, Lot Number 25DMJ266; Medline SKU DYNJRA0836A: UDI/DI 10889942833795 each, 40889942833796 case, Lot Number 24HMB245; Medline SKU DYNJRA0836A: UDI/DI 10889942833795 each, 40889942833796 case, Lot Number 24HMB241; Medline SKU DYNJRA0836A: UDI/DI 10889942833795 each, 40889942833796 case, Lot Number 24GMB114; Medline SKU DYNJRA0836A: UDI/DI 10889942833795 each, 40889942833796 case, Lot Number 24BME560; Medline SKU DYNJRA0978A: UDI/DI 10889942826827 each, 40889942826828 case, Lot Number 25KMD376; Medline SKU DYNJRA0978A: UDI/DI 10889942826827 each, 40889942826828 case, Lot Number 25JMC383; Medline SKU DYNJRA0978A: UDI/DI 10889942826827 each, 40889942826828 case, Lot Number 25FMH538; Medline SKU DYNJRA0978A: UDI/DI 10889942826827 each, 40889942826828 case, Lot Number 24KDB290; Medline SKU DYNJRA0978A: UDI/DI 10889942826827 each, 40889942826828 case, Lot Number 24EDB889; Medline SKU DYNJRA0978A: UDI/DI 10889942826827 each, 40889942826828 case, Lot Number 23JDC308; Medline SKU DYNJRA1034: UDI/DI 10889942760695 each, 40889942760696 case, Lot Number 26ABW292; Medline SKU DYNJRA1034: UDI/DI 10889942760695 each, 40889942760696 case, Lot Number 25KBT852; Medline SKU DYNJRA1034: UDI/DI 10889942760695 each, 40889942760696 case, Lot Number 25JBR203; Medline SKU DYNJRA1034: UDI/DI 10889942760695 each, 40889942760696 case, Lot Number 25HBS729; Medline SKU DYNJRA1034: UDI/DI 10889942760695 each, 40889942760696 case, Lot Number 25HBJ284; Medline SKU DYNJRA1034: UDI/DI 10889942760695 each, 40889942760696 case, Lot Number 25EBD163; Medline SKU DYNJRA1034: UDI/DI 10889942760695 each, 40889942760696 case, Lot Number 24EDB670; Medline SKU DYNJRA1034: UDI/DI 10889942760695 each, 40889942760696 case, Lot Number 24CDA047; Medline SKU DYNJRA1034: UDI/DI 10889942760695 each, 40889942760696 case, Lot Number 24BDA117; Medline SKU DYNJRA1034: UDI/DI 10889942760695 each, 40889942760696 case, Lot Number 23JDB931; Medline SKU DYNJRA9028: UDI/DI 10884389285701 each, 40884389285702 case, Lot Number 26BBN630; Medline SKU DYNJRA9028: UDI/DI 10884389285701 each, 40884389285702 case, Lot Number 26BBN631; Medline SKU DYNJRA9028: UDI/DI 10884389285701 each, 40884389285702 case, Lot Number 26ABU477; Medline SKU DYNJRA9028: UDI/DI 10884389285701 each, 40884389285702 case, Lot Number 26ABU479; Medline SKU DYNJRA9028: UDI/DI 10884389285701 each, 40884389285702 case, Lot Number 26ABQ765; Medline SKU DYNJRA9028: UDI/DI 10884389285701 each, 40884389285702 case, Lot Number 26ABE062; Medline SKU DYNJRA9028: UDI/DI 10884389285701 each, 40884389285702 case, Lot Number 26ABE063; Medline SKU DYNJRA9028: UDI/DI 10884389285701 each, 40884389285702 case, Lot Number 25DBE494; Medline SKU DYNJRA9028: UDI/DI 10884389285701 each, 40884389285702 case, Lot Number 25DBE495; Medline SKU DYNJRA9028: UDI/DI 10884389285701 each, 40884389285702 case, Lot Number 25DBE493; Medline SKU DYNJRA9028: UDI/DI 10884389285701 each, 40884389285702 case, Lot Number 25BBC565; Medline SKU DYNJRA9028: UDI/DI 10884389285701 each, 40884389285702 case, Lot Number 24BBP041; Medline SKU DYNJRA9028: UDI/DI 10884389285701 each, 40884389285702 case, Lot Number 23HBS638; Medline SKU DYNJRA9028: UDI/DI 10884389285701 each, 40884389285702 case, Lot Number 23HBS639; Medline SKU DYNJRA9028: UDI/DI 10884389285701 each, 40884389285702 case, Lot Number 23GBC535; Medline SKU DYNJRA9030: UDI/DI 10889942785728 each, 40889942785729 case, Lot Number 26ABQ980; Medline SKU DYNJRA9030: UDI/DI 10889942785728 each, 40889942785729 case, Lot Number 26ABJ386; Medline SKU DYNJRA9030: UDI/DI 10889942785728 each, 40889942785729 case, Lot Number 25LBH067; Medline SKU DYNJRA9030: UDI/DI 10889942785728 each, 40889942785729 case, Lot Number 25KBR359; Medline SKU DYNJRA9030: UDI/DI 10889942785728 each, 40889942785729 case, Lot Number 25JBP383; Medline SKU DYNJRA9030: UDI/DI 10889942785728 each, 40889942785729 case, Lot Number 25IBK145; Medline SKU DYNJRA9030: UDI/DI 10889942785728 each, 40889942785729 case, Lot Number 25ABP041; Medline SKU DYNJRA9030: UDI/DI 10889942785728 each, 40889942785729 case, Lot Number 24GBD227; Medline SKU DYNJRA9030: UDI/DI 10889942785728 each, 40889942785729 case, Lot Number 24FBJ511; Medline SKU DYNJRA9030: UDI/DI 10889942785728 each, 40889942785729 case, Lot Number 24FBJ026; Medline SKU DYNJRA9030: UDI/DI 10889942785728 each, 40889942785729 case, Lot Number 24BBP046; Medline SKU DYNJRA9030: UDI/DI 10889942785728 each, 40889942785729 case, Lot Number 23IBG977; Medline SKU DYNJRA9030: UDI/DI 10889942785728 each, 40889942785729 case, Lot Number 23GBM182.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2233-2026%22", "url": "https://recallledger.net/recalls/device-z-2233-2026-medline-kits-containing-huons-co-bupivacaine-hcl-in-dextrose-injectio/"}, {"id": "fda-device-z-2232-2026", "source": "FDA", "category": "device", "recall_number": "Z-2232-2026", "title": "Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection recall (Medline Industries, LP)", "product": "Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) PAIN TRAY, Medline Kit SKU DYNJRA1555; 2) SPINAL BLOCK TRAY WHITACRE 24G, Medline Kit SKU DYNJRA1817; 3) TRAY, 25G WHIT SPINAL W/PHARM, Medline Kit SKU DYNJRA1920; 4) ULTRASOUND GUIDED NERVE BLOCK, Medline Kit SKU DYNJRA2013; 5) TRAY, 25G WHIT SPINAL W/PHARM, Medline Kit SKU DYNJRA2017; 6) 25G SPINAL BLOCK TRAY, Medline Kit SKU DYNJRA2067; 7) 25G SPINAL BLOCK TRAY, Medline Kit SKU DYNJRA2067A; 8) TRAY, 25G WHIT SPINAL W/PHARM, Medline Kit SKU DYNJRA2093; 9) SPINAL BLOCK 25G WHTCRE 5S BU, Medline Kit SKU DYNJRA2117A; 10) SPINAL BLOCK 25G WHTCRE 5S BU, Medline Kit SKU DYNJRA2124; 11) SPINAL BLOCK 25G WHTCRE 5S BU, Medline Kit SKU DYNJRA2124A; 12) PAIN TRAY, Medline Kit SKU DYNJRA2144; 13) TRAY, 24G WHIT SPINAL W/PHARM, Medline Kit SKU DYNJRA2221; 14) TRAY, SPINAL PENCIL POINT 25G, Medline Kit SKU DYNJRA2333; 15) SPINAL TRAY, Medline Kit SKU DYNJRA2390; 16) SPINAL BLOCK 25G WHTCRE 5S BU, Medline Kit SKU DYNJRA2402; 17) SPINAL ANESTHESIA TRAY, Medline Kit SKU DYNJRA2407; 18) SPINAL ANESTHESIA TRAY, Medline Kit SKU DYNJRA2407A; 19) SPINAL ANESTHESIA TRAY, Medline Kit SKU DYNJRA2407B; 20) TRAY, SPINAL PENCIL POINT 25G, Medline Kit SKU DYNJRA2447; 21) TRAY, SPINAL PENCIL POINT 25G, Medline Kit SKU DYNJRA2447A; 22) SPINAL TRAY 25G, Medline Kit SKU DYNJRA2488A; 23) J&S SPINAL TRAY, Medline Kit SKU DYNJRA2545; 24) SPINAL TRAY, Medline Kit SKU DYNJRA2549; 25) TRAY, 25G WHIT SPINAL W/PHARM, Medline Kit SKU DYNJRA2550; 26) TRAY, SPINAL PENCIL POINT 25G, Medline Kit SKU DYNJRA2552; 27) SPINAL BLOCK TRAY, Medline Kit SKU DYNJRA2554; 28) SPINAL BLOCK TRAY, Medline Kit SKU DYNJRA2554A; 29) SPINAL ANESTHESIA TRAY, Medline Kit SKU DYNJRA2578; 30) TRAY, 25G WHIT SPINAL W/PHARM, Medline Kit SKU DYNJRA2588; 31) TRAY, 25G WHIT SPINAL W/PHARM, Medline Kit SKU DYNJRA2602; 32) SPINAL TRAY, Medline Kit SKU DYNJRA2618; 33) SPINAL TRAY, Medline Kit SKU DYNJRA2619; 34) SPINAL TRAY, Medline Kit SKU DYNJRA2622; 35) SPINAL BLOCK 25 WHITACRE 5S ND, Medline Kit SKU DYNJRA2624; 36) SPINAL TRAY, Medline Kit SKU DYNJRA2631; 37) TRAY, SPINAL PENCIL POINT 25G, Medline Kit SKU DYNJRA2632; 38) TRAY, 25G WHIT SPINAL W/PHARM, Medline Kit SKU DYNJRA2633; 39) SPINAL TRAY, Medline Kit SKU DYNJRA2645; 40) TRAY, 25G WHIT SPINAL W/PHARM, Medline Kit SKU DYNJRA2654; 41) CSE PAIN MANAGEMENT TRAY, Medline Kit SKU DYNJRA2665; 42) SPINAL TRAY, Medline Kit SKU DYNJRA2667; 43) SPINAL TRAY 24G BD, Medline Kit SKU DYNJRA2675; 44) SPINAL TRAY W/ CHLORAPREP, Medline Kit SKU DYNJRA2680; 45) SPINAL TRAY, Medline Kit SKU DYNJRA2682; 46) TRAY, 24G WHIT SPINAL W/PHARM, Medline Kit SKU DYNJRA2684; 47) SPINAL TRAY, Medline Kit SKU DYNJRA2725; 48) 25G SPINAL BLOCK TRAY, Medline Kit SKU DYNJRA2757; 49) TRAY, 25G SPINAL W/RX DURAPREP, Medline Kit SKU DYNJRA9039; 50) TRAY, 25G SPINAL W/RX, Medline Kit SKU DYNJRA9045; 51) SLSYSTEM CSE TRAY, Medline Kit SKU PAIN2333; 52) 25G SPINAL BLOCK TRAY, Medline Kit SKU SAMPA0135.", "reason": "Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.", "hazard_level": "Class I", "company": "Medline Industries, LP", "company_location": "Northfield, IL, United States", "date": "2026-04-10", "report_date": "2026-06-03", "status": "Ongoing", "distribution": "Worldwide - US Nationwide distribution in the US Territory of Virgin Islands and the countries of Bahamas, Panama, Barbados.", "states": [], "nationwide": true, "quantity": "28106 kits", "codes": "Medline SKU DYNJRA1555: UDI/DI 10193489238723 each, 40193489238724 case, Lot Numbers: 25CLA724; Medline SKU DYNJRA1555: UDI/DI 10193489238723 each, 40193489238724 case, Lot Numbers: 25CLA306; Medline SKU DYNJRA1817: UDI/DI 10193489942354 each, 40193489942355 case, Lot Numbers: 25JMH667; Medline SKU DYNJRA1817: UDI/DI 10193489942354 each, 40193489942355 case, Lot Numbers: 25JMC856; Medline SKU DYNJRA1817: UDI/DI 10193489942354 each, 40193489942355 case, Lot Numbers: 25JMA370; Medline SKU DYNJRA1817: UDI/DI 10193489942354 each, 40193489942355 case, Lot Numbers: 25IMI402; Medline SKU DYNJRA1817: UDI/DI 10193489942354 each, 40193489942355 case, Lot Numbers: 25HME985; Medline SKU DYNJRA1817: UDI/DI 10193489942354 each, 40193489942355 case, Lot Numbers: 25AMI063; Medline SKU DYNJRA1817: UDI/DI 10193489942354 each, 40193489942355 case, Lot Numbers: 24JMI488; Medline SKU DYNJRA1817: UDI/DI 10193489942354 each, 40193489942355 case, Lot Numbers: 24JMA113; Medline SKU DYNJRA1817: UDI/DI 10193489942354 each, 40193489942355 case, Lot Numbers: 23KMD776; Medline SKU DYNJRA1920: UDI/DI 10195327111168 each, 40195327111169 case, Lot Numbers: 25FBQ144; Medline SKU DYNJRA2013: UDI/DI 10195327212049 each, 40195327212040 case, Lot Numbers: 26ABV382; Medline SKU DYNJRA2013: UDI/DI 10195327212049 each, 40195327212040 case, Lot Numbers: 24GBA206; Medline SKU DYNJRA2017: UDI/DI 10195327217402 each, 40195327217403 case, Lot Numbers: 26BMJ305; Medline SKU DYNJRA2017: UDI/DI 10195327217402 each, 40195327217403 case, Lot Numbers: 25LMA710; Medline SKU DYNJRA2017: UDI/DI 10195327217402 each, 40195327217403 case, Lot Numbers: 25JMI170; Medline SKU DYNJRA2017: UDI/DI 10195327217402 each, 40195327217403 case, Lot Numbers: 25JMA642; Medline SKU DYNJRA2017: UDI/DI 10195327217402 each, 40195327217403 case, Lot Numbers: 25GMH968; Medline SKU DYNJRA2017: UDI/DI 10195327217402 each, 40195327217403 case, Lot Numbers: 25EMJ739; Medline SKU DYNJRA2017: UDI/DI 10195327217402 each, 40195327217403 case, Lot Numbers: 25DMF107; Medline SKU DYNJRA2017: UDI/DI 10195327217402 each, 40195327217403 case, Lot Numbers: 25DMB676; Medline SKU DYNJRA2017: UDI/DI 10195327217402 each, 40195327217403 case, Lot Numbers: 24HMD119; Medline SKU DYNJRA2017: UDI/DI 10195327217402 each, 40195327217403 case, Lot Numbers: 24DMB563; Medline SKU DYNJRA2017: UDI/DI 10195327217402 each, 40195327217403 case, Lot Numbers: 23IBL595; Medline SKU DYNJRA2017: UDI/DI 10195327217402 each, 40195327217403 case, Lot Numbers: 23GBO103; Medline SKU DYNJRA2067: UDI/DI 10195327269142 each, 40195327269143 case, Lot Numbers: 25EMJ740; Medline SKU DYNJRA2067: UDI/DI 10195327269142 each, 40195327269143 case, Lot Numbers: 25EMB776; Medline SKU DYNJRA2067: UDI/DI 10195327269142 each, 40195327269143 case, Lot Numbers: 25DMH562; Medline SKU DYNJRA2067: UDI/DI 10195327269142 each, 40195327269143 case, Lot Numbers: 25DMD631; Medline SKU DYNJRA2067: UDI/DI 10195327269142 each, 40195327269143 case, Lot Numbers: 24JMA116; Medline SKU DYNJRA2067: UDI/DI 10195327269142 each, 40195327269143 case, Lot Numbers: 24FMI984; Medline SKU DYNJRA2067: UDI/DI 10195327269142 each, 40195327269143 case, Lot Numbers: 24EMC757; Medline SKU DYNJRA2067: UDI/DI 10195327269142 each, 40195327269143 case, Lot Numbers: 24CMH743; Medline SKU DYNJRA2067: UDI/DI 10195327269142 each, 40195327269143 case, Lot Numbers: 24BBP785; Medline SKU DYNJRA2067: UDI/DI 10195327269142 each, 40195327269143 case, Lot Numbers: 23HBQ128; Medline SKU DYNJRA2067A: UDI/DI 10198459371967 each, 40198459371968 case, Lot Numbers: 26BBJ400; Medline SKU DYNJRA2093: UDI/DI 10195327296797 each, 40195327296798 case, Lot Numbers: 23JBQ988; Medline SKU DYNJRA2117A: UDI/DI 10198459009273 each, 40198459009274 case, Lot Numbers: 26BMC993; Medline SKU DYNJRA2117A: UDI/DI 10198459009273 each, 40198459009274 case, Lot Numbers: 26AMF175; Medline SKU DYNJRA2117A: UDI/DI 10198459009273 each, 40198459009274 case, Lot Numbers: 25LMG019; Medline SKU DYNJRA2117A: UDI/DI 10198459009273 each, 40198459009274 case, Lot Numbers: 25JME838; Medline SKU DYNJRA2117A: UDI/DI 10198459009273 each, 40198459009274 case, Lot Numbers: 25FMD398; Medline SKU DYNJRA2117A: UDI/DI 10198459009273 each, 40198459009274 case, Lot Numbers: 25DMH259; Medline SKU DYNJRA2117A: UDI/DI 10198459009273 each, 40198459009274 case, Lot Numbers: 25BMJ032; Medline SKU DYNJRA2117A: UDI/DI 10198459009273 each, 40198459009274 case, Lot Numbers: 24KMH222; Medline SKU DYNJRA2117A: UDI/DI 10198459009273 each, 40198459009274 case, Lot Numbers: 24JMB172; Medline SKU DYNJRA2117A: UDI/DI 10198459009273 each, 40198459009274 case, Lot Numbers: 24HME068; Medline SKU DYNJRA2117A: UDI/DI 10198459009273 each, 40198459009274 case, Lot Numbers: 24HMA876; Medline SKU DYNJRA2124: UDI/DI 10195327332334 each, 40195327332335 case, Lot Numbers: 25KBT829; Medline SKU DYNJRA2124: UDI/DI 10195327332334 each, 40195327332335 case, Lot Numbers: 25HBU514; Medline SKU DYNJRA2124: UDI/DI 10195327332334 each, 40195327332335 case, Lot Numbers: 25FBB363; Medline SKU DYNJRA2124: UDI/DI 10195327332334 each, 40195327332335 case, Lot Numbers: 24FBT394; Medline SKU DYNJRA2124: UDI/DI 10195327332334 each, 40195327332335 case, Lot Numbers: 23HBE118; Medline SKU DYNJRA2124A: UDI/DI 10198459699856 each, 40198459699857 case, Lot Numbers: 26CBD127; Medline SKU DYNJRA2144: UDI/DI 10195327356255 each, 40195327356256 case, Lot Numbers: 23IBP002; Medline SKU DYNJRA2221: UDI/DI 10195327428174 each, 40195327428175 case, Lot Numbers: 25KMC852; Medline SKU DYNJRA2221: UDI/DI 10195327428174 each, 40195327428175 case, Lot Numbers: 25IMI404; Medline SKU DYNJRA2221: UDI/DI 10195327428174 each, 40195327428175 case, Lot Numbers: 25EMJ886; Medline SKU DYNJRA2221: UDI/DI 10195327428174 each, 40195327428175 case, Lot Numbers: 25DMF094; Medline SKU DYNJRA2221: UDI/DI 10195327428174 each, 40195327428175 case, Lot Numbers: 24JMA125; Medline SKU DYNJRA2221: UDI/DI 10195327428174 each, 40195327428175 case, Lot Numbers: 23HBX509; Medline SKU DYNJRA2333: UDI/DI 10195327572686 each, 40195327572687 case, Lot Numbers: 26BBH475; Medline SKU DYNJRA2333: UDI/DI 10195327572686 each, 40195327572687 case, Lot Numbers: 26BBB092; Medline SKU DYNJRA2333: UDI/DI 10195327572686 each, 40195327572687 case, Lot Numbers: 26ABQ762; Medline SKU DYNJRA2333: UDI/DI 10195327572686 each, 40195327572687 case, Lot Numbers: 25LBA381; Medline SKU DYNJRA2333: UDI/DI 10195327572686 each, 40195327572687 case, Lot Numbers: 25IBJ314; Medline SKU DYNJRA2390: UDI/DI 10195327675981 each, 40195327675982 case, Lot Numbers: 26CBI127; Medline SKU DYNJRA2390: UDI/DI 10195327675981 each, 40195327675982 case, Lot Numbers: 25JBD690; Medline SKU DYNJRA2390: UDI/DI 10195327675981 each, 40195327675982 case, Lot Numbers: 25HBD399; Medline SKU DYNJRA2390: UDI/DI 10195327675981 each, 40195327675982 case, Lot Numbers: 25GBL686; Medline SKU DYNJRA2390: UDI/DI 10195327675981 each, 40195327675982 case, Lot Numbers: 24FBT390; Medline SKU DYNJRA2402: UDI/DI 10198459003448 each, 40198459003449 case, Lot Numbers: 26BBP527; Medline SKU DYNJRA2402: UDI/DI 10198459003448 each, 40198459003449 case, Lot Numbers: 25HBS558; Medline SKU DYNJRA2402: UDI/DI 10198459003448 each, 40198459003449 case, Lot Numbers: 25HBJ268; Medline SKU DYNJRA2402: UDI/DI 10198459003448 each, 40198459003449 case, Lot Numbers: 24FBT392; Medline SKU DYNJRA2407: UDI/DI 10198459006401 each, 40198459006402 case, Lot Numbers: 24FBT391; Medline SKU DYNJRA2407A: UDI/DI 10198459342363 each, 40198459342364 case, Lot Numbers: 25LBL084; Medline SKU DYNJRA2407A: UDI/DI 10198459342363 each, 40198459342364 case, Lot Numbers: 25JBH939; Medline SKU DYNJRA2407B: UDI/DI 10198459660931 each, 40198459660932 case, Lot Numbers: 26CBF845; Medline SKU DYNJRA2447: UDI/DI 10198459048043 each, 40198459048044 case, Lot Numbers: 24GBJ538; Medline SKU DYNJRA2447A: UDI/DI 10198459340734 each, 40198459340735 case, Lot Numbers: 26CBD943; Medline SKU DYNJRA2447A: UDI/DI 10198459340734 each, 40198459340735 case, Lot Numbers: 25LBO163; Medline SKU DYNJRA2447A: UDI/DI 10198459340734 each, 40198459340735 case, Lot Numbers: 25JBE899; Medline SKU DYNJRA2447A: UDI/DI 10198459340734 each, 40198459340735 case, Lot Numbers: 25FBH740; Medline SKU DYNJRA2488A: UDI/DI 10198459221576 each, 40198459221577 case, Lot Numbers: 26BBG175; Medline SKU DYNJRA2488A: UDI/DI 10198459221576 each, 40198459221577 case, Lot Numbers: 25KBT792; Medline SKU DYNJRA2488A: UDI/DI 10198459221576 each, 40198459221577 case, Lot Numbers: 25HBN364; Medline SKU DYNJRA2488A: UDI/DI 10198459221576 each, 40198459221577 case, Lot Numbers: 25FBT533; Medline SKU DYNJRA2488A: UDI/DI 10198459221576 each, 40198459221577 case, Lot Numbers: 25EBS468; Medline SKU DYNJRA2488A: UDI/DI 10198459221576 each, 40198459221577 case, Lot Numbers: 25DBI026; Medline SKU DYNJRA2488A: UDI/DI 10198459221576 each, 40198459221577 case, Lot Numbers: 25ABV158; Medline SKU DYNJRA2545: UDI/DI 10198459218811 each, 40198459218812 case, Lot Numbers: 25IBS272; Medline SKU DYNJRA2545: UDI/DI 10198459218811 each, 40198459218812 case, Lot Numbers: 25GBQ078; Medline SKU DYNJRA2545: UDI/DI 10198459218811 each, 40198459218812 case, Lot Numbers: 25DBQ388; Medline SKU DYNJRA2549: UDI/DI 10198459223785 each, 40198459223786 case, Lot Numbers: 25HBJ272; Medline SKU DYNJRA2550: UDI/DI 10198459225192 each, 40198459225193 case, Lot Numbers: 26CBD941; Medline SKU DYNJRA2550: UDI/DI 10198459225192 each, 40198459225193 case, Lot Numbers: 26BBL404; Medline SKU DYNJRA2550: UDI/DI 10198459225192 each, 40198459225193 case, Lot Numbers: 26ABT283; Medline SKU DYNJRA2550: UDI/DI 10198459225192 each, 40198459225193 case, Lot Numbers: 25HBT630; Medline SKU DYNJRA2552: UDI/DI 10198459234972 each, 40198459234973 case, Lot Numbers: 26BBR448; Medline SKU DYNJRA2552: UDI/DI 10198459234972 each, 40198459234973 case, Lot Numbers: 26ABJ301; Medline SKU DYNJRA2552: UDI/DI 10198459234972 each, 40198459234973 case, Lot Numbers: 25KBN074; Medline SKU DYNJRA2552: UDI/DI 10198459234972 each, 40198459234973 case, Lot Numbers: 25IBQ405; Medline SKU DYNJRA2552: UDI/DI 10198459234972 each, 40198459234973 case, Lot Numbers: 25IBG233; Medline SKU DYNJRA2552: UDI/DI 10198459234972 each, 40198459234973 case, Lot Numbers: 25EBU153; Medline SKU DYNJRA2552: UDI/DI 10198459234972 each, 40198459234973 case, Lot Numbers: 25EBK087; Medline SKU DYNJRA2554: UDI/DI 10198459239243 each, 40198459239244 case, Lot Numbers: 25JBX901; Medline SKU DYNJRA2554: UDI/DI 10198459239243 each, 40198459239244 case, Lot Numbers: 25FBD587; Medline SKU DYNJRA2554A: UDI/DI 10198459694431 each, 40198459694432 case, Lot Numbers: 26BBM303; Medline SKU DYNJRA2578: UDI/DI 10198459275111 each, 40198459275112 case, Lot Numbers: 26BBO256; Medline SKU DYNJRA2578: UDI/DI 10198459275111 each, 40198459275112 case, Lot Numbers: 25LBJ013; Medline SKU DYNJRA2578: UDI/DI 10198459275111 each, 40198459275112 case, Lot Numbers: 25KBP759; Medline SKU DYNJRA2578: UDI/DI 10198459275111 each, 40198459275112 case, Lot Numbers: 25JBB370; Medline SKU DYNJRA2588: UDI/DI 10198459294624 each, 40198459294625 case, Lot Numbers: 26CBF842; Medline SKU DYNJRA2588: UDI/DI 10198459294624 each, 40198459294625 case, Lot Numbers: 26ABE836; Medline SKU DYNJRA2588: UDI/DI 10198459294624 each, 40198459294625 case, Lot Numbers: 25JBG955; Medline SKU DYNJRA2588: UDI/DI 10198459294624 each, 40198459294625 case, Lot Numbers: 25GBJ117; Medline SKU DYNJRA2588: UDI/DI 10198459294624 each, 40198459294625 case, Lot Numbers: 25DBQ696; Medline SKU DYNJRA2602: UDI/DI 10198459315855 each, 40198459315856 case, Lot Numbers: 26BBJ384; Medline SKU DYNJRA2602: UDI/DI 10198459315855 each, 40198459315856 case, Lot Numbers: 25JBH500; Medline SKU DYNJRA2602: UDI/DI 10198459315855 each, 40198459315856 case, Lot Numbers: 25IBE968; Medline SKU DYNJRA2602: UDI/DI 10198459315855 each, 40198459315856 case, Lot Numbers: 25DBQ059; Medline SKU DYNJRA2618: UDI/DI 10198459341731 each, 40198459341732 case, Lot Numbers: 25HBA436; Medline SKU DYNJRA2618: UDI/DI 10198459341731 each, 40198459341732 case, Lot Numbers: 25GBC673; Medline SKU DYNJRA2618: UDI/DI 10198459341731 each, 40198459341732 case, Lot Numbers: 25EBN435; Medline SKU DYNJRA2619: UDI/DI 10198459341793 each, 40198459341794 case, Lot Numbers: 25FBL039; Medline SKU DYNJRA2622: UDI/DI 10198459341885 each, 40198459341886 case, Lot Numbers: 26CBD468; Medline SKU DYNJRA2622: UDI/DI 10198459341885 each, 40198459341886 case, Lot Numbers: 26BBQ318; Medline SKU DYNJRA2622: UDI/DI 10198459341885 each, 40198459341886 case, Lot Numbers: 26BBF246; Medline SKU DYNJRA2622: UDI/DI 10198459341885 each, 40198459341886 case, Lot Numbers: 25FBD907; Medline SKU DYNJRA2624: UDI/DI 10198459341991 each, 40198459341992 case, Lot Numbers: 25FBG508; Medline SKU DYNJRA2631: UDI/DI 10198459347610 each, 40198459347611 case, Lot Numbers: 25FBF497; Medline SKU DYNJRA2632: UDI/DI 10198459347634 each, 40198459347635 case, Lot Numbers: 26BBJ396; Medline SKU DYNJRA2632: UDI/DI 10198459347634 each, 40198459347635 case, Lot Numbers: 26ABS300; Medline SKU DYNJRA2632: UDI/DI 10198459347634 each, 40198459347635 case, Lot Numbers: 25IBL870; Medline SKU DYNJRA2632: UDI/DI 10198459347634 each, 40198459347635 case, Lot Numbers: 25FBL040; Medline SKU DYNJRA2633: UDI/DI 10198459349461 each, 40198459349462 case, Lot Numbers: 26BBG178; Medline SKU DYNJRA2633: UDI/DI 10198459349461 each, 40198459349462 case, Lot Numbers: 26ABD972; Medline SKU DYNJRA2633: UDI/DI 10198459349461 each, 40198459349462 case, Lot Numbers: 25LBF464; Medline SKU DYNJRA2633: UDI/DI 10198459349461 each, 40198459349462 case, Lot Numbers: 25JBW886; Medline SKU DYNJRA2633: UDI/DI 10198459349461 each, 40198459349462 case, Lot Numbers: 25JBA813; Medline SKU DYNJRA2633: UDI/DI 10198459349461 each, 40198459349462 case, Lot Numbers: 25HBL703; Medline SKU DYNJRA2633: UDI/DI 10198459349461 each, 40198459349462 case, Lot Numbers: 25FBG791; Medline SKU DYNJRA2645: UDI/DI 10198459369629 each, 40198459369620 case, Lot Numbers: 26ABE851; Medline SKU DYNJRA2645: UDI/DI 10198459369629 each, 40198459369620 case, Lot Numbers: 26ABB344; Medline SKU DYNJRA2645: UDI/DI 10198459369629 each, 40198459369620 case, Lot Numbers: 26ABA200; Medline SKU DYNJRA2645: UDI/DI 10198459369629 each, 40198459369620 case, Lot Numbers: 25HBP475; Medline SKU DYNJRA2645: UDI/DI 10198459369629 each, 40198459369620 case, Lot Numbers: 25GBC666; Medline SKU DYNJRA2654: UDI/DI 10198459414114 each, 40198459414115 case, Lot Numbers: 25IBU953; Medline SKU DYNJRA2654: UDI/DI 10198459414114 each, 40198459414115 case, Lot Numbers: 25GBP675; Medline SKU DYNJRA2665: UDI/DI 10198459440618 each, 40198459440619 case, Lot Numbers: 25ILA934; Medline SKU DYNJRA2665: UDI/DI 10198459440618 each, 40198459440619 case, Lot Numbers: 25HLA408; Medline SKU DYNJRA2667: UDI/DI 10198459453656 each, 40198459453657 case, Lot Numbers: 25LBE224; Medline SKU DYNJRA2667: UDI/DI 10198459453656 each, 40198459453657 case, Lot Numbers: 25IBK727; Medline SKU DYNJRA2675: UDI/DI 10198459492600 each, 40198459492601 case, Lot Numbers: 25IBE846; Medline SKU DYNJRA2680: UDI/DI 10198459504365 each, 40198459504366 case, Lot Numbers: 25JBK134; Medline SKU DYNJRA2682: UDI/DI 10198459505317 each, 40198459505318 case, Lot Numbers: 25IBR245; Medline SKU DYNJRA2684: UDI/DI 10198459509148 each, 40198459509149 case, Lot Numbers: 26ABW308; Medline SKU DYNJRA2684: UDI/DI 10198459509148 each, 40198459509149 case, Lot Numbers: 25IBR247; Medline SKU DYNJRA2725: UDI/DI 10198459592386 each, 40198459592387 case, Lot Numbers: 25LBH997; Medline SKU DYNJRA2757: UDI/DI 10198459659676 each, 40198459659677 case, Lot Numbers: 26BBB965; Medline SKU DYNJRA9039: UDI/DI 10195327113834 each, 40195327113835 case, Lot Numbers: 25LBF214; Medline SKU DYNJRA9039: UDI/DI 10195327113834 each, 40195327113835 case, Lot Numbers: 25IBC977; Medline SKU DYNJRA9045: UDI/DI 10195327031251 each, 40195327031252 case, Lot Numbers: 25LBN162; Medline SKU DYNJRA9045: UDI/DI 10195327031251 each, 40195327031252 case, Lot Numbers: 25JBR086; Medline SKU DYNJRA9045: UDI/DI 10195327031251 each, 40195327031252 case, Lot Numbers: 25FBS501; Medline SKU DYNJRA9045: UDI/DI 10195327031251 each, 40195327031252 case, Lot Numbers: 25EBU898; Medline SKU PAIN2333: UDI/DI 10198459537981 each, 40198459537982 case, Lot Numbers: 26CLA730; Medline SKU PAIN2333: UDI/DI 10198459537981 each, 40198459537982 case, Lot Numbers: 25KLA519; Medline SKU SAMPA0135: UDI/DI 10198459018534 each, 40198459018535 case, Lot Numbers: 25DBQ390.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2232-2026%22", "url": "https://recallledger.net/recalls/device-z-2232-2026-medline-kits-containing-huons-co-bupivacaine-hcl-in-dextrose-injectio/"}, {"id": "fda-device-z-2231-2026", "source": "FDA", "category": "device", "recall_number": "Z-2231-2026", "title": "Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection recall (Medline Industries, LP)", "product": "Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) ANESTHESIA TRAY, Medline SKU DYNJRA1355A; 2) SPINAL ANESTHESIA TRAY, Medline SKU DYNJRA2151.", "reason": "Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.", "hazard_level": "Class I", "company": "Medline Industries, LP", "company_location": "Northfield, IL, United States", "date": "2026-04-10", "report_date": "2026-06-03", "status": "Ongoing", "distribution": "Worldwide - US Nationwide distribution in the US Territory of Virgin Islands and the countries of Bahamas, Panama, Barbados.", "states": [], "nationwide": true, "quantity": "1100 kits", "codes": "Medline SKU DYNJRA1355A: UDI/DI 10195327179830 each, FI case, Lot Numbers: 26CBA272; Medline SKU DYNJRA1355A: UDI/DI 10195327179830 each, FI case, Lot Numbers: 26ABS307; Medline SKU DYNJRA1355A: UDI/DI 10195327179830 each, FI case, Lot Numbers: 25HBE663; Medline SKU DYNJRA1355A: UDI/DI 10195327179830 each, FI case, Lot Numbers: 25FBA408; Medline SKU DYNJRA1355A: UDI/DI 10195327179830 each, FI case, Lot Numbers: 25CBG043; Medline SKU DYNJRA1355A: UDI/DI 10195327179830 each, FI case, Lot Numbers: 24FBT395; Medline SKU DYNJRA2151: UDI/DI 10195327365400 each, FI case, Lot Numbers: 24FBT396.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2231-2026%22", "url": "https://recallledger.net/recalls/device-z-2231-2026-medline-kits-containing-huons-co-bupivacaine-hcl-in-dextrose-injectio/"}, {"id": "fda-device-z-2230-2026", "source": "FDA", "category": "device", "recall_number": "Z-2230-2026", "title": "Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers: 48771 recall (O&M HALYARD INC)", "product": "Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers: 48771 (XS), 48772 (Sm.), 48773 (Md.), 48774 (Lg.), 48775 (Xl)", "reason": "Nitrile Exam Glove failed to meet specifications chemical permeation performance.", "hazard_level": "Class II", "company": "O&M HALYARD INC", "company_location": "Alpharetta, GA, United States", "date": "2026-04-13", "report_date": "2026-06-03", "status": "Ongoing", "distribution": "US Nationwide distribution in the states of GA, CA, NJ, MA, NY, NC.", "states": ["CA", "GA", "MA", "NC", "NJ", "NY"], "nationwide": true, "quantity": "452,500 units", "codes": "REF: 48771/UDI: 30680651487712 (Package)20680651487715 (Primary)90680651487714 (Unit of Use) ; 48772/30680651487729 (Package)20680651487722 (Primary)90680651487721 (Unit of Use);48773/30680651487736 (Package)20680651487739 (Primary)90680651487738 (Unit of Use);48774/UDI: 30680651487743 (Package)20680651487746 (Primary) 90680651487745 (Unit of Use);48775/UDI:30680651487750 (Package)20680651487753 (Primary)90680651487752 (Unit of Use)", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2230-2026%22", "url": "https://recallledger.net/recalls/device-z-2230-2026-halyard-purezero-ultraviolet-nitrile-exam-gloves-reference-numbers-4/"}, {"id": "fda-device-z-2211-2026", "source": "FDA", "category": "device", "recall_number": "Z-2211-2026", "title": "Automated Impella Controller recall (Abiomed, Inc.)", "product": "Automated Impella Controller (AIC); Product Code: 0042-0000-US;", "reason": "A retrospective review identified that there are AIC units requiring specific hardware updates to address potential safety concerns. These hardware updates have been implemented through Abiomed s servicing process; therefore, AICs that have not received service are pending these updates. Issue 1: The proximity of the internal Video Graphics Array cable to the Digital Signal Processor chipset on the Impellatronic printed circuit assembly could potentially result in Electrostatic Discharge coupling into the Digital Signal Processor which may interrupt motor controls. Issue 2: There is a potential for the Compact Flash Memory Card dislodgement due to external applied forces, which could result in AIC startup failures and data logging issues. Issue 3: Improper routing of the fan wire within the AIC could lead to fan wire damage, which may result in console boot-up failure. Issue 4: Potential capacitor related issues on the Power Battery Manager, including the potential for the capacitors to cause pump stop, purge stop, and/or single fan fuse failures.", "hazard_level": "Class I", "company": "Abiomed, Inc.", "company_location": "Danvers, MA, United States", "date": "2026-04-20", "report_date": "2026-06-03", "status": "Ongoing", "distribution": "Worldwide - US Nationwide distribution in the states of CA, CT, FL, LA, MA, MI, MO, MS, ND, NY, OH, PA, TX, WY and the countries of Brazil, Canada, Colombia, Hong Kong, Italy, Kuwait, Saudi Arabia, UAE, United Kingdom;", "states": ["CA", "CT", "FL", "LA", "MA", "MI", "MO", "MS", "ND", "NY", "OH", "PA", "TX", "WY"], "nationwide": true, "quantity": "91 units", "codes": "Product Code: 0042-0000-US; UDI-DI: 00813502010022; Serial Numbers: IC2449, IC2451, IC2452, IC2453, IC2459, IC2460, IC1096, IC1142, IC1202, IC1203, IC1224, IC1231, IC1238, IC1284, IC1285, IC1390, IC1545, IC1577, IC1665, IC1708, IC1741, IC1852, IC1853, IC2029, IC2071, IC2154, IC2277, IC2278, IC2314, IC2315, IC2368, IC2369, IC2370, IC2442, IC2443, IC2444, IC2461, IC2471, IC2476, IC2477, IC2478, IC2479, IC2575, IC2989, IC3127, IC3128, IC3129, IC3130, IC3166, IC3167, IC3213, IC3223, IC3306, IC3307, IC3308, IC3309, IC3342, IC3398, IC3475, IC3656, IC3658, IC3663, IC3664, IC3665, IC3666, IC3674, IC3675, IC3719, IC3720, IC3776, IC3812, IC3887, IC3888, IC4045, IC4060, IC1301, IC1544, IC1572, IC2686, IC2687, IC2848, IC3174, IC3269, IC3272, IC3277, IC3278, IC3281, IC3282, IC3284, IC3294, IC3783;", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2211-2026%22", "url": "https://recallledger.net/recalls/device-z-2211-2026-automated-impella-controller-aic-product-code-0042-0000-us/"}, {"id": "fda-device-z-2160-2026", "source": "FDA", "category": "device", "recall_number": "Z-2160-2026", "title": "RelayPro Thoracic Stent-Graft System recall (Bolton Medical Inc.)", "product": "RelayPro Thoracic Stent-Graft System (various sizes) Reference numbers: 28-N4-32-104-32U\t28-N4-32-164-28U\t28-N4-32-164-32U\t28-N4-32-209-28U\t28-N4-32-209-32U\t28-N4-32-259-32U\t28-N4-34-109-34U\t28-N4-34-154-30U\t28-N4-34-154-34U\t28-N4-34-209-30U\t28-N4-34-209-34U\t28-N4-34-259-34U\t28-N4-36-109-36U\t28-N4-36-154-32U\t28-N4-36-154-36U\t28-N4-36-199-32U\t28-N4-36-199-36U\t28-N4-36-259-36U\t28-N4-38-109-38U\t28-N4-38-154-34U\t28-N4-38-154-38U\t28-N4-38-199-34U\t28-N4-38-199-38U\t28-N4-38-259-38U\t28-N4-40-114-40U\t28-N4-40-154-36U\t28-N4-40-154-40U\t28-N4-40-204-36U\t28-N4-40-204-40U\t28-N4-40-259-40U\t28-N4-42-114-42U\t28-N4-42-159-38U\t28-N4-42-159-42U\t28-N4-42-204-38U\t28-N4-42-204-42U\t28-N4-42-259-42U\t28-N4-44-114-44U\t28-N4-44-164-40U\t28-N4-44-164-44U\t28-N4-44-209-40U\t28-N4-44-209-44U\t28-N4-44-259-40U\t28-N4-44-259-44U\t28-N4-46-114-46U\t28-N4-46-164-42U\t28-N4-46-164-46U\t28-N4-46-209-42U\t28-N4-46-209-46U\t28-N4-46-259-42U", "reason": "Labeling update concerning proximal clasp disconnection from the outer control tube which may prevent stent graft from being released from the delivery system.", "hazard_level": "Class I", "company": "Bolton Medical Inc.", "company_location": "Sunrise, FL, United States", "date": "2026-04-22", "report_date": "2026-06-03", "status": "Ongoing", "distribution": "Worldwide - distribution in the US Territory of Puerto Rico and the countries of Argentina, Chile, Canada, Colombia, Mexico, United Kingdom.", "states": ["PR"], "nationwide": false, "quantity": "", "codes": "All Lots/(Ref Number/Proximal Diameter/DI)28-N4-32-104-32U/ 32/ (01)00843576150461; 28-N4-32-164-28U/ 32/ (01)00843576150959; 28-N4-32-164-32U/ 32/ (01)00843576150591; 28-N4-32-209-28U/ 32/ (01)00843576151055; 28-N4-32-209-32U/ 32/ (01)00843576150720; 28-N4-32-259-32U/ 32/ (01)00843576150850; 28-N4-34-109-34U/ 34/ (01)00843576150478; 28-N4-34-154-30U/ 34/ (01)00843576150966; 28-N4-34-154-34U/ 34/ (01)00843576150607; 28-N4-34-209-30U/ 34/ (01)00843576151062; 28-N4-34-209-34U/ 34/ (01)00843576150737; 28-N4-34-259-34U/ 34/ (01)00843576150867; 28-N4-36-109-36U/ 36/ (01)00843576150485; 28-N4-36-154-32U/ 36/ (01)00843576150973; 28-N4-36-154-36U/ 36/ (01)00843576150614; 28-N4-36-199-32U/ 36/ (01)00843576151079; 28-N4-36-199-36U/ 36/ (01)00843576150744; 28-N4-36-259-36U/ 36/ (01)00843576150874; 28-N4-38-109-38U/ 38/ (01)00843576150492; 28-N4-38-154-34U/ 38/ (01)00843576150980; 28-N4-38-154-38U/ 38/ (01)00843576150621; 28-N4-38-199-34U/ 38/ (01)00843576151086; 28-N4-38-199-38U/ 38/ (01)00843576150751; 28-N4-38-259-38U/ 38/ (01)00843576150881; 28-N4-40-114-40U/ 40/ (01)00843576150508; 28-N4-40-154-36U/ 40/ (01)00843576150997; 28-N4-40-154-40U/ 40/ (01)00843576150638; 28-N4-40-204-36U/ 40/ (01)00843576151093; 28-N4-40-204-40U/ 40/ (01)00843576150768; 28-N4-40-259-40U/ 40/ (01)00843576150898; 28-N4-42-114-42U/ 42/ (01)00843576150515; 28-N4-42-159-38U/ 42/ (01)00843576151000; 28-N4-42-159-42U/ 42/ (01)00843576150645; 28-N4-42-204-38U/ 42/ (01)00843576151109; 28-N4-42-204-42U/ 42/ (01)00843576150775; 28-N4-42-259-42U/ 42/ (01)00843576150904; 28-N4-44-114-44U/ 44/ (01)00843576150522; 28-N4-44-164-40U/ 44/ (01)00843576151017; 28-N4-44-164-44U/ 44/ (01)00843576150652; 28-N4-44-209-40U/ 44/ (01)00843576151116; 28-N4-44-209-44U/ 44/ (01)00843576150782; 28-N4-44-259-40U/ 44/ (01)00843576151215; 28-N4-44-259-44U/ 44/ (01)00843576150911; 28-N4-46-114-46U/ 46/ (01)00843576150539; 28-N4-46-164-42U/ 46/ (01)00843576151024; 28-N4-46-164-46U/ 46/ (01)00843576150669; 28-N4-46-209-42U/ 46/ (01)00843576151123; 28-N4-46-209-46U/ 46/ (01)00843576150799; 28-N4-46-259-42U/ 46/ (01)00843576151222", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2160-2026%22", "url": "https://recallledger.net/recalls/device-z-2160-2026-relaypro-thoracic-stent-graft-system-various-sizes-reference-number/"}, {"id": "fda-food-h-0847-2026", "source": "FDA", "category": "food", "recall_number": "H-0847-2026", "title": "GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX CLASSIC WHITE recall (Ghirardelli Chocolate Company)", "product": "GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX CLASSIC WHITE NET WT 50oz (3lbs 2oz) 1.42kg Ingredients: *** nonfat dry milk *** GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX CLASSIC WHITE NET WT 10lbs (4.54kg) Ingredients: *** nonfat dry milk *** GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX CLASSIC WHITE NET WT 30LB (13.62kg) Ingredients: *** nonfat dry milk *** Distributed by Ghirardelli Chocolate Company, San Leandro, CA 94578, U.S.A. UPC (50oz): 747599662010 UPC (10lbs): 747599662034 UPC (30lbs): 747599419027", "reason": "Potential contamination with Salmonella.", "hazard_level": "Class I", "company": "Ghirardelli Chocolate Company", "company_location": "San Leandro, CA, United States", "date": "2026-04-26", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "U.S. Distribution Pattern: AK, AZ, CA, FL, GA, ID, IL, IN, KY, MD, ME, MN, NC, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI. Foreign Distribution Pattern: Canada, Guatemala, Japan, Philippines, United Kingdom, South Korea.", "states": ["AK", "AZ", "CA", "FL", "GA", "ID", "IL", "IN", "KY", "MD", "ME", "MN", "NC", "NJ", "NV", "NY", "OH", "OK", "OR", "PA", "SC", "TN", "TX", "UT", "VA", "WA", "WI"], "nationwide": false, "quantity": "24 cases (6-50oz units/case) = 144 units; 3,841 cases (10 lbs/case); 3,001 cases (30 lbs/case)", "codes": "---50oz--- Lot, Best if Used By: S193260, 6/30/2027; S193261, 7/31/2027. ---10lbs--- Lot, Best if Used By: S296260A03, 7/31/2027; S292260A03, 7/31/2027; S292260A03, 8/31/2027; S292261A03, 8/31/2027. ---30lbs--- Lot, Best if Used By: S396260A03, 7/31/2027; S496260A03, 7/31/2027.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0847-2026%22", "url": "https://recallledger.net/recalls/food-h-0847-2026-ghirardelli-perfectly-premium-frappe-mix-classic-white-net-wt-50oz-3l/"}, {"id": "fda-food-h-0846-2026", "source": "FDA", "category": "food", "recall_number": "H-0846-2026", "title": "GHIRARDELLI PREMIUM HOT COCOA MIX recall (Ghirardelli Chocolate Company)", "product": "GHIRARDELLI PREMIUM HOT COCOA MIX NET WT 32oz (2lbs) 907g Ingredients: *** nonfat dry milk *** Distributed by Ghirardelli Chocolate Company, San Leandro, CA 94578, U.S.A. UPC: 747599620126", "reason": "Potential contamination with Salmonella.", "hazard_level": "Class I", "company": "Ghirardelli Chocolate Company", "company_location": "San Leandro, CA, United States", "date": "2026-04-26", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "U.S. Distribution Pattern: AK, AZ, CA, FL, GA, ID, IL, IN, KY, MD, ME, MN, NC, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI. Foreign Distribution Pattern: Canada, Guatemala, Japan, Philippines, United Kingdom, South Korea.", "states": ["AK", "AZ", "CA", "FL", "GA", "ID", "IL", "IN", "KY", "MD", "ME", "MN", "NC", "NJ", "NV", "NY", "OH", "OK", "OR", "PA", "SC", "TN", "TX", "UT", "VA", "WA", "WI"], "nationwide": false, "quantity": "13,558 cases (4-2lb units/case); 54,232 units", "codes": "Lot, Best if Used By: S550250A04, 5/31/2027; S149250A04, 6/30/2027; S249250A04, 6/30/2027; S349250A04, 6/30/2027; S449250A04, 6/30/2027; S549250A04, 6/30/2027.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0846-2026%22", "url": "https://recallledger.net/recalls/food-h-0846-2026-ghirardelli-premium-hot-cocoa-mix-net-wt-32oz-2lbs-907g-ingredients/"}, {"id": "fda-food-h-0845-2026", "source": "FDA", "category": "food", "recall_number": "H-0845-2026", "title": "GHIRARDELLI SWEET GROUND POWDER CHOCOLATE & COCOA recall (Ghirardelli Chocolate Company)", "product": "GHIRARDELLI SWEET GROUND POWDER CHOCOLATE & COCOA NET WT 48oz (3lbs) 1.36kg Distributed by Ghirardelli Chocolate Company, San Leandro, CA 94578, U.S.A. UPC: 747599620232", "reason": "Potential contamination with Salmonella.", "hazard_level": "Class I", "company": "Ghirardelli Chocolate Company", "company_location": "San Leandro, CA, United States", "date": "2026-04-26", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "U.S. Distribution Pattern: AK, AZ, CA, FL, GA, ID, IL, IN, KY, MD, ME, MN, NC, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI. Foreign Distribution Pattern: Canada, Guatemala, Japan, Philippines, United Kingdom, South Korea.", "states": ["AK", "AZ", "CA", "FL", "GA", "ID", "IL", "IN", "KY", "MD", "ME", "MN", "NC", "NJ", "NV", "NY", "OH", "OK", "OR", "PA", "SC", "TN", "TX", "UT", "VA", "WA", "WI"], "nationwide": false, "quantity": "293 cases (6-48oz units/case); 1,758 units", "codes": "Lot, Best if Used By: S293260, 12/31/2027; S293261, 1/31/2028.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0845-2026%22", "url": "https://recallledger.net/recalls/food-h-0845-2026-ghirardelli-sweet-ground-powder-chocolate-cocoa-net-wt-48oz-3lbs-1/"}, {"id": "fda-food-h-0844-2026", "source": "FDA", "category": "food", "recall_number": "H-0844-2026", "title": "GHIRARDELLI SWEET GROUND POWDER WHITE CHOCOLATE FLAVORED recall (Ghirardelli Chocolate Company)", "product": "GHIRARDELLI SWEET GROUND POWDER WHITE CHOCOLATE FLAVORED NET WT 50oz (3lbs 2oz) 1.41kg Distributed by Ghirardelli Chocolate Company, San Leandro, CA 94578, U.S.A. UPC: 747599620386", "reason": "Potential contamination with Salmonella.", "hazard_level": "Class I", "company": "Ghirardelli Chocolate Company", "company_location": "San Leandro, CA, United States", "date": "2026-04-26", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "U.S. Distribution Pattern: AK, AZ, CA, FL, GA, ID, IL, IN, KY, MD, ME, MN, NC, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI. Foreign Distribution Pattern: Canada, Guatemala, Japan, Philippines, United Kingdom, South Korea.", "states": ["AK", "AZ", "CA", "FL", "GA", "ID", "IL", "IN", "KY", "MD", "ME", "MN", "NC", "NJ", "NV", "NY", "OH", "OK", "OR", "PA", "SC", "TN", "TX", "UT", "VA", "WA", "WI"], "nationwide": false, "quantity": "2,267 cases (6-50oz units/case); 13,602 units", "codes": "Lot, Best if Used By: S394260, 7/31/2027; S494260, 7/31/2027; S594260, 7/31/2027.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0844-2026%22", "url": "https://recallledger.net/recalls/food-h-0844-2026-ghirardelli-sweet-ground-powder-white-chocolate-flavored-net-wt-50oz/"}, {"id": "fda-food-h-0843-2026", "source": "FDA", "category": "food", "recall_number": "H-0843-2026", "title": "GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX VANILLA recall (Ghirardelli Chocolate Company)", "product": "GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX VANILLA NET WT 48oz (3lbs) 1.36kg Ingredients: *** nonfat dry milk *** Distributed by Ghirardelli Chocolate Company, San Leandro, CA 94578, U.S.A. UPC: 747599621055", "reason": "Potential contamination with Salmonella.", "hazard_level": "Class I", "company": "Ghirardelli Chocolate Company", "company_location": "San Leandro, CA, United States", "date": "2026-04-26", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "U.S. Distribution Pattern: AK, AZ, CA, FL, GA, ID, IL, IN, KY, MD, ME, MN, NC, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI. Foreign Distribution Pattern: Canada, Guatemala, Japan, Philippines, United Kingdom, South Korea.", "states": ["AK", "AZ", "CA", "FL", "GA", "ID", "IL", "IN", "KY", "MD", "ME", "MN", "NC", "NJ", "NV", "NY", "OH", "OK", "OR", "PA", "SC", "TN", "TX", "UT", "VA", "WA", "WI"], "nationwide": false, "quantity": "489 cases (6-48oz units/case); 2,934 units", "codes": "Lot, Best if Used By: S495260, 3/31/2027; S495261, 6/30/2027; S594262, 7/31/2027.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0843-2026%22", "url": "https://recallledger.net/recalls/food-h-0843-2026-ghirardelli-perfectly-premium-frappe-mix-vanilla-net-wt-48oz-3lbs-1/"}, {"id": "fda-food-h-0842-2026", "source": "FDA", "category": "food", "recall_number": "H-0842-2026", "title": "GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX CHOCOLATE FLAVORED recall (Ghirardelli Chocolate Company)", "product": "GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX CHOCOLATE FLAVORED NET WT 50oz (3lbs 2oz) 1.42kg Ingredients: *** nonfat dry milk *** Distributed by Ghirardelli Chocolate Company, San Leandro, CA 94578, U.S.A. UPC: 747599662003", "reason": "Potential contamination with Salmonella.", "hazard_level": "Class I", "company": "Ghirardelli Chocolate Company", "company_location": "San Leandro, CA, United States", "date": "2026-04-26", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "U.S. Distribution Pattern: AK, AZ, CA, FL, GA, ID, IL, IN, KY, MD, ME, MN, NC, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI. Foreign Distribution Pattern: Canada, Guatemala, Japan, Philippines, United Kingdom, South Korea.", "states": ["AK", "AZ", "CA", "FL", "GA", "ID", "IL", "IN", "KY", "MD", "ME", "MN", "NC", "NJ", "NV", "NY", "OH", "OK", "OR", "PA", "SC", "TN", "TX", "UT", "VA", "WA", "WI"], "nationwide": false, "quantity": "309 cases (6-50oz units/case); 1,854 units", "codes": "Lot, Best if Used By: S397261, 2/28/2027; S397262, 4/30/2027; S397263, 6/30/2027.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0842-2026%22", "url": "https://recallledger.net/recalls/food-h-0842-2026-ghirardelli-perfectly-premium-frappe-mix-chocolate-flavored-net-wt-50o/"}, {"id": "fda-food-h-0841-2026", "source": "FDA", "category": "food", "recall_number": "H-0841-2026", "title": "GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX CHOCOLATE FLAVORED recall (Ghirardelli Chocolate Company)", "product": "GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX CHOCOLATE FLAVORED NET WT 10lbs (4.54kg) Ingredients: *** nonfat dry milk *** GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX CHOCOLATE FLAVORED NET WT 30LB (13.61kg) Ingredients: *** nonfat dry milk *** Distributed by Ghirardelli Chocolate Company, San Leandro, CA 94578 UPC (10lbs): 747599662027 UPC (30lbs): 747599418983", "reason": "Potential contamination with Salmonella.", "hazard_level": "Class I", "company": "Ghirardelli Chocolate Company", "company_location": "San Leandro, CA, United States", "date": "2026-04-26", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "U.S. Distribution Pattern: AK, AZ, CA, FL, GA, ID, IL, IN, KY, MD, ME, MN, NC, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI. Foreign Distribution Pattern: Canada, Guatemala, Japan, Philippines, United Kingdom, South Korea.", "states": ["AK", "AZ", "CA", "FL", "GA", "ID", "IL", "IN", "KY", "MD", "ME", "MN", "NC", "NJ", "NV", "NY", "OH", "OK", "OR", "PA", "SC", "TN", "TX", "UT", "VA", "WA", "WI"], "nationwide": false, "quantity": "237 cases (10 lbs/case); 3,488 cases (30 lbs/case)", "codes": "---10lbs--- Lot, Best if Used By: S295260A03, 7/31/2027; S395260A03, 7/31/2027. ---30lbs--- Lot, Best if Used By: S195260A03, 5/31/2027; S195261A03, 7/31/2027; S291260A03, 7/31/2027; S295260A03, 7/31/2027; S596260A03, 7/31/2027; S191260A03, 8/31/2027; S291261A03, 8/31/2027.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0841-2026%22", "url": "https://recallledger.net/recalls/food-h-0841-2026-ghirardelli-perfectly-premium-frappe-mix-chocolate-flavored-net-wt-10l/"}, {"id": "fda-food-h-0840-2026", "source": "FDA", "category": "food", "recall_number": "H-0840-2026", "title": "GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX WHITE MOCHA recall (Ghirardelli Chocolate Company)", "product": "GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX WHITE MOCHA NET WT 50oz (3lbs 2oz) 1.42kg Ingredients: *** nonfat dry milk *** Distributed by Ghirardelli Chocolate Company, San Leandro, CA 94578, U.S.A. UPC: 747599662096", "reason": "Potential contamination with Salmonella.", "hazard_level": "Class I", "company": "Ghirardelli Chocolate Company", "company_location": "San Leandro, CA, United States", "date": "2026-04-26", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "U.S. Distribution Pattern: AK, AZ, CA, FL, GA, ID, IL, IN, KY, MD, ME, MN, NC, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI. Foreign Distribution Pattern: Canada, Guatemala, Japan, Philippines, United Kingdom, South Korea.", "states": ["AK", "AZ", "CA", "FL", "GA", "ID", "IL", "IN", "KY", "MD", "ME", "MN", "NC", "NJ", "NV", "NY", "OH", "OK", "OR", "PA", "SC", "TN", "TX", "UT", "VA", "WA", "WI"], "nationwide": false, "quantity": "111 cases (6-50oz units/case); 666 units", "codes": "Lot, Best if Used By: S297261, 5/31/2027; S297262, 6/30/2027; S393262, 7/31/2027.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0840-2026%22", "url": "https://recallledger.net/recalls/food-h-0840-2026-ghirardelli-perfectly-premium-frappe-mix-white-mocha-net-wt-50oz-3lbs/"}, {"id": "fda-food-h-0839-2026", "source": "FDA", "category": "food", "recall_number": "H-0839-2026", "title": "GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX MOCHA recall (Ghirardelli Chocolate Company)", "product": "GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX MOCHA NET WT 50oz (3lbs 2oz) 1.42kg Ingredients: *** nonfat dry milk *** Distributed by Ghirardelli Chocolate Company, San Leandro, CA 94578, U.S.A. UPC: 747599662119", "reason": "Potential contamination with Salmonella.", "hazard_level": "Class I", "company": "Ghirardelli Chocolate Company", "company_location": "San Leandro, CA, United States", "date": "2026-04-26", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "U.S. Distribution Pattern: AK, AZ, CA, FL, GA, ID, IL, IN, KY, MD, ME, MN, NC, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI. Foreign Distribution Pattern: Canada, Guatemala, Japan, Philippines, United Kingdom, South Korea.", "states": ["AK", "AZ", "CA", "FL", "GA", "ID", "IL", "IN", "KY", "MD", "ME", "MN", "NC", "NJ", "NV", "NY", "OH", "OK", "OR", "PA", "SC", "TN", "TX", "UT", "VA", "WA", "WI"], "nationwide": false, "quantity": "275 cases (6-50oz units/case); 1,650 units", "codes": "Lot, Best if Used By: S295261, 4/30/2027; S295262, 6/30/2027; S395260, 6/30/2027; S588260, 6/30/2027; S187260, 8/31/2027.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0839-2026%22", "url": "https://recallledger.net/recalls/food-h-0839-2026-ghirardelli-perfectly-premium-frappe-mix-mocha-net-wt-50oz-3lbs-2oz/"}, {"id": "fda-food-h-0838-2026", "source": "FDA", "category": "food", "recall_number": "H-0838-2026", "title": "GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX FROZEN HOT COCOA recall (Ghirardelli Chocolate Company)", "product": "GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX FROZEN HOT COCOA NET WT 50oz (3lbs 2oz) 1.42kg Ingredients: *** nonfat dry milk *** Distributed by Ghirardelli Chocolate Company, San Leandro, CA 94578, U.S.A. UPC: 747599662133", "reason": "Potential contamination with Salmonella.", "hazard_level": "Class I", "company": "Ghirardelli Chocolate Company", "company_location": "San Leandro, CA, United States", "date": "2026-04-26", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "U.S. Distribution Pattern: AK, AZ, CA, FL, GA, ID, IL, IN, KY, MD, ME, MN, NC, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI. Foreign Distribution Pattern: Canada, Guatemala, Japan, Philippines, United Kingdom, South Korea.", "states": ["AK", "AZ", "CA", "FL", "GA", "ID", "IL", "IN", "KY", "MD", "ME", "MN", "NC", "NJ", "NV", "NY", "OH", "OK", "OR", "PA", "SC", "TN", "TX", "UT", "VA", "WA", "WI"], "nationwide": false, "quantity": "3102 cases (6-50oz units/case); 18,612 units", "codes": "Lot, Best if Used By: S195260, 5/31/2027; S195261, 6/30/2027; S295260, 6/30/2027; S393260, 7/31/2027; S487260, 9/30/2027; S587260, 9/30/2027.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0838-2026%22", "url": "https://recallledger.net/recalls/food-h-0838-2026-ghirardelli-perfectly-premium-frappe-mix-frozen-hot-cocoa-net-wt-50oz/"}, {"id": "fda-food-h-0830-2026", "source": "FDA", "category": "food", "recall_number": "H-0830-2026", "title": "Pork King Good Onion & Sour Cream Seasoning. Net Wt. 3 oz recall (Pork King Good, LLC)", "product": "Pork King Good Onion & Sour Cream Seasoning. Net Wt. 3 oz (85G) bottle. UPC 8 50008-53861 2. Made by Pork King Good, Milwaukee, WI 53110.", "reason": "Seasoning was made with recalled California Dairies milk powder due to Salmonella contamination.", "hazard_level": "Class I", "company": "Pork King Good, LLC", "company_location": "Cudahy, WI, United States", "date": "2026-04-23", "report_date": "2026-05-27", "status": "Completed", "distribution": "AL, AZ, CA, FL, GA,IL, IN, MD, MI, MO, MS, MT, NC, ND, NE, NH, NY, OH, PA, RI, TN, TX, UT, VA, WA, WI", "states": ["AL", "AZ", "CA", "FL", "GA", "IL", "IN", "MD", "MI", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NY", "OH", "PA", "RI", "TN", "TX", "UT", "VA", "WA", "WI"], "nationwide": false, "quantity": "497.06 lbs.", "codes": "Lot Number 329-5, Best if Used By 5/30/2027; Lot Number 004-6, Best if Used By 6/30/2027; Lot Number 029-6, Best if Used By 6/30/2027.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0830-2026%22", "url": "https://recallledger.net/recalls/food-h-0830-2026-pork-king-good-onion-sour-cream-seasoning-net-wt-3-oz-85g-bottl/"}, {"id": "fda-food-h-0829-2026", "source": "FDA", "category": "food", "recall_number": "H-0829-2026", "title": "Solina 6022487 Garlic Herb Topping recall (Solina U.S. Holding)", "product": "Solina 6022487 Garlic Herb Topping, 50lb bag", "reason": "potential to be contaminated with Salmonella", "hazard_level": "Class I", "company": "Solina U.S. Holding", "company_location": "Eastvale, CA, United States", "date": "2026-04-24", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "MI WI PA IL GA CA KS", "states": ["CA", "GA", "IL", "KS", "MI", "PA", "WI"], "nationwide": false, "quantity": "41 bags", "codes": "Lot: 335367; Use by: 07/13/2026", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0829-2026%22", "url": "https://recallledger.net/recalls/food-h-0829-2026-solina-6022487-garlic-herb-topping-50lb-bag/"}, {"id": "fda-food-h-0828-2026", "source": "FDA", "category": "food", "recall_number": "H-0828-2026", "title": "YT 6027393 Spicy Ranch Blend recall (Solina U.S. Holding)", "product": "YT 6027393 Spicy Ranch Blend, 50lb bag", "reason": "potential to be contaminated with Salmonella", "hazard_level": "Class I", "company": "Solina U.S. Holding", "company_location": "Eastvale, CA, United States", "date": "2026-04-24", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "MI WI PA IL GA CA KS", "states": ["CA", "GA", "IL", "KS", "MI", "PA", "WI"], "nationwide": false, "quantity": "80 bags", "codes": "Lot: 334912; Use by: 10/04/2026", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0828-2026%22", "url": "https://recallledger.net/recalls/food-h-0828-2026-yt-6027393-spicy-ranch-blend-50lb-bag/"}, {"id": "fda-food-h-0827-2026", "source": "FDA", "category": "food", "recall_number": "H-0827-2026", "title": "Solina 6036087 Cr¿me Fraiche Spice Seasoning recall (Solina U.S. Holding)", "product": "Solina 6036087 Cr¿me Fraiche Spice Seasoning, 25lb bag", "reason": "potential to be contaminated with Salmonella", "hazard_level": "Class I", "company": "Solina U.S. Holding", "company_location": "Eastvale, CA, United States", "date": "2026-04-24", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "MI WI PA IL GA CA KS", "states": ["CA", "GA", "IL", "KS", "MI", "PA", "WI"], "nationwide": false, "quantity": "161 bags", "codes": "Lot: 334409; Use by: 06/21/2026", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0827-2026%22", "url": "https://recallledger.net/recalls/food-h-0827-2026-solina-6036087-crme-fraiche-spice-seasoning-25lb-bag/"}, {"id": "fda-food-h-0826-2026", "source": "FDA", "category": "food", "recall_number": "H-0826-2026", "title": "Solina 6036277 Garlic Cream Sauce Seasoning recall (Solina U.S. Holding)", "product": "Solina 6036277 Garlic Cream Sauce Seasoning, 40lb bag", "reason": "potential to be contaminated with Salmonella", "hazard_level": "Class I", "company": "Solina U.S. Holding", "company_location": "Eastvale, CA, United States", "date": "2026-04-24", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "MI WI PA IL GA CA KS", "states": ["CA", "GA", "IL", "KS", "MI", "PA", "WI"], "nationwide": false, "quantity": "180 bags", "codes": "Lot: 335086; Use By: 7/8/2026", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0826-2026%22", "url": "https://recallledger.net/recalls/food-h-0826-2026-solina-6036277-garlic-cream-sauce-seasoning-40lb-bag/"}, {"id": "fda-food-h-0825-2026", "source": "FDA", "category": "food", "recall_number": "H-0825-2026", "title": "Solina 6036786 Instant Country Gravy Seasoning recall (Solina U.S. Holding)", "product": "Solina 6036786 Instant Country Gravy Seasoning, 40lb bag", "reason": "potential to be contaminated with Salmonella", "hazard_level": "Class I", "company": "Solina U.S. Holding", "company_location": "Eastvale, CA, United States", "date": "2026-04-24", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "MI WI PA IL GA CA KS", "states": ["CA", "GA", "IL", "KS", "MI", "PA", "WI"], "nationwide": false, "quantity": "204 bags", "codes": "Lot: 334910,334911; Use by: 01/07/2027; 01/09/2027", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0825-2026%22", "url": "https://recallledger.net/recalls/food-h-0825-2026-solina-6036786-instant-country-gravy-seasoning-40lb-bag/"}, {"id": "fda-food-h-0824-2026", "source": "FDA", "category": "food", "recall_number": "H-0824-2026", "title": "Solina 6036554 Parmesan Breadstick Sauce Seasoning recall (Solina U.S. Holding)", "product": "Solina 6036554 Parmesan Breadstick Sauce Seasoning, 40lb bag", "reason": "potential to be contaminated with Salmonella", "hazard_level": "Class I", "company": "Solina U.S. Holding", "company_location": "Eastvale, CA, United States", "date": "2026-04-24", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "MI WI PA IL GA CA KS", "states": ["CA", "GA", "IL", "KS", "MI", "PA", "WI"], "nationwide": false, "quantity": "996 bags", "codes": "Lot: 334856-334860; Use By: 07/05/2026, 07/06/2026", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0824-2026%22", "url": "https://recallledger.net/recalls/food-h-0824-2026-solina-6036554-parmesan-breadstick-sauce-seasoning-40lb-bag/"}, {"id": "fda-food-h-0823-2026", "source": "FDA", "category": "food", "recall_number": "H-0823-2026", "title": "Solina 6036443 Cheddar Cheese Powder Seasoning recall (Solina U.S. Holding)", "product": "Solina 6036443 Cheddar Cheese Powder Seasoning, 50lb bag", "reason": "potential to be contaminated with Salmonella", "hazard_level": "Class I", "company": "Solina U.S. Holding", "company_location": "Eastvale, CA, United States", "date": "2026-04-24", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "MI WI PA IL GA CA KS", "states": ["CA", "GA", "IL", "KS", "MI", "PA", "WI"], "nationwide": false, "quantity": "25 bags", "codes": "Lot:335491; Use By: 07/14/2026", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0823-2026%22", "url": "https://recallledger.net/recalls/food-h-0823-2026-solina-6036443-cheddar-cheese-powder-seasoning-50lb-bag/"}, {"id": "fda-food-h-0822-2026", "source": "FDA", "category": "food", "recall_number": "H-0822-2026", "title": "Solina 6036195 Ranch Seasoning recall (Solina U.S. Holding)", "product": "Solina 6036195 Ranch Seasoning, 50lb bag", "reason": "potential to be contaminated with Salmonella", "hazard_level": "Class I", "company": "Solina U.S. Holding", "company_location": "Eastvale, CA, United States", "date": "2026-04-24", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "MI WI PA IL GA CA KS", "states": ["CA", "GA", "IL", "KS", "MI", "PA", "WI"], "nationwide": false, "quantity": "459 bags", "codes": "Lot: 334386, 334882-334883; Use by: 06/20/2026, 07/14/2026", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0822-2026%22", "url": "https://recallledger.net/recalls/food-h-0822-2026-solina-6036195-ranch-seasoning-50lb-bag/"}, {"id": "fda-food-h-0821-2026", "source": "FDA", "category": "food", "recall_number": "H-0821-2026", "title": "Solina 6035687 Bayou Blackened Ranch Seasoning recall (Solina U.S. Holding)", "product": "Solina 6035687 Bayou Blackened Ranch Seasoning, 25lb bag", "reason": "potential to be contaminated with Salmonella", "hazard_level": "Class I", "company": "Solina U.S. Holding", "company_location": "Eastvale, CA, United States", "date": "2026-04-24", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "MI WI PA IL GA CA KS", "states": ["CA", "GA", "IL", "KS", "MI", "PA", "WI"], "nationwide": false, "quantity": "327 bags", "codes": "Lot: 335314-335315; Use by 07/13/2026", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0821-2026%22", "url": "https://recallledger.net/recalls/food-h-0821-2026-solina-6035687-bayou-blackened-ranch-seasoning-25lb-bag/"}, {"id": "fda-food-h-0820-2026", "source": "FDA", "category": "food", "recall_number": "H-0820-2026", "title": "Solina 6035415 Sourdough Cheese Crouton Seasoning recall (Solina U.S. Holding)", "product": "Solina 6035415 Sourdough Cheese Crouton Seasoning, 50lb bag", "reason": "potential to be contaminated with Salmonella", "hazard_level": "Class I", "company": "Solina U.S. Holding", "company_location": "Eastvale, CA, United States", "date": "2026-04-24", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "MI WI PA IL GA CA KS", "states": ["CA", "GA", "IL", "KS", "MI", "PA", "WI"], "nationwide": false, "quantity": "30 bags", "codes": "Lot: 355048; Use by 7/8/2026", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0820-2026%22", "url": "https://recallledger.net/recalls/food-h-0820-2026-solina-6035415-sourdough-cheese-crouton-seasoning-50lb-bag/"}, {"id": "fda-food-h-0819-2026", "source": "FDA", "category": "food", "recall_number": "H-0819-2026", "title": "Non Fat Dry Milk 1# recall (PS Seasoning & Spices, Inc.)", "product": "Non Fat Dry Milk 1#, Part #: 02000014P. Net Wt 1 lb (453g) PS Seasoning & Spices 216 W Pleasant St Iron Ridge, WI 53035.", "reason": "Product was made with milk powder recalled by the supplier due to Salmonella contamination.", "hazard_level": "Class I", "company": "PS Seasoning & Spices, Inc.", "company_location": "Iron Ridge, WI, United States", "date": "2026-04-22", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "Nationwide", "states": [], "nationwide": true, "quantity": "264 lbs.", "codes": "Lot #: 2025-45065 Exp 06/06/2027", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0819-2026%22", "url": "https://recallledger.net/recalls/food-h-0819-2026-non-fat-dry-milk-1-part-02000014p-net-wt-1-lb-453g-ps-season/"}, {"id": "fda-food-h-0818-2026", "source": "FDA", "category": "food", "recall_number": "H-0818-2026", "title": "PSW21585 Save A Lot Bind 50# recall (PS Seasoning & Spices, Inc.)", "product": "PSW21585 Save A Lot Bind 50#, Part #: 20009709. PS Seasoning & Spices 216 W Pleasant St Iron Ridge, WI 53035.", "reason": "Product was made with milk powder recalled by the supplier due to Salmonella contamination.", "hazard_level": "Class I", "company": "PS Seasoning & Spices, Inc.", "company_location": "Iron Ridge, WI, United States", "date": "2026-04-22", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "Nationwide", "states": [], "nationwide": true, "quantity": "992.5 lbs.", "codes": "Lot #: 2025-44885 Exp 6/3/ 2028 Lot #: 2026-57603 Exp 09/21/2028", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0818-2026%22", "url": "https://recallledger.net/recalls/food-h-0818-2026-psw21585-save-a-lot-bind-50-part-20009709-ps-seasoning-spice/"}, {"id": "fda-food-h-0817-2026", "source": "FDA", "category": "food", "recall_number": "H-0817-2026", "title": "Blackstone Parmesan Ranch Seasoning recall (PS Seasoning & Spices, Inc.)", "product": "Blackstone Parmesan Ranch Seasoning, Net Wt 7.3 oz (207g). UPC 7 17604-04106 2. Manufactured for North Atlantic Imports, LLC, Logan, UT 84321.", "reason": "Product was made with milk powder recalled by the supplier due to Salmonella contamination.", "hazard_level": "Class I", "company": "PS Seasoning & Spices, Inc.", "company_location": "Iron Ridge, WI, United States", "date": "2026-04-22", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "Nationwide", "states": [], "nationwide": true, "quantity": "22532.4 lbs.", "codes": "Lot #: 2025-43282 Exp 07/04/2027 or 07/05/2027 Lot 2025-46172 Exp 08/05/2027 Lot 2026-54751 Exp 08/14/2027", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0817-2026%22", "url": "https://recallledger.net/recalls/food-h-0817-2026-blackstone-parmesan-ranch-seasoning-net-wt-7-3-oz-207g-upc-7-1760/"}, {"id": "fda-food-h-0816-2026", "source": "FDA", "category": "food", "recall_number": "H-0816-2026", "title": "1P Jalapeno Heat Unit for 300 lbs of Meat recall (PS Seasoning & Spices, Inc.)", "product": "1P Jalapeno Heat Unit for 300 lbs of Meat, Part #: 180002945. Net Wt 18 lbs (8.20kg). PS Seasoning & Spices 216W Pleasant St Iron Ridge, WI 53035.", "reason": "Product was made with milk powder recalled by the supplier due to Salmonella contamination.", "hazard_level": "Class I", "company": "PS Seasoning & Spices, Inc.", "company_location": "Iron Ridge, WI, United States", "date": "2026-04-22", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "Nationwide", "states": [], "nationwide": true, "quantity": "3744 lbs.", "codes": "Lot #: 2025-44769 Exp 05/27/2027", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0816-2026%22", "url": "https://recallledger.net/recalls/food-h-0816-2026-1p-jalapeno-heat-unit-for-300-lbs-of-meat-part-180002945-net-wt/"}, {"id": "fda-food-h-0815-2026", "source": "FDA", "category": "food", "recall_number": "H-0815-2026", "title": "1P Original Smokehouse Unit for 300 lbs. of Meat recall (PS Seasoning & Spices, Inc.)", "product": "1P Original Smokehouse Unit for 300 lbs. of Meat, Part #: 180002964. Net Wt 15.10 lbs (6.85kg). PS Seasoning & Spices 216W Pleasant St Iron Ridge, WI 53035.", "reason": "Product was made with milk powder recalled by the supplier due to Salmonella contamination.", "hazard_level": "Class I", "company": "PS Seasoning & Spices, Inc.", "company_location": "Iron Ridge, WI, United States", "date": "2026-04-22", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "Nationwide", "states": [], "nationwide": true, "quantity": "5375.6 lbs", "codes": "Lot #: 2025-44770 Exp 05/27/2027", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0815-2026%22", "url": "https://recallledger.net/recalls/food-h-0815-2026-1p-original-smokehouse-unit-for-300-lbs-of-meat-part-180002964/"}, {"id": "fda-food-h-0814-2026", "source": "FDA", "category": "food", "recall_number": "H-0814-2026", "title": "Ellsworth Sour Cream + Onion Seasoning recall (PS Seasoning & Spices, Inc.)", "product": "Ellsworth Sour Cream + Onion Seasoning, Part #: 180000113. Net Wt 25.00 lbs (11.3kg). PS Seasoning & Spices 216 W Pleasant St Iron Ridge WI 53035", "reason": "Product was made with milk powder recalled by the supplier due to Salmonella contamination.", "hazard_level": "Class I", "company": "PS Seasoning & Spices, Inc.", "company_location": "Iron Ridge, WI, United States", "date": "2026-04-22", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "Nationwide", "states": [], "nationwide": true, "quantity": "250 lbs.", "codes": "Lot #: 2026-51127", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0814-2026%22", "url": "https://recallledger.net/recalls/food-h-0814-2026-ellsworth-sour-cream-onion-seasoning-part-180000113-net-wt-25/"}, {"id": "fda-food-h-0813-2026", "source": "FDA", "category": "food", "recall_number": "H-0813-2026", "title": "C7139D1 Natural Parmesan Cheese Flavor recall (Fontana Flavors, Inc)", "product": "C7139D1 Natural Parmesan Cheese Flavor, Net Weight: 50 lbs. bags. Item #: 202405. For Further Processing. Fontana Foods, Janesville, WI.", "reason": "Product was made with milk powder recalled by the supplier due to Salmonella contamination.", "hazard_level": "Class I", "company": "Fontana Flavors, Inc", "company_location": "Janesville, WI, United States", "date": "2026-04-22", "report_date": "2026-05-27", "status": "Terminated", "distribution": "IL, TN, and outside the US to Canada", "states": ["IL", "TN"], "nationwide": false, "quantity": "1,700 lbs.", "codes": "Lot Numbers: 120925F02, 010726F02, 022426F03, 031226F08, 032426F04.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0813-2026%22", "url": "https://recallledger.net/recalls/food-h-0813-2026-c7139d1-natural-parmesan-cheese-flavor-net-weight-50-lbs-bags-it/"}, {"id": "fda-food-h-0812-2026", "source": "FDA", "category": "food", "recall_number": "H-0812-2026", "title": "VG7274D1 Natural Cream of Mushroom Type Flavor recall (Fontana Flavors, Inc)", "product": "VG7274D1 Natural Cream of Mushroom Type Flavor, Net Weight: 50 lbs. bag. Item #: R5302. For Further Processing. Fontana Flavors, Janesville, WI.", "reason": "Product was made with milk powder recalled by the supplier due to Salmonella contamination.", "hazard_level": "Class I", "company": "Fontana Flavors, Inc", "company_location": "Janesville, WI, United States", "date": "2026-04-22", "report_date": "2026-05-27", "status": "Terminated", "distribution": "IL, TN, and outside the US to Canada", "states": ["IL", "TN"], "nationwide": false, "quantity": "3,000 lbs.", "codes": "Lot Numbers: 110625F06, 112425F08, 032626F07.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0812-2026%22", "url": "https://recallledger.net/recalls/food-h-0812-2026-vg7274d1-natural-cream-of-mushroom-type-flavor-net-weight-50-lbs-b/"}, {"id": "fda-food-h-0811-2026", "source": "FDA", "category": "food", "recall_number": "H-0811-2026", "title": "C0017D Natural & Artificial White Cheddar Cheese Flavor recall (Fontana Flavors, Inc)", "product": "C0017D Natural & Artificial White Cheddar Cheese Flavor, Net Weight: 50 lbs. bag. Item #: 8500101. For Further Processing. Fontana Flavors, Janesville, WI.", "reason": "Product was made with milk powder recalled by the supplier due to Salmonella contamination.", "hazard_level": "Class I", "company": "Fontana Flavors, Inc", "company_location": "Janesville, WI, United States", "date": "2026-04-22", "report_date": "2026-05-27", "status": "Terminated", "distribution": "IL, TN, and outside the US to Canada", "states": ["IL", "TN"], "nationwide": false, "quantity": "45,000 lbs.", "codes": "Lot Numbers: 111925F01#1, 111925F01#2, 111925F01#3, 111925F01#4, 111925F02#1, 111925F02#2, 120925F01#1, 120925F01#2, 121725F01#1, 121725F01#2, 121725F01#3, 121725F01#4, 020426F03#1, 020426F03#2, 022426F02#1, 022426F02#2, 032426F02#1, 032426F02#2, 032426F03#1, 032426F03#2.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0811-2026%22", "url": "https://recallledger.net/recalls/food-h-0811-2026-c0017d-natural-artificial-white-cheddar-cheese-flavor-net-weight/"}, {"id": "fda-food-h-0810-2026", "source": "FDA", "category": "food", "recall_number": "H-0810-2026", "title": "MA Cohen's Kippered Herring vacuum packed recall (Shining Sea Fish Co. LLC)", "product": "MA Cohen's Kippered Herring vacuum packed, weight provided at retail, UPC 7232577992", "reason": "Clostridium botulinum is an uncontrolled hazard", "hazard_level": "Class I", "company": "Shining Sea Fish Co. LLC", "company_location": "Detroit, MI, United States", "date": "2026-04-28", "report_date": "2026-05-27", "status": "Terminated", "distribution": "MI", "states": ["MI"], "nationwide": false, "quantity": "675 pounds", "codes": "LOT 25079 Expiration May 03 2026, LOT 25055 Expiration May 12 2026, LOT 25028 Expiration June 03 2026, LOT 26344 Expiration July 22 2026", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0810-2026%22", "url": "https://recallledger.net/recalls/food-h-0810-2026-ma-cohen-s-kippered-herring-vacuum-packed-weight-provided-at-retail/"}, {"id": "fda-food-h-0808-2026", "source": "FDA", "category": "food", "recall_number": "H-0808-2026", "title": "Liposomal Sleep Spray. Dosage: 6 sprays Liquid. Packaging: Aluminum bottle. 30 ml.... recall (Wellnov Supplements LLC)", "product": "Liposomal Sleep Spray. Dosage: 6 sprays Liquid. Packaging: Aluminum bottle. 30 ml. Firm Address: VitaminAlly LLC Chandler, AZ 85225", "reason": "Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.", "hazard_level": "Class II", "company": "Wellnov Supplements LLC", "company_location": "Chandler, AZ, United States", "date": "2026-04-23", "report_date": "2026-05-27", "status": "Terminated", "distribution": "Products were distributed nationwide and the United States Territory of Puerto Rico.", "states": ["PR"], "nationwide": true, "quantity": "105 bottles", "codes": "Distribution Dates: 10/01/2025-04/08/2026 Lot Number SL0925 Expiry Date 09/2027", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0808-2026%22", "url": "https://recallledger.net/recalls/food-h-0808-2026-liposomal-sleep-spray-dosage-6-sprays-liquid-packaging-aluminum-bo/"}, {"id": "fda-food-h-0807-2026", "source": "FDA", "category": "food", "recall_number": "H-0807-2026", "title": "Liposomal B12 Spray. Dosage: 3 sprays Liquid. Packaging: Aluminum bottle. 30 ml. Firm... recall (Wellnov Supplements LLC)", "product": "Liposomal B12 Spray. Dosage: 3 sprays Liquid. Packaging: Aluminum bottle. 30 ml. Firm Address: VitaminAlly LLC Chandler, AZ 85225", "reason": "Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.", "hazard_level": "Class II", "company": "Wellnov Supplements LLC", "company_location": "Chandler, AZ, United States", "date": "2026-04-23", "report_date": "2026-05-27", "status": "Terminated", "distribution": "Products were distributed nationwide and the United States Territory of Puerto Rico.", "states": ["PR"], "nationwide": true, "quantity": "63 bottles", "codes": "Distribution Dates: 10/01/2024-04/08/2026 Lot Number MB1024 Expiry Date 10/2026", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0807-2026%22", "url": "https://recallledger.net/recalls/food-h-0807-2026-liposomal-b12-spray-dosage-3-sprays-liquid-packaging-aluminum-bott/"}, {"id": "fda-food-h-0806-2026", "source": "FDA", "category": "food", "recall_number": "H-0806-2026", "title": "Liposomal D3+B12 Spray. Dosage: 3 sprays Liquid. Packaging: Aluminum bottle. 30 ml.... recall (Wellnov Supplements LLC)", "product": "Liposomal D3+B12 Spray. Dosage: 3 sprays Liquid. Packaging: Aluminum bottle. 30 ml. Firm Address: VitaminAlly LLC Chandler, AZ 85225.", "reason": "Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.", "hazard_level": "Class II", "company": "Wellnov Supplements LLC", "company_location": "Chandler, AZ, United States", "date": "2026-04-23", "report_date": "2026-05-27", "status": "Terminated", "distribution": "Products were distributed nationwide and the United States Territory of Puerto Rico.", "states": ["PR"], "nationwide": true, "quantity": "23 bottles", "codes": "Distribution Dates: 10/01/2024-04/08/2026 Lot Number DB1024 Expiry Date 10/2026", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0806-2026%22", "url": "https://recallledger.net/recalls/food-h-0806-2026-liposomal-d3-b12-spray-dosage-3-sprays-liquid-packaging-aluminum-b/"}, {"id": "fda-food-h-0805-2026", "source": "FDA", "category": "food", "recall_number": "H-0805-2026", "title": "Liposomal D3-5000IU Spray Dosage: 3 sprays Liquid. Packaging: Aluminum bottle. 30 ml.... recall (Wellnov Supplements LLC)", "product": "Liposomal D3-5000IU Spray Dosage: 3 sprays Liquid. Packaging: Aluminum bottle. 30 ml. Firm Address: Vitaminally LLC Chandler, AZ 85225.", "reason": "Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. 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Dosage: 3mL... recall (Wellnov Supplements LLC)", "product": "Liposomal Prenatal+Postnatal Liquid Multivitamin Drops - Iron Free. Dosage: 3mL Liquid. Packaging: Aluminum bottle. 90 ml. Firm Address: Vitaminally LLC Chandler, AZ 85225", "reason": "Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. 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Dosage: 3ml Liquid.... recall (Wellnov Supplements LLC)", "product": "Liposomal Women's Liquid Multivitamin Drops - Iron Free. Dosage: 3ml Liquid. Packaging: Aluminum bottle. 90 ml. Firm Address: Vitaminally LLC Chandler, AZ 85225.", "reason": "Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. 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Packaging: Aluminum... recall (Wellnov Supplements LLC)", "product": "Liposomal Kids Liquid Multivitamin Drops. Dosage: 3mL Liquid. Packaging: Aluminum bottle. 90 ml. Firm Address: Vitaminally LLC Chandler, AZ 85225", "reason": "Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. 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Packaging: Aluminum bottle. 90 ml.... recall (Wellnov Supplements LLC)", "product": "Liposomal Collagen Booster. Dosage: 3mL Liquid. Packaging: Aluminum bottle. 90 ml. Firm Address: Vitaminally LLC Chandler, AZ 85225.", "reason": "Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. 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Packaging:... recall (Wellnov Supplements LLC)", "product": "Liposomal Women's Liquid Multivitamin Drops with Iron. Dosage: 3mL Liquid. Packaging: Aluminum bottle. 90 ml. Firm Address: Vitaminally LLC Chandler, AZ 85225.", "reason": "Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.", "hazard_level": "Class II", "company": "Wellnov Supplements LLC", "company_location": "Chandler, AZ, United States", "date": "2026-04-23", "report_date": "2026-05-27", "status": "Terminated", "distribution": "Products were distributed nationwide and the United States Territory of Puerto Rico.", "states": ["PR"], "nationwide": true, "quantity": "83 bottles", "codes": "Distribution dates: 06/01/2025-04/08/2026 Lot Number WM0625 Expiry Date 06/2027", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0800-2026%22", "url": "https://recallledger.net/recalls/food-h-0800-2026-liposomal-women-s-liquid-multivitamin-drops-with-iron-dosage-3ml-liq/"}, {"id": "fda-food-h-0799-2026", "source": "FDA", "category": "food", "recall_number": "H-0799-2026", "title": "Liposomal Mens 50+ Liquid Multivitamin Drops. Dosage: 3mL Liquid. Packaging: Aluminum... recall (Wellnov Supplements LLC)", "product": "Liposomal Mens 50+ Liquid Multivitamin Drops. Dosage: 3mL Liquid. Packaging: Aluminum bottle. 90 ml. Firm Address: Vitaminally LLC Chandler, AZ 85225.", "reason": "Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.", "hazard_level": "Class II", "company": "Wellnov Supplements LLC", "company_location": "Chandler, AZ, United States", "date": "2026-04-23", "report_date": "2026-05-27", "status": "Terminated", "distribution": "Products were distributed nationwide and the United States Territory of Puerto Rico.", "states": ["PR"], "nationwide": true, "quantity": "129 bottles", "codes": "Distribution dates: 06/01/2025-04/08/2026 Lot Number M+0625 Expiry Date 06/2027", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0799-2026%22", "url": "https://recallledger.net/recalls/food-h-0799-2026-liposomal-mens-50-liquid-multivitamin-drops-dosage-3ml-liquid-pack/"}, {"id": "fda-food-h-0798-2026", "source": "FDA", "category": "food", "recall_number": "H-0798-2026", "title": "Liposomal Mens Liquid Multivitamin Drops. Dosage: 3mL Liquid. Packaging: Aluminum... recall (Wellnov Supplements LLC)", "product": "Liposomal Mens Liquid Multivitamin Drops. Dosage: 3mL Liquid. Packaging: Aluminum bottle. 90 ml. Firm Address: Vitaminally LLC Chandler, AZ 85225.", "reason": "Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.", "hazard_level": "Class II", "company": "Wellnov Supplements LLC", "company_location": "Chandler, AZ, United States", "date": "2026-04-23", "report_date": "2026-05-27", "status": "Terminated", "distribution": "Products were distributed nationwide and the United States Territory of Puerto Rico.", "states": ["PR"], "nationwide": true, "quantity": "20 bottles", "codes": "Distribution dates: 10/01/2024-04/08/2026 Lot Number MM0925 Expiry Date 09/2027", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0798-2026%22", "url": "https://recallledger.net/recalls/food-h-0798-2026-liposomal-mens-liquid-multivitamin-drops-dosage-3ml-liquid-packagi/"}, {"id": "fda-food-h-0797-2026", "source": "FDA", "category": "food", "recall_number": "H-0797-2026", "title": "Liposomal Womens 50+ Liquid Multivitamin Drops. Dosage: 3ml Liquid. Packaging:... recall (Wellnov Supplements LLC)", "product": "Liposomal Womens 50+ Liquid Multivitamin Drops. Dosage: 3ml Liquid. Packaging: Aluminum bottle. 90 ml. Firm Address: Vitaminally LLC Chandler, AZ 85225.", "reason": "Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.", "hazard_level": "Class II", "company": "Wellnov Supplements LLC", "company_location": "Chandler, AZ, United States", "date": "2026-04-23", "report_date": "2026-05-27", "status": "Terminated", "distribution": "Products were distributed nationwide and the United States Territory of Puerto Rico.", "states": ["PR"], "nationwide": true, "quantity": "474 bottles", "codes": "Distribution dates: 10/01/2024-04/08/2026 Lot Number: W+0925 Expiry Date: 09/2027", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0797-2026%22", "url": "https://recallledger.net/recalls/food-h-0797-2026-liposomal-womens-50-liquid-multivitamin-drops-dosage-3ml-liquid-pa/"}, {"id": "fda-food-h-0796-2026", "source": "FDA", "category": "food", "recall_number": "H-0796-2026", "title": "FulviLife Complex. Dosage:2 tablespoons recall (Wellnov Supplements LLC)", "product": "FulviLife Complex. Dosage:2 tablespoons (30mL). Liquid. Packaging: Plastic Bottle. Net Volume:16 fl oz (480 ml). Firm Address: VitaminAlly LLC Chandler, AZ 85225.", "reason": "Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.", "hazard_level": "Class II", "company": "Wellnov Supplements LLC", "company_location": "Chandler, AZ, United States", "date": "2026-04-23", "report_date": "2026-05-27", "status": "Terminated", "distribution": "Products were distributed nationwide and the United States Territory of Puerto Rico.", "states": ["PR"], "nationwide": true, "quantity": "35 bottles", "codes": "Distribution dates: 10/01/2024-04/08/2026 Lot Number: FL1024 Expiry Date: 10/2026", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0796-2026%22", "url": "https://recallledger.net/recalls/food-h-0796-2026-fulvilife-complex-dosage-2-tablespoons-30ml-liquid-packaging-pla/"}, {"id": "fda-food-h-0795-2026", "source": "FDA", "category": "food", "recall_number": "H-0795-2026", "title": "Joint Nourish. Dosage:2 tablespoons recall (Wellnov Supplements LLC)", "product": "Joint Nourish. Dosage:2 tablespoons (30mL). Liquid. For Oral use. Packaging: Plastic Bottle. Net Volume:480 ml. Firm Address: VitaminAlly LLC Chandler, AZ 85225.", "reason": "Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen contamination and possible C. Botulinum concerns.", "hazard_level": "Class II", "company": "Wellnov Supplements LLC", "company_location": "Chandler, AZ, United States", "date": "2026-04-23", "report_date": "2026-05-27", "status": "Terminated", "distribution": "Products were distributed nationwide and the United States Territory of Puerto Rico.", "states": ["PR"], "nationwide": true, "quantity": "90 bottles", "codes": "Distribution dates: 10/01/2025-04/08/2026 Lot Number JN0925 Expiry Date 09/2027", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0795-2026%22", "url": "https://recallledger.net/recalls/food-h-0795-2026-joint-nourish-dosage-2-tablespoons-30ml-liquid-for-oral-use-pack/"}, {"id": "fda-food-h-0794-2026", "source": "FDA", "category": "food", "recall_number": "H-0794-2026", "title": "Liquid Blenz Good Brain Tonic 16 oz and 32 oz recall (LIQUID BLENZ CORP)", "product": "Liquid Blenz Good Brain Tonic 16 oz and 32 oz", "reason": "May be under-processed resulting in growth of Clostridium botulinum and lists health claims.", "hazard_level": "Class II", "company": "LIQUID BLENZ CORP", "company_location": "Rockville Centre, NY, United States", "date": "2026-04-06", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "NY and online sales", "states": ["NY"], "nationwide": false, "quantity": "18,190 bottles total", "codes": "16 oz with UPC: 860010984468 & 32 oz with UPC: 860010984475 Lots: not provided", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0794-2026%22", "url": "https://recallledger.net/recalls/food-h-0794-2026-liquid-blenz-good-brain-tonic-16-oz-and-32-oz/"}, {"id": "fda-food-h-0793-2026", "source": "FDA", "category": "food", "recall_number": "H-0793-2026", "title": "Flat Belly Bully 16 oz and 32 oz recall (LIQUID BLENZ CORP)", "product": "Flat Belly Bully 16 oz and 32 oz", "reason": "May be under-processed resulting in growth of Clostridium botulinum and lists health claims.", "hazard_level": "Class II", "company": "LIQUID BLENZ CORP", "company_location": "Rockville Centre, NY, United States", "date": "2026-04-06", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "NY and online sales", "states": ["NY"], "nationwide": false, "quantity": "18,190 bottles total", "codes": "16 oz with upc: 196852337118 & 32 oz with upc: 196852926770 Lots: : FBB5552, FBB6226, FBB8166, FBB8536, FBB7757, FBB5277", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0793-2026%22", "url": "https://recallledger.net/recalls/food-h-0793-2026-flat-belly-bully-16-oz-and-32-oz/"}, {"id": "fda-food-h-0792-2026", "source": "FDA", "category": "food", "recall_number": "H-0792-2026", "title": "Blood Pressure Bully 16 oz and 32 oz recall (LIQUID BLENZ CORP)", "product": "Blood Pressure Bully 16 oz and 32 oz", "reason": "May be under-processed resulting in growth of Clostridium botulinum and lists health claims.", "hazard_level": "Class II", "company": "LIQUID BLENZ CORP", "company_location": "Rockville Centre, NY, United States", "date": "2026-04-06", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "NY and online sales", "states": ["NY"], "nationwide": false, "quantity": "18,190 bottles total", "codes": "16 oz with upc: 196852985432 & 32 oz with upc: 196852553129 Lots: BP02581, BP83283, BP14888, BP95123, BP75660", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0792-2026%22", "url": "https://recallledger.net/recalls/food-h-0792-2026-blood-pressure-bully-16-oz-and-32-oz/"}, {"id": "fda-food-h-0791-2026", "source": "FDA", "category": "food", "recall_number": "H-0791-2026", "title": "Pure Shilajit Tonic 16 oz and 32 oz recall (LIQUID BLENZ CORP)", "product": "Pure Shilajit Tonic 16 oz and 32 oz", "reason": "May be under-processed resulting in growth of Clostridium botulinum and lists health claims.", "hazard_level": "Class II", "company": "LIQUID BLENZ CORP", "company_location": "Rockville Centre, NY, United States", "date": "2026-04-06", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "NY and online sales", "states": ["NY"], "nationwide": false, "quantity": "18,190 bottles total", "codes": "16 oz with upc: 860010984482 & 32 oz with upc: 860010984499 Lots: not provided", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0791-2026%22", "url": "https://recallledger.net/recalls/food-h-0791-2026-pure-shilajit-tonic-16-oz-and-32-oz/"}, {"id": "fda-food-h-0790-2026", "source": "FDA", "category": "food", "recall_number": "H-0790-2026", "title": "Prostate Bully 16 oz and 32 oz recall (LIQUID BLENZ CORP)", "product": "Prostate Bully 16 oz and 32 oz", "reason": "May be under-processed resulting in growth of Clostridium botulinum and lists health claims.", "hazard_level": "Class II", "company": "LIQUID BLENZ CORP", "company_location": "Rockville Centre, NY, United States", "date": "2026-04-06", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "NY and online sales", "states": ["NY"], "nationwide": false, "quantity": "18,190 bottles total", "codes": "16 oz with upc: 860010984444 & 32 oz with upc: 860010984451 Lots: PB11333, PB29969, PB57444, PB00880, PB48552;", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0790-2026%22", "url": "https://recallledger.net/recalls/food-h-0790-2026-prostate-bully-16-oz-and-32-oz/"}, {"id": "fda-food-h-0789-2026", "source": "FDA", "category": "food", "recall_number": "H-0789-2026", "title": "Fibroid Bully 16 oz and 32 oz. recall (LIQUID BLENZ CORP)", "product": "Fibroid Bully 16 oz and 32 oz.", "reason": "May be under-processed resulting in growth of Clostridium botulinum and lists health claims.", "hazard_level": "Class II", "company": "LIQUID BLENZ CORP", "company_location": "Rockville Centre, NY, United States", "date": "2026-04-06", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "NY and online sales", "states": ["NY"], "nationwide": false, "quantity": "18,190 bottles total", "codes": "16 oz with upc: 860010984406 & 32 oz with upc: 860010984413 Lots: not provided", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0789-2026%22", "url": "https://recallledger.net/recalls/food-h-0789-2026-fibroid-bully-16-oz-and-32-oz/"}, {"id": "fda-food-h-0788-2026", "source": "FDA", "category": "food", "recall_number": "H-0788-2026", "title": "Menopause Bully 16 oz and 32 oz. recall (LIQUID BLENZ CORP)", "product": "Menopause Bully 16 oz and 32 oz.", "reason": "May be under-processed resulting in growth of Clostridium botulinum and lists health claims.", "hazard_level": "Class II", "company": "LIQUID BLENZ CORP", "company_location": "Rockville Centre, NY, United States", "date": "2026-04-06", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "NY and online sales", "states": ["NY"], "nationwide": false, "quantity": "18,190 bottles total", "codes": "16oz with upc: 860010984420 & 32oz with upc: 860010984437 Lots: not provided", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0788-2026%22", "url": "https://recallledger.net/recalls/food-h-0788-2026-menopause-bully-16-oz-and-32-oz/"}, {"id": "fda-food-h-0787-2026", "source": "FDA", "category": "food", "recall_number": "H-0787-2026", "title": "Immunity Enhancer Elderberry 16 oz and 32 oz. recall (LIQUID BLENZ CORP)", "product": "Immunity Enhancer Elderberry 16 oz and 32 oz.", "reason": "May be under-processed resulting in growth of Clostridium botulinum and lists health claims.", "hazard_level": "Class II", "company": "LIQUID BLENZ CORP", "company_location": "Rockville Centre, NY, United States", "date": "2026-04-06", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "NY and online sales", "states": ["NY"], "nationwide": false, "quantity": "18,190 bottles total", "codes": "16 oz with upc: 860005735099 & 32 oz with upc: 195893965434 Lots: not provided", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0787-2026%22", "url": "https://recallledger.net/recalls/food-h-0787-2026-immunity-enhancer-elderberry-16-oz-and-32-oz/"}, {"id": "fda-food-h-0786-2026", "source": "FDA", "category": "food", "recall_number": "H-0786-2026", "title": "Pure Libido Drink 16 oz and 32 oz. recall (LIQUID BLENZ CORP)", "product": "Pure Libido Drink 16 oz and 32 oz.", "reason": "May be under-processed resulting in growth of Clostridium botulinum and lists health claims.", "hazard_level": "Class II", "company": "LIQUID BLENZ CORP", "company_location": "Rockville Centre, NY, United States", "date": "2026-04-06", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "NY and online sales", "states": ["NY"], "nationwide": false, "quantity": "18,190 bottles total", "codes": "16 oz with upc: 195893463176 & 32 oz with upc: 195893949991 Lots: LB08560, LB18863, LB76882, LB84633, LB55881", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0786-2026%22", "url": "https://recallledger.net/recalls/food-h-0786-2026-pure-libido-drink-16-oz-and-32-oz/"}, {"id": "fda-food-h-0785-2026", "source": "FDA", "category": "food", "recall_number": "H-0785-2026", "title": "Pure Diabetes Bully 16 oz and 32 oz. recall (LIQUID BLENZ CORP)", "product": "Pure Diabetes Bully 16 oz and 32 oz.", "reason": "May be under-processed resulting in growth of Clostridium botulinum and lists health claims.", "hazard_level": "Class II", "company": "LIQUID BLENZ CORP", "company_location": "Rockville Centre, NY, United States", "date": "2026-04-06", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "NY and online sales", "states": ["NY"], "nationwide": false, "quantity": "18,190 bottles total", "codes": "16 oz with upc: 195893374878 & 32 oz with upc: 195893984466 Lots: DB58525, DB58885, DB21000, DB58661, DB25909, DB09550, DB66236, DB52855", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0785-2026%22", "url": "https://recallledger.net/recalls/food-h-0785-2026-pure-diabetes-bully-16-oz-and-32-oz/"}, {"id": "fda-food-h-0784-2026", "source": "FDA", "category": "food", "recall_number": "H-0784-2026", "title": "Sea Moss Tonic 16 oz and 32. oz. recall (LIQUID BLENZ CORP)", "product": "Sea Moss Tonic 16 oz and 32. oz.", "reason": "May be under-processed resulting in growth of Clostridium botulinum and lists health claims.", "hazard_level": "Class II", "company": "LIQUID BLENZ CORP", "company_location": "Rockville Centre, NY, United States", "date": "2026-04-06", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "NY and online sales", "states": ["NY"], "nationwide": false, "quantity": "18,190 bottles total", "codes": "16 oz with upc: 196852654833 & 32 oz with upc: 196852456406 Lots: not provided", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0784-2026%22", "url": "https://recallledger.net/recalls/food-h-0784-2026-sea-moss-tonic-16-oz-and-32-oz/"}, {"id": "fda-food-h-0783-2026", "source": "FDA", "category": "food", "recall_number": "H-0783-2026", "title": "Blackseed Bitters 16 oz and 32 oz. recall (LIQUID BLENZ CORP)", "product": "Blackseed Bitters 16 oz and 32 oz.", "reason": "May be under-processed resulting in growth of Clostridium botulinum and lists health claims.", "hazard_level": "Class II", "company": "LIQUID BLENZ CORP", "company_location": "Rockville Centre, NY, United States", "date": "2026-04-06", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "NY and online sales", "states": ["NY"], "nationwide": false, "quantity": "18,190 bottles total", "codes": "16 oz. with upc: 860005735020 & 32 oz with upc: 860005735037 Lots: BS62367, BS25400, BS11595, BS75444, BS75721, BS90605, BS34888", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0783-2026%22", "url": "https://recallledger.net/recalls/food-h-0783-2026-blackseed-bitters-16-oz-and-32-oz/"}, {"id": "fda-food-h-0782-2026", "source": "FDA", "category": "food", "recall_number": "H-0782-2026", "title": "Liquid Blenz Soursop Bitters 16 oz and 32 oz. recall (LIQUID BLENZ CORP)", "product": "Liquid Blenz Soursop Bitters 16 oz and 32 oz.", "reason": "May be under-processed resulting in growth of Clostridium botulinum and lists health claims.", "hazard_level": "Class II", "company": "LIQUID BLENZ CORP", "company_location": "Rockville Centre, NY, United States", "date": "2026-04-06", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "NY and online sales", "states": ["NY"], "nationwide": false, "quantity": "18,190 bottles total", "codes": "16 oz with upc: 860005735006 & 32 oz with upc: 860005735013 Lots: SS75223, SS00669, SS95811, SS95114, SS11139, SS54495, SS81258, SS44886", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0782-2026%22", "url": "https://recallledger.net/recalls/food-h-0782-2026-liquid-blenz-soursop-bitters-16-oz-and-32-oz/"}, {"id": "fda-drug-d-0553-2026", "source": "FDA", "category": "drug", "recall_number": "D-0553-2026", "title": "MG217 Multi-Symptom Treatment Cream & Skin Protectant recall (Wisconsin Pharmacal Company)", "product": "MG217 Multi-Symptom Treatment Cream & Skin Protectant (colloidal oatmeal 2%), NET WT 6 oz (170 g), Manufactured by: Pharmacal 1 Pharmacal Way, P.O. Box 198, Jackson, WI 53037.", "reason": "Microbial Contamination of Non-Sterile Products: confirmed presence of Staphylococcus Aureus.", "hazard_level": "Class I", "company": "Wisconsin Pharmacal Company", "company_location": "Jackson, WI, United States", "date": "2026-04-24", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "USA Nationwide and Bahamas", "states": [], "nationwide": true, "quantity": "690 tubes", "codes": "Lot #: 1024088, Exp 11/30/2026", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0553-2026%22", "url": "https://recallledger.net/recalls/drug-d-0553-2026-mg217-multi-symptom-treatment-cream-skin-protectant-colloidal-oatme/"}, {"id": "fda-drug-d-0545-2026", "source": "FDA", "category": "drug", "recall_number": "D-0545-2026", "title": "Erythromycin Tablets recall (Zydus Pharmaceuticals (USA) Inc)", "product": "Erythromycin Tablets, USP, 500 mg, 30 tablets per bottle, Rx only, Manufactured by: Zydus Lifesciences Ltd., Ahmedabad, India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534; (NDC 70710-1048-3).", "reason": "CGMP Deviations; presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit", "hazard_level": "Class II", "company": "Zydus Pharmaceuticals (USA) Inc", "company_location": "Pennington, NJ, United States", "date": "2026-04-29", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "Nationwide within the U.S", "states": [], "nationwide": true, "quantity": "10,992 bottles", "codes": "Lots: a) M411147, Expires: 08/2026; M502100, M502099, Expires: 01/2027.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0545-2026%22", "url": "https://recallledger.net/recalls/drug-d-0545-2026-erythromycin-tablets-usp-500-mg-30-tablets-per-bottle-rx-only-man/"}, {"id": "fda-drug-d-0544-2026", "source": "FDA", "category": "drug", "recall_number": "D-0544-2026", "title": "Erythromycin Tablets recall (Zydus Pharmaceuticals (USA) Inc)", "product": "Erythromycin Tablets, USP, 250 mg, 30 tablets per bottle, Rx only, Manufactured by: Zydus Lifesciences Ltd., Ahmedabad, India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534; a) 30 count bottles (NDC 70710-1047-3); b) 100 count bottles (NDC 70710-1047-1).", "reason": "CGMP Deviations; presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit", "hazard_level": "Class II", "company": "Zydus Pharmaceuticals (USA) Inc", "company_location": "Pennington, NJ, United States", "date": "2026-04-29", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "Nationwide within the U.S", "states": [], "nationwide": true, "quantity": "23,880 bottles", "codes": "Lots: a) M411146, Expires: 08/2026; M502098, M502097, Expires: 01/2027; b) M411145, Expires: 08/2026.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0544-2026%22", "url": "https://recallledger.net/recalls/drug-d-0544-2026-erythromycin-tablets-usp-250-mg-30-tablets-per-bottle-rx-only-man/"}, {"id": "fda-drug-d-0541-2026", "source": "FDA", "category": "drug", "recall_number": "D-0541-2026", "title": "Liraglutide Injection recall (Lupin Pharmaceuticals Inc.)", "product": "Liraglutide Injection, 18 mg/3 mL (6 mg/mL), Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Naples, FL 34108, Manufactured by: Lupin Limited, Nagpur 441108, INDIA, a) 2 Pens- NDC 70748-346-02; b) 3 Pens - NDC 70748-346-03.", "reason": "Presence of particulate matter: a white thread-like structure in the cartridge", "hazard_level": "Class II", "company": "Lupin Pharmaceuticals Inc.", "company_location": "Naples, FL, United States", "date": "2026-04-24", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "Nationwide within U.S", "states": [], "nationwide": true, "quantity": "217,621 pen injectors", "codes": "Lots: a) WB00097, WB00094, WB00088, Expires: Jul. 2027; WB00103, Expires: Oct. 2027; WC00016, Expires: Dec. 2027; b) WB00098, WB00092, WB00093, Expires: Jul. 2027; WB00104, WB00106, WB00105, Expires: Oct. 2027.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0541-2026%22", "url": "https://recallledger.net/recalls/drug-d-0541-2026-liraglutide-injection-18-mg-3-ml-6-mg-ml-rx-only-manufactured-for/"}, {"id": "fda-drug-d-0538-2026", "source": "FDA", "category": "drug", "recall_number": "D-0538-2026", "title": "Atomoxetine Capsules HCL recall (Safecor Health, LLC)", "product": "Atomoxetine Capsules HCL, 10 mg Capsules in unit dose foil strip, strips are packed in cartons of 100, Rx Only, Pkg by: Safecor, Columbus, OH 43204. NDC: 64380-474-01", "reason": "Labeling: Label Mix-Up: Atomoxetine HCl 25mg Capsule incorrectly labeled as Atomoxetine HCl 10mg Capsule.", "hazard_level": "Class II", "company": "Safecor Health, LLC", "company_location": "Columbus, OH, United States", "date": "2026-04-30", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "TX only", "states": ["TX"], "nationwide": false, "quantity": "149 capsules", "codes": "Lot #: 25530722", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0538-2026%22", "url": "https://recallledger.net/recalls/drug-d-0538-2026-atomoxetine-capsules-hcl-10-mg-capsules-in-unit-dose-foil-strip-stri/"}, {"id": "fda-drug-d-0535-2026", "source": "FDA", "category": "drug", "recall_number": "D-0535-2026", "title": "Primidone Tablets recall (Golden State Medical Supply Inc.)", "product": "Primidone Tablets, USP, 250 mg, 100-count bottle, RX only, Manufactured by: Lannett Company, Inc., Marketed by: GSMS, Incorporated, Camarillo, CA 93012. NDC 51407-638-01", "reason": "Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.", "hazard_level": "Class III", "company": "Golden State Medical Supply Inc.", "company_location": "Camarillo, CA, United States", "date": "2026-04-27", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "USA Nationwide", "states": [], "nationwide": true, "quantity": "1,620 bottles", "codes": "Lot #: GS067909, Exp 4/30/2028; GS068646, Exp 8/31/2026", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0535-2026%22", "url": "https://recallledger.net/recalls/drug-d-0535-2026-primidone-tablets-usp-250-mg-100-count-bottle-rx-only-manufacture/"}, {"id": "fda-drug-d-0534-2026", "source": "FDA", "category": "drug", "recall_number": "D-0534-2026", "title": "Primidone Tablets recall (Golden State Medical Supply Inc.)", "product": "Primidone Tablets, USP, 50 mg, 50-count bottle, RX only, Manufactured by: Lannett Company, Inc., Marketed by: GSMS, Incorporated, Camarillo, CA 93012. NDC 51407-637-05", "reason": "Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.", "hazard_level": "Class III", "company": "Golden State Medical Supply Inc.", "company_location": "Camarillo, CA, United States", "date": "2026-04-27", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "USA Nationwide", "states": [], "nationwide": true, "quantity": "8,526 bottles", "codes": "Lot#: GS066750, GS067084, GS067710, GS067873, Exp 3/31/2028; GS068339, GS068897, Exp 8/31/2028", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0534-2026%22", "url": "https://recallledger.net/recalls/drug-d-0534-2026-primidone-tablets-usp-50-mg-50-count-bottle-rx-only-manufactured/"}, {"id": "fda-drug-d-0533-2026", "source": "FDA", "category": "drug", "recall_number": "D-0533-2026", "title": "Primidone Tablets USP recall (Lannett Company Inc.)", "product": "Primidone Tablets USP, 250mg, 100-count bottle, Rx only, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136, NDC 0527-1231-01.", "reason": "Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.", "hazard_level": "Class III", "company": "Lannett Company Inc.", "company_location": "Seymour, IN, United States", "date": "2026-04-24", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "USA Nationwide", "states": [], "nationwide": true, "quantity": "44865 bottles", "codes": "Lot#: 25283038A, Exp 1/31/2028; 25283564A, 25283565A, Exp 3/31/2028; 25285712A Exp 08/31/2028; 25284105A, Exp 4/30/2028; 25284874A, 25284875A, Exp 08/31/2028.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0533-2026%22", "url": "https://recallledger.net/recalls/drug-d-0533-2026-primidone-tablets-usp-250mg-100-count-bottle-rx-only-distributed-b/"}, {"id": "fda-device-z-2229-2026", "source": "FDA", "category": "device", "recall_number": "Z-2229-2026", "title": "Integris-Allura system recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)", "product": "Integris-Allura system; System Code Description (Model Numbers): Integris CV Cesar-Powerpack-Visub-Nicol (722030), Integris Allura 15 & 12 (monoplane) (722043), INTEGRIS Allura 15-12 (biplane) (722044), Integris-Allura 9 (722018), Integris-Allura 9 (Biplane) (722021), Integris CV Cesar-Powerpack (722030), Integris H5000 C / Allura 9C (722016);", "reason": "The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in oil leakage. Oil leakage may affect the cooling performance of the X-ray tube. When the oil flow drops below a certain threshold, the system automatically switches to low-dose fluoroscopy and displays the message Low load fluoroscopy flavor selected: Tube cooler problem . This condition cannot be resolved by restarting the system.", "hazard_level": "Class II", "company": "PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.", "company_location": "Best, Netherlands", "date": "2026-04-28", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "Domestic: Nationwide; International: Canada, Algeria, Argentina, Australia, Austria, Bahrain, Bangladesh, Belarus, Belgium, Bolivia, Bosnia and Herzegovina, Brazil, Brunei Darussalam, Bulgaria, Chile, China, Colombia, Costa Rica, Croatia, Cuba, Cyprus, Czech Republic, Denmark, Dominican Republic, Ecuador, Egypt, Ethiopia, Finland, France, French Polynesia, Georgia, Germany, Greece, Hong Kong, Hungary, India, Indonesia, Iran, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan, Korea, Republic of, Kosovo, Kuwait, Kyrgyzstan, Lao People's Democratic Republic, Latvia, Lebanon, Libya, Lithuania, Malaysia, Maldives, Malta, Martinique, Mexico, Moldova, Mongolia, Morocco, Myanmar, Nepal, Netherlands, New Caledonia, New Zealand, Nigeria, Norway, Oman, Pakistan, Palestine, State of, Panama, Paraguay, Peru, Philippines, Poland, Portugal, Qatar, R¿union, Romania, Russian Federation, Saudi Arabia, Senegal, Serbia, Singapore, Slovakia, Slovenia, South Africa, Spain, Sri Lanka, Sudan, Sweden, Switzerland, Taiwan, Thailand, Trinidad and Tobago, Tunisia, Turkey, Ukraine, United Arab Emirates, United Kingdom, Uruguay, Uzbekistan, Viet Nam, Yemen;", "states": ["GA"], "nationwide": true, "quantity": "25 units (11 US, 14 OUS)", "codes": "1. Integris CV Cesar-Powerpack-Visub-Nicol; Model: 722030; UDI-DI: N/A; Serial Numbers: 4888270, 59, 0, 33; 2. Integris Allura 15 & 12 (monoplane) (722043); UDI-DI: N/A; Serial Numbers: 365, 18151, 176, 239, 407, 426, 0; 3. INTEGRIS Allura 15-12 (biplane) (722044); UDI-DI: N/A; Serial Numbers: 86322, 30, 66; 4. Integris-Allura 9 (722018); UDI-DI: N/A; Serial Numbers: 26, 85; 5. Integris-Allura 9 (Biplane) (722021); UDI-DI: N/A; Serial numbers: 22, 75, 25, 108; 6. Integris H5000 C / Allura 9C (722016); UDI-DI: N/A; Serial Numbers: 4059001008, 4807240, S01H003553/000001;", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2229-2026%22", "url": "https://recallledger.net/recalls/device-z-2229-2026-integris-allura-system-system-code-description-model-numbers-integ/"}, {"id": "fda-device-z-2228-2026", "source": "FDA", "category": "device", "recall_number": "Z-2228-2026", "title": "Allura system recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)", "product": "Allura system; System Code Description (Model Numbers): Allura Xper FD10C (722001), Allura Xper FD10F (722002), Allura Xper FD10 (722003, 722010, 722026), Allura Xper FD10/10 (722005, 722011, 722027), Allura Xper FD20 (722006, 722012, 722028), Allura Xper FD20 Biplane (722008, 722013), Allura Xper FD20 OR Table (722015, 722023, 722035), Allura Xper FD20 Biplane OR Table (722025), Allura Xper FD20/10 (722029), Allura Xper FD20/15 (722058), Allura Xper FD20/15 OR Table (722059), Allura Xper FD20/20 (722038), Allura Xper FD20/20 OR Table (722039), Cardio Vascular-Allura (722400);", "reason": "The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in oil leakage. Oil leakage may affect the cooling performance of the X-ray tube. When the oil flow drops below a certain threshold, the system automatically switches to low-dose fluoroscopy and displays the message Low load fluoroscopy flavor selected: Tube cooler problem . This condition cannot be resolved by restarting the system.", "hazard_level": "Class II", "company": "PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.", "company_location": "Best, Netherlands", "date": "2026-04-28", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "Domestic: Nationwide; International: Canada, Algeria, Argentina, Australia, Austria, Bahrain, Bangladesh, Belarus, Belgium, Bolivia, Bosnia and Herzegovina, Brazil, Brunei Darussalam, Bulgaria, Chile, China, Colombia, Costa Rica, Croatia, Cuba, Cyprus, Czech Republic, Denmark, Dominican Republic, Ecuador, Egypt, Ethiopia, Finland, France, French Polynesia, Georgia, Germany, Greece, Hong Kong, Hungary, India, Indonesia, Iran, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan, Korea, Republic of, Kosovo, Kuwait, Kyrgyzstan, Lao People's Democratic Republic, Latvia, Lebanon, Libya, Lithuania, Malaysia, Maldives, Malta, Martinique, Mexico, Moldova, Mongolia, Morocco, Myanmar, Nepal, Netherlands, New Caledonia, New Zealand, Nigeria, Norway, Oman, Pakistan, Palestine, State of, Panama, Paraguay, Peru, Philippines, Poland, Portugal, Qatar, R¿union, Romania, Russian Federation, Saudi Arabia, Senegal, Serbia, Singapore, Slovakia, Slovenia, South Africa, Spain, Sri Lanka, Sudan, Sweden, Switzerland, Taiwan, Thailand, Trinidad and Tobago, Tunisia, Turkey, Ukraine, United Arab Emirates, United Kingdom, Uruguay, Uzbekistan, Viet Nam, Yemen;", "states": ["GA"], "nationwide": true, "quantity": "3314 units (816 US, 2498 OUS)", "codes": "Code Information: Allura: 1. Allura Xper FD10C; Model: 722001; UDI-DI: N/A; Serial Numbers: 170, 242, 267, 142, 206, 316, 9, 306, 103, 33, 220; 2. Allura Xper FD10F; Model: 722002; UDI-DI: N/A; Serial Numbers: 0, 81, 47; 3. Allura Xper FD10; Model: 722003; UDI-DI: N/A; Serial Numbers: 208, 392, 109, 45, 1953, 1471, 1551, 485, 152, 928, 501, 90, 1435, 81, 939, 160, 472, 1349, 439, 1958, 1525, 72, 1187, 912, 368, 328A, 37, 1286, 1223, 487, 1061, 833, 688, 317, 157, 639, 375, 420, 225, 1338, 614, 214, 230, 736, 64, 1090, 1094, 1932, 1531, 421, 984, 373, 313, 918, 602, 374, 750, 1934, 1751, 1661, 961, 791, 454, 868, 416, 1329, 241; 4. Allura Xper FD10; Model: 722010; UDI: (01)00884838059030(21)921, (01)00884838059030(21)1440, (01)00884838059030(21)1328, (01)00884838059030(21)1292, (01)00884838059030(21)1428, (01)00884838059030(21)1396, (01)00884838059030(21)298, (01)00884838059030(21)1432, (01)00884838059030(21)1425, (01)00884838059030(21)1398, (01)00884838059030(21)1397, (01)00884838059030(21)1391, (01)00884838059030(21)1395, (01)00884838059030(21)314, (01)00884838059030(21)1297, (01)00884838059030(21)946, (01)00884838059030(21)1424, (01)00884838059030(21)1244, (01)00884838059030(21)1122, (01)00884838059030(21)1198, (01)00884838059030(21)1421, (01)00884838059030(21)1423, (01)00884838059030(21)1438, (01)00884838059030(21)697, (01)00884838059030(21)1192, (01)00884838059030(21)1326, (01)00884838059030(21)402, (01)00884838059030(21)1148, (01)00884838059030(21)1439, (01)00884838059030(21)1431, (01)00884838059030(21)1404, (01)00884838059030(21)1140, (01)00884838059030(21)1429, (01)00884838059030(21)1430, (01)00884838059030(21)1403, (01)00884838059030(21)1393, (01)00884838059030(21)1402, (01)00884838059030(21)406, (01)00884838059030(21)71, (01)00884838059030(21)1434, (01)00884838059030(21)1392, (01)00884838059030(21)1379, (01)00884838059030(21)1401, (01)00884838059030(21)1197, (01)00884838059030(21)1435, (01)00884838059030(21)1346, (01)00884838059030(21)232, (01)00884838059030(21)231, (01)00884838059030(21)248, (01)00884838059030(21)1137, (01)00884838059030(21)1446, (01)00884838059030(21)1422, (01)00884838059030(21)1433, (01)00884838059030(21)1131, (01)00884838059030(21)1218; 5. Allura Xper FD10; Model: 722026; UDI: (01)00884838054189(21)683, (01)00884838054189(21)1052, (01)00884838054189(21)1051, (01)00884838054189(21)786, (01)00884838054189(21)654, (01)00884838054189(21)1132, (01)00884838054189(21)1100, (01)00884838054189(21)770, (01)00884838054189(21)1338, (01)00884838054189(21)1068, (01)00884838054189(21)1072, (01)00884838054189(21)796, (01)00884838054189(21)1248, (01)00884838054189(21)1129, (01)00884838054189(21)781, (01)00884838054189(21)634, (01)00884838054189(21)908, (01)00884838054189(21)969, (01)00884838054189(21)1246, (01)00884838054189(21)877, (01)00884838054189(21)843, (01)00884838054189(21)1231, (01)00884838054189(21)1038, (01)00884838054189(21)1287, (01)00884838054189(21)878, (01)00884838054189(21)558, (01)00884838054189(21)633, (01)00884838054189(21)1050, (01)00884838054189(21)1000, (01)00884838054189(21)909, (01)00884838054189(21)841, (01)00884838054189(21)713, (01)00884838054189(21)731, (01)00884838054189(21)646, (01)00884838054189(21)728, (01)00884838054189(21)765, (01)00884838054189(21)959, (01)00884838054189(21)825, (01)00884838054189(21)942, (01)00884838054189(21)1192, (01)00884838054189(21)990, (01)00884838054189(21)774, (01)00884838054189(21)648, (01)00884838054189(21)966, (01)00884838054189(21)1268, (01)00884838054189(21)627, (01)00884838054189(21)604, (01)00884838054189(21)716, (01)00884838054189(21)1182, (01)00884838054189(21)965, (01)00884838054189(21)1189, (01)00884838054189(21)1126, (01)00884838054189(21)1210, (01)00884838054189(21)1239, (01)00884838054189(21)1215, (01)00884838054189(21)696, (01)00884838054189(21)664, (01)00884838054189(21)845, (01)00884838054189(21)778, (01)00884838054189(21)935, (01)00884838054189(21)782, (01)00884838054189(21)694, (01)00884838054189(21)838, (01)00884838054189(21)973, (01)00884838054189(21)985, (01)00884838054189(21)855, (01)00884838054189(21)612, (01)00884838054189(21)725, (01)00884838054189(21)805, (01)00884838054189(21)622, (01)00884838054189(21)1293, 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(01)00884838054189(21)1138, (01)00884838054189(21)814, (01)00884838054189(21)1234, (01)00884838054189(21)691, (01)00884838054189(21)1174, (01)00884838054189(21)1136, (01)00884838054189(21)789, (01)00884838054189(21)672, (01)00884838054189(21)640, (01)00884838054189(21)641, (01)00884838054189(21)642, (01)00884838054189(21)1119, (01)00884838054189(21)873, (01)00884838054189(21)868, (01)00884838054189(21)816, (01)00884838054189(21)1086, (01)00884838054189(21)898, (01)00884838054189(21)551, (01)00884838054189(21)766, (01)00884838054189(21)1150, (01)00884838054189(21)574, (01)00884838054189(21)1155, (01)00884838054189(21)1213, (01)00884838054189(21)970, (01)00884838054189(21)1352, (01)00884838054189(21)1226, (01)00884838054189(21)988, (01)00884838054189(21)994, (01)00884838054189(21)1169, (01)00884838054189(21)752, (01)00884838054189(21)732, (01)00884838054189(21)659, (01)00884838054189(21)956, (01)00884838054189(21)1120, (01)00884838054189(21)1022, (01)00884838054189(21)901, (01)00884838054189(21)815, (01)00884838054189(21)1133, (01)00884838054189(21)1354, (01)00884838054189(21)735, (01)00884838054189(21)1267, (01)00884838054189(21)1318, (01)00884838054189(21)1261, (01)00884838054189(21)1035, (01)00884838054189(21)1010, (01)00884838054189(21)1315, (01)00884838054189(21)1314, (01)00884838054189(21)1116, (01)00884838054189(21)1217, (01)00884838054189(21)1282, (01)00884838054189(21)1009, (01)00884838054189(21)1302, (01)00884838054189(21)1076, (01)00884838054189(21)1346, (01)00884838054189(21)833, (01)00884838054189(21)1331, (01)00884838054189(21)1028, (01)00884838054189(21)1062, (01)00884838054189(21)1358, (01)00884838054189(21)1154, (01)00884838054189(21)989, (01)00884838054189(21)1336, (01)00884838054189(21)1319, (01)00884838054189(21)1310, (01)00884838054189(21)1309, (01)00884838054189(21)891, (01)00884838054189(21)1262, (01)00884838054189(21)1334, (01)00884838054189(21)1339, (01)00884838054189(21)1283, (01)00884838054189(21)1109, (01)00884838054189(21)1252, (01)00884838054189(21)1342, (01)00884838054189(21)708, (01)00884838054189(21)1335, (01)00884838054189(21)987, (01)00884838054189(21)1159, (01)00884838054189(21)1266, (01)00884838054189(21)1153, (01)00884838054189(21)1063, (01)00884838054189(21)1292, (01)00884838054189(21)981, (01)00884838054189(21)948, (01)00884838054189(21)859, (01)00884838054189(21)1007, (01)00884838054189(21)1328, (01)00884838054189(21)1332, (01)00884838054189(21)1351, (01)00884838054189(21)760, (01)00884838054189(21)1256, (01)00884838054189(21)984, (01)00884838054189(21)1161, (01)00884838054189(21)636, (01)00884838054189(21)1294, (01)00884838054189(21)1122, (01)00884838054189(21)939, (01)00884838054189(21)1274, (01)00884838054189(21)1176, (01)00884838054189(21)767, (01)00884838054189(21)1269, (01)00884838054189(21)1214, (01)00884838054189(21)1348, (01)00884838054189(21)1270, (01)00884838054189(21)1164, (01)00884838054189(21)1259, (01)00884838054189(21)1260, (01)00884838054189(21)1135, (01)00884838054189(21)1312, (01)00884838054189(21)1209, (01)00884838054189(21)992, (01)00884838054189(21)844, (01)00884838054189(21)1317, (01)00884838054189(21)621, (01)00884838054189(21)1219, (01)00884838054189(21)875, (01)00884838054189(21)937, (01)00884838054189(21)971, (01)00884838054189(21)714, (01)00884838054189(21)742, (01)00884838054189(21)1224, (01)00884838054189(21)1137, (01)00884838054189(21)651, (01)00884838054189(21)1168, (01)00884838054189(21)701, (01)00884838054189(21)777, (01)00884838054189(21)776, (01)00884838054189(21)1149, (01)00884838054189(21)1207, (01)00884838054189(21)1206, (01)00884838054189(21)1330, (01)00884838054189(21)919, (01)00884838054189(21)741, (01)00884838054189(21)1279, (01)00884838054189(21)1066, (01)00884838054189(21)922, (01)00884838054189(21)808, (01)00884838054189(21)1125, (01)00884838054189(21)338, (01)00884838054189(21)1156, (01)00884838054189(21)1222, (01)00884838054189(21)673, (01)00884838054189(21)835, (01)00884838054189(21)737, (01)00884838054189(21)811, (01)00884838054189(21)1144, (01)00884838054189(21)1143, (01)00884838054189(21)867, (01)00884838054189(21)869, (01)00884838054189(21)702, (01)00884838054189(21)918, (01)00884838054189(21)1140, (01)00884838054189(21)790, (01)00884838054189(21)660, (01)00884838054189(21)1370, (01)00884838054189(21)1045, (01)00884838054189(21)824, (01)00884838054189(21)712, (01)00884838054189(21)1027, (01)00884838054189(21)582, (01)00884838054189(21)1020, (01)00884838054189(21)684, (01)00884838054189(21)736, (01)00884838054189(21)652, (01)00884838054189(21)1225, (01)00884838054189(21)758, (01)00884838054189(21)926, (01)00884838054189(21)724, (01)00884838054189(21)950, (01)00884838054189(21)549, (01)00884838054189(21)819, (01)00884838054189(21)983, (01)00884838054189(21)921, (01)00884838054189(21)821, (01)00884838054189(21)1311, (01)00884838054189(21)1158, (01)00884838054189(21)1157, (01)00884838054189(21)772, (01)00884838054189(21)1023, (01)00884838054189(21)784, (01)00884838054189(21)1004, (01)00884838054189(21)886, (01)00884838054189(21)887, (01)00884838054189(21)1102, (01)00884838054189(21)1002, (01)00884838054189(21)308, (01)00884838054189(21)1058, (01)00884838054189(21)896, (01)00884838054189(21)710, (01)00884838054189(21)1151, (01)00884838054189(21)706, (01)00884838054189(21)443, (01)00884838054189(21)442, (01)00884838054189(21)547, (01)00884838054189(21)870, (01)00884838054189(21)1365, (01)00884838054189(21)889, (01)00884838054189(21)412, (01)00884838054189(21)862, (01)00884838054189(21)1369, (01)00884838054189(21)1090, (01)00884838054189(21)1273, (01)00884838054189(21)788, (01)00884838054189(21)1345, (01)00884838054189(21)1344, (01)00884838054189(21)827, (01)00884838054189(21)1030, (01)00884838054189(21)1178, (01)00884838054189(21)1131, (01)00884838054189(21)675, (01)00884838054189(21)1322, (01)00884838054189(21)623, (01)00884838054189(21)853, (01)00884838054189(21)1172, (01)00884838054189(21)892, (01)00884838054189(21)588, (01)00884838054189(21)1257, (01)00884838054189(21)743, (01)00884838054189(21)1162, (01)00884838054189(21)1323, (01)00884838054189(21)1325, (01)00884838054189(21)876, (01)00884838054189(21)655, (01)00884838054189(21)974, (01)00884838054189(21)793, (01)00884838054189(21)907, (01)00884838054189(21)1251, (01)00884838054189(21)669; 6. Allura Xper FD10/10; Model: 722005; UDI-DI: N/A: Serial Numbers: 51, 22, 259, 196, 530, 435, 233, 309, 89, 29, 399, 480, 6, 41, 71, 124, 458, 54, 55, 528, 80, 556, 74, 203, 60, 125, 426, 123, 64, 299; 7. Allura Xper FD10/10; Model: 722011; UDI: (01)00884838059047(21)49, (01)00884838059047(21)196, (01)00884838059047(21)157, (01)00884838059047(21)82, (01)00884838059047(21)83, (01)00884838059047(21)275, (01)00884838059047(21)101, (01)00884838059047(21)347, (01)00884838059047(21)198, (01)00884838059047(21)94, (01)00884838059047(21)176, (01)00884838059047(21)329, (01)00884838059047(21)337; 8. Allura Xper FD10/10; Model: 722027; UDI: (01)00884838054196(21)351, (01)00884838054196(21)332, (01)00884838054196(21)71, (01)00884838054196(21)240, (01)00884838054196(21)241, (01)00884838054196(21)298, (01)00884838054196(21)175, (01)00884838054196(21)280, (01)00884838054196(21)222, (01)00884838054196(21)183, (01)00884838054196(21)202, (01)00884838054196(21)164, (01)00884838054196(21)335, (01)00884838054196(21)288, (01)00884838054196(21)342, (01)00884838054196(21)306, (01)00884838054196(21)307, (01)00884838054196(21)265, (01)00884838054196(21)169, (01)00884838054196(21)203, (01)00884838054196(21)234, (01)00884838054196(21)267, (01)00884838054196(21)209, (01)00884838054196(21)284, (01)00884838054196(21)263, (01)00884838054196(21)174, (01)00884838054196(21)305, (01)00884838054196(21)246, (01)00884838054196(21)255, (01)00884838054196(21)178, (01)00884838054196(21)266, (01)00884838054196(21)187, (01)00884838054196(21)321, (01)00884838054196(21)328, (01)00884838054196(21)282, (01)00884838054196(21)184, (01)00884838054196(21)337, (01)00884838054196(21)357, (01)00884838054196(21)213, (01)00884838054196(21)293, (01)00884838054196(21)292, (01)00884838054196(21)346, (01)00884838054196(21)211, (01)00884838054196(21)144, (01)00884838054196(21)238, (01)00884838054196(21)247, (01)00884838054196(21)347, (01)00884838054196(21)188, (01)00884838054196(21)196, (01)00884838054196(21)339, (01)00884838054196(21)343, (01)00884838054196(21)256, (01)00884838054196(21)338, (01)00884838054196(21)334, (01)00884838054196(21)294, (01)00884838054196(21)345, (01)00884838054196(21)172, (01)00884838054196(21)323, (01)00884838054196(21)324, (01)00884838054196(21)189, (01)00884838054196(21)212, (01)00884838054196(21)268, (01)00884838054196(21)356, (01)00884838054196(21)244, (01)00884838054196(21)254, (01)00884838054196(21)362, (01)00884838054196(21)271, (01)00884838054196(21)186, (01)00884838054196(21)259, (01)00884838054196(21)236, (01)00884838054196(21)201, (01)00884838054196(21)275, (01)00884838054196(21)277, (01)00884838054196(21)349, (01)00884838054196(21)350, (01)00884838054196(21)348, (01)00884838054196(21)273, (01)00884838054196(21)249, (01)00884838054196(21)149, (01)00884838054196(21)148, (01)00884838054196(21)316, (01)00884838054196(21)274, (01)00884838054196(21)205, (01)00884838054196(21)270, (01)00884838054196(21)223, (01)00884838054196(21)181, (01)00884838054196(21)221, (01)00884838054196(21)245, (01)00884838054196(21)352, (01)00884838054196(21)358, (01)00884838054196(21)361, (01)00884838054196(21)228, (01)00884838054196(21)142, (01)00884838054196(21)214, (01)00884838054196(21)299, (01)00884838054196(21)114, (01)00884838054196(21)204, (01)00884838054196(21)225, (01)00884838054196(21)297, (01)00884838054196(21)182, (01)00884838054196(21)177, (01)00884838054196(21)300, (01)00884838054196(21)130, (01)00884838054196(21)210, (01)00884838054196(21)261, (01)00884838054196(21)260, (01)00884838054196(21)322, (01)00884838054196(21)360, (01)00884838054196(21)310, (01)00884838054196(21)291, (01)00884838054196(21)180, (01)00884838054196(21)287, (01)00884838054196(21)264, (01)00884838054196(21)272, (01)00884838054196(21)207, (01)00884838054196(21)239, (01)00884838054196(21)308, (01)00884838054196(21)243, (01)00884838054196(21)242, (01)00884838054196(21)218, (01)00884838054196(21)197, (01)00884838054196(21)235, (01)00884838054196(21)278, (01)00884838054196(21)250, (01)00884838054196(21)227, (01)00884838054196(21)233, (01)00884838054196(21)329, (01)00884838054196(21)296, (01)00884838054196(21)193, (01)00884838054196(21)219, (01)00884838054196(21)276, (01)00884838054196(21)326, (01)00884838054196(21)312, (01)00884838054196(21)304, (01)00884838054196(21)311, (01)00884838054196(21)199, (01)00884838054196(21)192, (01)00884838054196(21)289, (01)00884838054196(21)217, (01)00884838054196(21)355, (01)00884838054196(21)232, (01)00884838054196(21)315, (01)00884838054196(21)309, (01)00884838054196(21)171, (01)00884838054196(21)191, (01)00884838054196(21)269, (01)00884838054196(21)206, (01)00884838054196(21)330, (01)00884838054196(21)195, (01)00884838054196(21)215, (01)00884838054196(21)220, (01)00884838054196(21)198, (01)00884838054196(21)208, (01)00884838054196(21)286; 9. Allura Xper FD20; Model: 722006; UDI-DI: N/A; Serial Numbers: 2051, 1936, 518, 326, 66, 2587, 332, 249, 2274, 1496, 2183, 579, 1044, 2336, 443, 1913, 1259, 79, 939, 283, 405, 2161, 2068, 560, 1747, 1601, 479, 970, 1586, 878, 2537, 658, 384, 1469, 588, 328, 235, 381, 1536, 2504, 103, 826, 962, 169, 1197, 223, 595, 934, 1364, 972, 2567, 2042, 2380, 828, 528, 288, 1889, 1578, 1000, 942, 104, 2257, 1977, 1594, 118, 2003, 226, 1978, 333, 52, 53, 1242, 203, 521, 2427, 191, 1611, 1287, 250, 1582, 301, 1615, 1007, 01H041985, 2301, 1276, 234, 655, 914, 1302, 767, 781, 1038, 1306, 346, 8, 1524, 598, 639, 434, 687, 1580, 157, 491, 393, 621, 63, 2465, 2206, 585, 2487, 608, 1793, 884, 955, 1529, 1678, 1106, 946, 1650, 408, 1893, 380, 873, 102, 1232, 430, 1990, 1450, 957, 507, 1192, 136, 940, 274, 581, 2592, 2379, 890, 602, 280, 2493, 640, 2, 511; 10. Allura Xper FD20; Model: 722012; UDI: (01)00884838059054(21)2942, (01)00884838059054(21)2265, (01)00884838059054(21)2735, (01)00884838059054(21)2707, (01)00884838059054(21)135, (01)00884838059054(21)2740, (01)00884838059054(21)2843, (01)00884838059054(21)2835, (01)00884838059054(21)760, (01)00884838059054(21)735, (01)00884838059054(21)174, (01)00884838059054(21)2855, (01)00884838059054(21)2856, (01)00884838059054(21)2712, (01)00884838059054(21)606, (01)00884838059054(21)2721, (01)00884838059054(21)2085, (01)00884838059054(21)695, (01)00884838059054(21)2202, (01)00884838059054(21)2828, (01)00884838059054(21)601, (01)00884838059054(21)1207, (01)00884838059054(21)2898, (01)00884838059054(21)334, (01)00884838059054(21)1656, (01)00884838059054(21)483, (01)00884838059054(21)2305, (01)00884838059054(21)2896, (01)00884838059054(21)2726, (01)00884838059054(21)2722, (01)00884838059054(21)451, (01)00884838059054(21)2883, (01)00884838059054(21)2755, (01)00884838059054(21)2741, (01)00884838059054(21)1301, (01)00884838059054(21)2736, (01)00884838059054(21)782, (01)00884838059054(21)2890, (01)00884838059054(21)2829, (01)00884838059054(21)1675, (01)00884838059054(21)412, (01)00884838059054(21)320, (01)00884838059054(21)1224, (01)00884838059054(21)453, (01)00884838059054(21)1964, (01)00884838059054(21)325, (01)00884838059054(21)2742, (01)00884838059054(21)2889, (01)00884838059054(21)2713, (01)00884838059054(21)2899, (01)00884838059054(21)1272, (01)00884838059054(21)2857, (01)00884838059054(21)2886, (01)00884838059054(21)100, (01)00884838059054(21)2875, (01)00884838059054(21)2888, (01)00884838059054(21)71, (01)00884838059054(21)1807, (01)00884838059054(21)418, (01)00884838059054(21)1329, (01)00884838059054(21)2873, (01)00884838059054(21)1075, (01)00884838059054(21)2842, (01)00884838059054(21)2841, (01)00884838059054(21)2849, (01)00884838059054(21)2840, (01)00884838059054(21)2901, (01)00884838059054(21)1226, (01)00884838059054(21)2774, (01)00884838059054(21)1441, (01)00884838059054(21)2723, (01)00884838059054(21)2900, (01)00884838059054(21)316, (01)00884838059054(21)2892, (01)00884838059054(21)527, (01)00884838059054(21)2876, (01)00884838059054(21)2881, (01)00884838059054(21)525, (01)00884838059054(21)1806, (01)00884838059054(21)2844, (01)00884838059054(21)1712, (01)00884838059054(21)2760, (01)00884838059054(21)2868, (01)00884838059054(21)2869, (01)00884838059054(21)718, (01)00884838059054(21)1282, (01)00884838059054(21)1946, (01)00884838059054(21)2912, (01)00884838059054(21)1622, (01)00884838059054(21)2874, (01)00884838059054(21)351, (01)00884838059054(21)1655, (01)00884838059054(21)2282, (01)00884838059054(21)2891, (01)00884838059054(21)2764, (01)00884838059054(21)2880, (01)00884838059054(21)1171, (01)00884838059054(21)1921, (01)00884838059054(21)2838, (01)00884838059054(21)2887, (01)00884838059054(21)2567, (01)00884838059054(21)2703, (01)00884838059054(21)2759, (01)00884838059054(21)2945, (01)00884838059054(21)1747, (01)00884838059054(21)2879, (01)00884838059054(21)2335, (01)00884838059054(21)2913, (01)00884838059054(21)537, (01)00884838059054(21)2897, (01)00884838059054(21)288, (01)00884838059054(21)191, (01)00884838059054(21)2917, (01)00884838059054(21)2915, (01)00884838059054(21)2850, (01)00884838059054(21)2825, (01)00884838059054(21)2579, (01)00884838059054(21)2916, (01)00884838059054(21)2667, (01)00884838059054(21)2681, (01)00884838059054(21)2784, (01)00884838059054(21)2747, (01)00884838059054(21)2914, (01)00884838059054(21)1911, (01)00884838059054(21)2831, (01)00884838059054(21)2749, (01)00884838059054(21)2801, (01)00884838059054(21)2771, (01)00884838059054(21)2724, (01)00884838059054(21)2877, (01)00884838059054(21)2788, (01)00884838059054(21)2702, (01)00884838059054(21)465, (01)00884838059054(21)309, (01)00884838059054(21)2827, (01)00884838059054(21)2806, (01)00884838059054(21)1628, (01)00884838059054(21)2934, (01)00884838059054(21)2763, (01)00884838059054(21)2810, (01)00884838059054(21)2581, (01)00884838059054(21)2623, (01)00884838059054(21)2647, (01)00884838059054(21)2854, (01)00884838059054(21)2548, (01)00884838059054(21)2745, (01)00884838059054(21)2812, (01)00884838059054(21)2676, (01)00884838059054(21)2599, (01)00884838059054(21)2789, (01)00884838059054(21)2818, (01)00884838059054(21)2678, (01)00884838059054(21)2701, (01)00884838059054(21)2756, (01)00884838059054(21)1256, (01)00884838059054(21)2830, (01)00884838059054(21)982, (01)00884838059054(21)2565, (01)00884838059054(21)2752, (01)00884838059054(21)2811, (01)00884838059054(21)2852, (01)00884838059054(21)2671, (01)00884838059054(21)2649, (01)00884838059054(21)2698, (01)00884838059054(21)2661, (01)00884838059054(21)2690, (01)00884838059054(21)2775, (01)00884838059054(21)2773, (01)00884838059054(21)2834, (01)00884838059054(21)2720, (01)00884838059054(21)2626, (01)00884838059054(21)2823, (01)00884838059054(21)374, (01)00884838059054(21)2782, (01)00884838059054(21)2766, (01)00884838059054(21)2776, (01)00884838059054(21)2826, (01)00884838059054(21)2738, (01)00884838059054(21)2851, (01)00884838059054(21)2777, (01)00884838059054(21)2739, (01)00884838059054(21)2847, (01)00884838059054(21)2832, (01)00884838059054(21)2725, (01)00884838059054(21)2650, (01)00884838059054(21)2813, (01)00884838059054(21)998, (01)00884838059054(21)2744, (01)00884838059054(21)2797, (01)00884838059054(21)2229, (01)00884838059054(21)2228, (01)00884838059054(21)2781, (01)00884838059054(21)2853, (01)00884838059054(21)2716, (01)00884838059054(21)2808, (01)00884838059054(21)2837, (01)00884838059054(21)2768, (01)00884838059054(21)2673, (01)00884838059054(21)2674, (01)00884838059054(21)2803, (01)00884838059054(21)2732, (01)00884838059054(21)2798, (01)00884838059054(21)2786, (01)00884838059054(21)2778, (01)00884838059054(21)2559, (01)00884838059054(21)2746, (01)00884838059054(21)2770, (01)00884838059054(21)2691, (01)00884838059054(21)2762, (01)00884838059054(21)2729, (01)00884838059054(21)2750, (01)00884838059054(21)2804, (01)00884838059054(21)2751, (01)00884838059054(21)2640, (01)00884838059054(21)2730, (01)00884838059054(21)2562, (01)00884838059054(21)2795, (01)00884838059054(21)2718, (01)00884838059054(21)2682, (01)00884838059054(21)2574, (01)00884838059054(21)2779, (01)00884838059054(21)2711, (01)00884838059054(21)2758, (01)00884838059054(21)2836, (01)00884838059054(21)2733, (01)00884838059054(21)2824, (01)00884838059054(21)2715, (01)00884838059054(21)2704, (01)00884838059054(21)2734, (01)00884838059054(21)2793, (01)00884838059054(21)2792, (01)00884838059054(21)2566, (01)00884838059054(21)2757, (01)00884838059054(21)2765, (01)00884838059054(21)2785, (01)00884838059054(21)2767, (01)00884838059054(21)2794, (01)00884838059054(21)240, (01)00884838059054(21)2719, (01)00884838059054(21)2708, (01)00884838059054(21)2882, (01)00884838059054(21)2169, (01)00884838059054(21)2802, (01)00884838059054(21)2761, (01)00884838059054(21)2799, (01)00884838059054(21)2652, (01)00884838059054(21)2743, (01)00884838059054(21)2790, (01)00884838059054(21)2748, (01)00884838059054(21)2911, (01)00884838059054(21)2714, (01)00884838059054(21)2688, (01)00884838059054(21)2780, (01)00884838059054(21)2791, (01)00884838059054(21)1547, (01)00884838059054(21)2772, (01)00884838059054(21)657; 11. Allura Xper FD20; Model: 722028; UDI: (01)00884838054202(21)1756, (01)00884838054202(21)1569, (01)00884838054202(21)1956, (01)00884838054202(21)2206, (01)00884838054202(21)1233, (01)00884838054202(21)928, (01)00884838054202(21)2502, (01)00884838054202(21)1774, (01)00884838054202(21)869, (01)00884838054202(21)1017, (01)00884838054202(21)1957, (01)00884838054202(21)2261, (01)00884838054202(21)866, (01)00884838054202(21)1310, (01)00884838054202(21)1043, (01)00884838054202(21)1077, (01)00884838054202(21)995, (01)00884838054202(21)896, (01)00884838054202(21)877, (01)00884838054202(21)1439, (01)00884838054202(21)1343, (01)00884838054202(21)895, (01)00884838054202(21)1154, (01)00884838054202(21)1000, (01)00884838054202(21)1909, (01)00884838054202(21)1716, (01)00884838054202(21)1983, (01)00884838054202(21)2061, (01)00884838054202(21)1393, (01)00884838054202(21)1656, (01)00884838054202(21)1461, (01)00884838054202(21)1751, (01)00884838054202(21)1050, (01)00884838054202(21)1428, 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(01)00884838054202(21)1275, (01)00884838054202(21)1142, (01)00884838054202(21)1111, (01)00884838054202(21)1122, (01)00884838054202(21)2151, (01)00884838054202(21)1352, (01)00884838054202(21)888, (01)00884838054202(21)1755, (01)00884838054202(21)1855, (01)00884838054202(21)842, (01)00884838054202(21)840, (01)00884838054202(21)2310, (01)00884838054202(21)655, (01)00884838054202(21)2007, (01)00884838054202(21)2008, (01)00884838054202(21)968, (01)00884838054202(21)781, (01)00884838054202(21)774, (01)00884838054202(21)1850, (01)00884838054202(21)1522, (01)00884838054202(21)1448, (01)00884838054202(21)1413, (01)00884838054202(21)1538, (01)00884838054202(21)1930, (01)00884838054202(21)535, (01)00884838054202(21)938, (01)00884838054202(21)990, (01)00884838054202(21)1081, (01)00884838054202(21)808, (01)00884838054202(21)1634, (01)00884838054202(21)1387, (01)00884838054202(21)1630, (01)00884838054202(21)989, (01)00884838054202(21)1824, (01)00884838054202(21)1481, (01)00884838054202(21)887, (01)00884838054202(21)1202, (01)00884838054202(21)2407, (01)00884838054202(21)2635, (01)00884838054202(21)1809, (01)00884838054202(21)874, (01)00884838054202(21)1049, (01)00884838054202(21)1333, (01)00884838054202(21)1264, (01)00884838054202(21)981, (01)00884838054202(21)1447, (01)00884838054202(21)1189, (01)00884838054202(21)1188, (01)00884838054202(21)696, (01)00884838054202(21)966, (01)00884838054202(21)1875, (01)00884838054202(21)1482, (01)00884838054202(21)1405, (01)00884838054202(21)930, (01)00884838054202(21)932, (01)00884838054202(21)1001, (01)00884838054202(21)1041, (01)00884838054202(21)1054, (01)00884838054202(21)1032, (01)00884838054202(21)2252, (01)00884838054202(21)1472, (01)00884838054202(21)1266, (01)00884838054202(21)917, (01)00884838054202(21)2070, (01)00884838054202(21)971, (01)00884838054202(21)1014, (01)00884838054202(21)1200, (01)00884838054202(21)1374, (01)00884838054202(21)1499, (01)00884838054202(21)1222, (01)00884838054202(21)1705, (01)00884838054202(21)1514, 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(01)00884838054202(21)832, (01)00884838054202(21)1851, (01)00884838054202(21)1554, (01)00884838054202(21)1105, (01)00884838054202(21)1346, (01)00884838054202(21)1309, (01)00884838054202(21)1361, (01)00884838054202(21)1689, (01)00884838054202(21)1792, (01)00884838054202(21)1209, (01)00884838054202(21)1221, (01)00884838054202(21)1884, (01)00884838054202(21)1825, (01)00884838054202(21)2546, (01)00884838054202(21)2503, (01)00884838054202(21)1913, (01)00884838054202(21)1320, (01)00884838054202(21)1064, (01)00884838054202(21)2531, (01)00884838054202(21)1960, (01)00884838054202(21)2015, (01)00884838054202(21)1595, (01)00884838054202(21)1901, (01)00884838054202(21)2357, (01)00884838054202(21)2356, (01)00884838054202(21)1073, (01)00884838054202(21)2274, (01)00884838054202(21)1602, (01)00884838054202(21)1372, (01)00884838054202(21)1045, (01)00884838054202(21)2101, (01)00884838054202(21)1037, (01)00884838054202(21)732, (01)00884838054202(21)1548, (01)00884838054202(21)1426, (01)00884838054202(21)919, (01)00884838054202(21)2467, (01)00884838054202(21)1265, (01)00884838054202(21)1268, (01)00884838054202(21)2496, (01)00884838054202(21)2082, (01)00884838054202(21)1547, (01)00884838054202(21)1546, (01)00884838054202(21)2294, (01)00884838054202(21)1858, (01)00884838054202(21)1429, (01)00884838054202(21)1101, (01)00884838054202(21)1926, (01)00884838054202(21)1145, (01)00884838054202(21)1791, (01)00884838054202(21)975, (01)00884838054202(21)2006, (01)00884838054202(21)2558, (01)00884838054202(21)1757, (01)00884838054202(21)1367, (01)00884838054202(21)1358, (01)00884838054202(21)1356, (01)00884838054202(21)2514, (01)00884838054202(21)2049, (01)00884838054202(21)2198, (01)00884838054202(21)2004, (01)00884838054202(21)2267, (01)00884838054202(21)1886, (01)00884838054202(21)2386, (01)00884838054202(21)1627, (01)00884838054202(21)2413, (01)00884838054202(21)2122, (01)00884838054202(21)1164, (01)00884838054202(21)2423, (01)00884838054202(21)1503, (01)00884838054202(21)2338, (01)00884838054202(21)2657, (01)00884838054202(21)1838, (01)00884838054202(21)2354, (01)00884838054202(21)791, (01)00884838054202(21)1784, (01)00884838054202(21)1874, (01)00884838054202(21)2149, (01)00884838054202(21)1585, (01)00884838054202(21)1615, (01)00884838054202(21)1934, (01)00884838054202(21)2046, (01)00884838054202(21)1868, (01)00884838054202(21)1896, (01)00884838054202(21)2434, (01)00884838054202(21)2330, (01)00884838054202(21)1712, (01)00884838054202(21)1982, (01)00884838054202(21)847, (01)00884838054202(21)1118, (01)00884838054202(21)1183, (01)00884838054202(21)2189, (01)00884838054202(21)1918, (01)00884838054202(21)1625, (01)00884838054202(21)1715, (01)00884838054202(21)2150, (01)00884838054202(21)2029, (01)00884838054202(21)1062, (01)00884838054202(21)1684, (01)00884838054202(21)2074, (01)00884838054202(21)1788, (01)00884838054202(21)2073, (01)00884838054202(21)429, (01)00884838054202(21)1685, (01)00884838054202(21)1731, (01)00884838054202(21)1799, (01)00884838054202(21)2170, (01)00884838054202(21)1102, (01)00884838054202(21)1557, (01)00884838054202(21)974, (01)00884838054202(21)2171, (01)00884838054202(21)1170, (01)00884838054202(21)2026, (01)00884838054202(21)1241, (01)00884838054202(21)2190, (01)00884838054202(21)1297, (01)00884838054202(21)1996, (01)00884838054202(21)2065, (01)00884838054202(21)2199, (01)00884838054202(21)1550, (01)00884838054202(21)1453, (01)00884838054202(21)1975, (01)00884838054202(21)1714, (01)00884838054202(21)898, (01)00884838054202(21)752, (01)00884838054202(21)1257, (01)00884838054202(21)2778, (01)00884838054202(21)2697, (01)00884838054202(21)2783, (01)00884838054202(21)2458, (01)00884838054202(21)2735, (01)00884838054202(21)2762, (01)00884838054202(21)2769, (01)00884838054202(21)2852, (01)00884838054202(21)2694; 12. Allura Xper FD20 Biplane; Model: 722008; UDI-DI: N/A; Serial Numbers: 445, 178, 420, 267, 245, 516, 67, 71, 379, 258, 124, 54, 142, 81, 33, 57, 447, 215, 122, 61, 58, 17, 31; 13. Allura Xper FD20 Biplane; Model: 722013; UDI: (01)00884838059061(21)441, (01)00884838059061(21)249, (01)00884838059061(21)410, (01)00884838059061(21)268, (01)00884838059061(21)124, (01)00884838059061(21)531, (01)00884838059061(21)316, (01)00884838059061(21)78, (01)00884838059061(21)564, (01)00884838059061(21)164, (01)00884838059061(21)422, (01)00884838059061(21)428, (01)00884838059061(21)634, (01)00884838059061(21)327, (01)00884838059061(21)313, (01)00884838059061(21)309, (01)00884838059061(21)35, (01)00884838059061(21)266, (01)00884838059061(21)633, (01)00884838059061(21)417, (01)00884838059061(21)390, (01)00884838059061(21)525, (01)00884838059061(21)542, (01)00884838059061(21)344, (01)00884838059061(21)465, (01)00884838059061(21)394; 14. Allura Xper FD20 OR Table; Model: 722023; UDI: (01)00884838059085(21)127, (01)00884838059085(21)177, (01)00884838059085(21)9, (01)00884838059085(21)38, (01)00884838059085(21)56, (01)00884838059085(21)126, (01)00884838059085(21)144; 15. Allura Xper FD20 OR Table; Model: 722035; UDI: (01)00884838054240(21)119, (01)00884838054240(21)126, (01)00884838054240(21)169, (01)00884838054240(21)124, (01)00884838054240(21)161, (01)00884838054240(21)183, (01)00884838054240(21)246, (01)00884838054240(21)245, (01)00884838054240(21)242, (01)00884838054240(21)196, (01)00884838054240(21)236, (01)00884838054240(21)172, (01)00884838054240(21)212, (01)00884838054240(21)222, (01)00884838054240(21)121, (01)00884838054240(21)131, (01)00884838054240(21)145, (01)00884838054240(21)127, (01)00884838054240(21)187, (01)00884838054240(21)243, (01)00884838054240(21)143, (01)00884838054240(21)244, (01)00884838054240(21)125, (01)00884838054240(21)117, (01)00884838054240(21)247, (01)00884838054240(21)165, (01)00884838054240(21)252, (01)00884838054240(21)192, (01)00884838054240(21)128, (01)00884838054240(21)111, (01)00884838054240(21)227, (01)00884838054240(21)144, (01)00884838054240(21)174, (01)00884838054240(21)130, (01)00884838054240(21)263, (01)00884838054240(21)132, (01)00884838054240(21)134, (01)00884838054240(21)226, (01)00884838054240(21)190, (01)00884838054240(21)249, (01)00884838054240(21)109, (01)00884838054240(21)251, (01)00884838054240(21)232, (01)00884838054240(21)207, (01)00884838054240(21)158, (01)00884838054240(21)160, (01)00884838054240(21)237, (01)00884838054240(21)163, (01)00884838054240(21)248, (01)00884838054240(21)253, (01)00884838054240(21)154, (01)00884838054240(21)170, (01)00884838054240(21)195, (01)00884838054240(21)166, (01)00884838054240(21)235, (01)00884838054240(21)230, (01)00884838054240(21)164, (01)00884838054240(21)221, (01)00884838054240(21)255, (01)00884838054240(21)229, (01)00884838054240(21)256, (01)00884838054240(21)254, (01)00884838054240(21)261, (01)00884838054240(21)218, (01)00884838054240(21)238, (01)00884838054240(21)113, (01)00884838054240(21)258, (01)00884838054240(21)241, (01)00884838054240(21)188, (01)00884838054240(21)259, (01)00884838054240(21)167, (01)00884838054240(21)204, (01)00884838054240(21)233, (01)00884838054240(21)153, (01)00884838054240(21)191, (01)00884838054240(21)225, (01)00884838054240(21)193, (01)00884838054240(21)185, (01)00884838054240(21)186, (01)00884838054240(21)129, (01)00884838054240(21)151, (01)00884838054240(21)92, (01)00884838054240(21)201, (01)00884838054240(21)149, (01)00884838054240(21)211, (01)00884838054240(21)198, (01)00884838054240(21)136, (01)00884838054240(21)194, (01)00884838054240(21)200, (01)00884838054240(21)116, (01)00884838054240(21)206, (01)00884838054240(21)168, (01)00884838054240(21)203, (01)00884838054240(21)146, (01)00884838054240(21)156, (01)00884838054240(21)173, (01)00884838054240(21)171, (01)00884838054240(21)184, (01)00884838054240(21)215, (01)00884838054240(21)231, (01)00884838054240(21)202; 16. Allura Xper FD20 Biplane OR Table; Model: 722025; UDI: (01)00884838059108(21)2; 17. Allura Xper FD20/10; Model: 722029; UDI: (01)00884838054219(21)88, (01)00884838054219(21)95, (01)00884838054219(21)126, (01)00884838054219(21)94, (01)00884838054219(21)97, (01)00884838054219(21)91, (01)00884838054219(21)110, (01)00884838054219(21)100, (01)00884838054219(21)114, (01)00884838054219(21)128, (01)00884838054219(21)108, (01)00884838054219(21)103, (01)00884838054219(21)107, (01)00884838054219(21)81, (01)00884838054219(21)119, (01)00884838054219(21)118, (01)00884838054219(21)80, (01)00884838054219(21)106, (01)00884838054219(21)123, (01)00884838054219(21)127, (01)00884838054219(21)122, (01)00884838054219(21)101, (01)00884838054219(21)116, (01)00884838054219(21)102, (01)00884838054219(21)109, (01)00884838054219(21)120, (01)00884838054219(21)92, (01)00884838054219(21)69, (01)00884838054219(21)93, (01)00884838054219(21)51, (01)00884838054219(21)124, (01)00884838054219(21)87, (01)00884838054219(21)104, (01)00884838054219(21)59, (01)00884838054219(21)79, (01)00884838054219(21)96, (01)00884838054219(21)82, (01)00884838054219(21)75, (01)00884838054219(21)98, (01)00884838054219(21)89; 18. Allura Xper FD20/15; Model: 722058; UDI: (01)00884838059115(21)239, (01)00884838059115(21)305, (01)00884838059115(21)203, (01)00884838059115(21)373, (01)00884838059115(21)290, (01)00884838059115(21)124, (01)00884838059115(21)274, (01)00884838059115(21)366, (01)00884838059115(21)340, (01)00884838059115(21)162, (01)00884838059115(21)186, (01)00884838059115(21)405, (01)00884838059115(21)196, (01)00884838059115(21)156, (01)00884838059115(21)146, (01)00884838059115(21)285, (01)00884838059115(21)277, (01)00884838059115(21)168, (01)00884838059115(21)178, (01)00884838059115(21)138, (01)00884838059115(21)212, (01)00884838059115(21)257, (01)00884838059115(21)337, (01)00884838059115(21)265, (01)00884838059115(21)134, (01)00884838059115(21)238, (01)00884838059115(21)190, (01)00884838059115(21)219, (01)00884838059115(21)197, (01)00884838059115(21)325, (01)00884838059115(21)123, (01)00884838059115(21)319, (01)00884838059115(21)378, (01)00884838059115(21)205, (01)00884838059115(21)149, (01)00884838059115(21)264, (01)00884838059115(21)167, (01)00884838059115(21)365, (01)00884838059115(21)199, (01)00884838059115(21)278, (01)00884838059115(21)215, (01)00884838059115(21)288, (01)00884838059115(21)254, (01)00884838059115(21)304, (01)00884838059115(21)279, (01)00884838059115(21)171, (01)00884838059115(21)202, (01)00884838059115(21)182, (01)00884838059115(21)200, (01)00884838059115(21)129, (01)00884838059115(21)59, (01)00884838059115(21)332, (01)00884838059115(21)142, (01)00884838059115(21)335, (01)00884838059115(21)151, (01)00884838059115(21)232, (01)00884838059115(21)292, (01)00884838059115(21)183, (01)00884838059115(21)349, (01)00884838059115(21)261, (01)00884838059115(21)375, (01)00884838059115(21)161, (01)00884838059115(21)368, (01)00884838059115(21)372, (01)00884838059115(21)252, (01)00884838059115(21)320, (01)00884838059115(21)213, (01)00884838059115(21)293, (01)00884838059115(21)389, (01)00884838059115(21)169, (01)00884838059115(21)336, (01)00884838059115(21)143, (01)00884838059115(21)133, (01)00884838059115(21)192, (01)00884838059115(21)201, (01)00884838059115(21)163, (01)00884838059115(21)170, (01)00884838059115(21)77, (01)00884838059115(21)273, (01)00884838059115(21)222, (01)00884838059115(21)229, (01)00884838059115(21)253, (01)00884838059115(21)248, (01)00884838059115(21)334, (01)00884838059115(21)384, (01)00884838059115(21)268, (01)00884838059115(21)240, (01)00884838059115(21)289, (01)00884838059115(21)258, (01)00884838059115(21)269, (01)00884838059115(21)226, (01)00884838059115(21)244, (01)00884838059115(21)141, (01)00884838059115(21)391, (01)00884838059115(21)241, (01)00884838059115(21)164, (01)00884838059115(21)381, (01)00884838059115(21)281, (01)00884838059115(21)154, (01)00884838059115(21)246, (01)00884838059115(21)315, (01)00884838059115(21)256, (01)00884838059115(21)233, (01)00884838059115(21)348, (01)00884838059115(21)204, (01)00884838059115(21)396, (01)00884838059115(21)185, (01)00884838059115(21)95, (01)00884838059115(21)131, (01)00884838059115(21)377, (01)00884838059115(21)206, (01)00884838059115(21)150, (01)00884838059115(21)333, (01)00884838059115(21)155, (01)00884838059115(21)313, (01)00884838059115(21)344, (01)00884838059115(21)376, (01)00884838059115(21)382, (01)00884838059115(21)360, (01)00884838059115(21)370, (01)00884838059115(21)387, (01)00884838059115(21)356, (01)00884838059115(21)392, (01)00884838059115(21)358, (01)00884838059115(21)385, (01)00884838059115(21)367, (01)00884838059115(21)331, (01)00884838059115(21)379, (01)00884838059115(21)369, (01)00884838059115(21)397, (01)00884838059115(21)357, (01)00884838059115(21)388, (01)00884838059115(21)211, (01)00884838059115(21)125, (01)00884838059115(21)301, (01)00884838059115(21)354, (01)00884838059115(21)355, (01)00884838059115(21)159, (01)00884838059115(21)139, (01)00884838059115(21)96, (01)00884838059115(21)343, (01)00884838059115(21)177, (01)00884838059115(21)311, (01)00884838059115(21)386, (01)00884838059115(21)132, (01)00884838059115(21)291, (01)00884838059115(21)327, (01)00884838059115(21)220, (01)00884838059115(21)214, (01)00884838059115(21)145, (01)00884838059115(21)223, (01)00884838059115(21)137, (01)00884838059115(21)136, (01)00884838059115(21)119, (01)00884838059115(21)103, (01)00884838059115(21)188, (01)00884838059115(21)350, (01)00884838059115(21)347, (01)00884838059115(21)55, (01)00884838059115(21)194, (01)00884838059115(21)189, (01)00884838059115(21)237, (01)00884838059115(21)230, (01)00884838059115(21)221, (01)00884838059115(21)247, (01)00884838059115(21)242, (01)00884838059115(21)276, (01)00884838059115(21)345, (01)00884838059115(21)166, (01)00884838059115(21)179, (01)00884838059115(21)303, (01)00884838059115(21)90, (01)00884838059115(21)112, (01)00884838059115(21)245, (01)00884838059115(21)148, (01)00884838059115(21)234, (01)00884838059115(21)208, (01)00884838059115(21)193, (01)00884838059115(21)236, (01)00884838059115(21)266, (01)00884838059115(21)130, (01)00884838059115(21)235, (01)00884838059115(21)251, (01)00884838059115(21)195, (01)00884838059115(21)144, (01)00884838059115(21)330, (01)00884838059115(21)295, (01)00884838059115(21)187, (01)00884838059115(21)361, (01)00884838059115(21)153, (01)00884838059115(21)284, (01)00884838059115(21)181, (01)00884838059115(21)351, (01)00884838059115(21)210, (01)00884838059115(21)243, (01)00884838059115(21)218; 19. Allura Xper FD20/15 OR Table; Model: 722059; UDI: (01)00884838059122(21)33, (01)00884838059122(21)7, (01)00884838059122(21)35, (01)00884838059122(21)38, (01)00884838059122(21)37, (01)00884838059122(21)2; 20. Allura Xper FD20/20; Model: 722038; UDI: (01)00884838054226(21)108, (01)00884838054226(21)173, (01)00884838054226(21)119, (01)00884838054226(21)126, (01)00884838054226(21)130, (01)00884838054226(21)157, (01)00884838054226(21)141, (01)00884838054226(21)137, (01)00884838054226(21)167, (01)00884838054226(21)120, (01)00884838054226(21)169, (01)00884838054226(21)134, (01)00884838054226(21)143, (01)00884838054226(21)133, (01)00884838054226(21)166, (01)00884838054226(21)147, (01)00884838054226(21)127, (01)00884838054226(21)135, (01)00884838054226(21)123, (01)00884838054226(21)129, (01)00884838054226(21)148, (01)00884838054226(21)153, (01)00884838054226(21)164, (01)00884838054226(21)111, (01)00884838054226(21)160, (01)00884838054226(21)172, (01)00884838054226(21)171, (01)00884838054226(21)159, (01)00884838054226(21)155, (01)00884838054226(21)144, (01)00884838054226(21)163, (01)00884838054226(21)168, (01)00884838054226(21)161, (01)00884838054226(21)158, (01)00884838054226(21)156, (01)00884838054226(21)138, (01)00884838054226(21)162, (01)00884838054226(21)150, (01)00884838054226(21)146, (01)00884838054226(21)154, (01)00884838054226(21)124, (01)00884838054226(21)136, (01)00884838054226(21)140, (01)00884838054226(21)170; 21. Cardio Vascular-Allura (722400); UDI-DI: N/A: Serial Numbers: 486, 480, 322, 280, 506, 507, 497, 502, 429, 413, 222, 510, 439, 382, 364, 209, 347, 552, 482, 414, 407, 338, 424, 273, 245, 307, 476, 533, 314, 432, 458, 491, 361, 272, 250, 252, 308, 321, 525, 519, 352, 434, 232, 471, 470, 440, 545, 279, 346, 317, 369, 495, 547, 348, 380, 438, 437, 341, 513, 459, 379, 355, 485, 290, 400, 498, 278, 283, 512, 487, 455, 448, 251, 319, 381, 504, 535, 479, 423, 473, 296, 539, 285, 419, 305, 430, 449, 329, 472, 356, 292, 398, 548, 523, 299, 494, 286, 300, 488, 541, 543, 427, 447, 344, 542, 262, 536, 469, 554, 555, 546, 375, 521, 433, 463, 443, 483, 357, 374, 277, 530, 337, 549, 441, 320, 445, 287, 556, 446, 527, 526, 532, 418, 544, 444, 511, 267, 393, 303, 550, 524, 540, 284, 557, 353, 553, 496, 368, 531, 297, 538, 415, 227, 528, 259, 330, 264, 386, 462, 551, 396, 460, 522, 412, 395, 478, 499, 515, 306, 271, 435, 501, 518, 226, 360, 370, 477;", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2228-2026%22", "url": "https://recallledger.net/recalls/device-z-2228-2026-allura-system-system-code-description-model-numbers-allura-xper-fd/"}, {"id": "fda-device-z-2227-2026", "source": "FDA", "category": "device", "recall_number": "Z-2227-2026", "title": "Azurion system recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)", "product": "Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063), Azurion 3 M15 (722064), Azurion 7 B12 (722067), Azurion 7 B20 (722068), Azurion 7 M12 (722078), Azurion 7 M20 (722079, 722224).", "reason": "The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in oil leakage. Oil leakage may affect the cooling performance of the X-ray tube. When the oil flow drops below a certain threshold, the system automatically switches to low-dose fluoroscopy and displays the message Low load fluoroscopy flavor selected: Tube cooler problem . This condition cannot be resolved by restarting the system.", "hazard_level": "Class II", "company": "PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.", "company_location": "Best, Netherlands", "date": "2026-04-28", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "Domestic: Nationwide; International: Canada, Algeria, Argentina, Australia, Austria, Bahrain, Bangladesh, Belarus, Belgium, Bolivia, Bosnia and Herzegovina, Brazil, Brunei Darussalam, Bulgaria, Chile, China, Colombia, Costa Rica, Croatia, Cuba, Cyprus, Czech Republic, Denmark, Dominican Republic, Ecuador, Egypt, Ethiopia, Finland, France, French Polynesia, Georgia, Germany, Greece, Hong Kong, Hungary, India, Indonesia, Iran, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan, Korea, Republic of, Kosovo, Kuwait, Kyrgyzstan, Lao People's Democratic Republic, Latvia, Lebanon, Libya, Lithuania, Malaysia, Maldives, Malta, Martinique, Mexico, Moldova, Mongolia, Morocco, Myanmar, Nepal, Netherlands, New Caledonia, New Zealand, Nigeria, Norway, Oman, Pakistan, Palestine, State of, Panama, Paraguay, Peru, Philippines, Poland, Portugal, Qatar, R¿union, Romania, Russian Federation, Saudi Arabia, Senegal, Serbia, Singapore, Slovakia, Slovenia, South Africa, Spain, Sri Lanka, Sudan, Sweden, Switzerland, Taiwan, Thailand, Trinidad and Tobago, Tunisia, Turkey, Ukraine, United Arab Emirates, United Kingdom, Uruguay, Uzbekistan, Viet Nam, Yemen;", "states": ["GA"], "nationwide": true, "quantity": "1651 units (592 US, 1359 OUS)", "codes": "1. Azurion 3 M12; Model: 722063; UDI: (01)00884838085275(21)64, (01)00884838085275(21)56, (01)00884838085275(21)77, (01)00884838085275(21)82, (01)00884838085275(21)47, (01)00884838085275(21)80, (01)00884838085275(21)102, (01)00884838085275(21)117, (01)00884838085275(21)2, (01)00884838085275(21)99, (01)00884838085275(21)44, (01)00884838085275(21)3, (01)00884838085275(21)62, (01)00884838085275(21)61, (01)00884838085275(21)22, (01)00884838085275(21)29, (01)00884838085275(21)40, (01)00884838085275(21)70, (01)00884838085275(21)30, (01)00884838085275(21)25, (01)00884838085275(21)19, (01)00884838085275(21)18, (01)00884838085275(21)17, (01)00884838085275(21)16, (01)00884838085275(21)14, (01)00884838085275(21)53, (01)00884838085275(21)103, (01)00884838085275(21)101, (01)00884838085275(21)41, (01)00884838085275(21)104, (01)00884838085275(21)93, (01)00884838085275(21)115, (01)00884838085275(21)73, (01)00884838085275(21)128, (01)00884838085275(21)4, (01)00884838085275(21)50, (01)00884838085275(21)72, (01)00884838085275(21)38, (01)00884838085275(21)21, (01)00884838085275(21)78, (01)00884838085275(21)23, (01)00884838085275(21)76, (01)00884838085275(21)63, (01)00884838085275(21)69, (01)00884838085275(21)59, (01)00884838085275(21)51, (01)00884838085275(21)92, (01)00884838085275(21)75, (01)00884838085275(21)94, (01)00884838085275(21)100, (01)00884838085275(21)54, (01)00884838085275(21)46, (01)00884838085275(21)26, (01)00884838085275(21)71, (01)00884838085275(21)106, (01)00884838085275(21)83, (01)00884838085275(21)37, (01)00884838085275(21)36, (01)00884838085275(21)27, (01)00884838085275(21)15, (01)00884838085275(21)85, (01)00884838085275(21)88, (01)00884838085275(21)86, (01)00884838085275(21)90, (01)00884838085275(21)91, (01)00884838085275(21)79, (01)00884838085275(21)81, (01)00884838085275(21)52, (01)00884838085275(21)48, (01)00884838085275(21)55, 2. Azurion 3 M15; Model: 722064; UDI: (01)00884838085282(21)209, (01)00884838085282(21)201, (01)00884838085282(21)64, (01)00884838085282(21)218, (01)00884838085282(21)61, (01)00884838085282(21)161, (01)00884838085282(21)162, (01)00884838085282(21)169, (01)00884838085282(21)131, (01)00884838085282(21)190, (01)00884838085282(21)220, (01)00884838085282(21)173, (01)00884838085282(21)89, (01)00884838085282(21)130, (01)00884838085282(21)60, (01)00884838085282(21)9, (01)00884838085282(21)102, (01)00884838085282(21)137, (01)00884838085282(21)84, (01)00884838085282(21)78, (01)00884838085282(21)49, (01)00884838085282(21)213, (01)00884838085282(21)212, (01)00884838085282(21)193, (01)00884838085282(21)214, (01)00884838085282(21)180, (01)00884838085282(21)185, (01)00884838085282(21)186, (01)00884838085282(21)127, (01)00884838085282(21)106, (01)00884838085282(21)58, (01)00884838085282(21)81, (01)00884838085282(21)200, (01)00884838085282(21)179, (01)00884838085282(21)156, (01)00884838085282(21)230, (01)00884838085282(21)176, (01)00884838085282(21)150, (01)00884838085282(21)149, (01)00884838085282(21)44, (01)00884838085282(21)184, (01)00884838085282(21)6, (01)00884838085282(21)10, (01)00884838085282(21)82, (01)00884838085282(21)35, (01)00884838085282(21)69, (01)00884838085282(21)39, (01)00884838085282(21)66, (01)00884838085282(21)45, (01)00884838085282(21)40, (01)00884838085282(21)125, (01)00884838085282(21)55, (01)00884838085282(21)36, (01)00884838085282(21)94, (01)00884838085282(21)104, (01)00884838085282(21)155, (01)00884838085282(21)132, (01)00884838085282(21)67, (01)00884838085282(21)183, (01)00884838085282(21)70, (01)00884838085282(21)50, (01)00884838085282(21)138, (01)00884838085282(21)151, (01)00884838085282(21)5, (01)00884838085282(21)208, (01)00884838085282(21)57, (01)00884838085282(21)222, (01)00884838085282(21)98, (01)00884838085282(21)79, (01)00884838085282(21)65, (01)00884838085282(21)87, (01)00884838085282(21)109, (01)00884838085282(21)75, (01)00884838085282(21)46, (01)00884838085282(21)101, (01)00884838085282(21)121, (01)00884838085282(21)68, (01)00884838085282(21)91, (01)00884838085282(21)74, (01)00884838085282(21)73, (01)00884838085282(21)124, (01)00884838085282(21)191, (01)00884838085282(21)122, (01)00884838085282(21)119, (01)00884838085282(21)11, (01)00884838085282(21)48, (01)00884838085282(21)147, (01)00884838085282(21)133, (01)00884838085282(21)7, (01)00884838085282(21)235, (01)00884838085282(21)120, (01)00884838085282(21)100, (01)00884838085282(21)51, (01)00884838085282(21)118, (01)00884838085282(21)62, (01)00884838085282(21)123, (01)00884838085282(21)177, (01)00884838085282(21)47, (01)00884838085282(21)272, (01)00884838085282(21)110, (01)00884838085282(21)59, (01)00884838085282(21)167, (01)00884838085282(21)174, (01)00884838085282(21)165, (01)00884838085282(21)41, (01)00884838085282(21)148, (01)00884838085282(21)182, (01)00884838085282(21)112, (01)00884838085282(21)86, (01)00884838085282(21)198, (01)00884838085282(21)206, (01)00884838085282(21)136, (01)00884838085282(21)143, (01)00884838085282(21)226, (01)00884838085282(21)43, (01)00884838085282(21)80, (01)00884838085282(21)12, (01)00884838085282(21)285, (01)00884838085282(21)215, (01)00884838085282(21)164, (01)00884838085282(21)114, (01)00884838085282(21)144, (01)00884838085282(21)227, (01)00884838085282(21)126, (01)00884838085282(21)92, (01)00884838085282(21)284, (01)00884838085282(21)175, (01)00884838085282(21)199, (01)00884838085282(21)188, (01)00884838085282(21)172, (01)00884838085282(21)210, (01)00884838085282(21)134, (01)00884838085282(21)207, (01)00884838085282(21)192, (01)00884838085282(21)116, (01)00884838085282(21)221, (01)00884838085282(21)189, (01)00884838085282(21)117, (01)00884838085282(21)187, (01)00884838085282(21)166, (01)00884838085282(21)96, (01)00884838085282(21)135, (01)00884838085282(21)108, (01)00884838085282(21)37, 3. Azurion 7 B12; Model: 722067; UDI: (01)00884838085350(21)42, (01)00884838085350(21)173, (01)00884838085350(21)109, (01)00884838085350(21)192, (01)00884838085350(21)92, (01)00884838085350(21)103, (01)00884838085350(21)114, (01)00884838085350(21)69, (01)00884838085350(21)41, (01)00884838085350(21)98, (01)00884838085350(21)81, (01)00884838085350(21)123, (01)00884838085350(21)46, (01)00884838085350(21)115, (01)00884838085350(21)150, (01)00884838085350(21)163, (01)00884838085350(21)131, (01)00884838085350(21)71, (01)00884838085350(21)75, (01)00884838085350(21)132, (01)00884838085350(21)147, (01)00884838085350(21)104, (01)00884838085350(21)36, (01)00884838085350(21)70, (01)00884838085350(21)141, (01)00884838085350(21)26, (01)00884838085350(21)148, (01)00884838085350(21)133, (01)00884838085350(21)57, (01)00884838085350(21)190, (01)00884838085350(21)128, (01)00884838085350(21)151, (01)00884838085350(21)68, (01)00884838085350(21)111, (01)00884838085350(21)43, (01)00884838085350(21)33, (01)00884838085350(21)146, (01)00884838085350(21)187, (01)00884838085350(21)74, (01)00884838085350(21)154, (01)00884838085350(21)157, (01)00884838085350(21)29, (01)00884838085350(21)59, (01)00884838085350(21)209, (01)00884838085350(21)95, (01)00884838085350(21)169, (01)00884838085350(21)127, (01)00884838085350(21)30, (01)00884838085350(21)23, (01)00884838085350(21)203, (01)00884838085350(21)138, (01)00884838085350(21)34, (01)00884838085350(21)53, (01)00884838085350(21)113, (01)00884838085350(21)140, (01)00884838085350(21)144, (01)00884838085350(21)60, (01)00884838085350(21)45, (01)00884838085350(21)107, (01)00884838085350(21)112, (01)00884838085350(21)134, (01)00884838085350(21)101, (01)00884838085350(21)100, (01)00884838085350(21)58, (01)00884838085350(21)47, (01)00884838085350(21)176, (01)00884838085350(21)64, (01)00884838085350(21)156, (01)00884838085350(21)52, (01)00884838099265(21)1, (01)00884838085350(21)55, (01)00884838085350(21)54, (01)00884838085350(21)165, (01)00884838085350(21)25, (01)00884838085350(21)35, (01)00884838085350(21)149, (01)00884838085350(21)32, (01)00884838085350(21)224, (01)00884838085350(21)76, (01)00884838085350(21)108, (01)00884838099265(21)17, (01)00884838085350(21)48, (01)00884838085350(21)102, (01)00884838085350(21)105, (01)00884838085350(21)99, (01)00884838085350(21)21, (01)00884838085350(21)159, (01)00884838085350(21)49, (01)00884838085350(21)185, (01)00884838085350(21)51, (01)00884838085350(21)239, (01)00884838085350(21)40, (01)00884838085350(21)94, (01)00884838085350(21)63, (01)00884838085350(21)96, (01)00884838085350(21)129, (01)00884838085350(21)186, (01)00884838085350(21)130, (01)00884838085350(21)161, (01)00884838085350(21)120, (01)00884838085350(21)170, (01)00884838085350(21)171, (01)00884838085350(21)80, (01)00884838085350(21)28, (01)00884838085350(21)145, (01)00884838085350(21)79, (01)00884838085350(21)93, (01)00884838085350(21)137, (01)00884838085350(21)50, (01)00884838085350(21)44, (01)00884838085350(21)38, (01)00884838085350(21)175, (01)00884838085350(21)167, (01)00884838085350(21)78, (01)00884838085350(21)86, (01)00884838085350(21)91, (01)00884838085350(21)37, (01)00884838085350(21)72, (01)00884838085350(21)88, (01)00884838085350(21)27, (01)00884838085350(21)121, (01)00884838085350(21)179, (01)00884838085350(21)183, (01)00884838085350(21)117, (01)00884838085350(21)118, (01)00884838085350(21)85, (01)00884838085350(21)89, (01)00884838085350(21)90, (01)00884838085350(21)119, (01)00884838085350(21)87, (01)00884838085350(21)31, (01)00884838085350(21)110, (01)00884838085350(21)178, (01)00884838085350(21)73, (01)00884838085350(21)39, (01)00884838085350(21)56, (01)00884838085350(21)139, (01)00884838085350(21)61; 4. Azurion 7 B20; Model: 722068; UDI: (01)00884838085367(21)178, (01)00884838085367(21)335, (01)00884838085367(21)147, (01)00884838085367(21)205, (01)00884838085367(21)170, (01)00884838085367(21)95, (01)00884838085367(21)440, (01)00884838085367(21)247, (01)00884838085367(21)225, (01)00884838085367(21)64, (01)00884838085367(21)149, (01)00884838085367(21)42, (01)00884838085367(21)324, (01)00884838085367(21)323, (01)00884838085367(21)320, (01)00884838085367(21)85, (01)00884838085367(21)89, (01)00884838085367(21)109, (01)00884838085367(21)239, (01)00884838085367(21)271, (01)00884838085367(21)104, (01)00884838085367(21)370, (01)00884838085367(21)322, (01)00884838085367(21)136, (01)00884838085367(21)373, (01)00884838085367(21)308, (01)00884838085367(21)354, (01)00884838085367(21)75, (01)00884838085367(21)279, (01)00884838085367(21)400, (01)00884838085367(21)196, (01)00884838085367(21)110, (01)00884838085367(21)78, (01)00884838085367(21)330, (01)00884838085367(21)73, (01)00884838085367(21)288, (01)00884838085367(21)285, (01)00884838085367(21)295, (01)00884838085367(21)329, (01)00884838085367(21)184, (01)00884838085367(21)350, (01)00884838085367(21)304, (01)00884838085367(21)319, (01)00884838085367(21)490, (01)00884838085367(21)243, (01)00884838085367(21)103, (01)00884838085367(21)262, (01)00884838085367(21)261, (01)00884838085367(21)277, (01)00884838085367(21)150, (01)00884838085367(21)172, (01)00884838085367(21)117, (01)00884838085367(21)356, (01)00884838085367(21)130, (01)00884838085367(21)146, (01)00884838085367(21)143, (01)00884838085367(21)84, (01)00884838085367(21)251, (01)00884838085367(21)361, (01)00884838085367(21)76, (01)00884838085367(21)270, (01)00884838085367(21)114, (01)00884838085367(21)232, (01)00884838085367(21)137, (01)00884838085367(21)107, (01)00884838085367(21)282, (01)00884838085367(21)337, (01)00884838085367(21)101, (01)00884838085367(21)213, (01)00884838085367(21)111, (01)00884838085367(21)82, (01)00884838085367(21)113, (01)00884838085367(21)275, (01)00884838085367(21)265, (01)00884838085367(21)459, (01)00884838085367(21)276, (01)00884838085367(21)62, (01)00884838085367(21)302, (01)00884838085367(21)88, (01)00884838085367(21)126, (01)00884838085367(21)211, (01)00884838085367(21)283, (01)00884838085367(21)231, (01)00884838085367(21)207, (01)00884838085367(21)167, (01)00884838085367(21)289, (01)00884838085367(21)233, (01)00884838085367(21)173, (01)00884838085367(21)204, (01)00884838085367(21)77, (01)00884838085367(21)313, (01)00884838085367(21)236, (01)00884838085367(21)237, (01)00884838085367(21)133, (01)00884838085367(21)280, (01)00884838085367(21)307, (01)00884838085367(21)210, (01)00884838085367(21)258, (01)00884838085367(21)328, (01)00884838085367(21)325, (01)00884838085367(21)199, (01)00884838085367(21)53, (01)00884838085367(21)364, (01)00884838085367(21)491, (01)00884838085367(21)246, (01)00884838085367(21)142, (01)00884838085367(21)257, (01)00884838085367(21)140, (01)00884838085367(21)369, (01)00884838085367(21)97, 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(01)00884838085367(21)50, (01)00884838085367(21)489, (01)00884838085367(21)37, (01)00884838085367(21)79, (01)00884838085367(21)254, (01)00884838085367(21)394, (01)00884838085367(21)71, (01)00884838085367(21)47, (01)00884838085367(21)292, (01)00884838085367(21)35, (01)00884838085367(21)293, (01)00884838085367(21)227, (01)00884838085367(21)359, (01)00884838085367(21)387, (01)00884838085367(21)168, (01)00884838085367(21)128, (01)00884838085367(21)129, (01)00884838085367(21)69, (01)00884838085367(21)174, (01)00884838085367(21)483, (01)00884838085367(21)334, (01)00884838085367(21)181, (01)00884838085367(21)166, (01)00884838085367(21)141, (01)00884838085367(21)365, (01)00884838085367(21)198, (01)00884838085367(21)228, (01)00884838085367(21)380, (01)00884838085367(21)420, (01)00884838085367(21)212, (01)00884838085367(21)180, (01)00884838085367(21)268, (01)00884838085367(21)269, (01)00884838085367(21)74, (01)00884838085367(21)115, (01)00884838085367(21)349, (01)00884838085367(21)291, 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Azurion 7 M12; Model: 722078; UDI: (01)00884838085251(21)302, (01)00884838085251(21)585, (01)00884838085251(21)410, (01)00884838085251(21)523, (01)00884838085251(21)293, (01)00884838085251(21)291, (01)00884838085251(21)536, (01)00884838085251(21)537, (01)00884838085251(21)613, (01)00884838085251(21)598, (01)00884838085251(21)224, (01)00884838085251(21)249, (01)00884838085251(21)546, (01)00884838085251(21)478, (01)00884838085251(21)479, (01)00884838085251(21)513, (01)00884838085251(21)278, (01)00884838085251(21)438, (01)00884838085251(21)437, (01)00884838085251(21)456, (01)00884838085251(21)566, (01)00884838085251(21)488, (01)00884838085251(21)550, (01)00884838085251(21)571, (01)00884838085251(21)545, (01)00884838085251(21)544, (01)00884838085251(21)465, (01)00884838085251(21)376, (01)00884838085251(21)31, (01)00884838085251(21)165, (01)00884838085251(21)445, (01)00884838085251(21)539, (01)00884838085251(21)654, (01)00884838085251(21)656, (01)00884838085251(21)658, 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(01)00884838085251(21)871, (01)00884838085251(21)18, (01)00884838085251(21)551, (01)00884838085251(21)543, (01)00884838085251(21)516, (01)00884838085251(21)12, (01)00884838085251(21)155, (01)00884838085251(21)446, (01)00884838085251(21)685, (01)00884838085251(21)715, (01)00884838085251(21)225, (01)00884838085251(21)582, (01)00884838085251(21)19, (01)00884838085251(21)435, (01)00884838085251(21)16, (01)00884838085251(21)11, (01)00884838085251(21)167, (01)00884838085251(21)664, (01)00884838085251(21)508, (01)00884838085251(21)530; 6. Azurion 7 M12; Model: 722223; UDI: (01)00884838099241(21)61, (01)00884838099241(21)6, (01)00884838099241(21)12, (01)00884838099241(21)2; 7. Azurion 7 M20; Model: 722079; UDI: (01)00884838085268(21)1023, (01)00884838085268(21)645, (01)00884838085268(21)646, (01)00884838085268(21)1013, (01)00884838085268(21)460, (01)00884838085268(21)43, (01)00884838085268(21)35, (01)00884838085268(21)890, (01)00884838085268(21)1137, (01)00884838085268(21)1048, (01)00884838085268(21)401, (01)00884838085268(21)1010, (01)00884838085268(21)1054, (01)00884838085268(21)536, (01)00884838085268(21)534, (01)00884838085268(21)535, (01)00884838085268(21)266, (01)00884838085268(21)818, (01)00884838085268(21)412, (01)00884838085268(21)617, (01)00884838085268(21)246, (01)00884838085268(21)488, (01)00884838085268(21)53, (01)00884838085268(21)57, (01)00884838085268(21)905, (01)00884838085268(21)55, (01)00884838085268(21)992, (01)00884838085268(21)691, (01)00884838085268(21)809, (01)00884838085268(21)848, (01)00884838085268(21)1033, (01)00884838085268(21)891, (01)00884838085268(21)836, (01)00884838085268(21)1155, (01)00884838085268(21)466, 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Azurion 7 M20; Model: 722079; UDI: (01)00884838099258(21)44, (01)00884838099258(21)56, (01)00884838099258(21)78, (01)00884838099258(21)6, (01)00884838099258(21)1595, (01)00884838099258(21)4, (01)00884838099258(21)2666, (01)00884838099258(21)132, (01)00884838099258(21)3;", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2227-2026%22", "url": "https://recallledger.net/recalls/device-z-2227-2026-azurion-system-system-code-description-model-numbers-azurion-3-m12/"}, {"id": "fda-device-z-2226-2026", "source": "FDA", "category": "device", "recall_number": "Z-2226-2026", "title": "Silastic Foley Catheters Silastic Brand Foley Catheter 30cc REF: 33416 33418 ... recall (C.R. Bard Inc)", "product": "Silastic Foley Catheters Silastic Brand Foley Catheter 30cc REF: 33416 33418 33420 33422 33424 Silastic Brand Foley Catheter 5cc REF: 33614 33616 33618 33620 33622 33624", "reason": "Due to stain present on the surface of affected foley catheters.", "hazard_level": "Class II", "company": "C.R. Bard Inc", "company_location": "Covington, GA, United States", "date": "2026-04-23", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "U.S.: AK, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, and WI O.U.S.: Canada", "states": ["AK", "AR", "AZ", "CA", "CO", "CT", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "WA", "WI"], "nationwide": false, "quantity": "106,160", "codes": "Silastic Brand Foley Catheter 30cc Catalog Number / UDI code: 33416 / 00801741019982 10801741019989 Lot Number: NGKX0444 33418 / 00801741019999 10801741019996 Lot Number: NGKW2813 33420 / 00801741020001 10801741020008 Lot Number: NGKQ1015 33422 / 00801741020018 10801741020015 Lot Number: NGKW3707 33424 / 00801741020025 10801741020022 Lot Number: NGKW2669 Silastic Brand Foley Catheter 5cc Catalog Number / UDI code: 33614 / 00801741020056 10801741020053 Lot Numbers: NGKN4037 NGKP1420 NGKQ0040 NGKQ3901 NGKS4937 NGKV3462 NGKW3897 33616 / 00801741020063 10801741020060 Lot Numbers: NGKQ0042 NGKQ3946 NGKR3420 NGKT3281 NGKU1015 NGKV0617 NGKV2275 NGKV2309 NGKW3771 33618 / 00801741020070 10801741020077 Lot Numbers: NGKQ3370 NGKS3753 NGKT3258 NGKT3309 NGKU4129 NGKV1446 NGKV2345 NGKV3478 NGKV5029 33620 / 00801741020087 10801741020084 Lot Numbers: NGKS5060 NGKT3308 NGKV3689 33622 / 00801741020094 10801741020091 Lot Numbers: NGKQ1016 NGKS0244 NGKU0967 NGKV5075 NGKX0441 33624 / 00801741020100 10801741020107 Lot Numbers: NGKQ1722 NGKQ3862 NGKT3259 NGKX0456", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2226-2026%22", "url": "https://recallledger.net/recalls/device-z-2226-2026-silastic-foley-catheters-silastic-brand-foley-catheter-30cc-ref-33/"}, {"id": "fda-device-z-2225-2026", "source": "FDA", "category": "device", "recall_number": "Z-2225-2026", "title": "Philips Azurion systems not configured with an optional auxiliary pan handle. Includes... recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)", "product": "Philips Azurion systems not configured with an optional auxiliary pan handle. Includes the below product descriptions and corresponding model numbers. 1. Azurion 3 M12; Model Numbers: 722063, 722229. 2. Azurion 3 M15; Model Numbers: 722222, 722064, 722280, 722230. 3. Azurion 5 M12; Model Numbers: 722227, 722231. 4. Azurion 5 M20; Model Numbers: 722228, 722232, 722281. 5. Azurion 7 B12; Model Numbers: 722067, 722225, 722235. 6. Azurion 7 B20; Model Numbers: 722068, 722226, 722236. 7. Azurion 7 M12; Model Numbers: 722078, 722223, 722233. 8. Azurion 7 M20; Model Numbers: 722079, 722224, 722234, 722282.", "reason": "Potential safety issue with Philips Azurion systems, where longitudinal and transverse table movements may be impacted due to mechanical wear of the Float Tabletop control on the control module.", "hazard_level": "Class II", "company": "PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.", "company_location": "Best, Netherlands", "date": "2026-04-28", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "Nationwide distribution. International distribution to Albania, Algeria, Argentina, Armenia, Australia, Austria, Azerbaijan, Bangladesh, Belarus, Belgium, Bolivia, Bosnia and Herzegovina, Brazil, Canada, Chile, C¿te D'Ivoire, El Salvador, Estonia, Greece, Honduras, Hong Kong, Iceland, Indonesia, Iraq, Japan, Kyrgyzstan, Malaysia, Malta, Moldova, Nepal, New Zealand, Philippines, Qatar, Singapore, South Africa, Sri Lanka, Syrian Arab Republic, Tanzania, Turkmenistan, Vietnam, Yemen", "states": [], "nationwide": true, "quantity": "5,537 units", "codes": "1. Model Number [UDI]: 722063 [(01)00884838085275(21)77, (01)00884838085275(21)47, (01)00884838085275(21)146, (01)00884838085275(21)102, (01)00884838085275(21)43, (01)00884838085275(21)2, (01)00884838085275(21)99, (01)00884838085275(21)28, (01)00884838085275(21)144, (01)00884838085275(21)62, (01)00884838085275(21)119, (01)00884838085275(21)61, (01)00884838085275(21)29, (01)00884838085275(21)40, (01)00884838085275(21)70, (01)00884838085275(21)120, (01)00884838085275(21)121, (01)00884838085275(21)110, (01)00884838085275(21)53, (01)00884838085275(21)103, (01)00884838085275(21)97, (01)00884838085275(21)101, (01)00884838085275(21)143, (01)00884838085275(21)116, (01)00884838085275(21)93, (01)00884838085275(21)141, (01)00884838085275(21)115, (01)00884838085275(21)137, (01)00884838085275(21)150, (01)00884838085275(21)128, (01)00884838085275(21)4, (01)00884838085275(21)50, (01)00884838085275(21)129, (01)00884838085275(21)78, (01)00884838085275(21)76, (01)00884838085275(21)69, (01)00884838085275(21)59, (01)00884838085275(21)92, (01)00884838085275(21)139, (01)00884838085275(21)130, (01)00884838085275(21)154, (01)00884838085275(21)75, (01)00884838085275(21)24, (01)00884838085275(21)94, (01)00884838085275(21)100, (01)00884838085275(21)26, (01)00884838085275(21)106, (01)00884838085275(21)37, (01)00884838085275(21)36, (01)00884838085275(21)27, (01)00884838085275(21)15, (01)00884838085275(21)135, (01)00884838085275(21)123, (01)00884838085275(21)87, (01)00884838085275(21)85, (01)00884838085275(21)89, (01)00884838085275(21)88, (01)00884838085275(21)86, (01)00884838085275(21)90, (01)00884838085275(21)91, (01)00884838085275(21)79, (01)00884838085275(21)133, (01)00884838085275(21)81, (01)00884838085275(21)52, (01)00884838085275(21)48, (01)00884838085275(21)148, (01)00884838085275(21)55]; 722229 [(01)00884838116726(21)7, (01)00884838116726(21)3, (01)00884838116726(21)10, (01)00884838116726(21)11, (01)00884838116726(21)21, (01)00884838116726(21)13]. 2. Model Number [UDI]: 722064 [(01)00884838085282(21)513, (01)00884838085282(21)61, (01)00884838085282(21)162, (01)00884838085282(21)161, (01)00884838085282(21)297, (01)00884838085282(21)169, (01)00884838085282(21)131, (01)00884838085282(21)479, (01)00884838085282(21)190, (01)00884838085282(21)359, (01)00884838085282(21)220, (01)00884838085282(21)375, (01)00884838085282(21)173, (01)00884838085282(21)256, (01)00884838085282(21)290, (01)00884838085282(21)502, (01)00884838085282(21)425, (01)00884838085282(21)89, (01)00884838085282(21)303, (01)00884838085282(21)130, (01)00884838085282(21)157, (01)00884838085282(21)60, (01)00884838085282(21)253, (01)00884838085282(21)280, (01)00884838085282(21)373, (01)00884838085282(21)417, (01)00884838085282(21)277, (01)00884838085282(21)102, (01)00884838085282(21)467, (01)00884838085282(21)461, (01)00884838085282(21)137, (01)00884838085282(21)84, (01)00884838085282(21)510, (01)00884838085282(21)49, (01)00884838085282(21)246, (01)00884838085282(21)282, 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(01)00884838099210(21)38, (01)00884838099210(21)10, (01)00884838099210(21)67, (01)00884838099210(21)165, (01)00884838099210(21)272, (01)00884838099210(21)326, (01)00884838099210(21)173, (01)00884838099210(21)90, (01)00884838099210(21)109, (01)00884838099210(21)291, (01)00884838099210(21)292, (01)00884838099210(21)288, (01)00884838099210(21)290, (01)00884838099210(21)295, (01)00884838099210(21)289, (01)00884838099210(21)294, (01)00884838099210(21)186, (01)00884838099210(21)181, (01)00884838099210(21)107, (01)00884838099210(21)379, (01)00884838099210(21)385, (01)00884838099210(21)296, (01)00884838099210(21)315, (01)00884838099210(21)314, (01)00884838099210(21)77, (01)00884838099210(21)380, (01)00884838099210(21)110, (01)00884838099210(21)184, (01)00884838099210(21)180, (01)00884838099210(21)131, (01)00884838099210(21)214, (01)00884838099210(21)116, (01)00884838099210(21)276, (01)00884838099210(21)73, (01)00884838099210(21)157, (01)00884838099210(21)87, (01)00884838099210(21)114, (01)00884838099210(21)274, (01)00884838099210(21)135, (01)00884838099210(21)159, (01)00884838099210(21)158, (01)00884838099210(21)78, (01)00884838099210(21)125, (01)00884838099210(21)218, (01)00884838099210(21)124, (01)00884838099210(21)126, (01)00884838099210(21)212]; 722230 [(01)00884838116733(21)20, (01)00884838116733(21)23, (01)00884838116733(21)19, (01)00884838116733(21)28, (01)00884838116733(21)38, (01)00884838116733(21)9, (01)00884838116733(21)39, (01)00884838116733(21)27, (01)00884838116733(21)13, (01)00884838116733(21)12, (01)00884838116733(21)1]; 722280 [(01)00884838103276(21)57, (01)00884838103276(21)161, (01)00884838103276(21)43, (01)00884838103276(21)179, (01)00884838103276(21)229, (01)00884838103276(21)249, (01)00884838103276(21)65, (01)00884838103276(21)76, (01)00884838103276(21)233, (01)00884838103276(21)232, (01)00884838103276(21)113, (01)00884838103276(21)167, (01)00884838103276(21)165, (01)00884838103276(21)80, (01)00884838103276(21)128, (01)00884838103276(21)158, (01)00884838103276(21)149, (01)00884838103276(21)194, (01)00884838103276(21)44, (01)00884838103276(21)100, (01)00884838103276(21)164, (01)00884838103276(21)240, (01)00884838103276(21)246, (01)00884838103276(21)66, (01)00884838103276(21)135, (01)00884838103276(21)175, (01)00884838103276(21)99, (01)00884838103276(21)112, (01)00884838103276(21)34, (01)00884838103276(21)79, (01)00884838103276(21)130, (01)00884838103276(21)48, (01)00884838103276(21)52, (01)00884838103276(21)141, (01)00884838103276(21)131, (01)00884838103276(21)189, (01)00884838103276(21)37, (01)00884838103276(21)83, (01)00884838103276(21)223, (01)00884838103276(21)139, (01)00884838103276(21)87, (01)00884838103276(21)61, (01)00884838103276(21)259, (01)00884838103276(21)218, (01)00884838103276(21)90, (01)00884838103276(21)188, (01)00884838103276(21)105, (01)00884838103276(21)23, (01)00884838103276(21)30, (01)00884838103276(21)132, (01)00884838103276(21)96, (01)00884838103276(21)107, (01)00884838103276(21)171, (01)00884838103276(21)118, (01)00884838103276(21)21, (01)00884838103276(21)174, (01)00884838103276(21)284, (01)00884838103276(21)220, (01)00884838103276(21)147, (01)00884838103276(21)133, (01)00884838103276(21)252, (01)00884838103276(21)38, (01)00884838103276(21)243, (01)00884838103276(21)177, (01)00884838103276(21)178, (01)00884838103276(21)150, (01)00884838103276(21)69, (01)00884838103276(21)148, (01)00884838103276(21)210, (01)00884838103276(21)207, (01)00884838103276(21)98, (01)00884838103276(21)211, (01)00884838103276(21)127, (01)00884838103276(21)222, (01)00884838103276(21)144, (01)00884838103276(21)143, (01)00884838103276(21)142, (01)00884838103276(21)198, (01)00884838103276(21)71, (01)00884838103276(21)146, (01)00884838103276(21)241, (01)00884838103276(21)206, (01)00884838103276(21)152, (01)00884838103276(21)247, (01)00884838103276(21)262, (01)00884838103276(21)279, (01)00884838103276(21)157, (01)00884838103276(21)40, (01)00884838103276(21)17, (01)00884838103276(21)204, (01)00884838103276(21)260, (01)00884838103276(21)275, (01)00884838103276(21)187, (01)00884838103276(21)208, (01)00884838103276(21)46, (01)00884838103276(21)271, (01)00884838103276(21)235, (01)00884838103276(21)234, (01)00884838103276(21)91, (01)00884838103276(21)162, (01)00884838103276(21)97, (01)00884838103276(21)153, (01)00884838103276(21)245, (01)00884838103276(21)106, (01)00884838103276(21)173, (01)00884838103276(21)258, (01)00884838103276(21)120, (01)00884838103276(21)45, (01)00884838103276(21)92, (01)00884838103276(21)226, (01)00884838103276(21)254, (01)00884838103276(21)213, (01)00884838103276(21)224, (01)00884838103276(21)95, (01)00884838103276(21)54, (01)00884838103276(21)126, (01)00884838103276(21)216, (01)00884838103276(21)19, (01)00884838103276(21)215, (01)00884838103276(21)93, (01)00884838103276(21)24, (01)00884838103276(21)129, (01)00884838103276(21)74, (01)00884838103276(21)219, (01)00884838103276(21)88, (01)00884838103276(21)85, (01)00884838103276(21)86, (01)00884838103276(21)170, (01)00884838103276(21)55, (01)00884838103276(21)102, (01)00884838103276(21)124, (01)00884838103276(21)125, (01)00884838103276(21)123, (01)00884838103276(21)151, (01)00884838103276(21)39, (01)00884838103276(21)47, (01)00884838103276(21)101, (01)00884838103276(21)209, (01)00884838103276(21)41, (01)00884838103276(21)42, (01)00884838103276(21)53, (01)00884838103276(21)250, (01)00884838103276(21)239, (01)00884838103276(21)248, (01)00884838103276(21)108, (01)00884838103276(21)119, (01)00884838103276(21)205, (01)00884838103276(21)197, (01)00884838103276(21)82, (01)00884838103276(21)33, (01)00884838103276(21)20, (01)00884838103276(21)231, (01)00884838103276(21)63, (01)00884838103276(21)261, (01)00884838103276(21)138, (01)00884838103276(21)255, (01)00884838103276(21)212, (01)00884838103276(21)84, (01)00884838103276(21)145, (01)00884838103276(21)221, (01)00884838103276(21)36, (01)00884838103276(21)256, (01)00884838103276(21)59, (01)00884838103276(21)196, (01)00884838103276(21)50, (01)00884838103276(21)110, (01)00884838103276(21)272, (01)00884838103276(21)199, (01)00884838103276(21)264, (01)00884838103276(21)140, (01)00884838103276(21)68, (01)00884838103276(21)117, (01)00884838103276(21)49, (01)00884838103276(21)257, (01)00884838103276(21)60, (01)00884838103276(21)103, (01)00884838103276(21)237, (01)00884838103276(21)72, (01)00884838103276(21)160, (01)00884838103276(21)81, (01)00884838103276(21)114, (01)00884838103276(21)137, (01)00884838103276(21)58, (01)00884838103276(21)73, (01)00884838103276(21)35, (01)00884838103276(21)22, (01)00884838103276(21)94]. 3. Model Number [UDI]: 722227 [(01)00884838099227(21)159, (01)00884838099227(21)197, (01)00884838099227(21)149, (01)00884838099227(21)54, (01)00884838099227(21)56, (01)00884838099227(21)230, (01)00884838099227(21)98, (01)00884838099227(21)31, (01)00884838099227(21)128, (01)00884838099227(21)81, (01)00884838099227(21)37, (01)00884838099227(21)320, (01)00884838099227(21)53, (01)00884838099227(21)246, (01)00884838099227(21)245, (01)00884838099227(21)84, (01)00884838099227(21)38, (01)00884838099227(21)28, (01)00884838099227(21)29, (01)00884838099227(21)170, (01)00884838099227(21)30, (01)00884838099227(21)108, (01)00884838099227(21)168, (01)00884838099227(21)172, (01)00884838099227(21)62, (01)00884838099227(21)236, (01)00884838099227(21)104, (01)00884838099227(21)59, (01)00884838099227(21)109, (01)00884838099227(21)101, (01)00884838099227(21)99, (01)00884838099227(21)247, (01)00884838099227(21)177, (01)00884838099227(21)138, (01)00884838099227(21)337, (01)00884838099227(21)61, (01)00884838099227(21)287, (01)00884838099227(21)55, (01)00884838099227(21)215, (01)00884838099227(21)216, (01)00884838099227(21)73, (01)00884838099227(21)318, (01)00884838099227(21)167, (01)00884838099227(21)85, (01)00884838099227(21)191, (01)00884838099227(21)20, (01)00884838099227(21)226, (01)00884838099227(21)83, (01)00884838099227(21)218, (01)00884838099227(21)195, (01)00884838099227(21)43, (01)00884838099227(21)18, (01)00884838099227(21)153, (01)00884838099227(21)351, (01)00884838099227(21)352, (01)00884838099227(21)120, (01)00884838099227(21)204, (01)00884838099227(21)258, (01)00884838099227(21)326, (01)00884838099227(21)348, (01)00884838099227(21)17, (01)00884838099227(21)141, (01)00884838099227(21)103, (01)00884838099227(21)355, (01)00884838099227(21)113, (01)00884838099227(21)315, (01)00884838099227(21)161, (01)00884838099227(21)194, (01)00884838099227(21)105, (01)00884838099227(21)171, (01)00884838099227(21)49, (01)00884838099227(21)71, (01)00884838099227(21)91, (01)00884838099227(21)187, (01)00884838099227(21)166, (01)00884838099227(21)210, (01)00884838099227(21)219, (01)00884838099227(21)222, (01)00884838099227(21)273, (01)00884838099227(21)205, (01)00884838099227(21)300, (01)00884838099227(21)335, (01)00884838099227(21)80, (01)00884838099227(21)123, (01)00884838099227(21)243, (01)00884838099227(21)344, (01)00884838099227(21)308, (01)00884838099227(21)22, (01)00884838099227(21)140, (01)00884838099227(21)362, (01)00884838099227(21)242, (01)00884838099227(21)323, (01)00884838099227(21)331, (01)00884838099227(21)136, (01)00884838099227(21)137, (01)00884838099227(21)89, (01)00884838099227(21)294, (01)00884838099227(21)2, (01)00884838099227(21)111, (01)00884838099227(21)221, (01)00884838099227(21)165, (01)00884838099227(21)1, (01)00884838099227(21)16, (01)00884838099227(21)12, (01)00884838099227(21)257, (01)00884838099227(21)330, (01)00884838099227(21)67, (01)00884838099227(21)260, (01)00884838099227(21)148, (01)00884838099227(21)281, (01)00884838099227(21)248, (01)00884838099227(21)333, (01)00884838099227(21)199, (01)00884838099227(21)183, (01)00884838099227(21)106, (01)00884838099227(21)253, (01)00884838099227(21)52, (01)00884838099227(21)26, (01)00884838099227(21)233, (01)00884838099227(21)301, (01)00884838099227(21)211, (01)00884838099227(21)154, (01)00884838099227(21)217, (01)00884838099227(21)332, (01)00884838099227(21)44, (01)00884838099227(21)198, (01)00884838099227(21)297, (01)00884838099227(21)206, (01)00884838099227(21)292, (01)00884838099227(21)58, (01)00884838099227(21)130, (01)00884838099227(21)203, (01)00884838099227(21)107, (01)00884838099227(21)93, (01)00884838099227(21)125, (01)00884838099227(21)240, (01)00884838099227(21)122, (01)00884838099227(21)118, (01)00884838099227(21)46, (01)00884838099227(21)252, (01)00884838099227(21)184, (01)00884838099227(21)57, (01)00884838099227(21)202, (01)00884838099227(21)100, (01)00884838099227(21)115, (01)00884838099227(21)133, (01)00884838099227(21)350, (01)00884838099227(21)175, (01)00884838099227(21)229, (01)00884838099227(21)304, (01)00884838099227(21)124, (01)00884838099227(21)220, (01)00884838099227(21)79, (01)00884838099227(21)60, (01)00884838099227(21)311, (01)00884838099227(21)147, (01)00884838099227(21)146, (01)00884838099227(21)319, (01)00884838099227(21)74, (01)00884838099227(21)188, (01)00884838099227(21)9, (01)00884838099227(21)8, (01)00884838099227(21)94, (01)00884838099227(21)82, (01)00884838099227(21)86, (01)00884838099227(21)286, (01)00884838099227(21)96, (01)00884838099227(21)227, (01)00884838099227(21)231, (01)00884838099227(21)126, (01)00884838099227(21)162, (01)00884838099227(21)299, (01)00884838099227(21)35, (01)00884838099227(21)11, (01)00884838099227(21)259, (01)00884838099227(21)180, (01)00884838099227(21)160, (01)00884838099227(21)196, (01)00884838099227(21)208, (01)00884838099227(21)282, (01)00884838099227(21)13, (01)00884838099227(21)132, (01)00884838099227(21)209]; 722231 [(01)00884838116740(21)49, (01)00884838116740(21)21, (01)00884838116740(21)34, (01)00884838116740(21)61, (01)00884838116740(21)26, (01)00884838116740(21)28, (01)00884838116740(21)45, (01)00884838116740(21)20, (01)00884838116740(21)51, (01)00884838116740(21)29, (01)00884838116740(21)27, (01)00884838116740(21)35, (01)00884838116740(21)54, (01)00884838116740(21)32]. 4. Model Number [UDI]: 722228 [(01)00884838099234(21)328, (01)00884838099234(21)522, (01)00884838099234(21)187, (01)00884838099234(21)113, (01)00884838099234(21)205, (01)00884838099234(21)567, (01)00884838099234(21)539, (01)00884838099234(21)156, (01)00884838099234(21)308, (01)00884838099234(21)335, (01)00884838099234(21)333, (01)00884838099234(21)570, (01)00884838099234(21)560, (01)00884838099234(21)44, (01)00884838099234(21)569, (01)00884838099234(21)418, (01)00884838099234(21)525, (01)00884838099234(21)280, (01)00884838099234(21)616, (01)00884838099234(21)387, (01)00884838099234(21)568, (01)00884838099234(21)428, (01)00884838099234(21)465, (01)00884838099234(21)556, (01)00884838099234(21)629, (01)00884838099234(21)102, (01)00884838099234(21)178, (01)00884838099234(21)299, (01)00884838099234(21)566, (01)00884838099234(21)508, (01)00884838099234(21)571, (01)00884838099234(21)493, (01)00884838099234(21)1, (01)00884838099234(21)434, (01)00884838099234(21)647, (01)00884838099234(21)317, 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(01)00884838110564(21)273, (01)00884838110564(21)340, (01)00884838110564(21)68, (01)00884838110564(21)151, (01)00884838110564(21)141, (01)00884838110564(21)221, (01)00884838110564(21)33, (01)00884838110564(21)41, (01)00884838110564(21)289, (01)00884838110564(21)59, (01)00884838110564(21)246, (01)00884838110564(21)83, (01)00884838110564(21)10, (01)00884838110564(21)284, (01)00884838110564(21)363, (01)00884838110564(21)177, (01)00884838110564(21)40, (01)00884838110564(21)39, (01)00884838110564(21)43, (01)00884838110564(21)326, (01)00884838110564(21)331, (01)00884838110564(21)57, (01)00884838110564(21)212, (01)00884838110564(21)304, (01)00884838110564(21)122, (01)00884838110564(21)178, (01)00884838110564(21)367, (01)00884838110564(21)323, (01)00884838110564(21)69, (01)00884838110564(21)191, (01)00884838110564(21)50, (01)00884838110564(21)13, (01)00884838110564(21)61, (01)00884838110564(21)194, (01)00884838110564(21)200, (01)00884838110564(21)250, (01)00884838110564(21)251, 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(01)00884838110564(21)385, (01)00884838110564(21)166, (01)00884838110564(21)72, (01)00884838110564(21)274, (01)00884838110564(21)47, (01)00884838110564(21)242, (01)00884838110564(21)324, (01)00884838110564(21)144, (01)00884838110564(21)355, (01)00884838110564(21)158, (01)00884838110564(21)234, (01)00884838110564(21)345, (01)00884838110564(21)22, (01)00884838110564(21)224, (01)00884838110564(21)197, (01)00884838110564(21)206, (01)00884838110564(21)198, (01)00884838110564(21)329, (01)00884838110564(21)249, (01)00884838110564(21)58, (01)00884838110564(21)133, (01)00884838110564(21)263, (01)00884838110564(21)193, (01)00884838110564(21)280, (01)00884838110564(21)118, (01)00884838110564(21)137, (01)00884838110564(21)303, (01)00884838110564(21)375, (01)00884838110564(21)439, (01)00884838110564(21)302, (01)00884838110564(21)103, (01)00884838110564(21)353, (01)00884838110564(21)196, (01)00884838110564(21)139, (01)00884838110564(21)408, (01)00884838110564(21)455, (01)00884838110564(21)173, (01)00884838110564(21)143, (01)00884838110564(21)29, (01)00884838110564(21)239, (01)00884838110564(21)15, (01)00884838110564(21)163, (01)00884838110564(21)437, (01)00884838110564(21)111, (01)00884838110564(21)252, (01)00884838110564(21)230, (01)00884838110564(21)42, (01)00884838110564(21)220, (01)00884838110564(21)213, (01)00884838110564(21)346, (01)00884838110564(21)347, (01)00884838110564(21)411, (01)00884838110564(21)362, (01)00884838110564(21)184, (01)00884838110564(21)185, (01)00884838110564(21)31, (01)00884838110564(21)30, (01)00884838110564(21)25, (01)00884838110564(21)106, (01)00884838110564(21)142, (01)00884838110564(21)128, (01)00884838110564(21)36, (01)00884838110564(21)84, (01)00884838110564(21)16, (01)00884838110564(21)431, (01)00884838110564(21)475, (01)00884838110564(21)257, (01)00884838110564(21)243, (01)00884838110564(21)241, (01)00884838110564(21)262, (01)00884838110564(21)165, (01)00884838110564(21)464, (01)00884838110564(21)147, (01)00884838110564(21)248, (01)00884838110564(21)288]. 5. Model Number [UDI]: 722067 [(01)00884838085350(21)128, (01)00884838085350(21)270, (01)00884838085350(21)251, (01)00884838085350(21)222, (01)00884838085350(21)262, (01)00884838085350(21)274, (01)00884838085350(21)218, (01)00884838085350(21)275, (01)00884838085350(21)127, (01)00884838085350(21)211, (01)00884838085350(21)212, (01)00884838085350(21)213, (01)00884838085350(21)210, (01)00884838085350(21)138, (01)00884838085350(21)254, (01)00884838085350(21)142, (01)00884838085350(21)60, (01)00884838085350(21)97, (01)00884838085350(21)45, (01)00884838085350(21)112, (01)00884838085350(21)134, (01)00884838085350(21)101, (01)00884838085350(21)100, (01)00884838085350(21)168, (01)00884838085350(21)235, (01)00884838085350(21)273, (01)00884838085350(21)176, (01)00884838085350(21)156, (01)00884838085350(21)276, (01)00884838085350(21)165, (01)00884838085350(21)25, (01)00884838085350(21)35, (01)00884838085350(21)202, (01)00884838085350(21)32, (01)00884838085350(21)38, (01)00884838085350(21)87, (01)00884838085350(21)56]; 722225 [(01)00884838099265(21)455, (01)00884838099265(21)284, (01)00884838099265(21)251, (01)00884838099265(21)468, (01)00884838099265(21)232, (01)00884838099265(21)230, (01)00884838099265(21)269, (01)00884838099265(21)345, (01)00884838099265(21)374, (01)00884838099265(21)241, (01)00884838099265(21)431, (01)00884838099265(21)450, (01)00884838099265(21)152, (01)00884838099265(21)145, (01)00884838099265(21)306, (01)00884838099265(21)140, (01)00884838099265(21)457, (01)00884838099265(21)314, (01)00884838099265(21)421, (01)00884838099265(21)422, (01)00884838099265(21)158, (01)00884838099265(21)267, (01)00884838099265(21)454, (01)00884838099265(21)438, (01)00884838099265(21)366, (01)00884838099265(21)173, (01)00884838099265(21)146, (01)00884838099265(21)196, (01)00884838099265(21)372, (01)00884838099265(21)254, (01)00884838099265(21)343, (01)00884838099265(21)201, (01)00884838099265(21)350, (01)00884838099265(21)373, (01)00884838099265(21)4, (01)00884838099265(21)385, (01)00884838099265(21)384, (01)00884838099265(21)214, (01)00884838099265(21)395, (01)00884838099265(21)427, (01)00884838099265(21)439, (01)00884838099265(21)133, (01)00884838099265(21)346, (01)00884838099265(21)471, (01)00884838099265(21)472, (01)00884838099265(21)253, (01)00884838099265(21)326, (01)00884838099265(21)252, (01)00884838099265(21)351, (01)00884838099265(21)309, (01)00884838099265(21)349, (01)00884838099265(21)342, (01)00884838099265(21)7, (01)00884838099265(21)159, (01)00884838099265(21)348, (01)00884838099265(21)17, (01)00884838099265(21)226, (01)00884838099265(21)114]; 722235 [(01)00884838116788(21)4, (01)00884838116788(21)3]. 6. Model Number [UDI]: 722068 [(01)00884838085367(21)455, (01)00884838085367(21)330, (01)00884838085367(21)608, (01)00884838085367(21)302, (01)00884838085367(21)126, (01)00884838085367(21)468, (01)00884838085367(21)410, (01)00884838085367(21)548, (01)00884838085367(21)495, (01)00884838085367(21)537, (01)00884838085367(21)237, (01)00884838085367(21)236, (01)00884838085367(21)307, (01)00884838085367(21)577, (01)00884838085367(21)325, (01)00884838085367(21)480, (01)00884838085367(21)53, (01)00884838085367(21)491, (01)00884838085367(21)423, (01)00884838085367(21)614, (01)00884838085367(21)142, (01)00884838085367(21)376, (01)00884838085367(21)539, (01)00884838085367(21)140, (01)00884838085367(21)369, (01)00884838085367(21)97, (01)00884838085367(21)87, (01)00884838085367(21)303, (01)00884838085367(21)48, (01)00884838085367(21)550, (01)00884838085367(21)551, (01)00884838085367(21)448, (01)00884838085367(21)160, (01)00884838085367(21)83, (01)00884838085367(21)68, (01)00884838085367(21)434, 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(01)00884838085367(21)397, (01)00884838085367(21)180, (01)00884838085367(21)269, (01)00884838085367(21)268, (01)00884838085367(21)414, (01)00884838085367(21)562, (01)00884838085367(21)115, (01)00884838085367(21)291, (01)00884838085367(21)532, (01)00884838085367(21)533, (01)00884838085367(21)618, (01)00884838085367(21)549, (01)00884838085367(21)46, (01)00884838085367(21)249, (01)00884838085367(21)531, (01)00884838085367(21)290, (01)00884838085367(21)125, (01)00884838085367(21)102, (01)00884838085367(21)124, (01)00884838085367(21)145, (01)00884838085367(21)299, (01)00884838085367(21)317, (01)00884838085367(21)90, (01)00884838085367(21)157, (01)00884838085367(21)100, (01)00884838085367(21)186, (01)00884838085367(21)296, (01)00884838085367(21)189]; 722226 [(01)00884838099272(21)209, (01)00884838099272(21)786, (01)00884838099272(21)814, (01)00884838099272(21)469, (01)00884838099272(21)219, (01)00884838099272(21)987, (01)00884838099272(21)880, (01)00884838099272(21)509, 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(01)00884838099272(21)745, (01)00884838099272(21)1033, (01)00884838099272(21)791, (01)00884838099272(21)591, (01)00884838099272(21)878, (01)00884838099272(21)86, (01)00884838099272(21)7, (01)00884838099272(21)768, (01)00884838099272(21)664, (01)00884838099272(21)85, (01)00884838099272(21)53, (01)00884838099272(21)52, (01)00884838099272(21)890, (01)00884838099272(21)815, (01)00884838099272(21)943, (01)00884838099272(21)729, (01)00884838099272(21)1079, (01)00884838099272(21)546, (01)00884838099272(21)753, (01)00884838099272(21)844, (01)00884838099272(21)276, (01)00884838099272(21)649, (01)00884838099272(21)618, (01)00884838099272(21)529]; 722236 [(01)00884838116801(21)10, (01)00884838116801(21)29, (01)00884838116801(21)244, (01)00884838116801(21)117, (01)00884838116801(21)201, (01)00884838116801(21)278, (01)00884838116801(21)34, (01)00884838116801(21)222, (01)00884838116801(21)216, (01)00884838116801(21)219, (01)00884838116801(21)156, (01)00884838116801(21)33, (01)00884838116801(21)66, (01)00884838116801(21)165, (01)00884838116801(21)234, (01)00884838116801(21)8, (01)00884838116801(21)102, (01)00884838116801(21)132, (01)00884838116801(21)157, (01)00884838116801(21)168, (01)00884838116801(21)30, (01)00884838116801(21)182, (01)00884838116801(21)27, (01)00884838116801(21)100, (01)00884838116801(21)23, (01)00884838116801(21)130, (01)00884838116801(21)154, (01)00884838116801(21)264, (01)00884838116801(21)128, (01)00884838116801(21)86, (01)00884838116801(21)94, (01)00884838116801(21)160, (01)00884838116801(21)41, (01)00884838116801(21)277, (01)00884838116801(21)240, (01)00884838116801(21)152]. 7. Model Number [UDI]: 722078 [(01)00884838085251(21)465, (01)00884838085251(21)700, (01)00884838085251(21)402, (01)00884838085251(21)360, (01)00884838085251(21)279, (01)00884838085251(21)162, (01)00884838085251(21)986, (01)00884838085251(21)561, (01)00884838085251(21)689, (01)00884838085251(21)499, (01)00884838085251(21)135, (01)00884838085251(21)38, (01)00884838085251(21)476, (01)00884838085251(21)380, (01)00884838085251(21)453, (01)00884838085251(21)24, (01)00884838085251(21)690, (01)00884838085251(21)943, (01)00884838085251(21)898, (01)00884838085251(21)378, (01)00884838085251(21)439, (01)00884838085251(21)628, (01)00884838085251(21)511, (01)00884838085251(21)178, (01)00884838085251(21)266, (01)00884838085251(21)526, (01)00884838085251(21)746, (01)00884838085251(21)264, (01)00884838085251(21)361, (01)00884838085251(21)348, (01)00884838085251(21)897, (01)00884838085251(21)845, (01)00884838085251(21)1036, (01)00884838085251(21)374, (01)00884838085251(21)375, (01)00884838085251(21)564, 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(01)00884838099241(21)1018, (01)00884838099241(21)513, (01)00884838099241(21)345, (01)00884838099241(21)95, (01)00884838099241(21)13, (01)00884838099241(21)927, (01)00884838099241(21)901, (01)00884838099241(21)1224, (01)00884838099241(21)297, (01)00884838099241(21)263, (01)00884838099241(21)539, (01)00884838099241(21)494, (01)00884838099241(21)1260, (01)00884838099241(21)319, (01)00884838099241(21)320, (01)00884838099241(21)586, (01)00884838099241(21)300, (01)00884838099241(21)276, (01)00884838099241(21)493, (01)00884838099241(21)624, (01)00884838099241(21)368, (01)00884838099241(21)394, (01)00884838099241(21)971]; 722233 [(01)00884838116764(21)76, (01)00884838116764(21)12, (01)00884838116764(21)82, (01)00884838116764(21)245, (01)00884838116764(21)141, (01)00884838116764(21)27, (01)00884838116764(21)235, (01)00884838116764(21)117, (01)00884838116764(21)7, (01)00884838116764(21)205, (01)00884838116764(21)204, (01)00884838116764(21)203, (01)00884838116764(21)120, 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Model Number [UDI]: 722079 [(01)00884838085268(21)35, (01)00884838085268(21)43, (01)00884838085268(21)40, (01)00884838085268(21)246, (01)00884838085268(21)420, (01)00884838085268(21)564, (01)00884838085268(21)838, (01)00884838085268(21)47, (01)00884838085268(21)1086, (01)00884838085268(21)877, (01)00884838085268(21)703395, (01)00884838085268(21)716, (01)00884838085268(21)483, (01)00884838085268(21)1392, (01)00884838085268(21)335, (01)00884838085268(21)1410, (01)00884838085268(21)1230, (01)00884838085268(21)703615, (01)00884838085268(21)944, (01)00884838085268(21)1005, (01)00884838085268(21)697, (01)00884838085268(21)621, (01)00884838085268(21)703426, (01)00884838085268(21)360, (01)00884838085268(21)469, (01)00884838085268(21)857, (01)00884838085268(21)34, (01)00884838085268(21)797, (01)00884838085268(21)281, (01)00884838085268(21)939, (01)00884838085268(21)703407, (01)00884838085268(21)866, (01)00884838085268(21)354, (01)00884838085268(21)1361, (01)00884838085268(21)921, 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"company_location": "Brooklyn Park, MN, United States", "date": "2026-04-21", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "Worldwide distribution - US Nationwide and the countries of Australia, Austria, Belgium, Canada, China, Colombia, Costa Rica, Cyprus, Denmark, France, Germany, Hong Kong, Hungary, Italy, Japan, Latvia, Lithuania, Malaysia, Moldova, Republic Of, Morocco, Netherlands, Norway, Panama, Poland, Russia, Serbia, Singapore, South Africa, South Korea, Spain, Suriname, Sweden, Taiwan, Thailand, Turkey, United Arab Emirates, United Kingdom, United States, Uruguay, Vietnam.", "states": [], "nationwide": true, "quantity": "280 units", "codes": "GTIN 20643169454808, Lot Numbers: 0231859673.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2221-2026%22", "url": "https://recallledger.net/recalls/device-z-2221-2026-medtronic-dlp-retrograde-cannula-manual-inflate-silicone-body-15fr/"}, {"id": "fda-device-z-2220-2026", "source": "FDA", "category": "device", "recall_number": "Z-2220-2026", "title": "Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR recall (Medtronic Perfusion Systems)", "product": "Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94913L; Cardiopulmonary bypass vascular catheter", "reason": "Certain lots of product have the potential for a sterile barrier breach.", "hazard_level": "Class II", "company": "Medtronic Perfusion Systems", "company_location": "Brooklyn Park, MN, United States", "date": "2026-04-21", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "Worldwide distribution - US Nationwide and the countries of Australia, Austria, Belgium, Canada, China, Colombia, Costa Rica, Cyprus, Denmark, France, Germany, Hong Kong, Hungary, Italy, Japan, Latvia, Lithuania, Malaysia, Moldova, Republic Of, Morocco, Netherlands, Norway, Panama, Poland, Russia, Serbia, Singapore, South Africa, South Korea, Spain, Suriname, Sweden, Taiwan, Thailand, Turkey, United Arab Emirates, United Kingdom, United States, Uruguay, Vietnam.", "states": [], "nationwide": true, "quantity": "481 units", "codes": "GTIN 00643169454460, Lot Numbers: 0231665646; GTIN 20643169454464, Lot Numbers: 0231665646, 0231665648.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2220-2026%22", "url": "https://recallledger.net/recalls/device-z-2220-2026-medtronic-dlp-retrograde-cannula-manual-inflate-silicone-body-13fr/"}, {"id": "fda-device-z-2219-2026", "source": "FDA", "category": "device", "recall_number": "Z-2219-2026", "title": "Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR recall (Medtronic Perfusion Systems)", "product": "Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94913; Cardiopulmonary bypass vascular catheter", "reason": "Certain lots of product have the potential for a sterile barrier breach.", "hazard_level": "Class II", "company": "Medtronic Perfusion Systems", "company_location": "Brooklyn Park, MN, United States", "date": "2026-04-21", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "Worldwide distribution - US Nationwide and the countries of Australia, Austria, Belgium, Canada, China, Colombia, Costa Rica, Cyprus, Denmark, France, Germany, Hong Kong, Hungary, Italy, Japan, Latvia, Lithuania, Malaysia, Moldova, Republic Of, Morocco, Netherlands, Norway, Panama, Poland, Russia, Serbia, Singapore, South Africa, South Korea, Spain, Suriname, Sweden, Taiwan, Thailand, Turkey, United Arab Emirates, United Kingdom, United States, Uruguay, Vietnam.", "states": [], "nationwide": true, "quantity": "3210 units", "codes": "GTIN 20643169454785, Lot Numbers: 0231757977, 0231757978, 0231757985, 0231758246, 0231758249, 0231758254, 0231758262, 0231772525, 0231792898, 0232066774, 0232112345, 0232114667, C232276641, C232277146, C232277149, C232949860, C232949864.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2219-2026%22", "url": "https://recallledger.net/recalls/device-z-2219-2026-medtronic-dlp-retrograde-cannula-manual-inflate-silicone-body-13fr/"}, {"id": "fda-device-z-2218-2026", "source": "FDA", "category": "device", "recall_number": "Z-2218-2026", "title": "Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall (Medtronic Perfusion Systems)", "product": "Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94725; Cardiopulmonary bypass vascular catheter", "reason": "Certain lots of product have the potential for a sterile barrier breach.", "hazard_level": "Class II", "company": "Medtronic Perfusion Systems", "company_location": "Brooklyn Park, MN, United States", "date": "2026-04-21", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "Worldwide distribution - US Nationwide and the countries of Australia, Austria, Belgium, Canada, China, Colombia, Costa Rica, Cyprus, Denmark, France, Germany, Hong Kong, Hungary, Italy, Japan, Latvia, Lithuania, Malaysia, Moldova, Republic Of, Morocco, Netherlands, Norway, Panama, Poland, Russia, Serbia, Singapore, South Africa, South Korea, Spain, Suriname, Sweden, Taiwan, Thailand, Turkey, United Arab Emirates, United Kingdom, United States, Uruguay, Vietnam.", "states": [], "nationwide": true, "quantity": "2620 units", "codes": "GTIN 00643169454736, Lot Numbers: 0231650787, 0231758255, 0231862812, C231966207; GTIN 00673978188713, Lot Numbers: 0231937422; GTIN 20643169454730, Lot Numbers: 0231650787, 0231650793, 0231758250, 0231758255, 0231758279, 0231758282, 0231823523, 0231862812, 0231937422, C231965721, C231966207, C232428221, C232430086.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2218-2026%22", "url": "https://recallledger.net/recalls/device-z-2218-2026-medtronic-dlp-retrograde-cannula-manual-inflate-silicone-body-15fr/"}, {"id": "fda-device-z-2217-2026", "source": "FDA", "category": "device", "recall_number": "Z-2217-2026", "title": "Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall (Medtronic Perfusion Systems)", "product": "Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94665; Cardiopulmonary bypass vascular catheter", "reason": "Certain lots of product have the potential for a sterile barrier breach.", "hazard_level": "Class II", "company": "Medtronic Perfusion Systems", "company_location": "Brooklyn Park, MN, United States", "date": "2026-04-21", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "Worldwide distribution - US Nationwide and the countries of Australia, Austria, Belgium, Canada, China, Colombia, Costa Rica, Cyprus, Denmark, France, Germany, Hong Kong, Hungary, Italy, Japan, Latvia, Lithuania, Malaysia, Moldova, Republic Of, Morocco, Netherlands, Norway, Panama, Poland, Russia, Serbia, Singapore, South Africa, South Korea, Spain, Suriname, Sweden, Taiwan, Thailand, Turkey, United Arab Emirates, United Kingdom, United States, Uruguay, Vietnam.", "states": [], "nationwide": true, "quantity": "840 units", "codes": "GTIN 00643169454705, Lot Numbers: 0231823435, 0231961203; GTIN 20643169454709, Lot Numbers: 0231823435, 0231823478, 0231961203.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2217-2026%22", "url": "https://recallledger.net/recalls/device-z-2217-2026-medtronic-dlp-retrograde-cannula-manual-inflate-silicone-body-15fr/"}, {"id": "fda-device-z-2216-2026", "source": "FDA", "category": "device", "recall_number": "Z-2216-2026", "title": "Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall (Medtronic Perfusion Systems)", "product": "Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94215T; Cardiopulmonary bypass vascular catheter", "reason": "Certain lots of product have the potential for a sterile barrier breach.", "hazard_level": "Class II", "company": "Medtronic Perfusion Systems", "company_location": "Brooklyn Park, MN, United States", "date": "2026-04-21", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "Worldwide distribution - US Nationwide and the countries of Australia, Austria, Belgium, Canada, China, Colombia, Costa Rica, Cyprus, Denmark, France, Germany, Hong Kong, Hungary, Italy, Japan, Latvia, Lithuania, Malaysia, Moldova, Republic Of, Morocco, Netherlands, Norway, Panama, Poland, Russia, Serbia, Singapore, South Africa, South Korea, Spain, Suriname, Sweden, Taiwan, Thailand, Turkey, United Arab Emirates, United Kingdom, United States, Uruguay, Vietnam.", "states": [], "nationwide": true, "quantity": "600 units", "codes": "GTIN 20643169454556, Lot Numbers: 0231881762, 0231881786, 0231931962, 0231962106, C233032040.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2216-2026%22", "url": "https://recallledger.net/recalls/device-z-2216-2026-medtronic-dlp-retrograde-cannula-manual-inflate-silicone-body-15fr/"}, {"id": "fda-device-z-2215-2026", "source": "FDA", "category": "device", "recall_number": "Z-2215-2026", "title": "Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 15FR recall (Medtronic Perfusion Systems)", "product": "Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94115T; Cardiopulmonary bypass vascular catheter", "reason": "Certain lots of product have the potential for a sterile barrier breach.", "hazard_level": "Class II", "company": "Medtronic Perfusion Systems", "company_location": "Brooklyn Park, MN, United States", "date": "2026-04-21", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "Worldwide distribution - US Nationwide and the countries of Australia, Austria, Belgium, Canada, China, Colombia, Costa Rica, Cyprus, Denmark, France, Germany, Hong Kong, Hungary, Italy, Japan, Latvia, Lithuania, Malaysia, Moldova, Republic Of, Morocco, Netherlands, Norway, Panama, Poland, Russia, Serbia, Singapore, South Africa, South Korea, Spain, Suriname, Sweden, Taiwan, Thailand, Turkey, United Arab Emirates, United Kingdom, United States, Uruguay, Vietnam.", "states": [], "nationwide": true, "quantity": "6572 units", "codes": "GTIN 00643169454521, Lot Numbers: 0231545565, C231958117; GTIN 20643169454525, Lot Numbers: 0231545557, 0231545560, 0231545565, 0231545567, 0231545569, 0231592142, 0231592228, 0231592241, 0231665664, 0231665707, 0231665708, 0231665711, 0231665712, 0231665713, 0231665714, 0231665715, 0231665716, 0231667178, 0231823613, 0231823689, 0231823700, 0231846134, 0231862819, 0231912810, C231958117, C231958118, C231958119, C231958120, C232287623.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2215-2026%22", "url": "https://recallledger.net/recalls/device-z-2215-2026-medtronic-gundry-retrograde-cannula-manual-inflate-silicone-body-15f/"}, {"id": "fda-device-z-2214-2026", "source": "FDA", "category": "device", "recall_number": "Z-2214-2026", "title": "Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 13FR recall (Medtronic Perfusion Systems)", "product": "Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94113T; Cardiopulmonary bypass vascular catheter", "reason": "Certain lots of product have the potential for a sterile barrier breach.", "hazard_level": "Class II", "company": "Medtronic Perfusion Systems", "company_location": "Brooklyn Park, MN, United States", "date": "2026-04-21", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "Worldwide distribution - US Nationwide and the countries of Australia, Austria, Belgium, Canada, China, Colombia, Costa Rica, Cyprus, Denmark, France, Germany, Hong Kong, Hungary, Italy, Japan, Latvia, Lithuania, Malaysia, Moldova, Republic Of, Morocco, Netherlands, Norway, Panama, Poland, Russia, Serbia, Singapore, South Africa, South Korea, Spain, Suriname, Sweden, Taiwan, Thailand, Turkey, United Arab Emirates, United Kingdom, United States, Uruguay, Vietnam.", "states": [], "nationwide": true, "quantity": "3790 units", "codes": "GTIN 00673978188447, Lot Numbers: 0231651336; GTIN 20643169454877, Lot Numbers: 0231651336, 0231651345, 0231651385, 0231651389, 0231651396, 0231667029, 0231667046, 0231757975, 0231758248, 0231758259, 0231936467, 0231982226, 0232274424, C232287618, C232287619, C232287620, C232598550, C232598552.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2214-2026%22", "url": "https://recallledger.net/recalls/device-z-2214-2026-medtronic-gundry-retrograde-cannula-manual-inflate-silicone-body-1/"}, {"id": "fda-device-z-2213-2026", "source": "FDA", "category": "device", "recall_number": "Z-2213-2026", "title": "OneLIF Interbody Cage recall (Novapproach Spine, LLC)", "product": "OneLIF Interbody Cage (REF/Description): 010-107-1007/Small 7 Degree 10mm X 7mm, 010-107-1007-2/Small 7 Degree 10mm X 7mm - Oblique, 010-107-1209/Small 7 Degree 12mm X 9mm, 010-107-1411/Small 7 Degree 14mm X 11mm, 010-107-1613/Small 7 Degree 16mm X 13mm, 010-113-1006/Small, 13 Degree 10mm X 6mm, 010-113-1006-2/Small, 13 Degree, 10mm X 6mm - Oblique, 010-113-1208/Small 13 Degree 12mm X 8mm, 010-113-1410/Small 13 Degree 14mm X 10mm, 010-113-1612/Small 13 Degree 16mm X 12mm, 010-119-1407/19 Degree 14mm X 7mm, 010-119-1609/Small 19 Degree 16mm X 9mm, 010-119-1811/Small 19 Degree 18mm X 11mm, 010-125-1606/Small 25 Degree 16mm X 6mm, 010-125-1808/Small 25 Degree 18mm X 8mm, 010-207-1007/Medium 7 Degree 10mm X 7mm, 010-207-1007-2/Medium 7 Degree 10mm X 7mm - Oblique, 010-207-1209/Medium 7 Degree 12mm X 9mm, 010-207-1411/Medium 7 Degree 14mm X 11mm, 010-207-1613/Medium 7 Degree 16mm X 13mm, 010-213-1206/Medium 13 Degree 12mm X 6mm, 010-213-1408/Medium 13 Degree 14mm X 8mm, 010-213-1610/Medium 13 Degree 16mm X 10mm, 010-213-1812/Medium 13 Degree 18mm X 12mm, 010-219-1406/Medium 19 Degree 14mm X 6mm, 010-219-1608/Medium 19 Degree 16mm X 8mm, 010-219-1810/Medium 19 Degree 18mm X 10mm, 010-225-1807/Medium 25 Degree 18mm X 7mm, 010-225-2009/Medium 25 Degree 20mm X 9mm, 010-307-1006/Large 7 Degree,10mm X 6mm, 010-307-1006-2/Large 7 Degree 10mm X 6mm - Oblique, 010-307-1208/ Large 7 Degree 12mm X 8mm, 010-307-1410/Large 7 Degree 14mm X 10mm, 010-307-1612/Large 7 Degree 16mm X 12mm, 010-313-1205/Large 13 Degree 12mm X 5mm, 010-313-1407/Large 13 Degree 14mm X 7mm, 010-313-1609/Large 13 Degree 16mm X 9mm, 010-313-1811/Large 13 Degree 18mm X 11mm, 010-313-2013/Large 13 Degree 20mm X 13mm, 010-319-1606/Large 19 Degree 16mm X 6mm, 010-319-1808/ Large 19 Degree 18mm X 8mm, 010-319-2010/ Large 19 Degree 20mm X 10mm, 010-325-2007/Large 25 Degree 20mm X 7mm, 010-325-2209/ Large 25 Degree 22mm X 9mm, Implant Kits containing OneLIF Interbody Cages, Name/Kit Family: Kit-OneLIF-10 mm (716)/Kit-OneLIF-10 mm, Kit-OneLIF-10 mm (717)/Kit-OneLIF-10 mm, Kit-OneLIF-10 mm (718)/Kit-OneLIF-10 mm, Kit-OneLIF-10 mm (719)/Kit-OneLIF-10 mm, Kit-OneLIF-10 mm (722)/Kit-OneLIF-10 mm, Kit-OneLIF-10 mm (723)/Kit-OneLIF-10 mm, Kit-OneLIF-10 mm (724)/Kit-OneLIF-10 mm, Kit-OneLIF-10 mm (733)/Kit-OneLIF-10 mm, Kit-OneLIF-10 mm (734)/Kit-OneLIF-10 mm, Kit-OneLIF-10 mm (737)/Kit-OneLIF-10 mm, Kit-OneLIF-10 mm (738)/Kit-OneLIF-10 mm, Kit-OneLIF-10 mm (746)/Kit-OneLIF-10 mm, Kit-OneLIF-10 mm (751)/Kit-OneLIF-10 mm, Kit-OneLIF-10 mm (761)/Kit-OneLIF-10 mm, Kit-OneLIF-10 mm (762)/Kit-OneLIF-10 mm, Kit-OneLIF-10 mm (787)/Kit-OneLIF-10 mm, Kit-OneLIF- IMPOneLIF Implant Kit (701)/Kit-OneLIF-IMP - OneLIF Implant Kit, Kit-OneLIF-IMP - OneLIF Implant Kit (702)/Kit-OneLIF-IMP - OneLIF Implant Kit, Kit-OneLIF-IMP - OneLIF Implant Kit (703) NL/Kit-OneLIF-IMP - OneLIF Implant Kit, Kit-OneLIF-IMP - OneLIF Implant Kit (704)/Kit-OneLIF-IMP - OneLIF Implant Kit, Kit-OneLIF-IMP - OneLIF Implant Kit (705)/Kit-OneLIF-IMP - OneLIF Implant Kit, Kit-OneLIF-IMP - OneLIF Implant Kit (706)/Kit-OneLIF-IMP - OneLIF Implant Kit, Kit-OneLIF-IMP - OneLIF Implant Kit (708)/Kit-OneLIF-IMP - OneLIF Implant Kit, Kit-OneLIF-IMP - OneLIF Implant Kit (709)/Kit-OneLIF-IMP - OneLIF Implant Kit,", "reason": "Intervertebral body fusion system straight inserter failed to properly attach to affected cages, which may result in an inability to securely engage the implant with the inserter, which could lead to procedural delay and/or the need to select an alternative implant.", "hazard_level": "Class II", "company": "Novapproach Spine, LLC", "company_location": "Alachua, FL, United States", "date": "2026-04-23", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "US Nationwide distribution in the states of NY, CT, CA, TX, FL, MI.", "states": ["CA", "CT", "FL", "MI", "NY", "TX"], "nationwide": true, "quantity": "1259", "codes": "REF/UDI-DI/ Cage Lots: 010-107-1007/G07001010710070/ 103003, 105701, 118001, 129301; 010-107-1007-2/G070010107100720/ 114301, 117509, 128703; 010-107-1209/G07001010712090/ 102714, 105702, 117501; 010-107-1411/G07001010714110/ 103019, 105703; 010-107-1613/G07001010716130/ 103020, 105704, 127701; 010-113-1006/G07001011310060/ 103021, 105705, 118002, 129801; 010-113-1006-2/G070010113100620/ 117510, 127716, 114302; 010-113-1208/G07001011312080/ 103022, 105706, 117502, 126902; 010-113-1410/G07001011314100/ 102715, 105707, 127702; 010-113-1612/G07001011316120/ 103023, 105708, 127703; 010-119-1407/G07001011914070/ 103024, 105709, 125101, 128701; 010-119-1609/G07001011916090/ 102716, 105710, 127001; 010-119-1811/G07001011918110/ 103025, 105711, 127003; 010-125-1606/G07001012516060/ 102717, 117901, 127002; 010-125-1808/G07001012518080/ 103005, 117902, 127704; 010-207-1007/G07001020710070/ 102702, 106201, 118003, 125102; 010-207-1007-2/G070010207100720/ 117511, 124106, 127717, 114303; 010-207-1209/G07001020712090/ 102701, 105401, 124101, 127705, 101201; 010-207-1411/G07001020714110/ 105001, 105402, 101203; 010-207-1613/G07001020716130/ 103007, 105403, 124102, 127706; 010-213-1206/G07001021312060/ 105002, 105404, 121202, 124103, 127707, 101204; 010-213-1408/G07001021314080/ 102704, 105405, 121203, 124104, 127708; 010-213-1610/G07001021316100/ 103008, 105406, 130101; 010-213-1812/G07001021318120/ 103009, 105407, 127709; 010-219-1406/G07001021914060/ 102705, 105408, 117503, 119301, 121201, 124105; 010-219-1608/G07001021916080/ 103010, 105409, 121204, 127710; 010-219-1810/G07001021918100/ 103011, 105410, 127711; 010-225-1807/G07001022518070/ 102706, 113701, 117001, 121205; 010-225-2009/G07001022520090/ 103001, 117903, 127004, 127712; 010-307-1006/G07001030710060/ 102707, 106202, 118004, 129302; 010-307-1006-2/G070010307100620/ 117512, 127718, 114304; 010-307-1208/G07001030712080/ 102709, 105601, 117504; 010-307-1410/G07001030714100/ 102710, 105602, 127713; 010-307-1612/G07001030716120/ 103012, 105603, 117505; 010-313-1205/G07001031312050/ 103013, 105604, 117506, 129303; 010-313-1407/G07001031314070/ 102711, 105605, 117507, 124107, 128702, 130102; 010-313-1609/G07001031316090/ 103014, 105606; 010-313-1811/G07001031318110/ 103015, 105607, 127714; 010-313-2013/G07001031320130/ 103016, 105608, 127715; 010-319-1606/G07001031916060/ 102712, 105609, 114905, 117508; 010-319-1808/G07001031918080/ 103017, 105610, 125103; 010-319-2010/G07001031920100/ 103018, 105611, 125104; 010-325-2007/G07001032520070/ 102713, 105612, 121206; 010-325-2209/G07001032522090/ 105613, 121207, 101206, 101207, 101208", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2213-2026%22", "url": "https://recallledger.net/recalls/device-z-2213-2026-onelif-interbody-cage-ref-description-010-107-1007-small-7-degree/"}, {"id": "fda-device-z-2204-2026", "source": "FDA", "category": "device", "recall_number": "Z-2204-2026", "title": "Swan-Ganz Pacing Catheter recall (Becton, Dickinson and Company)", "product": "Swan-Ganz Pacing Catheter, Models: D200F7;", "reason": "Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood loss.", "hazard_level": "Class II", "company": "Becton, Dickinson and Company", "company_location": "Irvine, CA, United States", "date": "2026-04-08", "report_date": "2026-05-27", "status": "Ongoing", "distribution": "Worldwide - US Nationwide distribution including in the states of TX, SC, CT, GA, VA, MO, NM, UT, NJ, CA, FL, PA, IN, TN, WA, KY, MD, WV, MI, MA, NC, MN, NY, AZ, AL, LA, CO, OK, HI, MS, IL, OH, NE, DC, KS, NV, WI, SD, IA, AR, ID, OR, WY, MT, RI, VT, DE, AK, NH, ND, ME, PR and the countries of Japan, Brazil, Colombia, Australia, New Zealand, Poland, Czech Republic, South Africa, Mauritius, Germany, Israel, Iran, Slovakia, Switzerland, Slovenia, Bulgaria, Cyprus, Saudi Arabia, United Arab Emirates (UAE), Kuwait, Malta, Bahrain, Qatar, Hungary, Morocco, Romania, Lebanon, Tunisia, Oman, Turkey, Austria, Belgium, Luxembourg, France, Netherlands, Italy, Spain, Canary Islands, Portugal, United Kingdom, Northern Ireland, Ireland, Denmark, Sweden, Iceland, Norway, Estonia, Finland, Greece, Chile, Puerto Rico, Canada.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", 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"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2202-2026%22", "url": "https://recallledger.net/recalls/device-z-2202-2026-swan-ganz-catheter-models-131f7-131f7p-131f7j-141f7-151f7-834f75/"}, {"id": "fda-food-h-0853-2026", "source": "FDA", "category": "food", "recall_number": "H-0853-2026", "title": "Pure Ground Ingredients-Organic Peppermint Leaf Powder. wholesale bulk recall (Pure Ground Ingredients, Inc.)", "product": "Pure Ground Ingredients-Organic Peppermint Leaf Powder. wholesale bulk; tea/food manufacturers. Closed container stored in a cool settings at ambient/room temperature, free of direct sunlight. Packaging: Box with poly liner. Net wt: total produced 581 lbs. Firm Name/Address: Pure Ground Ingredients; 2535 Business Parkway, Minden NV 89423", "reason": "Product has the potential to be contaminated with Salmonella.", "hazard_level": "Class I", "company": "Pure Ground Ingredients, Inc.", "company_location": "Minden, NV, United States", "date": "2026-04-08", "report_date": "2026-05-20", "status": "Terminated", "distribution": "Distributed to CA.", "states": ["CA"], "nationwide": false, "quantity": "578 lbs (-pack size: boxes 16 @35 lbs and 1@18 lbs)", "codes": "Lot#: PEPO-5234171TZM-PW-858Q, Best if used by: January 2028", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0853-2026%22", "url": "https://recallledger.net/recalls/food-h-0853-2026-pure-ground-ingredients-organic-peppermint-leaf-powder-wholesale-bulk/"}, {"id": "fda-food-h-0781-2026", "source": "FDA", "category": "food", "recall_number": "H-0781-2026", "title": "Kroger HOMESTYLE Cheese AND Garlic CROUTONS recall (Sugar Foods LLC)", "product": "Kroger HOMESTYLE Cheese AND Garlic CROUTONS NET WT 5 OZ (141g) UPC 0 11110 81353 4 DISTRIBUTED BY THE KROGER CO., CINCINNATI, OHIO 45202", "reason": "Possible Salmonella in croutons. The firm was notified by their supplier that the non-fat milk powder used to manufacture the product was recalled due to possible salmonella.", "hazard_level": "Class I", "company": "Sugar Foods LLC", "company_location": "Villa Rica, GA, United States", "date": "2026-04-27", "report_date": "2026-05-20", "status": "Completed", "distribution": "Product was shipped to distribution centers in the following states: IN, TN & WI.", "states": ["IN", "TN", "WI"], "nationwide": false, "quantity": "13,739cs/12/5oz pouches", "codes": "BEST IF USED BY FEB 17 27 BEST IF USED BY FEB 18 27 BEST IF USED BY FEB 27 27 BEST IF USED BY FEB 28 27 BEST IF USED BY MAR 6 27 BEST IF USED BY MAR 9 27 BEST IF USED BY MAR 21 27 BEST IF USED BY APR 1 27 BEST IF USED BY APR 7 27", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0781-2026%22", "url": "https://recallledger.net/recalls/food-h-0781-2026-kroger-homestyle-cheese-and-garlic-croutons-net-wt-5-oz-141g-upc-0-1/"}, {"id": "fda-food-h-0779-2026", "source": "FDA", "category": "food", "recall_number": "H-0779-2026", "title": "Prospector Popcorn brand Belgian Chocolate Toffee flavored popcorn recall (Prospector Popcorn, LLC)", "product": "Prospector Popcorn brand Belgian Chocolate Toffee flavored popcorn; Ingredients: Non-GMO popcorn, brown sugar, corn syrup, butter, vanilla, baking soda, sea salt, white chocolate (sugar, palm kernel fat, skimmed milk powder [12%], emulsifier [lecithins], natural vanilla flavoring), dark chocolate (sugar, palm kernel fat, fat reduced cocoa powder [20%], emulsifiers [lecithins], natural vanilla flavoring), pretzels (flour, water, salt, malt, dextrose, canola oil, yeast, soda), tofee bits (sugar, butter, almonds), coarse sea salt.; CONTAINS: MILK, TREE NUTS (ALMONDS), WHEAT; Produced in a facility that is shared with gluten, nuts, dairy, and soy.; Manufactured by: Prospector Popcord, LLC, Ridgefield, CT 06877; UPC: 850073852125", "reason": "Products contain undeclared soy, specifically soy lecithin.", "hazard_level": "Class II", "company": "Prospector Popcorn, LLC", "company_location": "Ridgefield, CT, United States", "date": "2026-04-28", "report_date": "2026-05-20", "status": "Completed", "distribution": "CT and NY", "states": ["CT", "NY"], "nationwide": false, "quantity": "140 - 3.5 oz bags", "codes": "Expiration dates August 5 - October 24, 2026", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0779-2026%22", "url": "https://recallledger.net/recalls/food-h-0779-2026-prospector-popcorn-brand-belgian-chocolate-toffee-flavored-popcorn-in/"}, {"id": "fda-food-h-0778-2026", "source": "FDA", "category": "food", "recall_number": "H-0778-2026", "title": "Swad Mango Flavored Masala Candy recall (Raja Foods and Vegetables Inc.)", "product": "Swad Mango Flavored Masala Candy", "reason": "Contains undeclared Blue 1", "hazard_level": "Class II", "company": "Raja Foods and Vegetables Inc.", "company_location": "Maspeth, NY, United States", "date": "2026-04-13", "report_date": "2026-05-20", "status": "Terminated", "distribution": "NY, NJ, DE, MA, PA, MD, CT, CA, NH, VT,", "states": ["CA", "CT", "DE", "MA", "MD", "NH", "NJ", "NY", "PA", "VT"], "nationwide": false, "quantity": "205 cases (24 units per case)", "codes": "Lot: RF CA25301 UPC: 5117939557 Use by: APRIL 2027", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0778-2026%22", "url": "https://recallledger.net/recalls/food-h-0778-2026-swad-mango-flavored-masala-candy/"}, {"id": "fda-food-h-0777-2026", "source": "FDA", "category": "food", "recall_number": "H-0777-2026", "title": "Swad Orange Flavored Masala Candy recall (Raja Foods and Vegetables Inc.)", "product": "Swad Orange Flavored Masala Candy", "reason": "Contains undeclared FD&C Yellow 6", "hazard_level": "Class II", "company": "Raja Foods and Vegetables Inc.", "company_location": "Maspeth, NY, United States", "date": "2026-04-13", "report_date": "2026-05-20", "status": "Terminated", "distribution": "NY, NJ, DE, MA, PA, MD, CT, CA, NH, VT,", "states": ["CA", "CT", "DE", "MA", "MD", "NH", "NJ", "NY", "PA", "VT"], "nationwide": false, "quantity": "205 CASES (24 units per case)", "codes": "Lot: RF CA25233 UPC Codes: 5117939577 Use by: FEBRUARY 2027", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0777-2026%22", "url": "https://recallledger.net/recalls/food-h-0777-2026-swad-orange-flavored-masala-candy/"}, {"id": "fda-food-h-0775-2026", "source": "FDA", "category": "food", "recall_number": "H-0775-2026", "title": "Uncle Giuseppe's Marketplace Milk Chocolate Bridge Mix recall (WE R NUTS)", "product": "Uncle Giuseppe's Marketplace Milk Chocolate Bridge Mix, 11 oz Net Wt, packed in clear tamper resistant plastic container. UPC 812235023309. Distributed by: WE R NUTS LLC, 99 Seaview Blvd, Port Washington, NY 11050", "reason": "Contains undeclared allergens (cashews, milk, and soy).", "hazard_level": "Class II", "company": "WE R NUTS", "company_location": "Port Washington, NY, United States", "date": "2026-04-20", "report_date": "2026-05-20", "status": "Ongoing", "distribution": "NY, NJ", "states": ["NJ", "NY"], "nationwide": false, "quantity": "254 (11oz units)", "codes": "Sell By dates range from 9/4/26-11/6/26. UPC: 812235023309", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0775-2026%22", "url": "https://recallledger.net/recalls/food-h-0775-2026-uncle-giuseppe-s-marketplace-milk-chocolate-bridge-mix-11-oz-net-wt/"}, {"id": "fda-food-h-0774-2026", "source": "FDA", "category": "food", "recall_number": "H-0774-2026", "title": "Frederik's by meijer Vanilla Bourbon Trail Mix recall (Ferris Coffee and Nut Company, Inc.)", "product": "Frederik's by meijer Vanilla Bourbon Trail Mix, packed in plastic retail-sized black bag NET WT 9 OZ (255g). On the back of the bag is both lot number and a stamped expiration date. UPC 719283 357212; 12-9oz retail units per case.", "reason": "Undeclared allergens (wheat and soy).", "hazard_level": "Class II", "company": "Ferris Coffee and Nut Company, Inc.", "company_location": "Grand Rapids, MI, United States", "date": "2026-04-21", "report_date": "2026-05-20", "status": "Terminated", "distribution": "Distributed in IL, IN, KY, MI, OH, and WI.", "states": ["IL", "IN", "KY", "MI", "OH", "WI"], "nationwide": false, "quantity": "125 cases (12-9oz retail units/case)", "codes": "lot # 6069-1, expiration date of 12/10/26.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0774-2026%22", "url": "https://recallledger.net/recalls/food-h-0774-2026-frederik-s-by-meijer-vanilla-bourbon-trail-mix-packed-in-plastic-reta/"}, {"id": "fda-food-h-0772-2026", "source": "FDA", "category": "food", "recall_number": "H-0772-2026", "title": "Dakota Honey Company the Honey Flight. 4 Flavors of Spreadable Spun Honey Original -... recall (Dakota Honey Company)", "product": "Dakota Honey Company the Honey Flight. 4 Flavors of Spreadable Spun Honey Original - Salted Caramel - Cinnamon - Jalapeno. UPC 8 60010-57968 8. 4 - 4 oz (340g) jars. Net Wt 16 oz (454g). Produced in Winner, SD.", "reason": "Foreign object (stainless steel dust/flakes or shreds of plastic)", "hazard_level": "Class II", "company": "Dakota Honey Company", "company_location": "Winner, SD, United States", "date": "2026-04-04", "report_date": "2026-05-20", "status": "Ongoing", "distribution": "Retail locations in FL, GA, and SD Internet sales Nationwide", "states": ["FL", "GA", "SD"], "nationwide": true, "quantity": "1897 - 4 oz containers, 286 - 12 oz containers Total.", "codes": "Honey does not have any code on container. 4 oz spun honey Flights purchased from December 19, 2025 to April 3, 2026", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0772-2026%22", "url": "https://recallledger.net/recalls/food-h-0772-2026-dakota-honey-company-the-honey-flight-4-flavors-of-spreadable-spun-h/"}, {"id": "fda-food-h-0771-2026", "source": "FDA", "category": "food", "recall_number": "H-0771-2026", "title": "Dakota Honey Company Spreadable Spun Honey recall (Dakota Honey Company)", "product": "Dakota Honey Company Spreadable Spun Honey, Jalapeno. Stir before use. Produced in Winner, SD. Packaged in the following sized plastic jars: 1. Net Wt 4 oz (113g) UPC 8 60012-41982 1. 2. Net Wt 12 oz (340g) UPC 8 60010-57965 7.", "reason": "Foreign object (stainless steel dust/flakes or shreds of plastic)", "hazard_level": "Class II", "company": "Dakota Honey Company", "company_location": "Winner, SD, United States", "date": "2026-04-04", "report_date": "2026-05-20", "status": "Ongoing", "distribution": "Retail locations in FL, GA, and SD Internet sales Nationwide", "states": ["FL", "GA", "SD"], "nationwide": true, "quantity": "1897 - 4 oz containers, and 286 - 12 oz containers Total.", "codes": "Honey does not have any code on container. 1. 4 oz spun honey purchased from December 19, 2025 to April 3, 2026 2. 12 oz spun honey purchased from February 25, 2026 to April 3, 2026", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0771-2026%22", "url": "https://recallledger.net/recalls/food-h-0771-2026-dakota-honey-company-spreadable-spun-honey-jalapeno-stir-before-use/"}, {"id": "fda-food-h-0770-2026", "source": "FDA", "category": "food", "recall_number": "H-0770-2026", "title": "Dakota Honey Company Spreadable Spun Honey recall (Dakota Honey Company)", "product": "Dakota Honey Company Spreadable Spun Honey, Salted Caramel. Stir before use. Produced in Winner, SD. Packaged in the following sized plastic jars: 1. Net Wt 4 oz (113g) UPC 8 60012-41981 4. 2. Net Wt 12 oz (340g) UPC 8 60010-57964 0.", "reason": "Foreign object (stainless steel dust/flakes or shreds of plastic)", "hazard_level": "Class II", "company": "Dakota Honey Company", "company_location": "Winner, SD, United States", "date": "2026-04-04", "report_date": "2026-05-20", "status": "Ongoing", "distribution": "Retail locations in FL, GA, and SD Internet sales Nationwide", "states": ["FL", "GA", "SD"], "nationwide": true, "quantity": "1897 - 4 oz containers, and 286 - 12 oz containers Total.", "codes": "Honey does not have any code on container. 1. 4 oz spun honey purchased from December 19, 2025 to April 3, 2026 2. 12 oz spun honey purchased from February 25, 2026 to April 3, 2026", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0770-2026%22", "url": "https://recallledger.net/recalls/food-h-0770-2026-dakota-honey-company-spreadable-spun-honey-salted-caramel-stir-befo/"}, {"id": "fda-food-h-0769-2026", "source": "FDA", "category": "food", "recall_number": "H-0769-2026", "title": "Dakota Honey Company Spreadable Spun Honey recall (Dakota Honey Company)", "product": "Dakota Honey Company Spreadable Spun Honey, Cinnamon-Infused. Stir before use. Produced in Winner, SD. Packaged in the following sized plastic jars: 1. Net Wt 4 oz (113g) UPC 8 60012-41980 7. 2. Net Wt 12 oz (340g) UPC 8 60010-57963 3.", "reason": "Foreign object (stainless steel dust/flakes or shreds of plastic)", "hazard_level": "Class II", "company": "Dakota Honey Company", "company_location": "Winner, SD, United States", "date": "2026-04-04", "report_date": "2026-05-20", "status": "Ongoing", "distribution": "Retail locations in FL, GA, and SD Internet sales Nationwide", "states": ["FL", "GA", "SD"], "nationwide": true, "quantity": "1897 - 4 oz containers and 286 - 12 oz containers Total.", "codes": "Honey does not have any code on container. 1. 4 oz spun honey purchased from December 19, 2025 to April 3, 2026 2. 12 oz spun honey purchased from February 25, 2026 to April 3, 2026", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0769-2026%22", "url": "https://recallledger.net/recalls/food-h-0769-2026-dakota-honey-company-spreadable-spun-honey-cinnamon-infused-stir-be/"}, {"id": "fda-food-h-0768-2026", "source": "FDA", "category": "food", "recall_number": "H-0768-2026", "title": "Dakota Honey Company Spreadable Spun Honey recall (Dakota Honey Company)", "product": "Dakota Honey Company Spreadable Spun Honey, Original. Stir before use. Produced in Winner, SD. Packaged in the following sized plastic jars: 1. Net Wt 4 oz (113g) UPC 8 60010-57969 5. 2. Net Wt 12 oz (340g) UPC 8 60010-57961 9.", "reason": "Foreign object (stainless steel dust/flakes or shreds of plastic)", "hazard_level": "Class II", "company": "Dakota Honey Company", "company_location": "Winner, SD, United States", "date": "2026-04-04", "report_date": "2026-05-20", "status": "Ongoing", "distribution": "Retail locations in FL, GA, and SD Internet sales Nationwide", "states": ["FL", "GA", "SD"], "nationwide": true, "quantity": "1897 - 4 oz containers, 286 - 12 oz containers Total.", "codes": "Honey does not have any code on container. 1. 4 oz spun honey purchased from December 19, 2025 to April 3, 2026 2. 12 oz spun honey purchased from February 25, 2026 to April 3, 2026", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0768-2026%22", "url": "https://recallledger.net/recalls/food-h-0768-2026-dakota-honey-company-spreadable-spun-honey-original-stir-before-use/"}, {"id": "fda-drug-d-0547-2026", "source": "FDA", "category": "drug", "recall_number": "D-0547-2026", "title": "Ascend Laboratories recall (Ascend Laboratories, LLC)", "product": "Ascend Laboratories, LLC, Metoprolol Succinate Extended-Release Tablets, USP, 25 mg* Rx Only, Manufactured by: Alkem Laboratories Ltd., India, Distributed by: Ascend Laboratories, LLC, Parsippany, NJ 07054, NDC 67877-590-01.", "reason": "Failed Dissolution Specifications", "hazard_level": "Class II", "company": "Ascend Laboratories, LLC", "company_location": "Bedminster, NJ, United States", "date": "2026-04-27", "report_date": "2026-05-20", "status": "Ongoing", "distribution": "U.S. Nationwide", "states": [], "nationwide": true, "quantity": "17,304 100-count bottles", "codes": "Lot # 25140859; Exp. Date: Jan 2027", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0547-2026%22", "url": "https://recallledger.net/recalls/drug-d-0547-2026-ascend-laboratories-llc-metoprolol-succinate-extended-release-tablet/"}, {"id": "fda-drug-d-0525-2026", "source": "FDA", "category": "drug", "recall_number": "D-0525-2026", "title": "Oasis Tears PF recall (Oasis Medical, Inc.)", "product": "Oasis Tears PF, Preservative-Free Lubricant Eye Drops, 10mL/0.34 Fl OZ Bottle, Sterile, Manufactured for: OASIS Medical, Inc., 514 S. Vermont Ave., Glendora, CA 91741, USA, Made in France, NDC 42126-6400-1.", "reason": "Lack of Assurance of Sterility: The recall is being initiated out of an abundance of caution following FDA observations noted during a recent inspection of Excelvision.", "hazard_level": "Class II", "company": "Oasis Medical, Inc.", "company_location": "Glendora, CA, United States", "date": "2026-04-27", "report_date": "2026-05-20", "status": "Ongoing", "distribution": "Nationwide within the United States", "states": [], "nationwide": true, "quantity": "", "codes": "Lot # 1V59, Exp Date: 05/31/26; Lot # 3V12, 3V69, Exp Date: 08/31/26.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0525-2026%22", "url": "https://recallledger.net/recalls/drug-d-0525-2026-oasis-tears-pf-preservative-free-lubricant-eye-drops-10ml-0-34-fl-oz/"}, {"id": "fda-device-z-2201-2026", "source": "FDA", "category": "device", "recall_number": "Z-2201-2026", "title": "Medtronic SynchroMed Flex Infusion Mode - A810 Clinician Programmer Software Application recall (Medtronic Neuromodulation)", "product": "Medtronic SynchroMed Flex Infusion Mode - A810 Clinician Programmer Software Application, loaded on the following devices: 1. PROG CT900A CLINICIAN TABLET US, Model Number CT900A; 2. PROG CT900B CLINICIAN TABLET EU -UK, Model Number CT900B; 3. PROG CT900C CLINICIAN TABLET UK, Model Number CT900C; 4. PROG CT900D CLINICIAN TABLET GLOBAL, Model Number CT900D; 5. PROG CT900E CLINICIAN TABLET GLBL SMSNG, Model Number CT900E; 6. PROG CT900F CLINICIAN TABLET GLBL SMSNG, Model Number CT900F; implanted programmable infusion pump", "reason": "Software issue: When programming the SynchroMed Pump with the A810 CP App in Flex Infusion Mode, the infusion steps should automatically be arranged in consecutive order, from earliest to latest. However, in rare cases, the steps may be displayed out of order. If this occurs, the programmed Flex Infusion schedule will not be delivered at the intended time, if at all.", "hazard_level": "Class II", "company": "Medtronic Neuromodulation", "company_location": "Minneapolis, MN, United States", "date": "2026-04-08", "report_date": "2026-05-20", "status": "Ongoing", "distribution": "Worldwide distribution.", "states": [], "nationwide": false, "quantity": "10165 units", "codes": "Software application (app) version 1.x and 2.x, loaded on the following units: 1. Model Number CT900A, GTIN 00643169890923, Serial Numbers: NPL0004445; 2. Model Number CT900B, GTIN 00643169890947, Serial Numbers: NPL1000042, NPL1000045, NPL1000046, NPL1000048, NPL1000050, NPL1000051, NPL1000053, NPL1000054, NPL1000059, NPL1000060, NPL1000062, NPL1000065, NPL1000069, NPL1000070, NPL1000071, NPL1000072, NPL1000073, NPL1000074, NPL1000075, NPL1000077, NPL1000081, NPL1000082, NPL1000083, NPL1000085, NPL1000086, NPL1000087, NPL1000090, NPL1000091, NPL1000093, NPL1000094, NPL1000098, NPL1000117, NPL1000133, NPL1000135, NPL1000137, NPL1000138, NPL1000151, NPL1000159, NPL1000160, NPL1000164, NPL1000166, NPL1000167, NPL1000169, NPL1000173, NPL1000174, NPL1000179, NPL1000180, NPL1000183, NPL1000185, NPL1000186, NPL1000187, NPL1000188, NPL1000191, NPL1000192, NPL1000193, NPL1000194, NPL1000195, NPL1000196, NPL1000230, NPL1000235, NPL1000237, NPL1000242, NPL1000244, NPL1000245, NPL1000246, NPL1000248, NPL1000249, NPL1000252, NPL1000254, NPL1000257, NPL1000258, NPL1000281, NPL1000292, NPL1000297, NPL1000301, NPL1000303, NPL1000307, NPL1000321, NPL1000322, NPL1000323, NPL1000325, NPL1000326, NPL1000332, NPL1000334, NPL1000343, NPL1000361, NPL1000362, NPL1000363, NPL1000364, NPL1000365, NPL1000366, NPL1000367, NPL1000369, NPL1000370, NPL1000381, NPL1000483, NPL1000486, NPL1000487, NPL1000501, NPL1000502, NPL1000505, NPL1000506, NPL1000507, NPL1000509, NPL1000510, NPL1000512, NPL1000515, NPL1000516, NPL1000518, NPL1000519, NPL1000528, NPL1000529, NPL1000539, NPL1000540, NPL1000555, NPL1000556, NPL1000558, NPL1000560, NPL1000561, NPL1000562, NPL1000563, NPL1000564, NPL1000571, NPL1000573, NPL1000574, NPL1000575, NPL1000576, NPL1000577, NPL1000578, NPL1000580, NPL1000585, NPL1000592, NPL1000603, NPL1000606, NPL1000612, NPL1000627, NPL1000630, NPL1000631, NPL1000632, NPL1000634, NPL1000637, NPL1000641, NPL1000652, NPL1000653, NPL1001194, NPL1001195, NPL1001201, NPL1001204, NPL1001205, NPL1001206, NPL1001207, NPL1001208, NPL1001210, NPL1001211, NPL1001212, NPL1001216, NPL1001223, NPL1001224, NPL1001225, NPL1001226, NPL1001228, NPL1001229, NPL1001230, NPL1001231, NPL1001235, NPL1001236, NPL1001237, NPL1001238, NPL1001240, NPL1001241, NPL1001243, NPL1001244, NPL1001250, NPL1001251, NPL1001254, NPL1001259, NPL1001264, NPL1001265, NPL1001272, NPL1001273, NPL1001274, NPL1001277, NPL1001282, NPL1001283, NPL1001290, NPL1001291, NPL1001306, NPL1001307, NPL1001313, NPL1001314, NPL1001328, NPL1001330, NPL1001332, NPL1001333, NPL1001334, NPL1001336, NPL1001337, NPL1001339, NPL1001341, NPL1001345, NPL1001349, NPL1001350, NPL1001351, NPL1001353, NPL1001354, NPL1001360, NPL1001361, NPL1001362, NPL1001366, NPL1001367, NPL1001369, NPL1001372, NPL1001375, NPL1001380, NPL1001381, NPL1001385, NPL1001386, NPL1001389, NPL1001398, NPL1001407, NPL1001408, NPL1001410, NPL1001412, NPL1001419, NPL1001421, NPL1001423, NPL1001430, NPL1001431, NPL1001434, NPL1001435, NPL1001436, NPL1001439, NPL1001445, NPL1001449, NPL1001458, NPL1001461, NPL1001464, NPL1001465, NPL1001468, NPL1001482, NPL1001483, NPL1001486, NPL1001499, NPL1001500, NPL1001505, NPL1001507, NPL1001510, NPL1001512, NPL1001513, NPL1001514, NPL1001518, NPL1001520, NPL1001524, NPL1001526, NPL1001531, NPL1001532, NPL1001537, NPL1001539, NPL1001540, NPL1001541, NPL1001542, NPL1001544, NPL1001545, NPL1001546, NPL1001547, NPL1001549, NPL1001550, NPL1001678, NPL1001689, NPL1001694, NPL1001695, NPL1001697, NPL1001699, NPL1001700, NPL1001701, NPL1001702, NPL1001705, NPL1001707, NPL1001708, NPL1001709, NPL1001710, NPL1001711, NPL1001716, NPL1001717, NPL1001723, NPL1001724, NPL1001727, NPL1001728, NPL1001739, NPL1001740, NPL1001741, NPL1001742, NPL1001743, NPL1001744, NPL1001745, NPL1001748, NPL1001749, NPL1001750, NPL1001754, NPL1001755, NPL1001756, NPL1001757, NPL1001759, NPL1001760, NPL1001761, NPL1001763, NPL1001764, NPL1001765, NPL1001766, NPL1001767, NPL1001769, NPL1001770, NPL1001773, NPL1001777, NPL1001784, NPL1001787, NPL1001789, NPL1001792, NPL1001794, NPL1001795, NPL1001797, NPL1001798, NPL1001799, NPL1001800, NPL1001801, NPL1001803, NPL1001804, NPL1001805, NPL1001806, NPL1001811, NPL1001812, NPL1001815, NPL1001816, NPL1001817, NPL1001820, NPL1001823, NPL1001824, NPL1001825, NPL1001829, NPL1001830, NPL1001833, NPL1001841, NPL1001842, NPL1001843, NPL1001844, NPL1001847, NPL1001875, NPL1001876, NPL1001877, NPL1001879, NPL1001880, NPL1001881, NPL1001882, NPL1001884, NPL1001885, NPL1001886, NPL1001887, NPL1001888, NPL1001889, NPL1001891, NPL1001897, NPL1001899, NPL1001900, NPL1001901, NPL1001903, NPL1001904, NPL1001905, NPL1001937, NPL1001940, NPL1001946, NPL1001947, NPL1001948, NPL1001950, NPL1001955, NPL1001957, NPL1001959, NPL1001963, NPL1001966, NPL1001968, NPL1001969, NPL1001970, NPL1001971, NPL1001972, NPL1001973, NPL1001974, NPL1001975, NPL1001976, NPL1001977, NPL1001995, NPL1001996, NPL1002004, NPL1002007, NPL1002010, NPL1002016, NPL1002020, NPL1002021, NPL1002025, NPL1002034, NPL1002035, NPL1002038, NPL1002048, NPL1002049, NPL1002050, NPL1002051, NPL1002053, NPL1002054, NPL1002064, NPL1002065, NPL1002066, NPL1002067, NPL1002068, NPL1002088, NPL1002089, NPL1002090, NPL1002091, NPL1002092, NPL1002093, NPL1002094, NPL1002095, NPL1002124, NPL1002126, NPL1002132, NPL1002137, NPL1002146, NPL1002152, NPL1002190, NPL1002191, NPL1002192, NPL1002194, NPL1002200, NPL1002203, NPL1002211, NPL1002214, NPL1002219, NPL1002221, NPL1002222, NPL1002223, NPL1002224, NPL1002225, NPL1002226, NPL1002227, NPL1002228, NPL1002229, NPL1002230, NPL1002231, NPL1002232, NPL1002233, NPL1002234, NPL1002236, NPL1002238, NPL1002239, NPL1002240, NPL1002243, NPL1002244, NPL1002245, NPL1002246, NPL1002247, NPL1002254, NPL1002255, NPL1002256, NPL1002311, NPL1002312, NPL1002313, NPL1002316, NPL1002324, NPL1002329, NPL1002330, NPL1002334, NPL1002335, NPL1002337, NPL1002338, NPL1002339, NPL1002340, NPL1002341, NPL1002342, NPL1002343, NPL1002344, NPL1002347, NPL1002349, NPL1002355, NPL1002356, NPL1002357, NPL1002358, NPL1002359, NPL1002360, NPL1002361, NPL1002362, NPL1002363, NPL1002364, NPL1002367, NPL1002368, NPL1002369, NPL1002370, NPL1002371, NPL1002373, NPL1002375, NPL1002380, NPL1002381, NPL1002382, NPL1002383, NPL1002386, NPL1002392, NPL1002396, NPL1002399, NPL1002401, NPL1002405, NPL1002408, NPL1002409, NPL1002410, NPL1002411, NPL1002412, NPL1002413, NPL1002414, NPL1002415, NPL1002416, NPL1002417, NPL1002418, NPL1002421, NPL1002427, NPL1002428, NPL1002431, NPL1002436, NPL1002438, NPL1002443, NPL1002445, NPL1002460, NPL1002461, NPL1002462, NPL1002464, NPL1002465, NPL1002466, NPL1002467, NPL1002470, NPL1002471, NPL1002474, NPL1002482, NPL1002484, NPL1002490, NPL1002491, NPL1002495, NPL1002496, NPL1002499, NPL1002500, NPL1002501, NPL1002502, NPL1002503, NPL1002505, NPL1002508, NPL1002521, NPL1002530, NPL1002537, NPL1002540, NPL1002544, NPL1002545, NPL1002548, NPL1002549, NPL1002555, NPL1002556, NPL1002557, NPL1002564, NPL1002567, NPL1002568, NPL1002572, NPL1002592, NPL1002593, NPL1002594, NPL1002595, NPL1002596, NPL1002613, NPL1002616, NPL1002617, NPL1002618, NPL1002620, NPL1002626, NPL1002628, NPL1002630, NPL1002631, NPL1002632, NPL1002636, NPL1002637, NPL1002638, NPL1002639, NPL1002640, NPL1002642, NPL1002646, NPL1002648, NPL1002650, NPL1002651, NPL1002652, NPL1002653, NPL1002654, NPL1002656, NPL1002659, NPL1002661, NPL1002666, NPL1002668, NPL1002669, NPL1002671, NPL1002673, NPL1002677, NPL1002679, NPL1002684, NPL1002685, NPL1002686, NPL1002687, NPL1002689, NPL1002690, NPL1002693, NPL1002695, NPL1002696, NPL1002698, NPL1002706, NPL1002709, NPL1002710, NPL1002711, NPL1002712, NPL1002714, NPL1002718, NPL1002719, NPL1002720, NPL1002721, NPL1002728, NPL1002729, NPL1002730, NPL1002731, NPL1002732, NPL1002733, NPL1002735, NPL1002736, NPL1002737, NPL1002739, NPL1002740, NPL1002741, NPL1002743, NPL1002753, NPL1002756, NPL1002757, NPL1002760, NPL1002761, NPL1002778, NPL1002779, NPL1002780, NPL1002781, NPL1002784, NPL1002786, NPL1002787, NPL1002789, NPL1002791, NPL1002792, NPL1002794, NPL1002796, NPL1002800; 3. Model Number CT900C, GTIN 00643169890961, Serial Numbers: NPL1000429, NPL1000430, NPL1000442, NPL1000443, NPL1000444, NPL1000445, NPL1000446, NPL1000447, NPL1000448, NPL1000451, NPL1000453, NPL1000771, NPL1000774, NPL1000776, NPL1000777, NPL1000780, NPL1000781, NPL1000794, NPL1000795, NPL1000797, NPL1000798, NPL1000799, NPL1000802, NPL1000804, NPL1000805, NPL1000806, NPL1000808, NPL1000809, NPL1000810, NPL1000811, NPL1000813, NPL1000814, NPL1000815, NPL1000817, NPL1000818, NPL1000819, NPL1000827, NPL1000830, NPL1000832, NPL1000833, NPL1000834, NPL1000835, NPL1000838, NPL1000845, NPL1000847, NPL1000854, NPL1000855, NPL1000858, NPL1001552, NPL1001562, NPL1001564, NPL1001565, NPL1001566, NPL1001570, NPL1001571, NPL1001574, NPL1001582, NPL1001583, NPL1001588, NPL1001590, NPL1001591, NPL1001592, NPL1001594, NPL1001595, NPL1001596, NPL1001601, NPL1001602, NPL1001605, NPL1001606, NPL1001607, NPL1001608, NPL1001609, NPL1001610, NPL1001611, NPL1001615, NPL1001617, NPL1001618, NPL1001620, NPL1001621, NPL1001627, NPL1001629, NPL1001630, NPL1001631, NPL1001632, NPL1001637, NPL1001638, NPL1001644, NPL1001645, NPL1001647, NPL1001649, NPL1001650, NPL1001651, NPL1001652, NPL1001656, NPL1001657, NPL1001670, NPL1001673, NPL1001675, NPL1002257, NPL1002259, NPL1002260, NPL1002262, NPL1002264, NPL1002265, NPL1002266, NPL1002267, NPL1002268, NPL1002275, NPL1002279, NPL1002280, NPL1002281, NPL1002282, NPL1002284, NPL1002285, NPL1002286, NPL1002288, NPL1002294, NPL1002295, NPL1002297, NPL1002298, NPL1002306, NPL1002307, NPL1002308, NPL1002309, NPL1002310; 4. Model Number CT900D, (1) GTIN 00763000077730, Serial Numbers: NPL3000277, NPL3000278, NPL3000279, NPL3000280, NPL3000281, NPL3000282, NPL3000283, NPL3000285, NPL3000290, NPL3000292, NPL3000293, NPL3000298, NPL3000299, NPL3000300, NPL3000301, NPL3000304, NPL3000305, NPL3000309, NPL3000310, NPL3000312, NPL3000460, NPL3000555, NPL3000563, NPL3000582, NPL3000590, NPL3000591, NPL3002090, NPL3002102, NPL3002311, NPL3002312, NPL3002313, NPL3002314, NPL3002315, NPL3002316, NPL3002318, NPL3002760, NPL3002761, NPL3002762, NPL3002763, NPL3002816, NPL3002995, NPL3002997, NPL3002998, NPL3002999, NPL3003000, NPL3003001, NPL3003002, NPL3003003, NPL3003004, NPL3003005, NPL3003009, NPL3003010, NPL3003011, NPL3003012, NPL3003013, NPL3003014, NPL3003015, NPL3003016, NPL3003018, NPL3003021, NPL3003022, NPL3003023, NPL3003024, NPL3003026, NPL3003028, NPL3003029, NPL3003030, NPL3003031, NPL3003032, NPL3003036, NPL3003037, NPL3003038, NPL3003042, NPL3003046, NPL3003048, NPL3003050, NPL3003051, NPL3003054, NPL3003059, NPL3003060, NPL3003062, NPL3003065, NPL3003067, NPL3003068, NPL3003070, NPL3003072, NPL3003073, NPL3003074, NPL3003076, NPL3003077, NPL3003078, NPL3003086, NPL3003260, NPL3003267, NPL3003268, NPL3003271, NPL3003275, NPL3003277, NPL3003280, NPL3003282, NPL3003283, NPL3003284, NPL3003402, NPL3003409, NPL3003412, NPL3003413, NPL3003415, NPL3003416, NPL3003417, NPL3003418, NPL3003419, NPL3003420, NPL3003422, NPL3003423, NPL3003425, NPL3003427, NPL3003513, NPL3003517, NPL3003518, NPL3003521, NPL3003524, NPL3003528, NPL3003529, NPL3003530, NPL3003532, NPL3003533, NPL3003534, NPL3003535, NPL3003536, NPL3003537, NPL3003538, NPL3003539, NPL3003540, NPL3003542, NPL3003543, NPL3003544, NPL3003545, NPL3003546, NPL3003547, NPL3003548, NPL3003549, NPL3003551, NPL3003552, NPL3003558, NPL3003560, NPL3003566, NPL3003567, NPL3003569, NPL3003570, NPL3003576, NPL3003577, NPL3003578, NPL3003579, NPL3003580, NPL3003581, NPL3003598, NPL3003599, NPL3003601, NPL3003745, NPL3003756, NPL3003766, NPL3003817, NPL3003821, NPL3003823, NPL3003824, NPL3003850, NPL3003885, NPL3003886, NPL3003887, NPL3003890, NPL3003891, NPL3003892, NPL3003893, NPL3003894, NPL3003895, NPL3003896, NPL3003897, NPL3003899, NPL3003900, NPL3003901, NPL3003904, NPL3003905, NPL3003906, NPL3003907, NPL3003921, NPL3003923, NPL3003924, NPL3003929, NPL3003943, NPL3003944, NPL3003951, NPL3003952, NPL3003954, NPL3004050, NPL3004052, NPL3004053, NPL3004057, NPL3004061, NPL3004062, NPL3004063, NPL3004064, NPL3004066, NPL3004067, NPL3004068, NPL3004069, NPL3004071, NPL3004072, NPL3004076, NPL3004078, NPL3004081, NPL3004082, NPL3004087, NPL3004095, NPL3004096, NPL3004102, NPL3004114, NPL3004117, NPL3004118, NPL3004139, NPL3004140, NPL3004141, NPL3004143, NPL3004144, NPL3004145, NPL3004146, NPL3004148, NPL3004149, NPL3004151, NPL3004152, NPL3004153, NPL3004340, NPL3004342, NPL3004344, NPL3004345, NPL3004352, NPL3004353, NPL3004417, NPL3004421, NPL3004436, NPL3004793, NPL3004841, NPL3004860, NPL3004871, NPL3004879, NPL3004895, NPL3004897, NPL3004905, NPL3004910, NPL3004913, NPL3004914, NPL3004918, NPL3004925, NPL3004942, NPL3004951, NPL3004952, NPL3004960, NPL3004969, NPL3004971, NPL3004992, NPL3005006, NPL3005009, NPL3005010, NPL3005018, NPL3005025, NPL3005033, NPL3005044, NPL3005053, NPL3005054, NPL3005059, NPL3005060, NPL3005061, NPL3005065, NPL3005075, NPL3005136, NPL3005187, NPL3005199, NPL3005750, NPL3005752, NPL3005760, NPL3005769, NPL3005773, NPL3005779, NPL3005782, NPL3005783, NPL3005785, NPL3005790, NPL3005799, NPL3005801, NPL3005811, NPL3005814, NPL3005817, NPL3005818, NPL3005866, NPL3005876, NPL3005889, NPL3005893, NPL3006002, NPL3006011, NPL3006027, NPL3006033, NPL3006069, NPL3006072, NPL3006084, NPL3006132, NPL3006142, NPL3006146, NPL3006147, NPL3006148, NPL3006151, NPL3006152, NPL3006153, NPL3006155, NPL3006160, NPL3006161, NPL3006167, NPL3006168, NPL3006176, NPL3006179, NPL3006181, NPL3006188, NPL3006189, NPL3006190, NPL3006192, NPL3006194, NPL3006198, NPL3006203, NPL3006205, NPL3006209, NPL3006213, NPL3006217, NPL3006221, NPL3006225, NPL3006230, NPL3006237, NPL3006238, NPL3006242, NPL3006245, NPL3006247, NPL3006248, NPL3006249, NPL3006250, NPL3006253, NPL3006254, NPL3006255, NPL3006267, NPL3006279, NPL3006280, NPL3006289, NPL3006305, NPL3006309, NPL3006310, NPL3006312, NPL3006359, NPL3006360, NPL3006361, NPL3006366, NPL3006372, NPL3006374, NPL3006375, NPL3006377, NPL3006379, NPL3006380, NPL3006381, NPL3006389, NPL3006391, NPL3006392, NPL3006393, NPL3006394, NPL3006399, NPL3006400, NPL3006406, NPL3006407, NPL3006408, NPL3006410, NPL3006413, NPL3006414, NPL3006416, NPL3006417, NPL3006433, NPL3006443, NPL3006445, NPL3006446, NPL3006448, NPL3006449, NPL3006450, NPL3006452, NPL3006453, NPL3006454, NPL3006457, NPL3006458, NPL3006461, NPL3006465, NPL3006468, NPL3006469, NPL3006475, NPL3006476, NPL3006485, NPL3006486, NPL3006487, NPL3006489, NPL3006490, NPL3006491, NPL3006492, NPL3006494, NPL3006495, NPL3006496, NPL3006498, NPL3006513, NPL3006516, NPL3006518, NPL3006519, NPL3006520, NPL3006522, NPL3006523, NPL3006524, NPL3006525, NPL3006526, NPL3006527, NPL3006531, NPL3006532, NPL3006533, NPL3006534, NPL3006536, NPL3006572, NPL3006581, NPL3006586, NPL3006587, NPL3006600, NPL3006601, NPL3006602, NPL3006604, NPL3006605, NPL3006608, NPL3006612, NPL3006620, NPL3006625, NPL3006626, NPL3006627, NPL3006634, NPL3006825, NPL3006827, NPL3006885, NPL3006886, NPL3006887, NPL3006888, NPL3006889, NPL3006900, NPL3006902, NPL3006904, NPL3006909, NPL3006911, NPL3006917, NPL3006918, NPL3006920, NPL3006921, NPL3006922, NPL3006923, NPL3006924, NPL3006930, NPL3006932, NPL3006933, NPL3006934, NPL3006936, NPL3006938, NPL3006944, NPL3006946, NPL3006947, NPL3006948, NPL3006949, NPL3006950, NPL3006951, NPL3006952, NPL3006953, NPL3006954, NPL3006955, NPL3006962, NPL3006963, NPL3006964, NPL3006966, NPL3006967, NPL3006968, NPL3006971, NPL3006972, NPL3006974, NPL3006977, NPL3006979, NPL3006982, NPL3006983, NPL3006985, NPL3006986, NPL3007004, NPL3007011, NPL3007012, NPL3007053, NPL3007268, NPL3007269, NPL3007272, NPL3007273, NPL3007274, NPL3007276, NPL3007277, NPL3007362, NPL3007363, NPL3007365, NPL3007366, NPL3007367, NPL3007368, NPL3007370, NPL3007371, NPL3007372, NPL3007384, NPL3007385, NPL3007393, NPL3007439, NPL3007451, NPL3007453, NPL3007455, NPL3007456, NPL3007457, NPL3007458, NPL3007464, NPL3007465, NPL3007583, NPL3007584, NPL3007585, NPL3007589, NPL3007592, NPL3007593, NPL3007594, NPL3007596, NPL3007601, NPL3007605, NPL3007608, NPL3007611, NPL3007617, NPL3007619, NPL3007621, NPL3007672, NPL3007677, NPL3007679, NPL3007685, NPL3007688, NPL3007776, NPL3007867, NPL3007869, NPL3007873, NPL3007875, NPL3007877, NPL3007878, NPL3007886, NPL3007887, NPL3007889, NPL3007890, NPL3007895, NPL3007900, NPL3007901, NPL3007904, NPL3007907, NPL3007908, NPL3007909, NPL3007910, NPL3007914, NPL3007916, NPL3007917, NPL3007918, NPL3007921, NPL3007924, NPL3007926, NPL3007927, NPL3007929, NPL3007930, NPL3007937, NPL3007947, NPL3007948, NPL3008029, NPL3008031, NPL3008033, NPL3008034, NPL3008036, NPL3008039, NPL3008046, NPL3008048, NPL3008053, NPL3008058, NPL3008068, NPL3010566, NPL3010568, NPL3010569, NPL3010570, NPL3010573, NPL3010578, NPL3010588, NPL3010593, NPL3010607, NPL3010628, NPL3010629, NPL3010631, NPL3010642, NPL3010645, NPL3010647, NPL3010652, NPL3010653, NPL3010658, NPL3010660, NPL3010665, NPL3010683, NPL3010688, NPL3010690, NPL3010691, NPL3010692, NPL3010782, NPL3010784, NPL3010786, NPL3010793, NPL3010800, NPL3010806, NPL3010817, NPL3010820, NPL3010824, NPL3010828, NPL3010829, NPL3010831, NPL3010833, NPL3010835, NPL3010866, NPL3010874, NPL3010876, NPL3010877, NPL3010879, NPL3010880, NPL3010887, NPL3010891, NPL3010892, NPL3010901, NPL3010902, NPL3010904, NPL3010907, NPL3010908, NPL3010910, NPL3010911, NPL3010914, NPL3010915, NPL3010927, NPL3010928, NPL3010934, NPL3010940, NPL3010945, NPL3010946, NPL3010953, NPL3010954, NPL3010955, NPL3010958, NPL3010968, NPL3010991, NPL3010996, NPL3010997, NPL3010998, NPL3011008, NPL3011104, NPL3011106, NPL3011107, NPL3011108, NPL3011109, NPL3011113, NPL3011169, NPL3011217, NPL3011219, NPL3011221, NPL3011224, NPL3011226, NPL3011227, NPL3011228, NPL3011234, NPL3011235, NPL3011236, NPL3011239, NPL3011240, NPL3011241, NPL3011242, NPL3011243, NPL3011244, NPL3011245, NPL3011246, NPL3011247, NPL3011249, NPL3011267, NPL3011269, NPL3011286, NPL3011287, NPL3011367, NPL3011426, NPL3011427, NPL3011428, NPL3011429, NPL3011430, NPL3011434, NPL3011435, NPL3011436, NPL3011437, NPL3011445, NPL3011446, NPL3011447, NPL3011448, NPL3011449, NPL3011452, NPL3011459, NPL3011460, NPL3011462, NPL3011463, NPL3011481, NPL3011482, NPL3011485, NPL3011487, NPL3011489, NPL3011490, NPL3011568, NPL3011569, NPL3011572, NPL3011573, NPL3011574, NPL3011575, NPL3011587, NPL3011589, NPL3011590, NPL3011600, NPL3011602, NPL3011605, NPL3011606, NPL3011607, NPL3011632, NPL3011633, NPL3011637, NPL3011639, NPL3011651, NPL3011652, NPL3011653, NPL3011656, NPL3011701, NPL3011703, NPL3011704, NPL3011705, NPL3011706, NPL3011707, NPL3011708, NPL3011709, NPL3011716, NPL3011718, NPL3011719, NPL3011720, NPL3011725, NPL3011734, NPL3011738, NPL3011739, NPL3011741, NPL3011749, NPL3011750, NPL3011753, NPL3011754, NPL3011756, NPL3011757, NPL3011762, NPL3013178, NPL3013655, NPL3013656, NPL3013665, NPL3013669, NPL3013670, NPL3013671, NPL3013674, NPL3013675, NPL3013676, NPL3013679, NPL3013680, NPL3013683, NPL3013684, NPL3013687, NPL3013699, NPL3013702, NPL3013712, NPL3013713, NPL3013714, NPL3013715, NPL3013717, NPL3013719, NPL3013721, NPL3013740, NPL3013743, NPL3013746, NPL3013748, NPL3013751, NPL3013754, NPL3013755, NPL3013758, NPL3013759, NPL3013760, NPL3013762, NPL3013763, NPL3013764, NPL3013766, NPL3013767, NPL3013768, NPL3013769, NPL3013773, NPL3013781, NPL3013783, NPL3013786, NPL3013795, NPL3013796, NPL3013797, NPL3013798, NPL3013799, NPL3013817, NPL3013818, NPL3013819, NPL3013821, NPL3013825, NPL3013826, NPL3013827, NPL3013830, NPL3013856, NPL3013857, NPL3013858, NPL3013860, NPL3013861, NPL3013862, NPL3013863, NPL3013864, NPL3013865, NPL3013871, NPL3013875, NPL3013876, NPL3013877, NPL3013878, NPL3013879, NPL3013890, NPL3013895, NPL3013896, NPL3013897, NPL3013901, NPL3013903, NPL3013904, NPL3013905, NPL3013906, NPL3013913, NPL3013916, NPL3013920, NPL3013923, NPL3013931, NPL3013932, NPL3013933, NPL3013935, NPL3013936, NPL3013937, NPL3013938, NPL3013939, NPL3013940, NPL3013941, NPL3013942, NPL3013943, NPL3013944, NPL3013949, NPL3013952, NPL3013953, NPL3013954, NPL3013960, NPL3013961, NPL3013962, NPL3013963, NPL3013964, NPL3013965, NPL3013966, NPL3013967, NPL3013969, NPL3013970, NPL3013971, NPL3013979, NPL3014238, NPL3014289, NPL3014291, NPL3014296, NPL3014297, NPL3014298, NPL3014299, NPL3014304, NPL3014307, NPL3014309, NPL3014311, NPL3014315, NPL3014317, NPL3014319, NPL3014321, NPL3014322, NPL3014323, NPL3014324, NPL3014326, NPL3014328, NPL3014330, NPL3014334, NPL3014335, NPL3014340, NPL3014343, NPL3014344, NPL3014457, NPL3014459, NPL3014462, NPL3014466, NPL3014467, NPL3014468, NPL3014521, NPL3014522, NPL3014526, NPL3014543, NPL3014544, NPL3014546, NPL3014573, NPL3014574, NPL3014575, NPL3014580, NPL3014584, NPL3014586, NPL3014588, NPL3014629, NPL3014630, NPL3014638, NPL3014770, NPL3014771, NPL3014772, NPL3014773, NPL3014774, NPL3014775, NPL3014776, NPL3014777, NPL3014778, NPL3014782, NPL3014784, NPL3014785, NPL3014788, NPL3014789, NPL3014791, NPL3014792, NPL3014793, NPL3014794, NPL3014796, NPL3014798, NPL3014799, NPL3014800, NPL3014869, NPL3014886, NPL3014887, NPL3014888, NPL3014889, NPL3014891, NPL3014892, NPL3014895, NPL3014971, NPL3014974, NPL3014975, NPL3014976, NPL3014977, NPL3014978, NPL3014980, NPL3014984, NPL3014988, NPL3014989, NPL3014990, NPL3014991, NPL3014997, NPL3015001, NPL3015005, NPL3015006, NPL3015007, NPL3015008, NPL3015010, NPL3015011, NPL3015014, NPL3015018, NPL3015071, NPL3015072, NPL3015074, NPL3015075, NPL3015076, NPL3015077, NPL3015078, NPL3015079, NPL3015081, NPL3015082, NPL3015083, NPL3015085, NPL3015086, NPL3015087, NPL3015088, NPL3015090, NPL3015091, NPL3015094, NPL3015095, NPL3015096, NPL3015097, NPL3015098, NPL3015099, NPL3015100, NPL3015101, NPL3015105, NPL3015107, NPL3015112, NPL3015113, NPL3015114, NPL3015116, NPL3015127, NPL3015128, NPL3015139, NPL3015140, NPL3015141, NPL3015142, NPL3015143, NPL3015144, NPL3015145, NPL3015146, NPL3015147, NPL3015148, NPL3015149, NPL3015150, NPL3015151, NPL3015152, NPL3015153, NPL3015154, NPL3015155, NPL3015156, NPL3015158, NPL3015160, NPL3015161, NPL3015162, NPL3015165, NPL3015166, NPL3015167, NPL3015168, NPL3015169, NPL3015170, NPL3015171, NPL3015178, NPL3015179, NPL3015184, NPL3015186, NPL3015187, NPL3015188, NPL3015189, NPL3015190, NPL3015261, NPL3015264, NPL3015266, NPL3015267, NPL3015270, NPL3015274, NPL3015275, NPL3015277, NPL3015278, NPL3015279, NPL3015310, NPL3015384, NPL3015385, NPL3015386, NPL3015387, NPL3015388, NPL3015389, NPL3015390, NPL3015391, NPL3015392, NPL3015393, NPL3015394, NPL3015396, NPL3015398, NPL3015399, NPL3015401, NPL3015402, NPL3015403, NPL3015404, NPL3015405, NPL3015406, NPL3015407, NPL3015512, NPL3015559, NPL3015561, NPL3015565; (2) GTIN 00763000094027, Serial Numbers: NPL3000006, NPL3000007, NPL3000009, NPL3000010, NPL3000011, NPL3000012, NPL3000014, NPL3000016, NPL3000017, NPL3000018, NPL3000021, NPL3000023, NPL3000025, NPL3000026, NPL3000029, NPL3000030, NPL3000031, NPL3000033, NPL3000035, NPL3000040, NPL3000043, NPL3000046, NPL3000047, NPL3000048, NPL3000049, NPL3000050, NPL3000055, NPL3000057, NPL3000059, NPL3000062, NPL3000063, NPL3000068, NPL3000071, NPL3000074, NPL3000076, NPL3000077, NPL3000079, NPL3000083, NPL3000093, NPL3000094, NPL3000097, NPL3000103, NPL3000105, NPL3000109, NPL3000111, NPL3000125, NPL3000128, NPL3000129, NPL3000134, NPL3000135, NPL3000143, NPL3000184, NPL3000186, NPL3000188, NPL3000189, NPL3000196, NPL3000197, NPL3000198, NPL3000199, NPL3000202, NPL3000203, NPL3000205, NPL3000206, NPL3000208, NPL3000209, NPL3000210, NPL3000212, NPL3000213, NPL3000214, NPL3000215, NPL3000216, NPL3000219, NPL3000220, NPL3000221, NPL3000222, NPL3000223, NPL3000224, NPL3000226, NPL3000227, NPL3000229, NPL3000230, NPL3000232, NPL3000233, NPL3000236, NPL3000237, NPL3000240, NPL3000241, NPL3000242, NPL3000246, NPL3000248, NPL3000249, NPL3000250, NPL3000252, NPL3000253, NPL3000255, NPL3000258, NPL3000259, NPL3000260, NPL3000261, NPL3000262, NPL3000264, NPL3000265, NPL3002259, NPL3002261, NPL3002262, NPL3002263, NPL3002266, NPL3002270, NPL3002274, NPL3002282, NPL3002284, NPL3002288, NPL3002291, NPL3002293, NPL3002294, NPL3002296, NPL3002300, NPL3002304, NPL3002655, NPL3002659, NPL3002660, NPL3002661, NPL3002662, NPL3002663, NPL3002664, NPL3002665, NPL3002666, NPL3002667, NPL3002668, NPL3002669, NPL3002670, NPL3002671, NPL3002672, NPL3002673, NPL3002674, NPL3002675, NPL3002676, NPL3002677, NPL3002679, NPL3002680, NPL3002681, NPL3002682, NPL3002684, NPL3002685, NPL3002686, NPL3002687, NPL3002688, NPL3002691, NPL3002692, NPL3002693, NPL3002694, NPL3002696, NPL3002697, NPL3002699, NPL3002700, NPL3002701, NPL3002702, NPL3002703, NPL3002704, NPL3002705, NPL3002706, NPL3002707, NPL3002709, NPL3002710, NPL3002711, NPL3002712, NPL3002713, NPL3002715, NPL3002716, NPL3002717, NPL3002718, NPL3002719, NPL3002720, NPL3002721, NPL3002722, NPL3002723, NPL3002724, NPL3002725, NPL3002726, NPL3002727, NPL3002728, NPL3002729, NPL3002730, NPL3002731, NPL3002732, NPL3002733, NPL3002734, NPL3002736, NPL3002737, NPL3002738, NPL3002739, NPL3002741, NPL3002742, NPL3002743, NPL3002745, NPL3002746, NPL3002747, NPL3002749, NPL3002750, NPL3002751, NPL3002752, NPL3002753, NPL3002754, NPL3002755, NPL3002756, NPL3002757, NPL3002872, NPL3002873, NPL3002874, NPL3002875, NPL3002877, NPL3002878, NPL3002879, NPL3002880, NPL3002881, NPL3002882, NPL3002883, NPL3002884, NPL3002885, NPL3002887, NPL3002888, NPL3002891, NPL3002892, NPL3002894, NPL3002898, NPL3002899, NPL3002900, NPL3002901, NPL3002902, NPL3002904, NPL3002906, NPL3002907, NPL3002908, NPL3002909, NPL3002910, NPL3002911, NPL3002913, NPL3002914, NPL3002915, NPL3002918, NPL3002919, NPL3002922, NPL3002924, NPL3002925, NPL3002927, NPL3002928, NPL3002929, NPL3002935, NPL3002940, NPL3002941, NPL3002942, NPL3002949, NPL3002950, NPL3002954, NPL3002955, NPL3002960, NPL3002961, NPL3003298, NPL3003304, NPL3003308, NPL3003310, NPL3003311, NPL3003313, NPL3003315, NPL3003317, NPL3003319, NPL3003324, NPL3003331, NPL3003332, NPL3003334, NPL3003337, NPL3003338, NPL3003339, NPL3003342, NPL3003345, NPL3003346, NPL3003347, NPL3003353, NPL3003354, NPL3003355, NPL3003356, NPL3003357, NPL3003359, NPL3003694, NPL3003696, NPL3003704, NPL3003705, NPL3003708, NPL3003711, NPL3003712, NPL3003713, NPL3003715, NPL3003717, NPL3003718, NPL3003720, NPL3003723, NPL3003729, NPL3003730, NPL3003731, NPL3003735, NPL3003736, NPL3003737, NPL3003741, NPL3003742, NPL3003984, NPL3003987, NPL3003988, NPL3003989, NPL3003990, NPL3007387, NPL3007388, NPL3007390, NPL3007391, NPL3010714, NPL3010717, NPL3010721, NPL3010722, NPL3010724, NPL3010725, NPL3010726, NPL3010732, NPL3010735, NPL3010736, NPL3010739, NPL3010748, NPL3010750, NPL3010752, NPL3010753, NPL3010756, NPL3010758, NPL3010759, NPL3010760, NPL3010761, NPL3010764, NPL3010769, NPL3010770, NPL3010771, NPL3010772, NPL3010774, NPL3010779, NPL3011292, NPL3011296, NPL3011298, NPL3011304, NPL3011309, NPL3011310, NPL3011311, NPL3011313, NPL3011314, NPL3011316, NPL3011317, NPL3011319, NPL3011320, NPL3011323, NPL3011328, NPL3011329, NPL3011330, NPL3011331, NPL3011332, NPL3011333, NPL3011336, NPL3011338, NPL3011343, NPL3011344, NPL3011345, NPL3011346, NPL3011347, NPL3011349, NPL3011350, NPL3011352, NPL3011353, NPL3011357, NPL3011358, NPL3011362, NPL3011363, NPL3011365, NPL3014039, NPL3014040, NPL3014042, NPL3014043, NPL3014045, NPL3014052, NPL3014053, NPL3014054, NPL3014055, NPL3014056, NPL3014057, NPL3014058, NPL3014059, NPL3014061, NPL3014064, NPL3014065, NPL3014066, NPL3014070, NPL3014071, NPL3014072, NPL3014073, NPL3014074, NPL3014076, NPL3014079, NPL3014083, NPL3014085, NPL3014086, NPL3014087, NPL3014095, NPL3014096, NPL3014097, NPL3014098, NPL3014346, NPL3014347, NPL3014454, NPL3014455, NPL3014456, NPL3014501, NPL3014505, NPL3014506, NPL3014508, NPL3014529, NPL3014530, NPL3014537, NPL3014541, NPL3014542, NPL3017239, NPL3017240, NPL3017247, NPL3017252, NPL3017254, NPL3017257, NPL3017260, NPL3017265, NPL3017266, NPL3017267, NPL3017268, NPL3017269, NPL3017270, NPL3017272, NPL3017275, NPL3017284, NPL3017285, NPL3017286, NPL3017287, NPL3017289, NPL3017290, NPL3017932, NPL3017933, NPL3017991, NPL3017992, NPL3017993, NPL3018577, NPL3018578, NPL3018655, NPL3018709, NPL3018711, NPL3018715, NPL3018718, NPL3018719, NPL3018885, NPL3019477, NPL3019531, NPL3019532, NPL3019533, NPL3019534, NPL3019535, NPL3019537, NPL3019539, NPL3019541, NPL3019607, NPL3019660, NPL3019663, NPL3019664, NPL3019666, NPL3019668, NPL3019672, NPL3019677, NPL3019678, NPL3019769, NPL3020210, NPL3021261, NPL3021268, NPL3021270, NPL3021465, NPL3021466, NPL3021467, NPL3021468, NPL3021471, NPL3021479, NPL3021480, NPL3021481, NPL3021485, NPL3021487, NPL3021488, NPL3021490, NPL3021491, NPL3022395, NPL3022399; (3) GTIN 00763000421007, Serial Numbers: NPL3016404, NPL3016409, NPL3016410, NPL3016411, NPL3016418, NPL3016420, NPL3016421, NPL3016422, NPL3016423, NPL3016424, NPL3016428, NPL3016429, NPL3016431, NPL3016435, NPL3016436, NPL3016437, NPL3016438, NPL3016439, NPL3016440, NPL3016441, NPL3016443, NPL3016444, NPL3016446, NPL3016447, NPL3016448, NPL3016449, NPL3016457, NPL3016458, NPL3016460, NPL3016461, NPL3016464, NPL3016465, NPL3016469, NPL3016470, NPL3016475, NPL3016477, NPL3016478, NPL3016479, NPL3016481, NPL3016482, NPL3016484, NPL3016488, NPL3016492, NPL3016493, NPL3016495, NPL3016498, NPL3016499, NPL3016501, NPL3016502, NPL3016504, NPL3016507, NPL3016508, NPL3016513, NPL3016515, NPL3016516, NPL3016517, NPL3016518, NPL3016519, NPL3016522, NPL3016524, NPL3016525, NPL3016526, NPL3016527, NPL3016528, NPL3016529, NPL3016530, NPL3016531, NPL3016535, NPL3016536, NPL3016537, NPL3016539, NPL3016582, NPL3016584, NPL3016592, NPL3016594, NPL3016600, NPL3016601, NPL3016602, NPL3016603, NPL3016606, NPL3016607, NPL3016608, NPL3016613, NPL3016617, NPL3016621, NPL3016699, NPL3016702, NPL3016712, NPL3016713, NPL3016714, NPL3016715, NPL3016716, NPL3016737, NPL3016738, NPL3016743, NPL3016744, NPL3016745, NPL3016746, NPL3016747, NPL3016748, NPL3016749, NPL3016750, NPL3016757, NPL3016761, NPL3016762, NPL3016763, NPL3016765, NPL3016766, NPL3016775, NPL3016776, NPL3016778, NPL3016780, NPL3016784, NPL3016785, NPL3016787, NPL3016788, NPL3016790, NPL3016792, NPL3016793, NPL3016795, NPL3016796, NPL3016797, NPL3016798, NPL3016800, NPL3016801, NPL3016802, NPL3016933, NPL3016995, NPL3017043, NPL3017053, NPL3017201, NPL3017214, NPL3017221, NPL3017224, NPL3017231, NPL3017232, NPL3017303, NPL3017307, NPL3017308, NPL3017309, NPL3017310, NPL3017312, NPL3017313, NPL3017315, NPL3017316, NPL3017320, NPL3017324, NPL3017325, NPL3017333, NPL3017335, NPL3017344, NPL3017346, NPL3017347, NPL3017348, NPL3017349, NPL3017350, NPL3017367, NPL3017384, NPL3017392, NPL3017393, NPL3017402, NPL3017412, NPL3017414, NPL3017424, NPL3017425, NPL3017426, NPL3017427, NPL3017430, NPL3017431, NPL3017444, NPL3017506, NPL3017610, NPL3017611, NPL3017613, NPL3017614, NPL3017620, NPL3017625, NPL3017628, NPL3017629, NPL3017630, NPL3017654, NPL3017660, NPL3017662, NPL3017663, NPL3017664, NPL3017685, NPL3017686, NPL3017692, NPL3017693, NPL3017694, NPL3017695, NPL3017704, NPL3017705, NPL3017706, NPL3017707, NPL3017717, NPL3017726, NPL3017727, NPL3017739, NPL3017744, NPL3017748, NPL3017761, NPL3017767, NPL3017768, NPL3017769, NPL3017770, NPL3017771, NPL3017774, NPL3017779, NPL3017890, NPL3017891, NPL3017895, NPL3017897, NPL3017898, NPL3017900, NPL3017922, NPL3017924, NPL3017926, NPL3017927, NPL3017928, NPL3017942, NPL3017943, NPL3017944, NPL3017995, NPL3017996, NPL3017998, NPL3018002, NPL3018004, NPL3018005, NPL3018006, NPL3018007, NPL3018008, NPL3018009, NPL3018010, NPL3018011, NPL3018012, NPL3018013, NPL3018015, NPL3018016, NPL3018017, NPL3018018, NPL3018019, NPL3018020, NPL3018021, NPL3018022, NPL3018023, NPL3018024, NPL3018025, NPL3018026, NPL3018028, NPL3018045, NPL3018046, NPL3018048, NPL3018049, NPL3018050, NPL3018052, NPL3018053, NPL3018054, NPL3018058, NPL3018059, NPL3018062, NPL3018527, NPL3018528, NPL3018532, NPL3018534, NPL3018537, NPL3018538, NPL3018562, NPL3018563, NPL3018564, NPL3018579, NPL3018602, NPL3018607, NPL3018608, NPL3018609, NPL3018613, NPL3018614, NPL3018617, NPL3018619, NPL3018623, NPL3018626, NPL3018627, NPL3018657, NPL3018659, NPL3018677, NPL3018720, NPL3018721, NPL3018726, NPL3018727, NPL3018728, NPL3018729, NPL3018735, NPL3018736, NPL3018737, NPL3018743, NPL3018747, NPL3018748, NPL3018750, NPL3018751, NPL3018756, NPL3018757, NPL3018759, NPL3018760, NPL3018761, NPL3018762, NPL3018763, NPL3018765, NPL3018769, NPL3018775, NPL3018776, NPL3018777, NPL3018778, NPL3018780, NPL3018784, NPL3018792, NPL3018808, NPL3018809, NPL3018829, NPL3018830, NPL3018831, NPL3018832, NPL3018833, NPL3018834, NPL3018835, NPL3018836, NPL3018839, NPL3018840, NPL3018842, NPL3018843, NPL3018844, NPL3018892, NPL3018894, NPL3019405, NPL3019406, NPL3019407, NPL3019408, NPL3019409, NPL3019410, NPL3019483, NPL3019484, NPL3019485, NPL3019486, NPL3019487, NPL3019488, NPL3019489, NPL3019490, NPL3019491, NPL3019492, NPL3019493, NPL3019494, NPL3019496, NPL3019497, NPL3019501, NPL3019502, NPL3019503, NPL3019543, NPL3019547, NPL3019548, NPL3019552, NPL3019558, NPL3019561, NPL3019580, NPL3019581, NPL3019582, NPL3019583, NPL3019585, NPL3019586, NPL3019610, NPL3019613, NPL3019614, NPL3019629, NPL3019630, NPL3019632, NPL3019698, NPL3019699, NPL3019701, NPL3019703, NPL3019704, NPL3019705, NPL3019706, NPL3019731, NPL3019732, NPL3019733, NPL3019734, NPL3019735, NPL3019736, NPL3019737, NPL3019742, NPL3019765, NPL3019895, NPL3019898, NPL3019974, NPL3020003, NPL3020074, NPL3020103, NPL3020104, NPL3020105, NPL3020106, NPL3020107, NPL3020108, NPL3020112, NPL3020113, NPL3020121, NPL3020127, NPL3020129, NPL3020134, NPL3020136, NPL3020137, NPL3020138, NPL3020139, NPL3020141, NPL3020151, NPL3020155, NPL3020157, NPL3020164, NPL3020165, NPL3020170, NPL3020177, NPL3020222, NPL3020252, NPL3020925, NPL3020931, NPL3020944, NPL3020954, NPL3020958, NPL3020959, NPL3020960, NPL3020964, NPL3020969, NPL3020970, NPL3020980, NPL3020982, NPL3020983, NPL3020986, NPL3020987, NPL3020988, NPL3020990, NPL3020991, NPL3021002, NPL3021003, NPL3021004, NPL3021015, NPL3021025, NPL3021030, NPL3021031, NPL3021044, NPL3021045, NPL3021047, NPL3021048, NPL3021050, NPL3021052, NPL3021155, NPL3021157, NPL3021160, NPL3021162, NPL3021163, NPL3021168, NPL3021169, NPL3021170, NPL3021227, NPL3021229, NPL3021334, NPL3021337, NPL3021338, NPL3021352, NPL3021354, NPL3021367, NPL3021425, NPL3021492, NPL3021493, NPL3021495, NPL3021496, NPL3021497, NPL3021499, NPL3021501, NPL3021559, NPL3021560, NPL3021564, NPL3021565, NPL3021567, NPL3021568, NPL3021569, NPL3022374, NPL3022380, NPL3022441, NPL3022461, NPL3022489, NPL3022490, NPL3022515, NPL3022520; 5. Model Number CT900E, (1) GTIN 00763000447090, Serial Numbers: NPL3020725, NPL3022005, NPL3022030, NPL3022054, NPL3022062, NPL3022070, NPL3022114, NPL3022119, NPL3022131, NPL3022145, NPL3022174, NPL3022231, NPL3022236, NPL3022238, NPL3022245, NPL3022250, NPL3022257, NPL3022263, NPL3022278, NPL3022279, NPL3022280, NPL3022281, NPL3022298, NPL3022299, NPL3022300, NPL3022301, NPL3022304, NPL3022305, NPL3022306, NPL3022307, NPL3022308, NPL3022309, NPL3022310, NPL3022311, NPL3022313, NPL3022314, NPL3022324, NPL3022325, NPL3022328, NPL3022329, NPL3022330, NPL3022331, NPL3022332, NPL3022333, NPL3022334, NPL3022335, NPL3022336, NPL3022337, NPL3022338, NPL3022339, NPL3022340, NPL3022341, NPL3022342, NPL3022343, NPL3022344, NPL3022347, NPL3022349, NPL3022350, NPL3022351, NPL3022352, NPL3022357, NPL3022364, NPL3022365, NPL3022712, NPL3022716, NPL3022717, NPL3022720, NPL3022721, NPL3022724, NPL3022725, NPL3022730, NPL3022731, NPL3022732, NPL3022733, NPL3022735, NPL3022740, NPL3022741, NPL3022742, NPL3022743, NPL3022744, NPL3022745, NPL3022746, NPL3022747, NPL3022748, NPL3022749, NPL3022750, NPL3022751, NPL3022753, NPL3022754, NPL3022755, NPL3022756, NPL3022757, NPL3022761, NPL3022762, NPL3022769, NPL3022772, NPL3022773, NPL3022774, NPL3022776, NPL3022781, NPL3022784, NPL3022785, NPL3022786, NPL3022787, NPL3022788, NPL3022791, NPL3022792, NPL3022812, NPL3022858, NPL3022874, NPL3022900, NPL3022912, NPL3022949, NPL3023030, NPL3023059, NPL3023131, NPL3023148, NPL3023150, NPL3023197, NPL3023277, NPL3023279, NPL3023292, NPL3023300, NPL3023319, NPL3023323, NPL3023367, NPL3023425, NPL3023427, NPL3023429, NPL3023431, NPL3023433, NPL3023434, NPL3023437, NPL3023438, NPL3023439, NPL3023440, NPL3023442, NPL3023443, NPL3023446, NPL3023448, NPL3023450, NPL3023494, NPL3023530, NPL3023554, NPL3023583, NPL3023605, NPL3023615, NPL3023640, NPL3023659, NPL3023692, NPL3023701, NPL3023702, NPL3023704, NPL3023708, NPL3023710, NPL3023716, NPL3023722, NPL3023729, NPL3023734, NPL3023738, NPL3023740, NPL3023759, NPL3023769, NPL3023775, NPL3023776, NPL3023780, NPL3023784, NPL3023785, NPL3023792, NPL3023798, NPL3023805, NPL3023830, NPL3023846, NPL3023854, NPL3023858, NPL3023869, NPL3023873, NPL3023874, NPL3023891, NPL3023893, NPL3023932, NPL3023936, NPL3023938, NPL3023941, NPL3023946, NPL3023948, NPL3023952, NPL3023955, NPL3023957, NPL3023959, NPL3023966, NPL3023973, NPL3023974, NPL3023975, NPL3024015, NPL3024018, NPL3024022, NPL3024023, NPL3024026, NPL3024028, NPL3024033, NPL3024080, NPL3024157, NPL3024188, NPL3024189, NPL3024201, NPL3024206, NPL3024211, NPL3024221, NPL3024243, NPL3024256, NPL3024258, NPL3024286, NPL3024299, NPL3024303, NPL3024311, NPL3024312, NPL3024313, NPL3024314, NPL3024317, NPL3024319, NPL3024320, NPL3024322, NPL3024323, NPL3024327, NPL3024330, NPL3024357, NPL3024390, NPL3024399, NPL3024405, NPL3024408, NPL3024422, NPL3024426, NPL3024427, NPL3024431, NPL3024436, NPL3024445, NPL3024458, NPL3024460, NPL3024472, NPL3024478, NPL3024480, NPL3024482, NPL3024484, NPL3024485, NPL3024486, NPL3024487, NPL3024492, NPL3024495, NPL3024496, NPL3024504, NPL3024511, NPL3024527, NPL3024528, NPL3024531, NPL3024533, NPL3024575, NPL3024587, NPL3024602, NPL3024633, NPL3024637, NPL3024646, NPL3024699, NPL3024709, NPL3024712, NPL3024713, NPL3024719, NPL3024720, NPL3024722, NPL3024731, NPL3024735, NPL3024747, NPL3024748, NPL3024750, NPL3024751, NPL3024754, NPL3024755, NPL3024759, NPL3024760, NPL3024764, NPL3024765, NPL3024766, NPL3024771, NPL3024773, NPL3024774, NPL3024775, NPL3024777, NPL3024778, NPL3024780, NPL3024784, NPL3024786, NPL3024792, NPL3024794, NPL3024796, NPL3024797, NPL3024808, NPL3024832, NPL3024836, NPL3024837, NPL3024841, NPL3024843, NPL3024858, NPL3024861, NPL3024871, NPL3024872, NPL3024884, NPL3024888, NPL3024889, NPL3024890, NPL3024897, NPL3024900, NPL3024902, NPL3024903, NPL3024909, NPL3024912, NPL3024917, NPL3024919, NPL3024924, NPL3024929, NPL3024933, NPL3024934, NPL3024935, NPL3024936, NPL3024948, NPL3024965, NPL3024973, NPL3024978, NPL3024989, NPL3024998, NPL3025007, NPL3025012, NPL3025013, NPL3025017, NPL3025021, NPL3025023, NPL3025025, NPL3025027, NPL3025031, NPL3025033, NPL3025042, NPL3025044, NPL3025047, NPL3025057, NPL3025058, NPL3025067, NPL3025076, NPL3025082, NPL3025097, NPL3025155, NPL3025179, NPL3025184, NPL3025197, NPL3025205, NPL3025222, NPL3025224, NPL3025226, NPL3025241, NPL3025242, NPL3025253, NPL3025257, NPL3025265, NPL3025268, NPL3025270, NPL3025271, NPL3025275, NPL3025279, NPL3025281, NPL3025284, NPL3025285, NPL3025288, NPL3025292, NPL3025293, NPL3025301, NPL3025304, NPL3025313, NPL3025316, NPL3025326, NPL3025327, NPL3025329, NPL3025331, NPL3025335, NPL3025339, NPL3025349, NPL3025372, NPL3025384, NPL3025396, NPL3025482, NPL3025509, NPL3025533, NPL3025640, NPL3025641, NPL3025649, NPL3025650, NPL3025715, NPL3025743, NPL3025760, NPL3025890, NPL3025902, NPL3025908, NPL3025917, NPL3025920, NPL3025945, NPL3025947, NPL3025949, NPL3025958, NPL3025965, NPL3026034, NPL3026053, NPL3026077, NPL3026097, NPL3026159, NPL3026177, NPL3026188, NPL3026190, NPL3026191, NPL3026196, NPL3026201, NPL3026202, NPL3026203, NPL3026204, NPL3026205, NPL3026207, NPL3026208, NPL3026210, NPL3026212, NPL3026215, NPL3026218, NPL3026220, NPL3026223, NPL3026224, NPL3026233, NPL3026245, NPL3026250, NPL3026258, NPL3026260, NPL3026262, NPL3026294, NPL3026324, NPL3026341, NPL3026351, NPL3026356, NPL3026358, NPL3026360, NPL3026362, NPL3026367, NPL3026382, NPL3026383, NPL3026390, NPL3026391, NPL3026393, NPL3026396, NPL3026397, NPL3026402, NPL3026407, NPL3026408, NPL3026414, NPL3026428, NPL3026429, NPL3026435, NPL3026438, NPL3026441, NPL3026442, NPL3026443, NPL3026447, NPL3026449, NPL3026650, NPL3026936, NPL3027060, NPL3027340, NPL3027473, NPL3027482, NPL3027519, NPL3027595, NPL3027607, NPL3027623, NPL3027627, NPL3027697, NPL3027720, NPL3027747, NPL3027748, NPL3027803, NPL3027825, NPL3027838, NPL3027845, NPL3027858, NPL3027859, NPL3030796, NPL3030799, NPL3030820, NPL3030824, NPL3030828, NPL3030836, NPL3030848, NPL3030853, NPL3030861, NPL3030865, NPL3030869, NPL3030872, NPL3030913, NPL3030916, NPL3030919, NPL3030930, NPL3030932, NPL3030933, NPL3030934, NPL3030935, NPL3030936, NPL3030941, NPL3030942, NPL3031031, NPL3031073, NPL3031075, NPL3031079, NPL3031080, NPL3031083, NPL3031084, NPL3031085, NPL3031110, NPL3031128, NPL3031144, NPL3031167, NPL3031175, NPL3031197, NPL3031205, NPL3031221, NPL3031239, NPL3031245, NPL3031247, NPL3031248, NPL3031258, NPL3031261, NPL3031266, NPL3031269, NPL3031274, NPL3031280, NPL3031284, NPL3031289, NPL3031290, NPL3031310, NPL3031324, NPL3031326, NPL3031337, NPL3031379, NPL3031404, NPL3031435, NPL3031471, NPL3031475, NPL3031481, NPL3031492, NPL3031493, NPL3031494, NPL3031495, NPL3031499, NPL3031501, NPL3031518, NPL3031525, NPL3031529, NPL3031540, NPL3031546, NPL3031548, NPL3031552, NPL3031563, NPL3031569, NPL3031570, NPL3031591, NPL3031593, NPL3031594, NPL3031595, NPL3031596, NPL3031597, NPL3031600, NPL3031603, NPL3031604, NPL3031606, NPL3031622, NPL3031627, NPL3031628, NPL3031650, NPL3031655, NPL3031660, NPL3031666, NPL3031674, NPL3031680, NPL3031690, NPL3031709, NPL3031719, NPL3031727, NPL3031734, NPL3031738, NPL3031761, NPL3031763, NPL3031793, NPL3031796, NPL3031798, NPL3031840, NPL3031848, NPL3031874, NPL3031883, NPL3031884, NPL3031892, NPL3031924, NPL3031951, NPL3031966, NPL3031968, NPL3031973, NPL3031975, NPL3031986, NPL3031990, NPL3031991, NPL3031995, NPL3031999, NPL3032036, NPL3032043, NPL3032049, NPL3032066, NPL3032072, NPL3032074, NPL3032086, NPL3032088, NPL3032089, NPL3032091, NPL3032095, NPL3032098, NPL3032108, NPL3032110, NPL3032120, NPL3032145, NPL3032151, NPL3032163, NPL3032193, NPL3032195, NPL3032200, NPL3032202, NPL3032207, NPL3032211, NPL3032214, NPL3032219, NPL3032225, NPL3032235, NPL3032236, NPL3032237, NPL3032238, NPL3032239, NPL3032240, NPL3032241, NPL3032242, NPL3032243, NPL3032246, NPL3032250, NPL3032251, NPL3032252, NPL3032253, NPL3032261, NPL3032262, NPL3032265, NPL3032281, NPL3032299, NPL3032310, NPL3032311, NPL3032320, NPL3032329, NPL3032330, NPL3032331, NPL3032332, NPL3032334, NPL3032342, NPL3032344, NPL3032355, NPL3032360, NPL3032378, NPL3032450, NPL3032457, NPL3032483, NPL3032488, NPL3032491, NPL3032497, NPL3032502, NPL3032513, NPL3032516, NPL3032568, NPL3032587, NPL3032600, NPL3032610, NPL3032611, NPL3032613, NPL3032614, NPL3032616, NPL3032622, NPL3032628, NPL3032642, NPL3032648, NPL3032650, NPL3032665, NPL3032678, NPL3032683, NPL3032687, NPL3032696, NPL3032707, NPL3032729, NPL3032747, NPL3032763, NPL3032771, NPL3032776, NPL3032781, NPL3032790, NPL3032807, NPL3032816, NPL3032834, NPL3032839, NPL3032883, NPL3032891, NPL3032894, NPL3032907, NPL3032917, NPL3032928, NPL3032939, NPL3032945, NPL3032954, NPL3032978, NPL3032980, NPL3032983, NPL3032991, NPL3032997, NPL3032998, NPL3033001, NPL3033004, NPL3033013, NPL3033017, NPL3033020, NPL3033036, NPL3033038, NPL3033039, NPL3033040, NPL3033042, NPL3033047, NPL3033049, NPL3033057, NPL3033062, NPL3033072, NPL3033077, NPL3033090, NPL3033091, NPL3033094, NPL3033107, NPL3033113, NPL3033134, NPL3033139, NPL3033143, NPL3033187, NPL3033196, NPL3033216, NPL3033218, NPL3033221, NPL3033229, NPL3033248, NPL3033249, NPL3033268, NPL3033274, NPL3033276, NPL3033277, NPL3033282, NPL3033285, NPL3033291, NPL3033339, NPL3033342, NPL3033365, NPL3033371, NPL3033379, NPL3033380, NPL3033400, NPL3033401, NPL3033402, NPL3033403, NPL3033499, NPL3033521, NPL3033560, NPL3033606, NPL3033620, NPL3033623, NPL3033624, NPL3033650, NPL3033680, NPL3033681, NPL3033687, NPL3033729, NPL3033742, NPL3033751, NPL3033753, NPL3033755, NPL3033765, NPL3033773, NPL3033791, NPL3033840, NPL3033846, NPL3033848, NPL3033862, NPL3033869, NPL3033871, NPL3033880, NPL3033883, NPL3033895, NPL3033900, NPL3033901, NPL3033902, NPL3033905, NPL3033910, NPL3033911, NPL3033914, NPL3033921, NPL3033925, NPL3033949, NPL3033952, NPL3033955, NPL3033958, NPL3033960, NPL3033962, NPL3033968, NPL3033975, NPL3033977, NPL3033979, NPL3033980, NPL3033989, NPL3033994, NPL3033995, NPL3033996, NPL3034000, NPL3034004, NPL3034007, NPL3034008, NPL3034009, NPL3034017, NPL3034018, NPL3034020, NPL3034021, NPL3034022, NPL3034046, NPL3034047, NPL3034048, NPL3034050, NPL3034058, NPL3034066, NPL3034068, NPL3034074, NPL3034075, NPL3034081, NPL3034084, NPL3034090, NPL3034093, NPL3034095, NPL3034108, NPL3034109, NPL3034112, NPL3034126, NPL3034134, NPL3034135, NPL3034142, NPL3034152, NPL3034165, NPL3034167, NPL3034168, NPL3034171, NPL3034174, NPL3034178, NPL3034179, NPL3034183, NPL3034186, NPL3034188, NPL3034191, NPL3034200, NPL3034202, NPL3034205, NPL3034206, NPL3034208, NPL3034210, NPL3034216, NPL3034226, NPL3034227, NPL3034229, NPL3034230, NPL3034231, NPL3034232, NPL3034239, NPL3034243, NPL3034244, NPL3034247, NPL3034248, NPL3034250, NPL3034252, NPL3034257, NPL3034260, NPL3034264, NPL3034269, NPL3034270, NPL3034271, NPL3034272, NPL3034273, NPL3034275, NPL3034277, NPL3034280, NPL3034281, NPL3034283, NPL3034284, NPL3034285, NPL3034287, NPL3034288, NPL3034290, NPL3034294, NPL3034301, NPL3034303, NPL3034306, NPL3034308, NPL3034310, NPL3034323, NPL3034324, NPL3034325, NPL3034326, NPL3034331, NPL3034332, NPL3034334, NPL3034338, NPL3034342, NPL3034349, NPL3034351, NPL3034360, NPL3034365, NPL3034368, NPL3034372, NPL3034374, NPL3034376, NPL3034383, NPL3034396, NPL3034397, NPL3034404, NPL3034407, NPL3034427, NPL3034431, NPL3034448, NPL3034452, NPL3034469, NPL3034477, NPL3034484, NPL3034512, NPL3034514, NPL3034515, NPL3034516, NPL3034517, NPL3034520, NPL3034521, NPL3034523, NPL3034526, NPL3034528, NPL3034535, NPL3034539, NPL3034540, NPL3034549, NPL3034550, NPL3034556, NPL3034557, NPL3034560, NPL3034566, NPL3034571, NPL3034582, NPL3034597, NPL3034605, NPL3034613, NPL3034617, NPL3034621, NPL3034648, NPL3034656, NPL3034673, NPL3034717, NPL3034740, NPL3034744, NPL3034752, NPL3034761, NPL3034774, NPL3034777, NPL3036810, NPL3036833, NPL3036840, NPL3036854, NPL3036887, NPL3036905, NPL3036926, NPL3036942, NPL3036944, NPL3036945, NPL3036946, NPL3036947, NPL3036948, NPL3036954, NPL3036957, NPL3036959, NPL3036960, NPL3036975, NPL3036985, NPL3036992, NPL3037094, NPL3037107, NPL3037112, NPL3037117, NPL3037131, NPL3037196, NPL3037216, NPL3037218, NPL3037223, NPL3037225, NPL3037240, NPL3037241, NPL3037245, NPL3037246, NPL3037251, NPL3037252, NPL3037254, NPL3037255, NPL3037262, NPL3037278, NPL3037307, NPL3037310, NPL3037311, NPL3037323, NPL3037325, NPL3037326, NPL3037327, NPL3037335, NPL3037379, NPL3037381, NPL3037382, NPL3037384, NPL3037391, NPL3037397, NPL3037398, NPL3037399, NPL3037400, NPL3037403, NPL3037405, NPL3037406, NPL3037412, NPL3037419, NPL3037420, NPL3037429, NPL3037430, NPL3037431, NPL3037440, NPL3037444, NPL3037461, NPL3037492, NPL3037494, NPL3037499, NPL3037509, NPL3037516, NPL3037526, NPL3037528, NPL3037529, NPL3037549, NPL3037559, NPL3037563, NPL3037567, NPL3037568, NPL3037569, NPL3037571, NPL3037604, NPL3037615, NPL3037621, NPL3037623, NPL3037624, NPL3037626, NPL3037662, NPL3037668, NPL3037697, NPL3037700, NPL3037707, NPL3037714, NPL3037715, NPL3037721, NPL3037729, NPL3037730, NPL3037740, NPL3037753, NPL3037756, NPL3037764, NPL3037779, NPL3037850, NPL3037880, NPL3037902, NPL3037966, NPL3037967, NPL3037996, NPL3038006, NPL3038010, NPL3038066, NPL3038078, NPL3038092, NPL3038112, NPL3038127, NPL3038177, NPL3038188, NPL3038218, NPL3038334, NPL3038335, NPL3038336, NPL3038345, NPL3038361, NPL3038372, NPL3038374, NPL3038375, NPL3038381, NPL3038385, NPL3038386, NPL3038412, NPL3038419, NPL3038422, NPL3038437, NPL3038440, NPL3038443, NPL3038446, NPL3038449, NPL3038450, NPL3038452, NPL3038456, NPL3038457, NPL3038460, NPL3038461, NPL3038462, NPL3038465, NPL3038471, NPL3038474, NPL3038478, NPL3038479, NPL3038480; (2) GTIN 00763000729141, Serial Numbers: NPL3022833, NPL3022835, NPL3022836, NPL3022838, NPL3022839, NPL3022840, NPL3022841, NPL3022954, NPL3022973, NPL3022974, NPL3022975, NPL3023250, NPL3023254, NPL3023256, NPL3023257, NPL3023288, NPL3023459, NPL3023460, NPL3023461, NPL3023463, NPL3023464, NPL3023465, NPL3023466, NPL3023467, NPL3023471, NPL3023473, NPL3023474, NPL3024180, NPL3024181, NPL3024187, NPL3024192, NPL3024195, NPL3024224, NPL3024227, NPL3024229, NPL3024251, NPL3024290, NPL3024302, NPL3024344, NPL3025010, NPL3025032, NPL3025045, NPL3025053, NPL3025054, NPL3038210, NPL3038230, NPL3038351, NPL3038714, NPL3038718, NPL3038719, NPL3038736, NPL3038737, NPL3038738, NPL3038741, NPL3038742, NPL3038779, NPL3038780, NPL3038781, NPL3038867, NPL3039871, NPL3040070, NPL3040071, NPL3040073, NPL3040080, NPL3040083, NPL3040084, NPL3040099, NPL3040100, NPL3040101, NPL3040103, NPL3040104, NPL3040105, NPL3040106, NPL3040107, NPL3040109, NPL3040111, NPL3040112, NPL3040175, NPL3040176, NPL3040177, NPL3040178, NPL3040179, NPL3040242, NPL3040243, NPL3040245, NPL3040246, NPL3040247, NPL3040251, NPL3040252, NPL3040256, NPL3040257, NPL3040261, NPL3040262, NPL3040263, NPL3040266, NPL3040268, NPL3040271, NPL3040307, NPL3040523, NPL3040725, NPL3040728, NPL3040729, NPL3040730, NPL3040731, NPL3040732, NPL3040733, NPL3040734, NPL3040735, NPL3040736, NPL3040737, NPL3040738, NPL3040739, NPL3040741, NPL3040743, NPL3040744, NPL3040745, NPL3040746, NPL3040747, NPL3040748, NPL3040846, NPL3040855, NPL3040928, NPL3040932, NPL3040933, NPL3040935, NPL3040938, NPL3040939, NPL3044955, NPL3044969, NPL3044970, NPL3044971, NPL3044972, NPL3044973, NPL3045026, NPL3045027, NPL3045028, NPL3045029, NPL3045030, NPL3045031, NPL3045032; (3) GTIN 00763000737290, Serial Numbers: NPL3038512, NPL3038518, NPL3038519, NPL3038520, NPL3038522, NPL3038526, NPL3038530, NPL3038531, NPL3038533, NPL3038534, NPL3038539, NPL3038543, NPL3038545, NPL3038549, NPL3038553, NPL3038556, NPL3038559, NPL3038561, NPL3038567, NPL3038575, NPL3038576, NPL3038578, NPL3038581, NPL3038585, NPL3038604, NPL3038657, NPL3038746, NPL3038747, NPL3038748, NPL3038750, NPL3038751, NPL3038752, NPL3038753, NPL3038754, NPL3038755, NPL3038756, NPL3038757, NPL3038758, NPL3038759, NPL3038760, NPL3038761, NPL3038762, NPL3038763, NPL3038764, NPL3038765, NPL3038766, NPL3038767, NPL3038768, NPL3038769, NPL3038770, NPL3038771, NPL3038775, NPL3038777, NPL3038778, NPL3038784, NPL3038786, NPL3038802, NPL3038805, NPL3038812, NPL3038827, NPL3038828, NPL3038829, NPL3038830, NPL3038831, NPL3038832, NPL3038843, NPL3038844, NPL3038846, NPL3038847, NPL3038849, NPL3038851, NPL3038854, NPL3038856, NPL3038865, NPL3038873, NPL3038875, NPL3038876, NPL3038877, NPL3038878, NPL3038879, NPL3038887, NPL3038888, NPL3038889, NPL3038891, NPL3038892, NPL3038895, NPL3038896, NPL3038898, NPL3038899, NPL3038900, NPL3038901, NPL3038902, NPL3038903, NPL3038905, NPL3038908, NPL3038909, NPL3038911, NPL3038916, NPL3038917, NPL3038918, NPL3038919, NPL3038920, NPL3038921, NPL3038922, NPL3038924, NPL3038928, NPL3038929, NPL3038946, NPL3038947, NPL3038948, NPL3038949, NPL3038951, NPL3038953, NPL3038955, NPL3038956, NPL3038957, NPL3038958, NPL3038959, NPL3038960, NPL3038965, NPL3038966, NPL3038970, NPL3038971, NPL3038972, NPL3038973, NPL3038974, NPL3038975, NPL3038976, NPL3038982, NPL3038984, NPL3038985, NPL3038987, NPL3038989, NPL3038990, NPL3038992, NPL3038994, NPL3038997, NPL3038999, NPL3039000, NPL3039002, NPL3039003, NPL3039005, NPL3039006, NPL3039007, NPL3039008, NPL3039018, NPL3039043, NPL3039061, NPL3039065, NPL3039066, NPL3039071, NPL3039072, NPL3039073, NPL3039074, NPL3039076, NPL3039084, NPL3039085, NPL3039086, NPL3039087, NPL3039088, NPL3039094, NPL3039097, NPL3039101, NPL3039109, NPL3039119, NPL3039120, NPL3039121, NPL3039127, NPL3039132, NPL3039134, NPL3039136, NPL3039137, NPL3039138, NPL3039149, NPL3039150, NPL3039151, NPL3039152, NPL3039156, NPL3039164, NPL3039168, NPL3039169, NPL3039174, NPL3039176, NPL3039177, NPL3039178, NPL3039179, NPL3039180, NPL3039182, NPL3039186, NPL3039194, NPL3039195, NPL3039196, NPL3039197, NPL3039202, NPL3039245, NPL3039246, NPL3039255, NPL3039267, NPL3039280, NPL3039334, NPL3039345, NPL3039346, NPL3039347, NPL3039363, NPL3039364, NPL3039374, NPL3039378, NPL3039388, NPL3039393, NPL3039395, NPL3039396, NPL3039404, NPL3039413, NPL3039426, NPL3039427, NPL3039428, NPL3039444, NPL3039446, NPL3039447, NPL3039448, NPL3039449, NPL3039450, NPL3039451, NPL3039452, NPL3039453, NPL3039454, NPL3039463, NPL3039464, NPL3039465, NPL3039466, NPL3039468, NPL3039472, NPL3039476, NPL3039477, NPL3039478, NPL3039510, NPL3039511, NPL3039512, NPL3039513, NPL3039514, NPL3039515, NPL3039516, NPL3039517, NPL3039518, NPL3039519, NPL3039530, NPL3039551, NPL3039555, NPL3039563, NPL3039564, NPL3039565, NPL3039566, NPL3039567, NPL3039568, NPL3039569, NPL3039570, NPL3039571, NPL3039572, NPL3039574, NPL3039575, NPL3039576, NPL3039577, NPL3039578, NPL3039580, NPL3039581, NPL3039582, NPL3039583, NPL3039584, NPL3039585, NPL3039587, NPL3039589, NPL3039590, NPL3039591, NPL3039592, NPL3039593, NPL3039594, NPL3039596, NPL3039597, NPL3039598, NPL3039599, NPL3039600, NPL3039601, NPL3039603, NPL3039604, NPL3039605, NPL3039607, NPL3039608, NPL3039609, NPL3039610, NPL3039611, NPL3039612, NPL3039613, NPL3039614, NPL3039615, NPL3039619, NPL3039620, NPL3039621, NPL3039622, NPL3039624, NPL3039625, NPL3039626, NPL3039627, NPL3039635, NPL3039636, NPL3039637, NPL3039638, NPL3039639, NPL3039640, NPL3039648, NPL3039703, NPL3039748, NPL3039749, NPL3039750, NPL3039751, NPL3039752, NPL3039754, NPL3039756, NPL3039762, NPL3039763, NPL3039764, NPL3039776, NPL3039777, NPL3039781, NPL3039785, NPL3039787, NPL3039792, NPL3039799, NPL3039801, NPL3039802, NPL3039804, NPL3039806, NPL3039807, NPL3039808, NPL3039810, NPL3039820, NPL3039822, NPL3039823, NPL3039829, NPL3039830, NPL3039832, NPL3039835, NPL3039837, NPL3039840, NPL3039843, NPL3039844, NPL3039850, NPL3039853, NPL3039857, NPL3039859, NPL3039860, NPL3039862, NPL3039865, NPL3039872, NPL3039873, NPL3039874, NPL3039877, NPL3039880, NPL3039881, NPL3039883, NPL3039885, NPL3039886, NPL3039887, NPL3039888, NPL3039890, NPL3039891, NPL3039892, NPL3039893, NPL3039894, NPL3039895, NPL3039899, NPL3039900, NPL3039901, NPL3039902, NPL3039903, NPL3039909, NPL3039913, NPL3039914, NPL3039916, NPL3039919, NPL3039920, NPL3039921, NPL3039923, NPL3039924, NPL3039925, NPL3039926, NPL3039927, NPL3039928, NPL3039935, NPL3039936, NPL3039941, NPL3039943, NPL3039944, NPL3039945, NPL3039950, NPL3039960, NPL3039961, NPL3039963, NPL3039964, NPL3039966, NPL3039967, NPL3039968, NPL3039969, NPL3039970, NPL3039974, NPL3039977, NPL3039980, NPL3039981, NPL3039983, NPL3039984, NPL3039987, NPL3039988, NPL3039992, NPL3040006, NPL3040007, NPL3040008, NPL3040013, NPL3040017, NPL3040018, NPL3040019, NPL3040021, NPL3040022, NPL3040023, NPL3040026, NPL3040027, NPL3040028, NPL3040029, NPL3040030, NPL3040035, NPL3040036, NPL3040037, NPL3040038, NPL3040039, NPL3040041, NPL3040042, NPL3040043, NPL3040045, NPL3040046, NPL3040047, NPL3040049, NPL3040050, NPL3040051, NPL3040052, NPL3040053, NPL3040054, NPL3040055, NPL3040056, NPL3040057, NPL3040058, NPL3040060, NPL3040062, NPL3040063, NPL3040064, NPL3040065, NPL3040068, NPL3040069, NPL3040074, NPL3040076, NPL3040078, NPL3040085, NPL3040086, NPL3040087, NPL3040096, NPL3040097, NPL3040108, NPL3040113, NPL3040114, NPL3040118, NPL3040119, NPL3040120, NPL3040121, NPL3040123, NPL3040124, NPL3040125, NPL3040127, NPL3040129, NPL3040130, NPL3040131, NPL3040132, NPL3040133, NPL3040134, NPL3040135, NPL3040136, NPL3040139, NPL3040140, NPL3040145, NPL3040169, NPL3040173, NPL3040183, NPL3040184, NPL3040186, NPL3040187, NPL3040188, NPL3040195, NPL3040196, NPL3040200, NPL3040201, NPL3040202, NPL3040208, NPL3040215, NPL3040226, NPL3040230, NPL3040236, NPL3040249, NPL3040250, NPL3040264, NPL3040265, NPL3040267, NPL3040269, NPL3040279, NPL3040287, NPL3040288, NPL3040299, NPL3040302, NPL3040303, NPL3040316, NPL3040317, NPL3040320, NPL3040321, NPL3040325, NPL3040333, NPL3040334, NPL3040343, NPL3040347, NPL3040348, NPL3040350, NPL3040352, NPL3040356, NPL3040360, NPL3040372, NPL3040385, NPL3040388, NPL3040389, NPL3040391, NPL3040392, NPL3040407, NPL3040418, NPL3040426, NPL3040473, NPL3040488, NPL3040490, NPL3040496, NPL3040515, NPL3040569, NPL3040575, NPL3040606, NPL3040637, NPL3040645, NPL3040663, NPL3040692, NPL3040749, NPL3040752, NPL3040766, NPL3040787, NPL3040833, NPL3040836, NPL3040837, NPL3040839, NPL3040840, NPL3040841, NPL3040842, NPL3040843, NPL3040905, NPL3040958, NPL3044979, NPL3045061, NPL3045088, NPL3045127, NPL3045136, NPL3045141, NPL3045144, NPL3045162, NPL3045173, NPL3045179, NPL3045229, NPL3045236, NPL3045262; 6. Model Number CT900F, (1) GTIN 00763000926144, Serial Numbers: NPL3041229, NPL3041230, NPL3041231, NPL3041234, NPL3041235, NPL3041236, NPL3041237, NPL3041239, NPL3041240, NPL3041241, NPL3041244, NPL3041246, NPL3041248, NPL3041261, NPL3041264, NPL3041265, NPL3041266, NPL3041277, NPL3041278, NPL3041281, NPL3041282, NPL3041286, NPL3041288, NPL3041298, NPL3041301, NPL3041307, NPL3041311, NPL3041312, NPL3041324, NPL3041326, NPL3041335, NPL3041336, NPL3041337, NPL3041338, NPL3041339, NPL3041340, NPL3041352, NPL3041353, NPL3041356, NPL3041357, NPL3041359, NPL3041360, NPL3041457, NPL3041481, NPL3041486, NPL3041489, NPL3041491, NPL3041493, NPL3041505, NPL3041506, NPL3041527, NPL3041528, NPL3041532, NPL3041537, NPL3041545, NPL3041546, NPL3041551, NPL3041565, NPL3041566, NPL3041569, NPL3041585, NPL3041586, NPL3041589, NPL3041590, NPL3041614, NPL3041622, NPL3041632, NPL3041633, NPL3041640, NPL3041641, NPL3041651, NPL3041655, NPL3041656, NPL3041657, NPL3041661, NPL3041663, NPL3041682, NPL3041709, NPL3041713, NPL3041725, NPL3041728, NPL3041737, NPL3041744, NPL3041754, NPL3041763, NPL3041764, NPL3041788, NPL3041790, NPL3041793, NPL3041794, NPL3041795, NPL3041801, NPL3041807, NPL3041825, NPL3041868, NPL3041878, NPL3041884, NPL3041890, NPL3041891, NPL3041892, NPL3041893, NPL3041896, NPL3041897, NPL3041903, NPL3041910, NPL3041911, NPL3041942, NPL3041948, NPL3041959, NPL3041960, NPL3041966, NPL3041970, NPL3041975, NPL3041976, NPL3042017, NPL3042076, NPL3042095, NPL3042098, NPL3042261, NPL3042272, NPL3042283, NPL3042306, NPL3042308, NPL3042317, NPL3042326, NPL3042327, NPL3042329, NPL3042330, NPL3042331, NPL3042332, NPL3042354, NPL3042355, NPL3042361, NPL3042363, NPL3042366, NPL3042367, NPL3042368, NPL3042371, NPL3042376, NPL3042378, NPL3042416, NPL3042417, NPL3042419, NPL3042429, NPL3042432, NPL3042436, NPL3042449, NPL3042462, NPL3042476, NPL3042477, NPL3042479, NPL3042499, NPL3042509, NPL3042510, NPL3042514, NPL3042529, NPL3042532, NPL3042534, NPL3042537, NPL3042541, NPL3042553, NPL3042576, NPL3042621, NPL3042639, NPL3042644, NPL3042646, NPL3042661, NPL3042663, NPL3042665, NPL3042682, NPL3042713, NPL3042718, NPL3042730, NPL3043028, NPL3043034, NPL3043036, NPL3043037, NPL3043038, NPL3043044, NPL3043047, NPL3043049, NPL3043050, NPL3043051, NPL3043066, NPL3043075, NPL3043076, NPL3043078, NPL3043079, NPL3043080, NPL3043082, NPL3043083, NPL3043091, NPL3043092, NPL3043094, NPL3043095, NPL3043097, NPL3043100, NPL3043101, NPL3043113, NPL3043165, NPL3043167, NPL3043213, NPL3043217, NPL3043223, NPL3043224, NPL3043225, NPL3043226, NPL3043227, NPL3043229, NPL3043231, NPL3043233, NPL3043244, NPL3043249, NPL3043250, NPL3043251, NPL3043252, NPL3043253, NPL3043255, NPL3043257, NPL3043258, NPL3043259, NPL3043260, NPL3043261, NPL3043262, NPL3043263, NPL3043264, NPL3043265, NPL3043266, NPL3043267, NPL3043268, NPL3043271, NPL3043273, NPL3043274, NPL3043282, NPL3043288, NPL3043290, NPL3043321, NPL3043332, NPL3043339, NPL3043341, NPL3043342, NPL3043343, NPL3043344, NPL3043358, NPL3043360, NPL3043361, NPL3043363, NPL3043364, NPL3043366, NPL3043373, NPL3043381, NPL3043399, NPL3043400, NPL3043440, NPL3043441, NPL3043442, NPL3043444, NPL3043474, NPL3043475, NPL3043477, NPL3043488, NPL3043491, NPL3043503, NPL3043504, NPL3043505, NPL3043506, NPL3043507, NPL3043513, NPL3043517, NPL3043518, NPL3043519, NPL3043520, NPL3043526, NPL3043527, NPL3043529, NPL3043533, NPL3043535, NPL3043537, NPL3043538, NPL3043540, NPL3043541, NPL3043542, NPL3043543, NPL3043544, NPL3043574, NPL3043575, NPL3043580, NPL3043581, NPL3043582, NPL3043583, NPL3043590, NPL3043591, NPL3043597, NPL3043632, NPL3043660, NPL3043667, NPL3043668, NPL3043673, NPL3043698, NPL3043701, NPL3043719, NPL3043749, NPL3043751, NPL3043810, NPL3043811, NPL3043813, NPL3043816, NPL3043839, NPL3043840, NPL3043852, NPL3043857, NPL3043867, NPL3043873, NPL3043888, NPL3043894, NPL3043899, NPL3043903, NPL3043904, NPL3043921, NPL3043928, NPL3043961, NPL3043962, NPL3044007, NPL3044022, NPL3044024, NPL3044026, NPL3044029, NPL3044032, NPL3044033, NPL3044034, NPL3044035, NPL3044038, NPL3044039, NPL3044041, NPL3044042, NPL3044045, NPL3044053, NPL3044055, NPL3044057, NPL3044069, NPL3044073, NPL3044076, NPL3044090, NPL3044127, NPL3044128, NPL3044129, NPL3044137, NPL3044151, NPL3044153, NPL3044156, NPL3044169, NPL3044180, NPL3044181, NPL3044183, NPL3044208, NPL3044217, NPL3044239, NPL3044240, NPL3044241, NPL3044242, NPL3044243, NPL3044244, NPL3044253, NPL3044258, NPL3044260, NPL3044280, NPL3044290, NPL3044292, NPL3044300, NPL3044301, NPL3044345, NPL3044346, NPL3044347, NPL3044351, NPL3044352, NPL3044357, NPL3044358, NPL3044359, NPL3044360, NPL3044363, NPL3044364, NPL3044367, NPL3044368, NPL3044372, NPL3044373, NPL3044374, NPL3044375, NPL3044376, NPL3044378, NPL3044379, NPL3044380, NPL3044381, NPL3044382, NPL3044383, NPL3044384, NPL3044385, NPL3044386, NPL3044387, NPL3044388, NPL3044389, NPL3044390, NPL3044391, NPL3044392, NPL3044393, NPL3044394, NPL3044395, NPL3044396, NPL3044397, NPL3044398, NPL3044399, NPL3044400, NPL3044401, NPL3044402, NPL3044403, NPL3044404, NPL3044405, NPL3044406, NPL3044407, NPL3044408, NPL3044409, NPL3044410, NPL3044412, NPL3044415, NPL3044425, NPL3044431, NPL3044437, NPL3044438, NPL3044439, NPL3044467, NPL3044490, NPL3044493, NPL3044495, NPL3044505, NPL3044506, NPL3044512, NPL3044517, NPL3044518, NPL3044519, NPL3044520, NPL3044531, NPL3044533, NPL3044555, NPL3044557, NPL3044558, NPL3044559, NPL3044560, NPL3044562, NPL3044563, NPL3044564, NPL3044569, NPL3044571, NPL3044572, NPL3045323, NPL3045335, NPL3045359, NPL3045370, NPL3045404, NPL3045530, NPL3045549, NPL3045600, NPL3045696, NPL3045697, NPL3045698, NPL3045705, NPL3045706, NPL3045707, NPL3045708, NPL3045709, NPL3045710, NPL3045741, NPL3045744, NPL3045745, NPL3045746, NPL3045747, NPL3045763, NPL3045764, NPL3045770, NPL3045772, NPL3045773, NPL3045779, NPL3045783, NPL3045804, NPL3045805, NPL3045807, NPL3045808, NPL3045809, NPL3045810, NPL3045811, NPL3045812, NPL3045813, NPL3045814, NPL3045839, NPL3045840, NPL3045842, NPL3045849, NPL3045851, NPL3045852, NPL3045870, NPL3045878, NPL3045879, NPL3045881, NPL3045882, NPL3045883, NPL3045886, NPL3045889, NPL3045890, NPL3045891, NPL3045892, NPL3045897, NPL3045898, NPL3045911, NPL3045912, NPL3045924, NPL3045930, NPL3045933, NPL3045934, NPL3045937, NPL3045939, NPL3045940, NPL3045957, NPL3045958, NPL3045960, NPL3045965, NPL3045966, NPL3045973, NPL3045977, NPL3045984, NPL3045985, NPL3046034, NPL3046041, NPL3046042, NPL3046043, NPL3046045, NPL3046066, NPL3046078, NPL3046090, NPL3046091, NPL3046094, NPL3046095, NPL3046097, NPL3046099, NPL3046101, NPL3046103, NPL3046106, NPL3046107, NPL3046109, NPL3046110, NPL3046111, NPL3046112, NPL3046114, NPL3046115, NPL3046116, NPL3046121, NPL3046123, NPL3046125, NPL3046126, NPL3046134, NPL3046135, NPL3046136, NPL3046137, NPL3046138, NPL3046139, NPL3046140, NPL3046141, NPL3046142, NPL3046143, NPL3046144, NPL3046145, NPL3046146, NPL3046147, NPL3046148, NPL3046149, NPL3046150, NPL3046151, NPL3046153, NPL3046154, NPL3046156, NPL3046157, NPL3046159, NPL3046160, NPL3046161, NPL3046162, NPL3046163, NPL3046164, NPL3046165, NPL3046166, NPL3046168, NPL3046169, NPL3046170, NPL3046171, NPL3046172, NPL3046173, NPL3046174, NPL3046176, NPL3046177, NPL3046178, NPL3046179, NPL3046180, NPL3046181, NPL3046182, NPL3046183, NPL3046184, NPL3046185, NPL3046186, NPL3046187, NPL3046188, NPL3046189, NPL3046190, NPL3046191, NPL3046192, NPL3046193, NPL3046194, NPL3046196, NPL3046197, NPL3046198, NPL3046199, NPL3046201, NPL3046203, NPL3046204, NPL3046205, NPL3046206, NPL3046207, NPL3046208, NPL3046209, NPL3046210, NPL3046211, NPL3046212, NPL3046213, NPL3046214, NPL3046215, NPL3046216, NPL3046217, NPL3046218, NPL3046219, NPL3046220, NPL3046221, NPL3046223, NPL3046225, NPL3046226, NPL3046227, NPL3046228, NPL3046229, NPL3046230, NPL3046231, NPL3046232, NPL3046234, NPL3046236, NPL3046238, NPL3046239, NPL3046240, NPL3046241, NPL3046243, NPL3046245, NPL3046246, NPL3046247, NPL3046248, NPL3046249, NPL3046251, NPL3046252, NPL3046253, NPL3046254, NPL3046255, NPL3046256, NPL3046257, NPL3046258, NPL3046259, NPL3046260, NPL3046261, NPL3046262, NPL3046263, NPL3046264, NPL3046265, NPL3046266, NPL3046268, NPL3046269, NPL3046270, NPL3046271, NPL3046272, NPL3046274, NPL3046275, NPL3046276, NPL3046279, NPL3046280, NPL3046281, NPL3046282, NPL3046283, NPL3046284, NPL3046285, NPL3046286, NPL3046287, NPL3046288, NPL3046289, NPL3046290, NPL3046291, NPL3046292, NPL3046293, NPL3046294, NPL3046296, NPL3046297, NPL3046298, NPL3046299, NPL3046300, NPL3046302, NPL3046303, NPL3046304, NPL3046307, NPL3046310, NPL3046311, NPL3046313, NPL3046314, NPL3046316, NPL3046317, NPL3046318, NPL3046319, NPL3046320, NPL3046321, NPL3046323, NPL3046324, NPL3046325, NPL3046326, NPL3046327, NPL3046328, NPL3046329, NPL3046330, NPL3046331, NPL3046332, NPL3046334, NPL3046335, NPL3046338, NPL3046339, NPL3046341, NPL3046342, NPL3046343, NPL3046344, NPL3046345, NPL3046346, NPL3046347, NPL3046348, NPL3046349, NPL3046350, NPL3046351, NPL3046352, NPL3046353, NPL3046354, NPL3046355, NPL3046356, NPL3046357, NPL3046358, NPL3046359, NPL3046360, NPL3046361, NPL3046362, NPL3046363, NPL3046364, NPL3046365, NPL3046366, NPL3046367, NPL3046368, NPL3046369, NPL3046370, NPL3046371, NPL3046372, NPL3046373, NPL3046374, NPL3046376, NPL3046377, NPL3046378, NPL3046379, NPL3046380, NPL3046381, NPL3046382, NPL3046383, NPL3046384, NPL3046386, NPL3046389, NPL3046391, NPL3046393, NPL3046394, NPL3046396, NPL3046397, NPL3046398, NPL3046400, NPL3046401, NPL3046402, NPL3046403, NPL3046404, NPL3046406, NPL3046407, NPL3046408, NPL3046409, NPL3046410, NPL3046412, NPL3046413, NPL3046414, NPL3046415, NPL3046416, NPL3046417, NPL3046418, NPL3046419, NPL3046420, NPL3046422, NPL3046423, NPL3046424, NPL3046425, NPL3046427, NPL3046428, NPL3046430, NPL3046432, NPL3046433, NPL3046434, NPL3046435, NPL3046436, NPL3046437, NPL3046438, NPL3046439, NPL3046440, NPL3046441, NPL3046442, NPL3046443, NPL3046446, NPL3046447, NPL3046448, NPL3046449, NPL3046451, NPL3046452, NPL3046453, NPL3046454, NPL3046455, NPL3046457, NPL3046458, NPL3046459, NPL3046460, NPL3046461, NPL3046462, NPL3046463, NPL3046464, NPL3046465, NPL3046466, NPL3046467, NPL3046468, NPL3046469, NPL3046471, NPL3046472, NPL3046473, NPL3046474, NPL3046476, NPL3046477, NPL3046478, NPL3046479, NPL3046480, NPL3046481, NPL3046482, NPL3046483, NPL3046484, NPL3046485, NPL3046486, NPL3046492, NPL3046493, NPL3046494, NPL3046497, NPL3046498, NPL3046499, NPL3046500, NPL3046501, NPL3046502, NPL3046503, NPL3046504, NPL3046505, NPL3046517, NPL3046518, NPL3046519, NPL3046520, NPL3046521, NPL3046522, NPL3046523, NPL3046532, NPL3046533, NPL3046535, NPL3046537, NPL3046538, NPL3046540, NPL3046542, NPL3046543, NPL3046544, NPL3046545, NPL3046546, NPL3046547, NPL3046548, NPL3046549, NPL3046550, NPL3046551, NPL3046552, NPL3046553, NPL3046554, NPL3046560, NPL3046563, NPL3046564, NPL3046565, NPL3046566, NPL3046567, NPL3046568, NPL3046569, NPL3046570, NPL3046571, NPL3046572, NPL3046573, NPL3046574, NPL3046575, NPL3046577, NPL3046579, NPL3046580, NPL3046581, NPL3046582, NPL3046583, NPL3046584, NPL3046587, NPL3046588, NPL3046589, NPL3046590, NPL3046591, NPL3046592, NPL3046593, NPL3046595, NPL3046597, NPL3046599, NPL3046601, NPL3046603, NPL3046604, NPL3046605, NPL3046606, NPL3046607, NPL3046630, NPL3046631, NPL3046632, NPL3046633, NPL3046634, NPL3046635, NPL3046636, NPL3046637, NPL3046638, NPL3046639, NPL3046640, NPL3046641, NPL3046642, NPL3046643, NPL3046644, NPL3046645, NPL3046646, NPL3046647, NPL3046648, NPL3046649, NPL3046650, NPL3046651, NPL3046652, NPL3046653, NPL3046654, NPL3046655, NPL3046656, NPL3046657, NPL3046659, NPL3046660, NPL3046661, NPL3046662, NPL3046663, NPL3046664, NPL3046665, NPL3046667, NPL3046668, NPL3046669, NPL3046670, NPL3046671, NPL3046672, NPL3046674, NPL3046675, NPL3046676, NPL3046677, NPL3046678, NPL3046679, NPL3046680, NPL3046682, NPL3046684, NPL3046686, NPL3046689, NPL3046705, NPL3046709, NPL3046711, NPL3046712, NPL3046713, NPL3046714, NPL3046715, NPL3046716, NPL3046717, NPL3046719, NPL3046720, NPL3046721, NPL3046723, NPL3046724, NPL3046725, NPL3046726, NPL3046727, NPL3046728, NPL3046729, NPL3046748, NPL3046749, NPL3046750, NPL3046751, NPL3046752, NPL3046753, NPL3046754, NPL3046755, NPL3046756, NPL3046757, NPL3046758, NPL3046759, NPL3046760, NPL3046761, NPL3046762, NPL3046763, NPL3046764, NPL3046766, NPL3046767, NPL3046768, NPL3046771, NPL3046773, NPL3046774, NPL3046775, NPL3046776, NPL3046777, NPL3046779, NPL3046780, NPL3046781, NPL3046782, NPL3046783, NPL3046784, NPL3046785, NPL3046787, NPL3046788, NPL3046793, NPL3046795, NPL3046797, NPL3046800, NPL3046802, NPL3046803, NPL3046804, NPL3046805, NPL3046806, NPL3046807, NPL3046808, NPL3046809, NPL3046810, NPL3046811, NPL3046812, NPL3046813, NPL3046814, NPL3046815, NPL3046816, NPL3046817, NPL3046818, NPL3046819, NPL3046820, NPL3046821, NPL3046822, NPL3046824, NPL3046825, NPL3046826, NPL3046843, NPL3046844, NPL3046845, NPL3046846, NPL3046847, NPL3046848, NPL3046866, NPL3046870, NPL3046871, NPL3046872, NPL3046873, NPL3046874, NPL3046875, NPL3046876, NPL3046877, NPL3046878, NPL3046879, NPL3046880, NPL3046881, NPL3046882, NPL3046883, NPL3046884, NPL3046885, NPL3046886, NPL3046887, NPL3046888, NPL3046889, NPL3046890, NPL3046891, NPL3046892, NPL3046893, NPL3046894, NPL3046895, NPL3046896, NPL3046899, NPL3046900, NPL3046901, NPL3046902, NPL3046903, NPL3046904, NPL3046907, NPL3046908, NPL3046909, NPL3046910, NPL3046911, NPL3046912, NPL3046914, NPL3046915, NPL3046916, NPL3046917, NPL3046919, NPL3046920, NPL3046921, NPL3046922, NPL3046923, NPL3046925, NPL3046926, NPL3046927, NPL3046928, NPL3046929, NPL3046930, NPL3046931, NPL3046932, NPL3046933, NPL3046934, NPL3046935, NPL3046936, NPL3046937, NPL3046938, NPL3046939, NPL3046940, NPL3046941, NPL3046942, NPL3046948, NPL3046949, NPL3046950, NPL3046951, NPL3046952, NPL3046953, NPL3046954, NPL3046955, NPL3046956, NPL3046957, NPL3046958, NPL3046959, NPL3046960, NPL3046961, NPL3046962, NPL3046963, NPL3046964, NPL3046980, NPL3046981, NPL3046992, NPL3046993, NPL3046995, NPL3046997, NPL3046998, NPL3047003, NPL3047005, NPL3047006, NPL3047007, NPL3047010, NPL3047015, NPL3047016, NPL3047019, NPL3047020, NPL3047022, NPL3047023, NPL3047031, NPL3047032, NPL3047034, NPL3047036, NPL3047038, NPL3047041, NPL3047044, NPL3047045, NPL3047047, NPL3047048, NPL3047052, NPL3047053, NPL3047054, NPL3047055, NPL3047065, NPL3047087, NPL3047088, NPL3047090, NPL3047091, NPL3047092, NPL3047095, NPL3047096, NPL3047098, NPL3047099, NPL3047103, NPL3047104, NPL3047105, NPL3047106, NPL3047107, NPL3047108, NPL3047111, NPL3047113, NPL3047114, NPL3047116, NPL3047119, NPL3047123, NPL3047137, NPL3047138, NPL3047139, NPL3047140, NPL3047141, NPL3047142, NPL3047143, NPL3047144, NPL3047145, NPL3047146, NPL3047147, NPL3047148, NPL3047149, NPL3047150, NPL3047151, NPL3047152, NPL3047153, NPL3047154, NPL3047155, NPL3047156, NPL3047157, NPL3047158, NPL3047161, NPL3047162, NPL3047163, NPL3047164, NPL3047165, NPL3047166, NPL3047167, NPL3047168, NPL3047169, NPL3047170, NPL3047177, NPL3047179, NPL3047180, NPL3047182, NPL3047183, NPL3047184, NPL3047187, NPL3047189, NPL3047195, NPL3047203, NPL3047204, NPL3047225, NPL3047226, NPL3047227, NPL3047228, NPL3047231, NPL3047233, NPL3047234, NPL3047235, NPL3047237, NPL3047238, NPL3047239, NPL3047240, NPL3047241, NPL3047242, NPL3047243, NPL3047244, NPL3047245, NPL3047246, NPL3047247, NPL3047248, NPL3047249, NPL3047250, NPL3047253, NPL3047254, NPL3047255, NPL3047256, NPL3047258, NPL3047259, NPL3047260, NPL3047261, NPL3047262, NPL3047263, NPL3047264, NPL3047265, NPL3047266, NPL3047270, NPL3047271, NPL3047272, NPL3047273, NPL3047274, NPL3047275, NPL3047277, NPL3047278, NPL3047279, NPL3047280, NPL3047281, NPL3047282, NPL3047283, NPL3047284, NPL3047285, NPL3047286, NPL3047287, NPL3047288, NPL3047289, NPL3047290, NPL3047291, NPL3047292, NPL3047293, NPL3047294, NPL3047296, NPL3047297, NPL3047298, NPL3047301, NPL3047302, NPL3047303, NPL3047305, NPL3047314, NPL3047318, NPL3047322, NPL3047323, NPL3047325, NPL3047326, NPL3047327, NPL3047328, NPL3047331, NPL3047332, NPL3047333, NPL3047334, NPL3047335, NPL3047336, NPL3047337, NPL3047338, NPL3047339, NPL3047340, NPL3047341, NPL3047342, NPL3047343, NPL3047344, NPL3047345, NPL3047346, NPL3047347, NPL3047348, NPL3047349, NPL3047352, NPL3047353, NPL3047354, NPL3047355, NPL3047356, NPL3047357, NPL3047358, NPL3047359, NPL3047360, NPL3047361, NPL3047362, NPL3047368, NPL3047369, NPL3047370, NPL3047371, NPL3047372, NPL3047373, NPL3047374, NPL3047375, NPL3047376, NPL3047377, NPL3047378, NPL3047379, NPL3047380, NPL3047382, NPL3047383, NPL3047384, NPL3047386, NPL3047387, NPL3047388, NPL3047389, NPL3047390, NPL3047391, NPL3047392, NPL3047393, NPL3047395, NPL3047398, NPL3047399, NPL3047400, NPL3047402, NPL3047403, NPL3047406, NPL3047408, NPL3047409, NPL3047410, NPL3047411, NPL3047412, NPL3047413, NPL3047414, NPL3047415, NPL3047416, NPL3047417, NPL3047418, NPL3047420, NPL3047421, NPL3047422, NPL3047423, NPL3047424, NPL3047425, NPL3047426, NPL3047427, NPL3047428, NPL3047429, NPL3047430, NPL3047432, NPL3047433, NPL3047434, NPL3047435, NPL3047436, NPL3047437, NPL3047438, NPL3047439, NPL3047440, NPL3047442, NPL3047443, NPL3047446, NPL3047452, NPL3047453, NPL3047454, NPL3047455, NPL3047456, NPL3047457, NPL3047462, NPL3047463, NPL3047464, NPL3047466, NPL3047467, NPL3047468, NPL3047469, NPL3047470, NPL3047471, NPL3047472, NPL3047475, NPL3047476, NPL3047479, NPL3047480, NPL3047482, NPL3047483, NPL3047484, NPL3047486, NPL3047487, NPL3047488, NPL3047489, NPL3047491, NPL3047492, NPL3047494, NPL3047495, NPL3047499, NPL3047500, NPL3047501, NPL3047502, NPL3047503, NPL3047504, NPL3047505, NPL3047506, NPL3047507, NPL3047508, NPL3047509, NPL3047510, NPL3047511, NPL3047512, NPL3047513, NPL3047516, NPL3047517, NPL3047518, NPL3047521, NPL3047525, NPL3047526, NPL3047527, NPL3047528, NPL3047529, NPL3047532, NPL3047548, NPL3047549, NPL3047550, NPL3047551, NPL3047559, NPL3047560, NPL3047561, NPL3047562, NPL3047563, NPL3047565, NPL3047566, NPL3047567, NPL3047568, NPL3047569, NPL3047570, NPL3047572, NPL3047573, NPL3047575, NPL3047576, NPL3047577, NPL3047579, NPL3047611, NPL3047614, NPL3047615, NPL3047616, NPL3047617, NPL3047618, NPL3047619, NPL3047622, NPL3047623, NPL3047625, NPL3047626, NPL3047627, NPL3047628, NPL3047629, NPL3047635, NPL3047636, NPL3047638, NPL3047639, NPL3047640, NPL3047641, NPL3047642, NPL3047643, NPL3047644, NPL3047645, NPL3047646, NPL3047647, NPL3047649, NPL3047650, NPL3047651, NPL3047652, NPL3047654, NPL3047656, NPL3047657, NPL3047659, NPL3047662, NPL3047664, NPL3047665, NPL3047668, NPL3047671, NPL3047672, NPL3047673, NPL3047674, NPL3047675, NPL3047676, NPL3047677, NPL3047678, NPL3047679, NPL3047680, NPL3047681, NPL3047682, NPL3047683, NPL3047684, NPL3047685, NPL3047686, NPL3047687, NPL3047689, NPL3047691, NPL3047692, NPL3047693, NPL3047694, NPL3047696, NPL3047697, NPL3047698, NPL3047699, NPL3047700, NPL3047701, NPL3047702, NPL3047703, NPL3047704, NPL3047709, NPL3047710, NPL3047711, NPL3047712, NPL3047713, NPL3047714, NPL3047715, NPL3047716, NPL3047717, NPL3047718, NPL3047719, NPL3047720, NPL3047721, NPL3047722, NPL3047723, NPL3047724, NPL3047725, NPL3047726, NPL3047729, NPL3047731, NPL3047732, NPL3047733, NPL3047734, NPL3047735, NPL3047736, NPL3047738, NPL3047739, NPL3047740, NPL3047741, NPL3047743, NPL3047744, NPL3047745, NPL3047746, NPL3047747, NPL3047748, NPL3047752, NPL3047753, NPL3047754, NPL3047755, NPL3047756, NPL3047757, NPL3047758, NPL3047759, NPL3047760, NPL3047761, NPL3047762, NPL3047763, NPL3047764, NPL3047765, NPL3047769, NPL3047772, NPL3047773, NPL3047774, NPL3047775, NPL3047776, NPL3047777, NPL3047778, NPL3047779, NPL3047781, NPL3047782, NPL3047783, NPL3047784, NPL3047785, NPL3047786, NPL3047787, NPL3047788, NPL3047789, NPL3047790, NPL3047791, NPL3047792, NPL3047793, NPL3047794, NPL3047795, NPL3047796, NPL3047797, NPL3047798, NPL3047799, NPL3047800, NPL3047801, NPL3047802, NPL3047803, NPL3047804, NPL3047805, NPL3047806, NPL3047807, NPL3047808, NPL3047809, NPL3047810, NPL3047811, NPL3047814, NPL3047815, NPL3047816, NPL3047817, NPL3047818, NPL3047820, NPL3047822, NPL3047823, NPL3047824, NPL3047826, NPL3047829, NPL3047830, NPL3047833, NPL3047834, NPL3047835, NPL3047836, NPL3047837, NPL3047838, NPL3047839, NPL3047841, NPL3047842, NPL3047843, NPL3047848, NPL3047849, NPL3047853, NPL3047854, NPL3047855, NPL3047856, NPL3047857, NPL3047858, NPL3047859, NPL3047860, NPL3047861, NPL3047862, NPL3047863, NPL3047864, NPL3047866, NPL3047872, NPL3047875, NPL3047878, NPL3047879, NPL3047880, NPL3047882, NPL3047883, NPL3047884, NPL3047885, NPL3047886, NPL3047887, NPL3047908, NPL3047909, NPL3047910, NPL3047912, NPL3047914, NPL3047915, NPL3047917, NPL3047920, NPL3047921, NPL3047922, NPL3047924, NPL3047925, NPL3047926, NPL3047927, NPL3047928, NPL3047929, NPL3047930, NPL3047935, NPL3047936, NPL3047937, NPL3047938, NPL3047939, NPL3047941, NPL3047944, NPL3047945, NPL3047946, NPL3047947, NPL3047948, NPL3047949, NPL3047950, NPL3047951, NPL3047952, NPL3047954, NPL3047955, NPL3047956, NPL3047957, NPL3047958, NPL3047959, NPL3047960, NPL3047961, NPL3047962, NPL3047963, NPL3047964, NPL3047965, NPL3047966, NPL3047967, NPL3047968, NPL3047969, NPL3047970, NPL3047971, NPL3047972, NPL3047973, NPL3047975, NPL3047976, NPL3047977, NPL3047978, NPL3047979, NPL3047980, NPL3047981, NPL3047982, NPL3047983, NPL3047984, NPL3047987, NPL3047989, NPL3047990, NPL3047991, NPL3047992, NPL3047993, NPL3047994, NPL3047995, NPL3047996, NPL3047997, NPL3047998, NPL3047999, NPL3048000, NPL3048001, NPL3048002, NPL3048003, NPL3048004, NPL3048005, NPL3048011, NPL3048013, NPL3048014, NPL3048015, NPL3048016, NPL3048017, NPL3048019, NPL3048020, NPL3048021, NPL3048022, NPL3048023, NPL3048024, NPL3048025, NPL3048032, NPL3048033, NPL3048034, NPL3048035, NPL3048036, NPL3048038, NPL3048039, NPL3048041, NPL3048046, NPL3048047, NPL3048048, NPL3048052, NPL3048053, NPL3048054, NPL3048055, NPL3048062, NPL3048067, NPL3048068, NPL3048069, NPL3048071, NPL3048075, NPL3048082, NPL3048088, NPL3048089, NPL3048090, NPL3048091, NPL3048092, NPL3048094, NPL3048095, NPL3048096, NPL3048097, NPL3048098, NPL3048099, NPL3048100, NPL3048101, NPL3048102, NPL3048103, NPL3048104, NPL3048105, NPL3048106, NPL3048107, NPL3048109, NPL3048110, NPL3048111, NPL3048112, NPL3048113, NPL3048114, NPL3048115, NPL3048116, NPL3048117, NPL3048118, NPL3048119, NPL3048120, NPL3048121, NPL3048122, NPL3048123, NPL3048124, NPL3048125, NPL3048129, NPL3048130, NPL3048135, NPL3048136, NPL3048137, NPL3048138, NPL3048139, NPL3048142, NPL3048143, NPL3048148, NPL3048149, NPL3048150, NPL3048151, NPL3048152, NPL3048153, NPL3048154, NPL3048160, NPL3048161, NPL3048163, NPL3048164, NPL3048165, NPL3048166, NPL3048168, NPL3048169, NPL3048171, NPL3048173, NPL3048174, NPL3048175, NPL3048176, NPL3048177, NPL3048178, NPL3048180, NPL3048183, NPL3048185, NPL3048186, NPL3048187, NPL3048188, NPL3048193, NPL3048194, NPL3048197, NPL3048200, NPL3048206, NPL3048207, NPL3048208, NPL3048209, NPL3048210, NPL3048214, NPL3048217, NPL3048218, NPL3048219, NPL3048220, NPL3048221, NPL3048222, NPL3048223, NPL3048224, NPL3048225, NPL3048226, NPL3048227, NPL3048229, NPL3048230, NPL3048231, NPL3048232, NPL3048233, NPL3048236, NPL3048237, NPL3048239, NPL3048241, NPL3048243, NPL3048244, NPL3048245, NPL3048246, NPL3048248, NPL3048249, NPL3048250, NPL3048251, NPL3048252, NPL3048254, NPL3048255, NPL3048256, NPL3048257, NPL3048258, NPL3048259, NPL3048261, NPL3048262, NPL3048264, NPL3048265, NPL3048267, NPL3048268, NPL3048269, NPL3048270, NPL3048271, NPL3048272, NPL3048273, NPL3048274, NPL3048277, NPL3048278, NPL3048279, NPL3048283, NPL3048284, NPL3048285, NPL3048286, NPL3048287, NPL3048288, NPL3048289, NPL3048290, NPL3048291, NPL3048292, NPL3048294, NPL3048295, NPL3048296, NPL3048297, NPL3048298, NPL3048300, NPL3048301, NPL3048302, NPL3048303, NPL3048304, NPL3048305, NPL3048306, NPL3048307, NPL3048308, NPL3048310, NPL3048311, NPL3048313, NPL3048314, NPL3048315, NPL3048316, NPL3048318, NPL3048320, NPL3048321, NPL3048330, NPL3048331, NPL3048332, NPL3048333, NPL3048335, NPL3048336, NPL3048337, NPL3048338, NPL3048339, NPL3048340, NPL3048342, NPL3048343, NPL3048345, NPL3048347, NPL3048348, NPL3048350, NPL3048351, NPL3048352, NPL3048353, NPL3048354, NPL3048356, NPL3048357, NPL3048358, NPL3048359, NPL3048360, NPL3048363, NPL3048364, NPL3048365, NPL3048366, NPL3048368, NPL3048369, NPL3048370, NPL3048371, NPL3048372, NPL3048373, NPL3048375, NPL3048376, NPL3048377, NPL3048378, NPL3048379, NPL3048381, NPL3048382, NPL3048383, NPL3048384, NPL3048385, NPL3048386, NPL3048387, NPL3048389, NPL3048393, NPL3048394, NPL3048395, NPL3048396, NPL3048397, NPL3048398, NPL3048399, NPL3048400, NPL3048401, NPL3048402, NPL3048403, NPL3048404, NPL3048405, NPL3048406, NPL3048407, NPL3048409, NPL3048410, NPL3048411, NPL3048412, NPL3048413, NPL3048414, NPL3048415, NPL3048416, NPL3048417, NPL3048418, NPL3048419, NPL3048420, NPL3048421, NPL3048422, NPL3048423, NPL3048424, NPL3048425, NPL3048426, NPL3048427, NPL3048428, NPL3048429, NPL3048430, NPL3048431, NPL3048432, NPL3048433, NPL3048434, NPL3048435, NPL3048436, NPL3048437, NPL3048438, NPL3048439, NPL3048440, NPL3048441, NPL3048442, NPL3048443, NPL3048444, NPL3048445, NPL3048446, NPL3048447, NPL3048448, NPL3048450, NPL3048452, NPL3048453, NPL3048465, NPL3048466, NPL3048467, NPL3048468, NPL3048469, NPL3048470, NPL3048471, NPL3048472, NPL3048473, NPL3048474, NPL3048475, NPL3048476, NPL3048477, NPL3048478, NPL3048479, NPL3048480, NPL3048481, NPL3048482, NPL3048483, NPL3048484, NPL3048485, NPL3048486, NPL3048487, NPL3048488, NPL3048489, NPL3048490, NPL3048499, NPL3048504, NPL3048513, NPL3048514, NPL3048521, NPL3048523, NPL3048530, NPL3048533, NPL3048536, NPL3048544, NPL3048548, NPL3048549, NPL3048552, NPL3048561, NPL3048562, NPL3048563, NPL3048565, NPL3048571, NPL3048581, NPL3048587, NPL3048588, NPL3048594, NPL3048595, NPL3048598, NPL3048599, NPL3048600, NPL3048601, NPL3048602, NPL3048604, NPL3048612, NPL3048614, NPL3048615, NPL3048619, NPL3048621, NPL3048622, NPL3048623, NPL3048625, NPL3048634, NPL3048651, NPL3048652, NPL3048667, NPL3048668, NPL3048671, NPL3048672, NPL3048673, NPL3048674, NPL3048675, NPL3048677, NPL3048678, NPL3048679, NPL3048684, NPL3048685, NPL3048687, NPL3048690, NPL3048691, NPL3048694, NPL3048695, NPL3048706, NPL3048710, NPL3048715, NPL3048716, NPL3048717, NPL3048731, NPL3048732, NPL3048734, NPL3048737, NPL3048738, NPL3048739, NPL3048741, NPL3048742, NPL3048757, NPL3048766, NPL3048771, NPL3048775, NPL3048777, NPL3048783, NPL3048784, NPL3048787, NPL3048797, NPL3048799, NPL3048801, NPL3048806, NPL3048810, NPL3048814, NPL3048818, NPL3048821, NPL3048827, NPL3048829, NPL3048835, NPL3048836, NPL3048837, NPL3048838, NPL3048839, NPL3048840, NPL3048842, NPL3048843, NPL3048844, NPL3048846, NPL3048848, NPL3048849, NPL3048850, NPL3048851, NPL3048852, NPL3048853, NPL3048854, NPL3048855, NPL3048856, NPL3048857, NPL3048858, NPL3048859, NPL3048860, NPL3048861, NPL3048862, NPL3048863, NPL3048864, NPL3048868, NPL3048870, NPL3048871, NPL3048872, NPL3048873, NPL3048874, NPL3048875, NPL3048876, NPL3048877, NPL3048878, NPL3048879, NPL3048880, NPL3048881, NPL3048882, NPL3048883, NPL3048884, NPL3048885, NPL3048886, NPL3048887, NPL3048888, NPL3048889, NPL3048890, NPL3048891, NPL3048892, NPL3048893, NPL3048894, NPL3048895, NPL3048896, NPL3048897, NPL3048898, NPL3048899, NPL3048900, NPL3048901, NPL3048902, NPL3048903, NPL3048904, NPL3048905, NPL3048906, NPL3048907, NPL3048908, NPL3048909, NPL3048910, NPL3048911, NPL3048912, NPL3048913, NPL3048914, NPL3048915, NPL3048916, NPL3048917, NPL3048918, NPL3048919, NPL3048920, NPL3048921, NPL3048927, NPL3048928, NPL3048929, NPL3048930, NPL3048931, NPL3048933, NPL3048934, NPL3048935, NPL3048936, NPL3048938, NPL3048939, NPL3048940, NPL3048941, NPL3048942, NPL3048943, NPL3048944, NPL3048945, NPL3048946, NPL3048947, NPL3048948, NPL3048949, NPL3048951, NPL3048952, NPL3048953, NPL3048954, NPL3048955, NPL3048956, NPL3048957, NPL3048958, NPL3048959, NPL3048960, NPL3048964, NPL3048965, NPL3048966, NPL3048967, NPL3048971, NPL3048974, NPL3048975, NPL3048989, NPL3048990, NPL3049001, NPL3049004, NPL3049005, NPL3049006, NPL3049007, NPL3049008, NPL3049009, NPL3049010, NPL3049011, NPL3049013, NPL3049014, NPL3049015, NPL3049016, NPL3049017, NPL3049018, NPL3049039, NPL3049045, NPL3049046, NPL3049052, NPL3049053, NPL3049054, NPL3049058, NPL3049059, NPL3049064, NPL3049065, NPL3049099, NPL3049106, NPL3049107, NPL3049108, NPL3049109, NPL3049110, NPL3049117, NPL3049119, NPL3049120, NPL3049121, NPL3049122, NPL3049123, NPL3049124, NPL3049125, NPL3049126, NPL3049127, NPL3049128, NPL3049129, NPL3049130, NPL3049132, NPL3049133, NPL3049134, NPL3049135, NPL3049136, NPL3049137, NPL3049140, NPL3049142, NPL3049145, NPL3049146, NPL3049147, NPL3049148, NPL3049149, NPL3049150, NPL3049151, NPL3049153, NPL3049154, NPL3049156, NPL3049157, NPL3049158, NPL3049159, NPL3049160, NPL3049161, NPL3049163, NPL3049164, NPL3049165, NPL3049166, NPL3049167, NPL3049168, NPL3049169, NPL3049170, NPL3049171, NPL3049172, NPL3049173, NPL3049175, NPL3049176, NPL3049177, NPL3049178, NPL3049179, NPL3049180, NPL3049182, NPL3049183, NPL3049184, NPL3049185, NPL3049187, NPL3049188, NPL3049189, NPL3049192, NPL3049194, NPL3049199, NPL3049200, NPL3049202, NPL3049203, NPL3049204, NPL3049206, NPL3049217, NPL3049218, NPL3049219, NPL3049220, NPL3049221, NPL3049222, NPL3049223, NPL3049231, NPL3049234, NPL3049235, NPL3049243, NPL3049254, NPL3049255, NPL3049256, NPL3049257, NPL3049262, NPL3049263, NPL3049264, NPL3049265, NPL3049267, NPL3049269, NPL3049284, NPL3049289, NPL3049290, NPL3049291, NPL3049300, NPL3049303, NPL3049309, NPL3049310, NPL3049312, NPL3049320, NPL3049328, NPL3049329, NPL3049330, NPL3049332, NPL3049334, NPL3049336, NPL3049337, NPL3049346, NPL3049347, NPL3049359, NPL3049360, NPL3049361, NPL3049362, NPL3049364, NPL3049365, NPL3049377, NPL3049380, NPL3049381, NPL3049382, NPL3049383, NPL3049384, NPL3049398, NPL3049404, NPL3049409, NPL3049421, NPL3049429, NPL3049433, NPL3049434, NPL3049440, NPL3049450, NPL3049456, NPL3049457, NPL3049458, NPL3049459, NPL3049460, NPL3049461, NPL3049463, NPL3049464, NPL3049466, NPL3049467, NPL3049470, NPL3049471, NPL3049474, NPL3049475, NPL3049477, NPL3049479, NPL3049481, NPL3049482, NPL3049483, NPL3049484, NPL3049485, NPL3049486, NPL3049487, NPL3049489, NPL3049505, NPL3049508, NPL3049509, NPL3049510, NPL3049511, NPL3049512, NPL3049513, NPL3049514, NPL3049515, NPL3049516, NPL3049517, NPL3049518, NPL3049519, NPL3049520, NPL3049521, NPL3049522, NPL3049523, NPL3049524, NPL3049525, NPL3049526, NPL3049527, NPL3049528, NPL3049529, NPL3049530, NPL3049531, NPL3049532, NPL3049533, NPL3049534, NPL3049535, NPL3049536, NPL3049537, NPL3049538, NPL3049539, NPL3049540, NPL3049543, NPL3049550, NPL3049551, NPL3049552, NPL3049554, NPL3049555, NPL3049556, NPL3049557, NPL3049558, NPL3049559, NPL3049563, NPL3049564, NPL3049565, NPL3049566, NPL3049567, NPL3049568, NPL3049569, NPL3049571, NPL3049572, NPL3049576, NPL3049582, NPL3049587, NPL3049588, NPL3049589, NPL3049590, NPL3049591, NPL3049592, NPL3049593, NPL3049594, NPL3049595, NPL3049596, NPL3049597, NPL3049598, NPL3049599, NPL3049600, NPL3049601, NPL3049602, NPL3049604, NPL3049606, NPL3049607, NPL3049609, NPL3049611, NPL3049612, NPL3049613, NPL3049614, NPL3049615, NPL3049616, NPL3049617, NPL3049618, NPL3049619, NPL3049620, NPL3049621, NPL3049622, NPL3049623, NPL3049624, NPL3049625, NPL3049626, NPL3049627, NPL3049628, NPL3049629, NPL3049630, NPL3049631, NPL3049632, NPL3049633, NPL3049634, NPL3049635, NPL3049636, NPL3049637, NPL3049638, NPL3049639, NPL3049640, NPL3049641, NPL3049642, NPL3049643, NPL3049644, NPL3049645, NPL3049646, NPL3049647, NPL3049648, NPL3049649, NPL3049650, NPL3049651, NPL3049652, NPL3049653, NPL3049654, NPL3049655, NPL3049656, NPL3049657, NPL3049658, NPL3049659, NPL3049660, NPL3049661, NPL3049662, NPL3049663, NPL3049664, NPL3049665, NPL3049666, NPL3049667, NPL3049668, NPL3049669, NPL3049670, NPL3049671, NPL3049672, NPL3049673, NPL3049674, NPL3049675, NPL3049676, NPL3049677, NPL3049678, NPL3049679, NPL3049680, NPL3049681, NPL3049682, NPL3049683, NPL3049684, NPL3049685, NPL3049686, NPL3049687, NPL3049688, NPL3049690, NPL3049691, NPL3049692, NPL3049693, NPL3049694, NPL3049695, NPL3049696, NPL3049697, NPL3049698, NPL3049699, NPL3049700, NPL3049701, NPL3049702, NPL3049703, NPL3049704, NPL3049705, NPL3049706, NPL3049707, NPL3049708, NPL3049709, NPL3049710, NPL3049711, NPL3049712, NPL3049713, NPL3049714, NPL3049715, NPL3049716, NPL3049717, NPL3049718, NPL3049719, NPL3049720, NPL3049721, NPL3049722, NPL3049723, NPL3049724, NPL3049725, NPL3049726, NPL3049727, NPL3049728, NPL3049729, NPL3049730, NPL3049731, NPL3049732, NPL3049733, NPL3049734, NPL3049735, NPL3049737, NPL3049738, NPL3049739, NPL3049740, NPL3049741, NPL3049742, NPL3049743, NPL3049744, NPL3049745, NPL3049746, NPL3049747, NPL3049748, NPL3049749, NPL3049750, NPL3049751, NPL3049752, NPL3049753, NPL3049754, NPL3049755, NPL3049756, NPL3049757, NPL3049758, NPL3049759, NPL3049761, NPL3049763, NPL3049765, NPL3049770, NPL3049772, NPL3049774, NPL3049775, NPL3049777, NPL3049778, NPL3049779, NPL3049783, NPL3049786, NPL3049787, NPL3049788, NPL3049789, NPL3049793, NPL3049794, NPL3049795, NPL3049797, NPL3049798, NPL3049806, NPL3049819, NPL3049820, NPL3049821, NPL3049822, NPL3049823, NPL3049825, NPL3049826, NPL3049829, NPL3049830, NPL3049832, NPL3049833, NPL3049835, NPL3049837, NPL3049838, NPL3049839, NPL3049840, NPL3049843, NPL3049857, NPL3049876, NPL3050007, NPL3050117, NPL3050122, NPL3050146, NPL3050205, NPL3050212, NPL3050217, NPL3050275, NPL3050286, NPL3050310, NPL3050333, NPL3050349, NPL3050364, NPL3050392, NPL3050414, NPL3050424, NPL3050426, NPL3050443, NPL3050449, NPL3050497, NPL3050499, NPL3050508, NPL3050518, NPL3050538, NPL3050562, NPL3050575, NPL3050581, NPL3050583, NPL3050592, NPL3050607, NPL3050620, NPL3050674, NPL3050675, NPL3050677, NPL3050678, NPL3050679, NPL3050680, NPL3050682, NPL3050683, NPL3050685, NPL3050687, NPL3050689, NPL3050690, NPL3050692, NPL3050693, NPL3050694, NPL3050695, NPL3050697, NPL3050700, NPL3050701, NPL3050702, NPL3050703, NPL3050704, NPL3050705, NPL3050706, NPL3050707, NPL3050708, NPL3050709, NPL3050711, NPL3050712, NPL3050714, NPL3050715, NPL3050717, NPL3050721, NPL3050724, NPL3050725, NPL3050726, NPL3050735, NPL3050738, NPL3050739, NPL3050740, NPL3050742, NPL3050743, NPL3050746, NPL3050750, NPL3050751, NPL3050752, NPL3050753, NPL3050755, NPL3050756, NPL3050757, NPL3050758, NPL3050759, NPL3050760, NPL3050761, NPL3050762, NPL3050763, NPL3050764, NPL3050765, NPL3050766, NPL3050767, NPL3050768, NPL3050769, NPL3050770, NPL3050771, NPL3050772, NPL3050773, NPL3050774, NPL3050775, NPL3050776, NPL3050777, NPL3050778, NPL3050779, NPL3050780, NPL3050781, NPL3050782, NPL3050783, NPL3050784, NPL3050785, NPL3050786, NPL3050788, NPL3050789, NPL3050790, NPL3050792, NPL3050793, NPL3050795, NPL3050797, NPL3050799, NPL3050800, NPL3050801, NPL3050802, NPL3050804, NPL3050805, NPL3050806, NPL3050807, NPL3050808, NPL3050809, NPL3050810, NPL3050811, NPL3050812, NPL3050817, NPL3050820, NPL3050821, NPL3050823, NPL3050824, NPL3050830, NPL3050831, NPL3050832, NPL3050833, NPL3050836, NPL3050837, NPL3050839, NPL3050842, NPL3050843, NPL3050844, NPL3050845, NPL3050847, NPL3050848, NPL3050850, NPL3050851, NPL3050854, NPL3050856, NPL3050861, NPL3050862, NPL3050863, NPL3050864, NPL3050865, NPL3050867, NPL3050868, NPL3050873, NPL3050878, NPL3050882, NPL3050883, NPL3050885, NPL3050886, NPL3050887, NPL3050888, NPL3050889, NPL3050890, NPL3050892, NPL3050893, NPL3050895, NPL3050896, NPL3050897, NPL3050898, NPL3050899, NPL3050900, NPL3050902, NPL3050903, NPL3050904, NPL3050907, NPL3050909, NPL3050911, NPL3050912, NPL3050918, NPL3050928, NPL3050930, NPL3050931, NPL3050933, NPL3050934, NPL3050935, NPL3050937, NPL3050938, NPL3050950, NPL3050952, NPL3050953, NPL3050954, NPL3050955, NPL3050956, NPL3050957, NPL3050958, NPL3050962, NPL3050963, NPL3050964, NPL3050965, NPL3050967, NPL3050968, NPL3050969, NPL3050970, NPL3050971, NPL3050973, NPL3050974, NPL3050976, NPL3050979, NPL3050984, NPL3050992, NPL3050993, NPL3050995, NPL3051000, NPL3051005, NPL3051013, NPL3051015, NPL3051018, NPL3051019, NPL3051020, NPL3051021, NPL3051022, NPL3051026, NPL3051027, NPL3051028, NPL3051031, NPL3051032, NPL3051035, NPL3051036, NPL3051037, NPL3051038, NPL3051043, NPL3051046, NPL3051047, NPL3051050, NPL3051056, NPL3051057, NPL3051059, NPL3051060, NPL3051063, NPL3051066, NPL3051067, NPL3051068, NPL3051069, NPL3051071, NPL3051073, NPL3051074, NPL3051075, NPL3051083, NPL3051084, NPL3051087, NPL3051088, NPL3051089, NPL3051090, NPL3051091, NPL3051092, NPL3051095, NPL3051107, NPL3051109, NPL3051112, NPL3051114, NPL3051115, NPL3051117, NPL3051119, NPL3051120, NPL3051121, NPL3051123, NPL3051129, NPL3051130, NPL3051133, NPL3051134, NPL3051135, NPL3051136, NPL3051137, NPL3051138, NPL3051140, NPL3051142, NPL3051143, NPL3051144, NPL3051150, NPL3051155, NPL3051156, NPL3051157, NPL3051160, NPL3051161, NPL3051169, NPL3051173, NPL3051183, NPL3051184, NPL3051187, NPL3051192, NPL3051204, NPL3051208, NPL3051213, NPL3051222, NPL3051227, NPL3051235, NPL3051237, NPL3051239, NPL3051250, NPL3051256, NPL3051272, NPL3051274, NPL3051284, NPL3051286, NPL3051292, NPL3051295, NPL3051300, NPL3051306, NPL3051312, NPL3051313, NPL3051314, NPL3051324, NPL3051326, NPL3051332, NPL3051336, NPL3051338, NPL3051341, NPL3051343, NPL3051348, NPL3051361, NPL3051362, NPL3051368, NPL3051388, NPL3051392, NPL3051393, NPL3051394, NPL3051400, NPL3051401, NPL3051402, NPL3051403, NPL3051405, NPL3051406, NPL3051410, NPL3051411, NPL3051412, NPL3051413, NPL3051414, NPL3051415, NPL3051416, NPL3051417, NPL3051418, NPL3051419, NPL3051421, NPL3051422, NPL3051423, NPL3051424, NPL3051425, NPL3051427, NPL3051428, NPL3051429, NPL3051431, NPL3051432, NPL3051433, NPL3051442, NPL3051450, NPL3051451, NPL3051461, NPL3051462, NPL3051480, NPL3051486, NPL3051490, NPL3051518, NPL3051520, NPL3051521, NPL3051522, NPL3051523, NPL3051525, NPL3051526, NPL3051527, NPL3051532, NPL3051535, NPL3051536, NPL3051543, NPL3051545, NPL3051546, NPL3051547, NPL3051548, NPL3051549, NPL3051550, NPL3051551, NPL3051552, NPL3051556, NPL3051557, NPL3051562, NPL3051564, NPL3051569, NPL3051571, NPL3051573, NPL3051574, NPL3051575, NPL3051577, NPL3051578, NPL3051579, NPL3051580, NPL3051581, NPL3051582, NPL3051583, NPL3051584, NPL3051585, NPL3051586, NPL3051587, NPL3051588, NPL3051589, NPL3051590, NPL3051591, NPL3051592, NPL3051593, NPL3051595, NPL3051596, NPL3051597, NPL3051598, NPL3051599, NPL3051600, NPL3051601, NPL3051602, NPL3051603, NPL3051604, NPL3051605, NPL3051608, NPL3051609, NPL3051610, NPL3051611, NPL3051612, NPL3051613, NPL3051614, NPL3051615, NPL3051616, NPL3051617, NPL3051618, NPL3051619, NPL3051620, NPL3051622, NPL3051623, NPL3051624, NPL3051625, NPL3051626, NPL3051627, NPL3051628, NPL3051630, NPL3051631, NPL3051632, NPL3051633, NPL3051634, NPL3051635, NPL3051636, NPL3051637, NPL3051638, NPL3051639, NPL3051640, NPL3051641, NPL3051642, NPL3051643, NPL3051644, NPL3051645, NPL3051646, NPL3051647, NPL3051649, NPL3051650, NPL3051651, NPL3051652, NPL3051653, NPL3051654, NPL3051655, NPL3051656, NPL3051657, NPL3051658, NPL3051659, NPL3051660, NPL3051661, NPL3051662, NPL3051663, NPL3051664, NPL3051665, NPL3051666, NPL3051667, NPL3051670, NPL3051671, NPL3051673, NPL3051674, NPL3051677, NPL3051678, NPL3051679, NPL3051680, NPL3051681, NPL3051682, NPL3051683, NPL3051685, NPL3051687, NPL3051688, NPL3051690, NPL3051691, NPL3051693, NPL3051694, NPL3051695, NPL3051696, NPL3051697, NPL3051698, NPL3051699, NPL3051700, NPL3051701, NPL3051704, NPL3051706, NPL3051707, NPL3051709, NPL3051710, NPL3051711, NPL3051712, NPL3051714, NPL3051717, NPL3051718, NPL3051720, NPL3051721, NPL3051722, NPL3051723, NPL3051724, NPL3051725, NPL3051726, NPL3051727, NPL3051728, NPL3051730, NPL3051733, NPL3051734, NPL3051736, NPL3051737, NPL3051738, NPL3051739, NPL3051740, NPL3051743, NPL3051744, NPL3051745, NPL3051746, NPL3051747, NPL3051748, NPL3051750, NPL3051752, NPL3051753, NPL3051755, NPL3051757, NPL3051758, NPL3051759, NPL3051760, NPL3051761, NPL3051762, NPL3051763, NPL3051764, NPL3051767, NPL3051768, NPL3051769, NPL3051770, NPL3051771, NPL3051775, NPL3051776, NPL3051777, NPL3051778, NPL3051779, NPL3051780, NPL3051785, NPL3051799, NPL3051804, NPL3051805, NPL3051806, NPL3051810, NPL3051812, NPL3051813, NPL3051817, NPL3051820, NPL3051824, NPL3051826, NPL3051827, NPL3051828, NPL3051830, NPL3051832, NPL3051834, NPL3051835, NPL3051836, NPL3051837, NPL3051840, NPL3051842, NPL3051843, NPL3051844, NPL3051846, NPL3051847, NPL3051848, NPL3051850, NPL3051851, NPL3051852, NPL3051857, NPL3051858, NPL3051861, NPL3051866, NPL3051868, NPL3051869, NPL3051870, NPL3051871, NPL3051872, NPL3051874, NPL3051875, NPL3051877, NPL3051878, NPL3051879, NPL3051881, NPL3051883, NPL3051884, NPL3051885, NPL3051886, NPL3051887, NPL3051889, NPL3051890, NPL3051891, NPL3051892, NPL3051893, NPL3051896, NPL3051897, NPL3051898, NPL3051899, NPL3051900, NPL3051901, NPL3051908, NPL3051910, NPL3051911, NPL3051913, NPL3051919, NPL3051920, NPL3051921, NPL3051922, NPL3051923, NPL3051924, NPL3051 925, NPL3051926, NPL3051927, NPL3051928, NPL3051929, NPL3051930, NPL3051931, NPL3051932, NPL3051933, NPL3051935, NPL3051936, NPL3051937, NPL3051938, NPL3051940, NPL3051941, NPL3051943, NPL3051944, NPL3051946, NPL3051947, NPL3051949, NPL3051952, NPL3051956, NPL3051957, NPL3051959, NPL3051975, NPL3051977, NPL3051978, NPL3051979, NPL3051980, NPL3051981, NPL3051982, NPL3051983, NPL3051984, NPL3051985, NPL3051986, NPL3051987, NPL3051991, NPL3051992, NPL3051993, NPL3051994, NPL3051995, NPL3051996, NPL3051997, NPL3051998, NPL3051999, NPL3052000, NPL3052001, NPL3052002, NPL3052003, NPL3052004, NPL3052005, NPL3052006, NPL3052007, NPL3052008, NPL3052009, NPL3052010, NPL3052011, NPL3052013, NPL3052014, NPL3052015, NPL3052016, NPL3052017, NPL3052018, NPL3052019, NPL3052020, NPL3052021, NPL3052022, NPL3052023, NPL3052024, NPL3052026, NPL3052030, NPL3052031, NPL3052032, NPL3052033, NPL3052034, NPL3052038, NPL3052039, NPL3052042, NPL3052046, NPL3052047, NPL3052048, NPL3052049, NPL3052050, NPL3052051, NPL3052052, NPL3052054, NPL3052055, NPL3052056, NPL3052057, NPL3052058, NPL3052059, NPL3052060, NPL3052062, NPL3052063, NPL3052064, NPL3052070, NPL3052074, NPL3052077, NPL3052079, NPL3052080, NPL3052090, NPL3052092, NPL3052093, NPL3052095, NPL3052096, NPL3052098, NPL3052102, NPL3052103, NPL3052104, NPL3052105, NPL3052107, NPL3052108, NPL3052110, NPL3052111, NPL3052112, NPL3052114, NPL3052115, NPL3052120, NPL3052123, NPL3052130, NPL3052132, NPL3052133, NPL3052134, NPL3052137, NPL3052142, NPL3052143, NPL3052145, NPL3052151, NPL3052153, NPL3052172, NPL3052174, NPL3052177, NPL3052183, NPL3052186, NPL3052200, NPL3052207, NPL3052226, NPL3052241, NPL3052256, NPL3052265, NPL3052267, NPL3052269, NPL3052270, NPL3052277, NPL3052286, NPL3052290, NPL3052291, NPL3052292, NPL3052293, NPL3052294, NPL3052295, NPL3052297, NPL3052299, NPL3052301, NPL3052302, NPL3052305, NPL3052306, NPL3052317, NPL3052318, NPL3052320, NPL3052322, NPL3052323, NPL3052324, NPL3052325, NPL3052326, NPL3052327, NPL3052328, NPL3052329, NPL3052330, NPL3052331, NPL3052332, NPL3052333, NPL3052334, NPL3052335, NPL3052336, NPL3052337, NPL3052338, NPL3052339, NPL3052340, NPL3052341, NPL3052342, NPL3052343, NPL3052344, NPL3052345, NPL3052346, NPL3052347, NPL3052348, NPL3052349, NPL3052350, NPL3052351, NPL3052352, NPL3052353, NPL3052354, NPL3052355, NPL3052356, NPL3052357, NPL3052358, NPL3052359, NPL3052360, NPL3052361, NPL3052364, NPL3052365, NPL3052366, NPL3052367, NPL3052368, NPL3052374, NPL3052375, NPL3052377, NPL3052378, NPL3052381, NPL3052382, NPL3052383, NPL3052384, NPL3052385, NPL3052386, NPL3052389, NPL3052390, NPL3052391, NPL3052392, NPL3052394, NPL3052395, NPL3052396, NPL3052397, NPL3052398, NPL3052399, NPL3052400, NPL3052403, NPL3052404, NPL3052405, NPL3052407, NPL3052408, NPL3052415, NPL3052416, NPL3052418, NPL3052432, NPL3052436, NPL3052438, NPL3052442, NPL3052447, NPL3052453, NPL3052459, NPL3052461, NPL3052462, NPL3052479, NPL3052483, NPL3052484, NPL3052485, NPL3052491, NPL3052492, NPL3052495, NPL3052503, NPL3052504, NPL3052519, NPL3052521, NPL3052525, NPL3052527, NPL3052529, NPL3052530, NPL3052531, NPL3052532, NPL3052533, NPL3052536, NPL3052537, NPL3052546, NPL3052547, NPL3052552, NPL3052553, NPL3052554, NPL3052555, NPL3052557, NPL3052558, NPL3052567, NPL3052568, NPL3052569, NPL3052572, NPL3052576, NPL3052577, NPL3052579, NPL3052580, NPL3052581, NPL3052582, NPL3052583, NPL3052584, NPL3052585, NPL3052588, NPL3052590, NPL3052593, NPL3052594, NPL3052595, NPL3052596, NPL3052597, NPL3052598, NPL3052599, NPL3052600, NPL3052603, NPL3052604, NPL3052607, NPL3052608, NPL3052609, NPL3052610, NPL3052611, NPL3052612, NPL3052613, NPL3052614, NPL3052615, NPL3052616, NPL3052618, NPL3052625, NPL3052626, NPL3052627, NPL3052644, NPL3052646, NPL3052649, NPL3052653, NPL3052654, NPL3052683, NPL3052684, NPL3052708, NPL3052709, NPL3052710, NPL3052711, NPL3052712, NPL3052713, NPL3052715, NPL3052716, NPL3052717, NPL3052718, NPL3052719, NPL3052720, NPL3052721, NPL3052722, NPL3052723, NPL3052724, NPL3052725, NPL3052726, NPL3052727, NPL3052728, NPL3052729, NPL3052732, NPL3052733, NPL3052734, NPL3052737, NPL3052738, NPL3052739, NPL3052740, NPL3052742, NPL3052743, NPL3052745, NPL3052753, NPL3052766, NPL3052767, NPL3052769, NPL3052770, NPL3052772, NPL3052773, NPL3052774, NPL3052775, NPL3052776, NPL3052777, NPL3052778, NPL3052780, NPL3052781, NPL3052782, NPL3052783, NPL3052785, NPL3052786, NPL3052787, NPL3052788, NPL3052789, NPL3052790, NPL3052792, NPL3052793, NPL3052794, NPL3052796, NPL3052797, NPL3052800, NPL3052801, NPL3052802, NPL3052804, NPL3052808, NPL3052811, NPL3052812, NPL3052813, NPL3052814, NPL3052822, NPL3052824, NPL3052825, NPL3052828, NPL3052830, NPL3052831, NPL3052832, NPL3052833, NPL3052834, NPL3052837, NPL3052838, NPL3052840, NPL3052842, NPL3052846, NPL3052848, NPL3052849, NPL3052850, NPL3052851, NPL3052852, NPL3052856, NPL3052858, NPL3052861, NPL3052862, NPL3052864, NPL3052865, NPL3052868, NPL3052869, NPL3052870, NPL3052875, NPL3052877, NPL3052881, NPL3052883, NPL3052884, NPL3052885, NPL3052886, NPL3052887, NPL3052889, NPL3052890, NPL3052892, NPL3052898, NPL3052899, NPL3052901, NPL3052902, NPL3052903, NPL3052904, NPL3052908, NPL3052916, NPL3052928, NPL3052930, NPL3052931, NPL3052932, NPL3052933, NPL3052934, NPL3052935, NPL3052936, NPL3052937, NPL3052939, NPL3052940, NPL3052941, NPL3052946, NPL3052947, NPL3052949, NPL3052950, NPL3052951, NPL3052952, NPL3052953, NPL3052955, NPL3052956, NPL3052957, NPL3052958, NPL3052961, NPL3052963, NPL3052964, NPL3052965, NPL3052967, NPL3052968, NPL3052969, NPL3052970, NPL3052972, NPL3052973, NPL3052974, NPL3052975, NPL3052976, NPL3052977, NPL3052978, NPL3052980, NPL3052981, NPL3052982, NPL3052984, NPL3052985, NPL3052987, NPL3052988, NPL3052989, NPL3052990, NPL3052991, NPL3052992, NPL3052993, NPL3052994, NPL3052995, NPL3052996, NPL3052997, NPL3052998, NPL3052999, NPL3053000, NPL3053002, NPL3053003, NPL3053004, NPL3053005, NPL3053006, NPL3053007, NPL3053009, NPL3053010, NPL3053011, NPL3053012, NPL3053013, NPL3053014, NPL3053015, NPL3053016, NPL3053017, NPL3053018, NPL3053019, NPL3053020, NPL3053021, NPL3053022, NPL3053023, NPL3053024, NPL3053025, NPL3053026, NPL3053027, NPL3053028, NPL3053030, NPL3053031, NPL3053032, NPL3053035, NPL3053036, NPL3053037, NPL3053038, NPL3053043, NPL3053044, NPL3053045, NPL3053046, NPL3053047, NPL3053048, NPL3053049, NPL3053050, NPL3053051, NPL3053052, NPL3053053, NPL3053054, NPL3053056, NPL3053057, NPL3053058, NPL3053059, NPL3053060, NPL3053061, NPL3053062, NPL3053063, NPL3053064, NPL3053065, NPL3053067, NPL3053068, NPL3053069, NPL3053070, NPL3053071, NPL3053072, NPL3053073, NPL3053074, NPL3053075, NPL3053076, NPL3053077, NPL3053078, NPL3053079, NPL3053080, NPL3053081, NPL3053082, NPL3053084, NPL3053085, NPL3053086, NPL3053087, NPL3053092, NPL3053093, NPL3053095, NPL3053096, NPL3053099, NPL3053100, NPL3053103, NPL3053104, NPL3053111, NPL3053112, NPL3053113, NPL3053115, NPL3053117, NPL3053118, NPL3053119, NPL3053120, NPL3053121, NPL3053122, NPL3053123, NPL3053124, NPL3053125, NPL3053126, NPL3053134, NPL3053137, NPL3053141, NPL3053142, NPL3053143, NPL3053144, NPL3053145, NPL3053147, NPL3053149, NPL3053150, NPL3053152, NPL3053153, NPL3053154, NPL3053155, NPL3053157, NPL3053158, NPL3053159, NPL3053160, NPL3053161, NPL3053163, NPL3053166, NPL3053167, NPL3053172, NPL3053173, NPL3053175, NPL3053176, NPL3053177, NPL3053178, NPL3053179, NPL3053185, NPL3053187, NPL3053193, NPL3053194, NPL3053196, NPL3053197, NPL3053198, NPL3053204, NPL3053206, NPL3053207, NPL3053211, NPL3053212, NPL3053213, NPL3053215, NPL3053216, NPL3053217, NPL3053218, NPL3053219, NPL3053220, NPL3053221, NPL3053222, NPL3053223, NPL3053224, NPL3053225, NPL3053226, NPL3053227, NPL3053229, NPL3053230, NPL3053231, NPL3053232, NPL3053233, NPL3053234, NPL3053235, NPL3053238, NPL3053239, NPL3053240, NPL3053241, NPL3053246, NPL3053251, NPL3053252, NPL3053253, NPL3053254, NPL3053255, NPL3053257, NPL3053259, NPL3053260, NPL3053261, NPL3053262, NPL3053263, NPL3053264, NPL3053265, NPL3053266, NPL3053267, NPL3053268, NPL3053270, NPL3053271, NPL3053273, NPL3053274, NPL3053280, NPL3053287, NPL3053288, NPL3053289, NPL3053293, NPL3053294, NPL3053295, NPL3053296, NPL3053299, NPL3053300, NPL3053304, NPL3053305, NPL3053308, NPL3053310, NPL3053314, NPL3053316, NPL3053317, NPL3053318, NPL3053319, NPL3053320, NPL3053322, NPL3053323, NPL3053325, NPL3053326, NPL3053327, NPL3053329, NPL3053330, NPL3053331, NPL3053332, NPL3053333, NPL3053334, NPL3053335, NPL3053336, NPL3053340, NPL3053341, NPL3053342, NPL3053343, NPL3053344, NPL3053345, NPL3053346, NPL3053347, NPL3053348, NPL3053349, NPL3053350, NPL3053351, NPL3053352, NPL3053353, NPL3053359, NPL3053360, NPL3053364, NPL3053365, NPL3053366, NPL3053367, NPL3053368, NPL3053369, NPL3053370, NPL3053371, NPL3053373, NPL3053374, NPL3053375, NPL3053376, NPL3053377, NPL3053378, NPL3053379, NPL3053380, NPL3053381, NPL3053382, NPL3053383, NPL3053384, NPL3053386, NPL3053387, NPL3053388, NPL3053390, NPL3053391, NPL3053392, NPL3053393, NPL3053395, NPL3053396, NPL3053397, NPL3053399, NPL3053400, NPL3053401, NPL3053402, NPL3053403, NPL3053404, NPL3053405, NPL3053406, NPL3053407, NPL3053409, NPL3053411, NPL3053412, NPL3053413, NPL3053414, NPL3053415, NPL3053416, NPL3053417, NPL3053418, NPL3053419, NPL3053420, NPL3053421, NPL3053422, NPL3053425, NPL3053426, NPL3053427, NPL3053428, NPL3053429, NPL3053431, NPL3053432, NPL3053433, NPL3053434, NPL3053435, NPL3053436, NPL3053437, NPL3053438, NPL3053439, NPL3053441, NPL3053443, NPL3053444, NPL3053445, NPL3053446, NPL3053447, NPL3053448, NPL3053449, NPL3053450, NPL3053451, NPL3053452, NPL3053453, NPL3053454, NPL3053456, NPL3053457, NPL3053459, NPL3053460, NPL3053461, NPL3053462, NPL3053463, NPL3053465, NPL3053466, NPL3053470, NPL3053473, NPL3053474, NPL3053475, NPL3053477, NPL3053478, NPL3053479, NPL3053480, NPL3053481, NPL3053484, NPL3053485, NPL3053486, NPL3053487, NPL3053491, NPL3053494, NPL3053495, NPL3053496, NPL3053497, NPL3053502, NPL3053505, NPL3053509, NPL3053510, NPL3053517, NPL3053518, NPL3053521, NPL3053522, NPL3053528, NPL3053530, NPL3053531, NPL3053534, NPL3053535, NPL3053536, NPL3053538, NPL3053540, NPL3053542, NPL3053543, NPL3053545, NPL3053546, NPL3053547, NPL3053548, NPL3053560, NPL3053561, NPL3053563, NPL3053567, NPL3053568, NPL3053571, NPL3053575, NPL3053576, NPL3053577, NPL3053579, NPL3053581, NPL3053583, NPL3053584, NPL3053585, NPL3053586, NPL3053587, NPL3053588, NPL3053589, NPL3053590, NPL3053591, NPL3053592, NPL3053593, NPL3053594, NPL3053595, NPL3053596, NPL3053597, NPL3053599, NPL3053601, NPL3053602, NPL3053603, NPL3053605, NPL3053606, NPL3053607, NPL3053609, NPL3053611, NPL3053613, NPL3053614, NPL3053615, NPL3053616, NPL3053617, NPL3053618, NPL3053619, NPL3053620, NPL3053621, NPL3053622, NPL3053626, NPL3053627, NPL3053628, NPL3053631, NPL3053633, NPL3053634, NPL3053635, NPL3053636, NPL3053638, NPL3053640, NPL3053641, NPL3053642, NPL3053646, NPL3053648, NPL3053649, NPL3053651, NPL3053652, NPL3053653, NPL3053656, NPL3053658, NPL3053660, NPL3053661, NPL3053662, NPL3053664, NPL3053666, NPL3053667, NPL3053673, NPL3053674, NPL3053675, NPL3053676, NPL3053677, NPL3053678, NPL3053681, NPL3053684, NPL3053685, NPL3053686, NPL3053688, NPL3053689, NPL3053690, NPL3053691, NPL3053693, NPL3053694, NPL3053696, NPL3053697, NPL3053698, NPL3053701, NPL3053706, NPL3053712, NPL3053713, NPL3053716, NPL3053718, NPL3053719, NPL3053723, NPL3053725, NPL3053726, NPL3053734, NPL3053735, NPL3053736, NPL3053738, NPL3053741, NPL3053742, NPL3053745, NPL3053759, NPL3053760, NPL3053761, NPL3053762, NPL3053763, NPL3053764, NPL3053770, NPL3053771, NPL3053772, NPL3053773, NPL3053774, NPL3053775, NPL3053776, NPL3053777, NPL3053778, NPL3053779, NPL3053780, NPL3053781, NPL3053782, NPL3053783, NPL3053784, NPL3053785, NPL3053786, NPL3053787, NPL3053788, NPL3053789, NPL3053790, NPL3053791, NPL3053794, NPL3053795, NPL3053796, NPL3053797, NPL3053798, NPL3053799, NPL3053800, NPL3053801, NPL3053802, NPL3053803, NPL3053804, NPL3053805, NPL3053806, NPL3053809, NPL3053810, NPL3053815, NPL3053816, NPL3053817, NPL3053818, NPL3053819, NPL3053820, NPL3053821, NPL3053824, NPL3053825, NPL3053826, NPL3053829, NPL3053830, NPL3053832, NPL3053834, NPL3053835, NPL3053836, NPL3053837, NPL3053841, NPL3053844, NPL3053845, NPL3053848, NPL3053851, NPL3053853, NPL3053854, NPL3053855, NPL3053856, NPL3053857, NPL3053858, NPL3053859, NPL3053860, NPL3053861, NPL3053862, NPL3053863, NPL3053865, NPL3053868, NPL3053871, NPL3053872, NPL3053873, NPL3053877, NPL3053879, NPL3053881, NPL3053882, NPL3053884, NPL3053886, NPL3053888, NPL3053889, NPL3053892, NPL3053894, NPL3053895, NPL3053896, NPL3053897, NPL3053898, NPL3053899, NPL3053901, NPL3053902, NPL3053903, NPL3053905, NPL3053906, NPL3053907, NPL3053908, NPL3053910, NPL3053912, NPL3053913, NPL3053915, NPL3053916, NPL3053917, NPL3053919, NPL3053920, NPL3053921, NPL3053922, NPL3053923, NPL3053924, NPL3053925, NPL3053926, NPL3053927, NPL3053928, NPL3053929, NPL3053930, NPL3053931, NPL3053932, NPL3053934, NPL3053936, NPL3053937, NPL3053938, NPL3053939, NPL3053940, NPL3053945, NPL3053946, NPL3053948, NPL3053949, NPL3053951, NPL3053952, NPL3053953, NPL3053954, NPL3053955, NPL3053956, NPL3053957, NPL3053958, NPL3053959, NPL3053960, NPL3053961, NPL3053963, NPL3053964, NPL3053965, NPL3053966, NPL3053967, NPL3053968, NPL3053969, NPL3053971, NPL3053972, NPL3053973, NPL3053975, NPL3053976, NPL3053983, NPL3053984, NPL3053985, NPL3053988, NPL3053989, NPL3053990, NPL3053991, NPL3053992, NPL3053994, NPL3053996, NPL3054010, NPL3054012, NPL3054013, NPL3054016, NPL3054017, NPL3054019, NPL3054020, NPL3054021, NPL3054022, NPL3054023, NPL3054024, NPL3054025, NPL3054026, NPL3054027, NPL3054028, NPL3054032, NPL3054033, NPL3054034, NPL3054035, NPL3054036, NPL3054037, NPL3054038, NPL3054043, NPL3054046, NPL3054047, NPL3054048, NPL3054049, NPL3054050, NPL3054051, NPL3054053, NPL3054054, NPL3054055, NPL3054056, NPL3054057, NPL3054058, NPL3054059, NPL3054060, NPL3054061, NPL3054070, NPL3054076, NPL3054077, NPL3054078, NPL3054079, NPL3054080, NPL3054084, NPL3054085, NPL3054087, NPL3054090, NPL3054092, NPL3054093, NPL3054096, NPL3054098, NPL3054102, NPL3054103, NPL3054104, NPL3054138, NPL3054147, NPL3054150, NPL3054159, NPL3054167, NPL3054175, NPL3054186, NPL3054191, NPL3054194, NPL3054199, NPL3054200, NPL3054202, NPL3054203, NPL3054204, NPL3054205, NPL3054206, NPL3054217, NPL3054223, NPL3054225, NPL3054229, NPL3054231, NPL3054235, NPL3054238, NPL3054239, NPL3054245, NPL3054257, NPL3054260, NPL3054262, NPL3054266, NPL3054269, NPL3054276, NPL3054277, NPL3054283, NPL3054284, NPL3054287, NPL3054290, NPL3054292, NPL3054293, NPL3054294, NPL3054295, NPL3054296, NPL3054297, NPL3054298, NPL3054299, NPL3054300, NPL3054301, NPL3054302, NPL3054303, NPL3054307, NPL3054309, NPL3054311, NPL3054313, NPL3054316, NPL3054318, NPL3054321, NPL3054322, NPL3054325, NPL3054326, NPL3054327, NPL3054328, NPL3054329, NPL3054330, NPL3054331, NPL3054332, NPL3054333, NPL3054341, NPL3054357, NPL3054361, NPL3054362, NPL3054363, NPL3054364, NPL3054365, NPL3054366, NPL3054377, NPL3054378, NPL3054379, NPL3054381, NPL3054385, NPL3054386, NPL3054387, NPL3054388, NPL3054391, NPL3054393, NPL3054396, NPL3054397, NPL3054398, NPL3054399, NPL3054402, NPL3054403, NPL3054404, NPL3054405, NPL3054406, NPL3054407, NPL3054408, NPL3054409, NPL3054410, NPL3054411, NPL3054413, NPL3054414, NPL3054415, NPL3054425, NPL3054426, NPL3054427, NPL3054459, NPL3054463, NPL3054464, NPL3054465, NPL3054467, NPL3054469, NPL3054470, NPL3054472, NPL3054473, NPL3054479, NPL3054480, NPL3054481, NPL3054483, NPL3054484, NPL3054485, NPL3054486, NPL3054491, NPL3054496, NPL3054497, NPL3054498, NPL3054500, NPL3054501, NPL3054502, NPL3054504, NPL3054505, NPL3054507, NPL3054508, NPL3054509, NPL3054510, NPL3054511, NPL3054512, NPL3054514, NPL3054515, NPL3054525, NPL3054527, NPL3054539, NPL3054543, NPL3054545, NPL3054546, NPL3054547, NPL3054548, NPL3054549, NPL3054550, NPL3054571, NPL3054572, NPL3054574, NPL3054577, NPL3054578, NPL3054579, NPL3054583, NPL3054584, NPL3054585, NPL3054587, NPL3054588, NPL3054589, NPL3054591, NPL3054592, NPL3054595, NPL3054605, NPL3054609, NPL3054610, NPL3054611, NPL3054612, NPL3054621, NPL3054622, NPL3054623, NPL3054624, NPL3054626, NPL3054627, NPL3054630, NPL3054632, NPL3054634, NPL3054636, NPL3054640, NPL3054642, NPL3054643, NPL3054644, NPL3054714, NPL3054715, NPL3054724, NPL3054726, NPL3054744, NPL3054746, NPL3054747, NPL3054753, NPL3054754, NPL3054761, NPL3054762, NPL3054763, NPL3054764, NPL3054767, NPL3054768, NPL3054778, NPL3054779, NPL3054788, NPL3054789, NPL3054790, NPL3054793, NPL3054794, NPL3054796, NPL3054797, NPL3054799, NPL3054800, NPL3054801, NPL3054804, NPL3054805, NPL3054806, NPL3054807, NPL3054810, NPL3054814, NPL3054815, NPL3054820, NPL3054821, NPL3054822, NPL3054823, NPL3054832, NPL3054845, NPL3054858, NPL3054859, NPL3054860, NPL3054866, NPL3054867, NPL3054868, NPL3054869, NPL3054871, NPL3054879, NPL3054880, NPL3054881, NPL3054882, NPL3054884, NPL3054885, NPL3054886, NPL3054887, NPL3054908, NPL3054909, NPL3054910, NPL3054911, NPL3054912, NPL3054913, NPL3054938, NPL3054988, NPL3054989, NPL3055007, NPL3055008, NPL3055011, NPL3055012, NPL3055013, NPL3055014, NPL3055015, NPL3055023, NPL3055025, NPL3055026, NPL3055027, NPL3055032, NPL3055034, NPL3055035, NPL3055037, NPL3055039, NPL3055040, NPL3055041, NPL3055042, NPL3055046, NPL3055050, NPL3055051, NPL3055054, NPL3055057, NPL3055059, NPL3055061, NPL3055063, NPL3055064, NPL3055066, NPL3055067, NPL3055068, NPL3055069, NPL3055071, NPL3055072, NPL3055073, NPL3055074, NPL3055078, NPL3055079, NPL3055080, NPL3055081, NPL3055082, NPL3055083, NPL3055084, NPL3055085, NPL3055086, NPL3055087, NPL3055088, NPL3055090, NPL3055091, NPL3055092, NPL3055093, NPL3055094, NPL3055096, NPL3055097, NPL3055098, NPL3055114, NPL3055122, NPL3055123, NPL3055130, NPL3055131, NPL3055132, NPL3055135, NPL3055140, NPL3055141, NPL3055142, NPL3055143, NPL3055144, NPL3055145, NPL3055146, NPL3055147, NPL3055151, NPL3055152, NPL3055156, NPL3055157, NPL3055163, NPL3055165, NPL3055166, NPL3055167, NPL3055168, NPL3055169, NPL3055170, NPL3055171, NPL3055172, NPL3055173, NPL3055175, NPL3055176, NPL3055177, NPL3055178, NPL3055186, NPL3055187, NPL3055190, NPL3055193, NPL3055194, NPL3055197, NPL3055198, NPL3055199, NPL3055202, NPL3055203, NPL3055204, NPL3055205, NPL3055206, NPL3055207, NPL3055208, NPL3055209, NPL3055210, NPL3055212, NPL3055214, NPL3055215, NPL3055216, NPL3055217, NPL3055218, NPL3055219, NPL3055225, NPL3055226, NPL3055227, NPL3055229, NPL3055232, NPL3055233, NPL3055234, NPL3055235, NPL3055236, NPL3055237, NPL3055238, NPL3055239, NPL3055240, NPL3055241, NPL3055242, NPL3055243, NPL3055244, NPL3055245, NPL3055246, NPL3055253, NPL3055254, NPL3055255, NPL3055257, NPL3055258, NPL3055259, NPL3055260, NPL3055261, NPL3055262, NPL3055263, NPL3055265, NPL3055267, NPL3055268, NPL3055271, NPL3055273, NPL3055275, NPL3055276, NPL3055277, NPL3055278, NPL3055279, NPL3055281, NPL3055282, NPL3055283, NPL3055284, NPL3055287, NPL3055288, NPL3058210, NPL3058213, NPL3058214, NPL3058215, NPL3058216, NPL3058224, NPL3058229, NPL3058230, NPL3058231, NPL3058232, NPL3058233, NPL3058234, NPL3058236, NPL3058238, NPL3058240, NPL3058244, NPL3058247, NPL3058248, NPL3058250, NPL3058252, NPL3058253, NPL3058254, NPL3058255, NPL3058256, NPL3058257, NPL3058258, NPL3058260, NPL3058261, NPL3058263, NPL3058264, NPL3058267, NPL3058268, NPL3058269, NPL3058270, NPL3058271, NPL3058273, NPL3058274, NPL3058275, NPL3058276, NPL3058277, NPL3058278, NPL3058280, NPL3058282, NPL3058283, NPL3058284, NPL3058287, NPL3058288, NPL3058289, NPL3058291, NPL3058292, NPL3058293, NPL3058294, NPL3058295, NPL3058296, NPL3058297, NPL3058298, NPL3058299, NPL3058300, NPL3058301, NPL3058302, NPL3058304, NPL3058305, NPL3058306, NPL3058307, NPL3058309, NPL3058310, NPL3058311, NPL3058312, NPL3058313, NPL3058314, NPL3058315, NPL3058316, NPL3058318, NPL3058321, NPL3058322, NPL3058323, NPL3058324, NPL3058328, NPL3058333, NPL3058335, NPL3058342, NPL3058343, NPL3058344, NPL3058346, NPL3058347, NPL3058348, NPL3058349, NPL3058355, NPL3058356, NPL3058357, NPL3058359, NPL3058360, NPL3058361, NPL3058364, NPL3058366, NPL3058469, NPL3058470, NPL3058471, NPL3058472, NPL3058477, NPL3058481, NPL3058482, NPL3058486, NPL3058631, NPL3058632, NPL3058634, NPL3058635, NPL3058636, NPL3058637, NPL3058655, NPL3058657, NPL3058658, NPL3058659, NPL3058660, NPL3058662, NPL3058663, NPL3058666, NPL3058667, NPL3058670, NPL3058677, NPL3058681, NPL3058682, NPL3058683, NPL3058684, NPL3058685, NPL3058686, NPL3058687, NPL3058688, NPL3058689, NPL3058690, NPL3058691, NPL3058692, NPL3058693, NPL3058694, NPL3058695, NPL3058698, NPL3058699, NPL3058701, NPL3058709, NPL3058710, NPL3058713, NPL3058714, NPL3058717, NPL3058719, NPL3058721, NPL3058723, NPL3058727, NPL3058728, NPL3058729, NPL3058730, NPL3058739, NPL3058741, NPL3058742, NPL3058748, NPL3058749, NPL3058764, NPL3058765, NPL3058766, NPL3058767, NPL3058768, NPL3058774, NPL3058775, NPL3058897, NPL3058903, NPL3058917, NPL3058921, NPL3058925, NPL3058928, NPL3058929, NPL3058931, NPL3058936, NPL3058938, NPL3058944, NPL3058945, NPL3058948, NPL3058950, NPL3058951, NPL3058964, NPL3058965, NPL3058967, NPL3058969, NPL3058970, NPL3058971, NPL3058976, NPL3058977, NPL3058980, NPL3058984, NPL3058985, NPL3058986, NPL3058987, NPL3058999, NPL3059006, NPL3059007, NPL3059027, NPL3059030, NPL3059031, NPL3059033, NPL3059036, NPL3059042, NPL3059050, NPL3059051, NPL3059053, NPL3059061, NPL3059066, NPL3059074, NPL3059075, NPL3059076, NPL3059077, NPL3059078, NPL3059087, NPL3059093, NPL3059094, NPL3059095, NPL3059105, NPL3059106, NPL3059110, NPL3059111, NPL3059112, NPL3059113, NPL3059114, NPL3059115, NPL3059116, NPL3059119, NPL3059120, NPL3059123, NPL3059124, NPL3059137, NPL3059151, NPL3059154, NPL3059155, NPL3059157, NPL3059158, NPL3059163, NPL3059174, NPL3059177, NPL3059178, NPL3059183, NPL3059184, NPL3059185, NPL3059186, NPL3059187, NPL3059188, NPL3059189, NPL3059190, NPL3059192, NPL3059195, NPL3059203, NPL3059208, NPL3059232, NPL3059293, NPL3059297, NPL3059389, NPL3059440, NPL3059516, NPL3059553, NPL3059711, NPL3059717, NPL3059748, NPL3059777, NPL3059806, NPL3059814, NPL3059837, NPL3059840, NPL3059867, NPL3059911, NPL3059920, NPL3059925, NPL3059928, NPL3059929, NPL3059933, NPL3059937, NPL3059945, NPL3059947, NPL3059949, NPL3059954, NPL3059957, NPL3059962, NPL3059972, NPL3059987, NPL3059990, NPL3059994, NPL3060001, NPL3060031, NPL3060033, NPL3060041, NPL3060043, NPL3060060, NPL3060063, NPL3060072, NPL3060073, NPL3060075, NPL3060081, NPL3060083, NPL3060091, NPL3060112, NPL3060125, NPL3060126, NPL3060127, NPL3060130, NPL3060136, NPL3060140, NPL3060141, NPL3060143, NPL3060144, NPL3060145, NPL3060174, NPL3060176, NPL3060178, NPL3060179, NPL3060180, NPL3060191, NPL3060194, NPL3060201, NPL3060202, NPL3060205, NPL3060208, NPL3060213, NPL3060217, NPL3060218, NPL3060245, NPL3060275, NPL3060617, NPL3060638, NPL3060755, NPL3060814, NPL3060815; (2) GTIN 00763000984649, Serial Numbers: NPL3049809, NPL3049810, NPL3049811, NPL3049812, NPL3049814, NPL3049815, NPL3049816, NPL3049817, NPL3049818, NPL3049862, NPL3049898, NPL3049900, NPL3049906, NPL3049931, NPL3049939, NPL3049940, NPL3049969, NPL3050484, NPL3050493, NPL3051007, NPL3051010, NPL3051054, NPL3051096, NPL3051097, NPL3051099, NPL3051100, NPL3051104, NPL3051170, NPL3051171, NPL3051172, NPL3051178, NPL3051179, NPL3051180, NPL3051181, NPL3051195, NPL3051196, NPL3051200, NPL3051202, NPL3051209, NPL3051211, NPL3051212, NPL3051214, NPL3051219, NPL3051224, NPL3051229, NPL3051230, NPL3051231, NPL3051233, NPL3051234, NPL3051238, NPL3051241, NPL3051244, NPL3051245, NPL3051246, NPL3051247, NPL3051248, NPL3051249, NPL3051251, NPL3051253, NPL3051254, NPL3051257, NPL3051260, NPL3051261, NPL3051262, NPL3051263, NPL3051265, NPL3051266, NPL3051267, NPL3051269, NPL3051270, NPL3051275, NPL3051276, NPL3051277, NPL3051278, NPL3051279, NPL3051281, NPL3051282, NPL3051287, NPL3051288, NPL3051289, NPL3051290, NPL3051291, NPL3051296, NPL3051297, NPL3051298, NPL3051299, NPL3051301, NPL3051303, NPL3051304, NPL3051305, NPL3051307, NPL3051310, NPL3051311, NPL3051316, NPL3051317, NPL3051318, NPL3051319, NPL3051322, NPL3051325, NPL3051327, NPL3051328, NPL3051329, NPL3051333, NPL3051334, NPL3051337, NPL3051339, NPL3051340, NPL3051342, NPL3051345, NPL3051347, NPL3051349, NPL3051350, NPL3051351, NPL3051352, NPL3051353, NPL3051354, NPL3051355, NPL3051358, NPL3051359, NPL3051360, NPL3051363, NPL3051365, NPL3051366, NPL3051369, NPL3051370, NPL3051371, NPL3051381, NPL3051382, NPL3051385, NPL3051386, NPL3051435, NPL3051437, NPL3051438, NPL3051439, NPL3051440, NPL3051441, NPL3051443, NPL3051444, NPL3051446, NPL3051447, NPL3051452, NPL3051453, NPL3051456, NPL3051457, NPL3051458, NPL3051459, NPL3051460, NPL3051464, NPL3051465, NPL3051466, NPL3051467, NPL3051469, NPL3051495, NPL3051498, NPL3051505, NPL3051506, NPL3051507, NPL3051509, NPL3051510, NPL3051511, NPL3051512, NPL3051513, NPL3051516, NPL3051519, NPL3059593.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2201-2026%22", "url": "https://recallledger.net/recalls/device-z-2201-2026-medtronic-synchromed-flex-infusion-mode-a810-clinician-programmer-so/"}, {"id": "fda-device-z-2200-2026", "source": "FDA", "category": "device", "recall_number": "Z-2200-2026", "title": "LVIS Intraluminal Support Device recall (MICROVENTION INC.)", "product": "LVIS Intraluminal Support Device, REF/Outside Diameter(OD)xTotal Length(TL)xWorking Length(WL): 214022-CAS/4.0 mm x 22 mm x 18 mm, 214518-CAS/4.5 mm x 18 mm x 14 mm, 213517-CAS/3.5 mm x 17 mm x 13 mm", "reason": "Stent-assisted coiling device may due to commingling during manufacturing have dimensional nonconformance and/or incorrect device configuration. If device is oversized may lead to increased vessel wall stress, neointimal hyperplasia, vessel injury/rupture; if undersized may lead to incomplete expansion/malposition, acute stent thrombosis, distal embolization, ischemic neurological events", "hazard_level": "Class II", "company": "MICROVENTION INC.", "company_location": "Aliso Viejo, CA, United States", "date": "2026-04-06", "report_date": "2026-05-20", "status": "Ongoing", "distribution": "International distribution to the country of China.", "states": [], "nationwide": false, "quantity": "38", "codes": "Lots: 0000616462, 0000619851, 0000552987, 0000551725. 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4559835, 4655625, 4813669, 4881109, 4984797, 5032163, 5086512, 4149227, 4302668, 4455040, 4559836, 4656012, 4813671, 4881254, 4986193, 5032164, 5086711, 4149969, 4303896, 4455168, 4559837, 4656013, 4813770, 4881440, 4986194, 5032187, 5086717, 4150815, 4303903, 4455169, 4559890, 4656020, 4814782, 4881442, 4986195, 5032188, 5086720, 4150816, 4304007, 4456588, 4559892, 4656023, 4814791, 4881453, 4986546, 5032369, 4152114, 4304318, 4456589, 4559941, 4656112, 4814850, 4881454, 4986547, 5032370, 4153497, 4304319, 4456591, 4559942, 4656116, 4815412, 4881455, 4986548, 5032387, 4153504, 4304355, 4457636, 4559943, 4656119, 4815413, 4881457, 4986565, 5032388, 4154957, 4304924, 4457638, 4559944, 4658880, 4815457, 4881458, 4986566, 5032389, 4155772, 4305035, 4457639, 4559946, 4658881, 4815460, 4881593, 4987016, 5032934.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2174-2026%22", "url": "https://recallledger.net/recalls/device-z-2174-2026-bard-dynamic-deca-steerable-product-number-201101-reprocessed-electr/"}, {"id": "fda-device-z-2173-2026", "source": "FDA", "category": "device", "recall_number": "Z-2173-2026", "title": "Codman CerebroFlo EVD Catheter with Endexo Technology. Contains 5 sets. Product ID:... recall (Integra LifeSciences Corp. (NeuroSciences))", "product": "Codman CerebroFlo EVD Catheter with Endexo Technology. Contains 5 sets. Product ID: 37.550.501. The CerebroFlo EVD Catheter is a 3.3 mm diameter (10 Fr.), 35 cm long polyurethane catheter for diverting cerebrospinal fluid (CSF) from the ventricles of the brain through a series of drainage holes near the catheter's bullet shaped tip.", "reason": "Out-of-specification endotoxin result that did not meet the acceptance criteria.", "hazard_level": "Class II", "company": "Integra LifeSciences Corp. (NeuroSciences)", "company_location": "Princeton, NJ, United States", "date": "2026-04-10", "report_date": "2026-05-20", "status": "Ongoing", "distribution": "US Nationwide distribution in the states of Arizona (AZ), Arkansas (AR), California (CA), Connecticut (CT), Florida (FL), Kentucky (KY), Louisiana (LA), Michigan (MI), Minnesota (MN), Missouri (MO), North Carolina (NC), North Dakota (ND), Oklahoma (OK), Oregon (OR), Texas (TX), Washington (WA).", "states": ["AR", "AZ", "CA", "CT", "FL", "KY", "LA", "MI", "MN", "MO", "NC", "ND", "OK", "OR", "TX", "WA"], "nationwide": true, "quantity": "40 packs (200 units)", "codes": "Product ID: 37.550.501. UDI-DI: 10381780530138. Lot Number: 45322.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2173-2026%22", "url": "https://recallledger.net/recalls/device-z-2173-2026-codman-cerebroflo-evd-catheter-with-endexo-technology-contains-5-sets/"}, {"id": "fda-device-z-2171-2026", "source": "FDA", "category": "device", "recall_number": "Z-2171-2026", "title": "ZYMUTEST HIA IgG recall (Aniara Diagnostica LLC)", "product": "ZYMUTEST HIA IgG, in vitro diagnostic ELISA kit, Ref. RK040A", "reason": "Kits from lot FD1265 had been packaged on 17 October 2024 and put on the market with an outdated flyer (8 October 2024), containing incorrect values for the positive control.", "hazard_level": "Class II", "company": "Aniara Diagnostica LLC", "company_location": "West Chester, OH, United States", "date": "2026-04-01", "report_date": "2026-05-20", "status": "Ongoing", "distribution": "US Nationwide distribution in the states of CA, GA, MN, MO, NC, NM, NY, VA, WA, and WI", "states": ["CA", "GA", "MN", "MO", "NC", "NM", "NY", "VA", "WA", "WI"], "nationwide": true, "quantity": "359 units", "codes": "UDI-DI: 03663537018763; Lot Number: FD1265", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2171-2026%22", "url": "https://recallledger.net/recalls/device-z-2171-2026-zymutest-hia-igg-in-vitro-diagnostic-elisa-kit-ref-rk040a/"}, {"id": "fda-device-z-2169-2026", "source": "FDA", "category": "device", "recall_number": "Z-2169-2026", "title": "QuickVue Dipstick Strep A Test recall (Quidel Corporation)", "product": "QuickVue Dipstick Strep A Test, 50T, REF 20108, antigens, all groups, streptococcus spp.", "reason": "Product has the potential for false positive results", "hazard_level": "Class II", "company": "Quidel Corporation", "company_location": "San Diego, CA, United States", "date": "2026-04-06", "report_date": "2026-05-20", "status": "Ongoing", "distribution": "US Nationwide distribution in the states of AL, CA, FL, ID, IL, LA, MA, MD, MN, MO, NY, PA, SC, TN, TX, VA.", "states": ["AL", "CA", "FL", "ID", "IL", "LA", "MA", "MD", "MN", "MO", "NY", "PA", "SC", "TN", "TX", "VA"], "nationwide": true, "quantity": "12279 units", "codes": "UDI/DI 30014613201083, Lot Numbers: 225788, 228322, 233274.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2169-2026%22", "url": "https://recallledger.net/recalls/device-z-2169-2026-quickvue-dipstick-strep-a-test-50t-ref-20108-antigens-all-groups/"}, {"id": "fda-device-z-2168-2026", "source": "FDA", "category": "device", "recall_number": "Z-2168-2026", "title": "3DIMENSIONS MAMMOGRAPHY SYSTEM recall (Hologic, Inc)", "product": "3DIMENSIONS MAMMOGRAPHY SYSTEM; Model Numbers: 3DM-SYS-INTL2D, 3DM-SYS-INTL2D-MOB, 3DM-SYS-INTL2D-NS, 3DM-SYS-INTL3D, 3DM-SYS-INTL3D-MOB, 3DM-SYS-INTL3D-NS, 3DM-SYS-STD, 3DM-SYS-STD-MOB, 3DM-SYS-STD-NS.", "reason": "Complaints have been received of systems developing loose, missing, or broken internal bolts over time.", "hazard_level": "Class II", "company": "Hologic, Inc", "company_location": "Marlborough, MA, United States", "date": "2026-04-08", "report_date": "2026-05-20", "status": "Ongoing", "distribution": "US Nationwide distribution.", "states": [], "nationwide": true, "quantity": "14837 units", "codes": "\"[Model No.; UDI]: [3DM-SYS-INTL2D;15420045510609], [3DM-SYS-INTL2D-MOB;15420045510593], [3DM-SYS-INTL2D-NS;15420045510586], [3DM-SYS-INTL3D;15420045510579], [3DM-SYS-INTL3D-MOB;15420045510562], [3DM-SYS-INTL3D-NS;15420045510555], [3DM-SYS-STD;15420045510524], [3DM-SYS-STD-MOB;15420045510531], [3DM-SYS-STD-NS;15420045510548]; All Serial No.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2168-2026%22", "url": "https://recallledger.net/recalls/device-z-2168-2026-3dimensions-mammography-system-model-numbers-3dm-sys-intl2d-3dm-sys/"}, {"id": "fda-device-z-2167-2026", "source": "FDA", "category": "device", "recall_number": "Z-2167-2026", "title": "SELENIA DIMENSIONS MAMMOGRAPHY SYSTEMS. Model Numbers: SDA-SYS-3000-2D-HTC recall (Hologic, Inc)", "product": "SELENIA DIMENSIONS MAMMOGRAPHY SYSTEMS. Model Numbers: SDA-SYS-3000-2D-HTC, SDA-SYS-3000-3D, SDM-SYS-6000-2D, SDM-SYS-6000-3D, SDM-00001-2D, SDM-00001-3D, SDM-00001-M2D, SDM-00001-M3D, SDM-05000-2A2, SDM-05000-2A3, SDM-05000-2AC, SDM-05000-2D2, SDM-05000-2D3, SDM-05000-2DC, SDM-05000-3D2, SDM-05000-3D3, SDM-05000-3DC, SDM-SYS-9000-2D, SDM-SYS-9000-3D.", "reason": "Complaints have been received of systems developing loose, missing, or broken internal bolts over time.", "hazard_level": "Class II", "company": "Hologic, Inc", "company_location": "Marlborough, MA, United States", "date": "2026-04-08", "report_date": "2026-05-20", "status": "Ongoing", "distribution": "US Nationwide distribution.", "states": [], "nationwide": true, "quantity": "4,305 units", "codes": "\"Model No.; UDI\": [SDA-SYS-3000-2D-HTC;15420045510616], [SDA-SYS-3000-3D;15420045517783], [SDM-SYS-6000-2D;15420045510753], [SDM-SYS-6000-3D;15420045510760], [SDM-00001-2D;15420045510623], [SDM-00001-3D;15420045510630], [SDM-00001-M2D;15420045510647], [SDM-00001-M3D;15420045510654], [SDM-05000-2A2;15420045510661], [SDM-05000-2A3;15420045510678], [SDM-05000-2AC;15420045510685], [SDM-05000-2D2;15420045510692], [SDM-05000-2D3;15420045510708], [SDM-05000-2DC;15420045510715], [SDM-05000-3D2;15420045510722], [SDM-05000-3D3;15420045510739], [SDM-05000-3DC;15420045510746], [SDM-SYS-9000-2D;15420045510777], [SDM-SYS-9000-3D;15420045510784]; All Serial No.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2167-2026%22", "url": "https://recallledger.net/recalls/device-z-2167-2026-selenia-dimensions-mammography-systems-model-numbers-sda-sys-3000-2d/"}, {"id": "fda-device-z-2166-2026", "source": "FDA", "category": "device", "recall_number": "Z-2166-2026", "title": "Thermedx FluidSmart Urology Tube Set REF LL0006 UDI-DI code: 00860936000365 The... recall (Stryker Corporation)", "product": "Thermedx FluidSmart Urology Tube Set REF LL0006 UDI-DI code: 00860936000365 The FluidSmart Tube Sets are intended to be used with the FluidSmart Fluid Management System, which is intended for irrigation and fluid warming in laparoscopic procedures, and distention, fluid warming, and volume/deficit measurements in endoscopic procedures within gynecology, urology, and orthopedic disciplines.", "reason": "Due to nonconforming products being inadvertently distributed.", "hazard_level": "Class II", "company": "Stryker Corporation", "company_location": "San Jose, CA, United States", "date": "2026-04-09", "report_date": "2026-05-20", "status": "Ongoing", "distribution": "U.S. Nationwide distribution in the state of GA.", "states": ["GA"], "nationwide": true, "quantity": "10 tube sets", "codes": "Catalog Number: LL0006 UDI-DI code: 00860936000365 Lot Number: B000576601", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2166-2026%22", "url": "https://recallledger.net/recalls/device-z-2166-2026-thermedx-fluidsmart-urology-tube-set-ref-ll0006-udi-di-code-00860936/"}, {"id": "fda-device-z-2165-2026", "source": "FDA", "category": "device", "recall_number": "Z-2165-2026", "title": "Brand Name: Dexcom ONE+ Continuous Glucose Monitoring System Product Name: Dexcom... recall (Dexcom, Inc.)", "product": "Brand Name: Dexcom ONE+ Continuous Glucose Monitoring System Product Name: Dexcom ONE+ iOS CGM App Model/Catalog Number: SW14244 Software Version: versions 1.5.0 and 1.6.0 Product Description: Dexcom ONE+ iOS CGM App Component: Dexcom ONE+ Continuous Glucose Monitoring System", "reason": "A software defect in which a low-priority file I/O check blocks the higher-priority thread responsible for processing estimated glucose values (EGVs) and trend arrows. When the app is running in the background, EGV notifications may queue up and then \"replay\" sequentially when the user brings the app to the foreground, causing the Glucose Compass to flicker through previous EGVs. In more severe instances, the app may perceive signal loss and deploy signal loss mitigations. This delay in EGV and alert processing creates a risk that users may miss detection of a hypoglycemic or hyperglycemic event, or make treatment decisions based on outdated glucose information.", "hazard_level": "Class II", "company": "Dexcom, Inc.", "company_location": "San Diego, CA, United States", "date": "2026-04-14", "report_date": "2026-05-20", "status": "Ongoing", "distribution": "SW12300 & SW13355 Dexcom G7 iOS and watchOS app versions 2.9.0 through 2.11.2: Worldwide - US Nationwide including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, and WY. The countries of Austria, Australia, Belgium, Bahrain, Canada, Czech Republic, Germany, Denmark, Estonia, Finland, France, Hong Kong, Ireland, Israel, Iceland, Italy, Jordan, Japan, Kuwait, Luxembourg, Malta, Netherlands, Norway, New Zealand, Oman, Poland, Portugal, Qatar, Saudi Arabia, Singapore, Slovenia, Slovakia, South Africa, South Korea, Spain, Sweden, Switzerland, Turkey, United Arab Emirates, United Kingdom. SW14245 Dexcom ONE iOS App versions 1.5.0 and 1.6.0 - Only International distribution to the countries of Andorra, Australia, Belgium, Bulgaria, Czech Republic, Estonia, France, Greece, Croatia, Ireland, Italy, Lithuania, Latvia, Malaysia, Monaco, Netherlands, New Zealand, Poland, Qatar, Romania, Saudi Arabia, Spain, Sweden, United Kingdom.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "70212", "codes": "Lot Code: SW14244 versions 1.5.0 and 1.6.0 - UDI-DI: 00386270004307", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2165-2026%22", "url": "https://recallledger.net/recalls/device-z-2165-2026-brand-name-dexcom-one-continuous-glucose-monitoring-system-product/"}, {"id": "fda-device-z-2164-2026", "source": "FDA", "category": "device", "recall_number": "Z-2164-2026", "title": "Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7... recall (Dexcom, Inc.)", "product": "Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM watchOS App Model/Catalog Number: SW13355 Software Version: Versions 2.9.0 through 2.11.2 Product Description: Dexcom G7 CGM watchOS App - The watchOS app is installed along with the iOS phone app and the versions used are the same for each user. The watchOS app cannot be installed independently from the iOS phone app. Component: Dexcom G7 Continuous Glucose Monitoring System, Dexcom G7 15 Day Continuous Glucose Monitoring System", "reason": "A software defect in which a low-priority file I/O check blocks the higher-priority thread responsible for processing estimated glucose values (EGVs) and trend arrows. When the app is running in the background, EGV notifications may queue up and then \"replay\" sequentially when the user brings the app to the foreground, causing the Glucose Compass to flicker through previous EGVs. In more severe instances, the app may perceive signal loss and deploy signal loss mitigations. This delay in EGV and alert processing creates a risk that users may miss detection of a hypoglycemic or hyperglycemic event, or make treatment decisions based on outdated glucose information.", "hazard_level": "Class II", "company": "Dexcom, Inc.", "company_location": "San Diego, CA, United States", "date": "2026-04-14", "report_date": "2026-05-20", "status": "Ongoing", "distribution": "SW12300 & SW13355 Dexcom G7 iOS and watchOS app versions 2.9.0 through 2.11.2: Worldwide - US Nationwide including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, and WY. The countries of Austria, Australia, Belgium, Bahrain, Canada, Czech Republic, Germany, Denmark, Estonia, Finland, France, Hong Kong, Ireland, Israel, Iceland, Italy, Jordan, Japan, Kuwait, Luxembourg, Malta, Netherlands, Norway, New Zealand, Oman, Poland, Portugal, Qatar, Saudi Arabia, Singapore, Slovenia, Slovakia, South Africa, South Korea, Spain, Sweden, Switzerland, Turkey, United Arab Emirates, United Kingdom. SW14245 Dexcom ONE iOS App versions 1.5.0 and 1.6.0 - Only International distribution to the countries of Andorra, Australia, Belgium, Bulgaria, Czech Republic, Estonia, France, Greece, Croatia, Ireland, Italy, Lithuania, Latvia, Malaysia, Monaco, Netherlands, New Zealand, Poland, Qatar, Romania, Saudi Arabia, Spain, Sweden, United Kingdom.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "58582", "codes": "Lot Code: SW13355 versions 2.9.0 through 2.11.2 - UDI-DI: 00386270005168", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2164-2026%22", "url": "https://recallledger.net/recalls/device-z-2164-2026-brand-name-dexcom-g7-continuous-glucose-monitoring-system-product-na/"}, {"id": "fda-device-z-2163-2026", "source": "FDA", "category": "device", "recall_number": "Z-2163-2026", "title": "Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7... recall (Dexcom, Inc.)", "product": "Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM iOS App Model/Catalog Number: SW12300 Software Version: Versions 2.9.0 through 2.11.2 Product Description: Dexcom G7 CGM iOS App Component: Dexcom G7 Continuous Glucose Monitoring System, Dexcom G7 15 Day Continuous Glucose Monitoring System", "reason": "A software defect in which a low-priority file I/O check blocks the higher-priority thread responsible for processing estimated glucose values (EGVs) and trend arrows. When the app is running in the background, EGV notifications may queue up and then \"replay\" sequentially when the user brings the app to the foreground, causing the Glucose Compass to flicker through previous EGVs. In more severe instances, the app may perceive signal loss and deploy signal loss mitigations. This delay in EGV and alert processing creates a risk that users may miss detection of a hypoglycemic or hyperglycemic event, or make treatment decisions based on outdated glucose information.", "hazard_level": "Class II", "company": "Dexcom, Inc.", "company_location": "San Diego, CA, United States", "date": "2026-04-14", "report_date": "2026-05-20", "status": "Ongoing", "distribution": "SW12300 & SW13355 Dexcom G7 iOS and watchOS app versions 2.9.0 through 2.11.2: Worldwide - US Nationwide including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, and WY. The countries of Austria, Australia, Belgium, Bahrain, Canada, Czech Republic, Germany, Denmark, Estonia, Finland, France, Hong Kong, Ireland, Israel, Iceland, Italy, Jordan, Japan, Kuwait, Luxembourg, Malta, Netherlands, Norway, New Zealand, Oman, Poland, Portugal, Qatar, Saudi Arabia, Singapore, Slovenia, Slovakia, South Africa, South Korea, Spain, Sweden, Switzerland, Turkey, United Arab Emirates, United Kingdom. SW14245 Dexcom ONE iOS App versions 1.5.0 and 1.6.0 - Only International distribution to the countries of Andorra, Australia, Belgium, Bulgaria, Czech Republic, Estonia, France, Greece, Croatia, Ireland, Italy, Lithuania, Latvia, Malaysia, Monaco, Netherlands, New Zealand, Poland, Qatar, Romania, Saudi Arabia, Spain, Sweden, United Kingdom.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "PR", "RI", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "58582", "codes": "Lot Code: SW12300 versions 2.9.0 through 2.11.2 - UDI-DI: 00386270001863", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2163-2026%22", "url": "https://recallledger.net/recalls/device-z-2163-2026-brand-name-dexcom-g7-continuous-glucose-monitoring-system-product-na/"}, {"id": "fda-device-z-2161-2026", "source": "FDA", "category": "device", "recall_number": "Z-2161-2026", "title": "LUCAS 2 Model Number: 99576 Catalog Numbers: 99576-000024 and 99576-000011 UDI-DI... recall (Jolife AB)", "product": "LUCAS 2 Model Number: 99576 Catalog Numbers: 99576-000024 and 99576-000011 UDI-DI code: 00883873904565 LUCAS 3 Model Number: 99576 Catalog Number: 99576-000043 UDI-DI code: 00883873861875 LUCAS 3.1 Model Number: 99576 Catalog Number: 99576-000063 UDI-DI code: 00883873834329 LUCAS chest compression System is to be used for performing external cardiac compressions on adult patients who have acute circulatory arrest defined as absence of spontaneous breathing and pulse, and loss of consciousness.", "reason": "Due to a subset of chest compression systems/devices where the service performed on the systems were not appropriately documented (The documents for the service performed to justify the passing results were not include in the service records).", "hazard_level": "Class II", "company": "Jolife AB", "company_location": "Lund, Sweden", "date": "2026-04-13", "report_date": "2026-05-20", "status": "Ongoing", "distribution": "U.S. Nationwide distribution in the states of AL, AZ, CA, FL, HI, IA, KS, KY, LA, MA, MD, MN, NC, NV, OH, SC, TX, UT, VA, WA, and WY.", "states": ["AL", "AZ", "CA", "FL", "HI", "IA", "KS", "KY", "LA", "MA", "MD", "MN", "NC", "NV", "OH", "SC", "TX", "UT", "VA", "WA", "WY"], "nationwide": true, "quantity": "153 systems", "codes": "LUCAS 2 Model Number: 99576 Catalog Numbers: 99576-000024 and 99576-000011 UDI-DI code: 00883873904565 Serial Numbers: 30100846 30112125 30123845 30124348 30124440 30124475 30124991 30136605 30148155 30148365 3015B568 3015B682 3015C276 3015C722 3015C723 3015C724 3015F246 3015F587 3016G845 3016H983 3017K078 3017K079 3017K080 LUCAS 3 Model Number: 99576 Catalog Number: 99576-000043 UDI-DI code: 00883873861875 Serial Numbers: 35160778 35173272 35173461 35185820 35185817 35175040 35175039 35173347 35160921 35175373 35174279 35172701 35161449 LUCAS 3.1 Model Number: 99576 Catalog Number: 99576-000063 UDI-DI code: 00883873834329 Serial Numbers: 3520R763 3522AN95 3519F615 3520N419 3522DK48 3521S574 3521T901 3520R187 3518B300 3522EG06 3520P749 3520R206 3520S005 3520P512 3520P691 3520P741 3520P742 3520P744 3520P745 3520P746 3520P748 3520P810 3520S006 3520P747 3520S003 3521AF21 3518B131 3520L408 3519E743 3521AC18 3521U379 3520O364 3520S292 3519F035 3520S149 3521Z495 3521Z496 3520P082 3520L957 3520R180 3519G235 3519G633 3519H568 3519E607 3522BI32 3518D028 3522CN47 3520K867 3519I425 3520K923 3523FA45 3520O771 3520R123 3521W020 3520K966 3522AV78 3521T568 3520O776 3518A707 3521T325 3521T329 3518C485 3518D396 3522BU41 3519G180 3522AR04 3522AR05 3520R135 3522CR96 3523EN71 3520R209 3520L915 3520L916 3520N979 3520O026 3520O298 3520P109 3520P559 3520S287 3521V691 3522AR01 3522AR03 3518D017 3519E728 3520N729 3519F039 3520L676 3520N364 3520N366 3521S486 3520P539 3521V200 3522BZ70 3523FL02 3523FL03 3521T704 3521T575 3520O549 3520P906 3520P928 3520P930 3522AR07 3520R138 3523EN74 3521V688 3519F034 3523FA47 3520P907 3520S285 3521S487 3522AR00 3522AR06 3523FD33 3519F038 3523FH21 3520N010 3520N505", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2161-2026%22", "url": "https://recallledger.net/recalls/device-z-2161-2026-lucas-2-model-number-99576-catalog-numbers-99576-000024-and-99576/"}, {"id": "fda-device-z-2159-2026", "source": "FDA", "category": "device", "recall_number": "Z-2159-2026", "title": "NextStep Antegrade Chronic Hemodialysis Catheter recall (ARROW INTERNATIONAL, LLC)", "product": "NextStep Antegrade Chronic Hemodialysis Catheter, REF: AC-15192-SFX, AC-15232-SFX, CS-15192-SFX, CS-15232-SFX, CS-15272-SFX, CS-15312-SFX, CS-15422-SFX, CS-15502-SFX; NextStep Antegrade Hemodialysis Catheter with Arrow Simplicity Micro-Introducer, REF: CS-15192-SFXM, CS-15232-SFXM; NextStep Retrograde Hemodialysis Catheter, REF: AC-15192-X, AC-15232-X, AC-15272-X, CS-15192-X, CS-15232-X, CS-15272-X, CS-15312-X; NextStep Retrograde Hemodialysis Catheter with Arrow Simplicity Micro-Introducer, REF: CS-15192-XM, CS-15232-XM, CS-15272-XM, CS-15312-XM", "reason": "16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets. Sheath introducer may not split as intended, and may result in withdrawal resistance, prolonged procedure time, pain, bleeding, hematoma, tissue injury, vessel wall injury.", "hazard_level": "Class I", "company": "ARROW INTERNATIONAL, LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-10", "report_date": "2026-05-20", "status": "Ongoing", "distribution": "Worldwide distribution: US nationwide and countries of: AE, AL, AR, AT, AU, BE, BG, BS, BR, BW, CA, CH, CL, CN, CO, CZ, DE, EC, EE, ES, FR, GB, GR, GT, HU, ID, IE, IN, IT, JP, KW, KZ, LB, LT, LU, MN, MZ, NA, NL, NO, NP, NZ, PA, PE, PF, PH, PL, PT, QA, RO, RS, RU, SA, SG, SL, SK, SZ, TH, TN, TR, TT, UA, VN, ZA, ZM, and ZW", "states": ["AL", "AR", "CA", "MN", "TN"], "nationwide": true, "quantity": "19,687", "codes": "REF/UDI-DI/Lots: AC-15192-SFX/30801902197758/AC-15192-SFX; AC-15232-SFX/00801902095909/33F23H1018; CS-15192-SFX/30801902195297/33F23E0575, 33F23G0530, 33F23K0187, 33F23K1104, 33F23L0929, 33F24A0275, 33F24C0068, 33F24D1012, 33F25C0020, 33F25E1083, 33F25G0636, 33F25H0292, 33F25H0790, 33F25L0038; CS-15232-SFX/30801902195549/33F23E0576, 33F23G0534, 33F23L0936, 33F24A0279, 33F24C0067, 33F24D1006, 33F24E0684, 33F24H0258, 33F24J0033, 33F24J0085, 33F24J0342, 33F24L0056, 33F24M0231, 33F25A0405, 33F25C0036, 33F25C0664, 33F25D0739, 33F25E0433, 33F25G0716, 33F25H0248; CS-15272-SFX/10801902195217/33F23B0321, 33F23D0859, 33F23H0500, 33F23K0177, 33F23L0943, 33F24A0280, 33F24C0083, 33F24H0042, 33F24H0260, 33F24J0022, 33F24J0038, 33F24J0088, 33F24L0177, 33F25C0028, 33F25E1090, 33F25F0301, 33F25F0514; CS-15312-SFX/30801902197529/33F23G0541, 33F23H0984, 33F23L0951, 33F24A0283; CS-15422-SFX/30801902195327/33F23K0179, 33F23L0956, 33F24A0290, 33F24E0814; CS-15502-SFX/30801902195563/33F23L0959, 33F24A0286, 33F24J0060; CS-15192-SFXM/10801902127157/33F25C0015, 33F25E1084; CS-15232-SFXM/10801902127232/33F25C0671; AC-15192-X/ 00801902095879/33F23F0744, 33F24E0784, 33F25D0685; AC-15232-X/00801902095916/33F23H1013, 33F24J0068, 33F25C0675, 33F25J0589; AC-15272-X/00801902095954/33F23H1023; CS-15192-X/30801902195303/33F23C0886, 33F23E0564, 33F23G0263, 33F23G0533, 33F23K0712, 33F23L0935, 33F24E0187, 33F24E0793, 33F24G0171, 33F24J0017, 33F24J0041, 33F25D0701, 33F25E0476, 33F25F0486, 33F25H0783, 33F25H0857; CS-15232-X/30801902195556/33F23C0862, 33F23E0566, 33F23F0722, 33F23K0171, 33F23L0940, 33F24A0916, 33F24C0061, 33F24D1037, 33F24E0800, 33F24J0043, 33F24L0176, 33F25A0028, 33F25C0029, 33F25C0644, 33F25D0096, 33F25E0352, 33F25F0300, 33F25F0513, 33F25E0477, 33F25J0745; CS-15272-X/10801902195224/33F23C0887, 33F23F0731, 33F23H0983, 33F23K0190, 33F23L0947, 33F24E0807, 33F24F0124, 33F24J0018, 33F24J0050, 33F24L0054, 33F24L0063, 33F24M0006, 33F25C0684, 33F25E0342, 33F25F0276, 33F25J0641; CS-15312-X/30801902195310/33F23C0863, 33F23D0858, 33F23G0544; CS-15192-XM/10801902127225/33F25D0711; CS-15232-XM/10801902127300/33F25E0435; CS-15272-XM/10801902127409/33F25C0680, 33F25K0272; CS-15312-XM/10801902127508/33F25E0442", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2159-2026%22", "url": "https://recallledger.net/recalls/device-z-2159-2026-nextstep-antegrade-chronic-hemodialysis-catheter-ref-ac-15192-sfx-a/"}, {"id": "fda-device-z-2158-2026", "source": "FDA", "category": "device", "recall_number": "Z-2158-2026", "title": "Cannon II Plus Hemodialysis Catheter recall (ARROW INTERNATIONAL, LLC)", "product": "Cannon II Plus Hemodialysis Catheter, REF: CS-15242-VSP, CS-15282-VSP, CS-15322-VSP, CS-15362-VSP, CS-15552-VSP, CSD-15242-SP, CSD-15282-SP; Cannon II Plus Hemodialysis Catheter with Arrow Simplicity Micro-Introducer, REF: CS-15242-SPM, CS-15282-SPM, CS-15322-SPM, CS-15362-SPM", "reason": "16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets. Sheath introducer may not split as intended, and may result in withdrawal resistance, prolonged procedure time, pain, bleeding, hematoma, tissue injury, vessel wall injury.", "hazard_level": "Class I", "company": "ARROW INTERNATIONAL, LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-10", "report_date": "2026-05-20", "status": "Ongoing", "distribution": "Worldwide distribution: US nationwide and countries of: AE, AL, AR, AT, AU, BE, BG, BS, BR, BW, CA, CH, CL, CN, CO, CZ, DE, EC, EE, ES, FR, GB, GR, GT, HU, ID, IE, IN, IT, JP, KW, KZ, LB, LT, LU, MN, MZ, NA, NL, NO, NP, NZ, PA, PE, PF, PH, PL, PT, QA, RO, RS, RU, SA, SG, SL, SK, SZ, TH, TN, TR, TT, UA, VN, ZA, ZM, and ZW", "states": ["AL", "AR", "CA", "MN", "TN"], "nationwide": true, "quantity": "34,568", "codes": "REF/UDI-DI/Lots: CS-15242-VSP/30801902195273/33F23C0870, 33F23D0857, 33F23F0719, 33F23K0182, 33F24A0265, 33F24C0062, 33F24D1000, 33F24D1039, 33F24E0803, 33F24H0038, 33F24H0261, 33F24K0505, 33F24M0039, 33F24M0218, 33F25A0141, 33F25C0657, 33F25D0125, 33F25E0305, 33F25E0429, 33F25E0430, 33F25E1131, 33F25F0042, 33F25G0070, 33F25H0295, 33F25H0366, 33F25H0674, 33F25J1015; CS-15282-VSP/30801902195518/33F23C0866, 33F23D0854, 33F23E0572, 33F23F0594, 33F23G0540, 33F23J0544, 33F23K0174, 33F23L0950, 33F24B0010, 33F24C0060, 33F24D0993, 33F24D1040, 33F24E0268, 33F24E0809, 33F24F0155, 33F24J0037, 33F24M0007, 33F24M0040, 33F24M0165, 33F24M0217, 33F25A0406, 33F25B0269, 33F25C0021, 33F25C0045, 33F25C0642, 33F25D0013, 33F25D0713, 33F25F0249, 33F25H0296, 33F25J0051; CS-15322-VSP/20801902195184/33F23C0869, 33F23D0862, 33F23F0723, 33F23H0985, 33F24A0272, 33F24C0066, 33F24E0813, 33F24G0170, 33F24G0185, 33F24H0256, 33F24J0040, 33F24L0183, 33F24M0222, 33F25A0426, 33F25C0022, 33F25C0593, 33F25E1082, 33F25G0024, 33F25H0297; CS-15362-VSP/30801902195525/33F23C0875, 33F23G0546, 33F23K0195, 33F24E0186, 33F24H0039, 33F24L0201, 33F24M0235, 33F25C0647, 33F25E0326, 33F25G0058, 33F25J0043; CS-15552-VSP/30801902195198/33F23G0552, 33F23H0987, 33F23L0961, 33F24C0070, 33F24E0820, 33F24H0257, 33F24L0068, 33F24M0227, 33F25C0654, 33F25E0432; CSD-15242-SP/20801902096610/33F24A0303, 33F25C0688; CSD-15282-SP/20801902096634/33F23K1087, 33F24A0297; CS-15242-SPM/10801902193527/33F23D0867, 33F23K0192, 33F24A0288, 33F24E0802, 33F24M0244, 33F25C0669, 33F25E0338, 33F25G0586; CS-15282-SPM/10801902193688/33F23C0872, 33F23D0864, 33F23G0539, 33F23L0949, 33F24A0278, 33F24C0075, 33F24E0808, 33F24H0254, 33F24J0036, 33F24L1166, 33F24M0233, 33F25A0413, 33F25C0666, 33F25H0824; CS-15322-SPM/30801902193538/33F23D0865, 33F23H1010, 33F23L0955, 33F24E0812, 33F25C0682, 33F25E0335; CS-15362-SPM/20801902193548/33F24G0062", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2158-2026%22", "url": "https://recallledger.net/recalls/device-z-2158-2026-cannon-ii-plus-hemodialysis-catheter-ref-cs-15242-vsp-cs-15282-vsp/"}, {"id": "fda-device-z-2157-2026", "source": "FDA", "category": "device", "recall_number": "Z-2157-2026", "title": "Arrow-Clark VectorFlow Antegrade Chronic Hemodialysis Catheter: REF: ACS-15192-VFI recall (ARROW INTERNATIONAL, LLC)", "product": "Arrow-Clark VectorFlow Antegrade Chronic Hemodialysis Catheter: REF: ACS-15192-VFI, ACS-15232-VFI, ACS-15272-VFI, CS-15192-VFI, CS-15192-VFIE, CS-15232-VFI, CS-15232-VFIE, CS-15272-VFI, CS-15272-VFIE, CS-15312-VFI, CS-15312-VFIE, CS-15422-VFI, CS-15422-VFIE, CS-15552-VFI, CS-15552-VFIE; Arrow-Clark VectorFlow Antegrade Hemodialysis Catheter with Arrow Simplicity Micro-Introducer: REF: CS-15192-VFIM, CS-15232-VFIM, CS-15272-VFIM; Arrow-Clark VectorFlow Retrograde Chronic Hemodialysis Catheter, REF: ACS-15192-VF, ACS-15232-VF, ACS-15272-VF, ACS-15552-VF, CS-15192-VF, CS-15192-VFE, CS-15232-VF, CS-15232-VFE, CS-15272-VF, CS-15272-VFE, CS-15312-VF, CS-15312-VFE, CS-15422-VF, CS-15422-VFE, CS-15552-VF, CS-15552-VFE; Arrow-Clark VectorFlow Retrograde Hemodialysis Catheter with Arrow Simplicity Micro-Introducer: CS-15192-VFM, CS-15232-VFM, CS-15272-VFM", "reason": "16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets. Sheath introducer may not split as intended, and may result in withdrawal resistance, prolonged procedure time, pain, bleeding, hematoma, tissue injury, vessel wall injury.", "hazard_level": "Class I", "company": "ARROW INTERNATIONAL, LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-10", "report_date": "2026-05-20", "status": "Ongoing", "distribution": "Worldwide distribution: US nationwide and countries of: AE, AL, AR, AT, AU, BE, BG, BS, BR, BW, CA, CH, CL, CN, CO, CZ, DE, EC, EE, ES, FR, GB, GR, GT, HU, ID, IE, IN, IT, JP, KW, KZ, LB, LT, LU, MN, MZ, NA, NL, NO, NP, NZ, PA, PE, PF, PH, PL, PT, QA, RO, RS, RU, SA, SG, SL, SK, SZ, TH, TN, TR, TT, UA, VN, ZA, ZM, and ZW", "states": ["AL", "AR", "CA", "MN", "TN"], "nationwide": true, "quantity": "92,827", "codes": "REF/UDI-DI/Lots: ACS-15192-VFI/ 10801902126709/33F23G0040, 33F25C0689; ACS-15232-VFI/10801902126723/33F23G0045, 33F25C0678; ACS-15272-VFI/ 10801902126747/33F24G0638; CS-15192-VFI/10801902127188, 10801902193572/33F23E0579, 33F23G0042, 33F23K0170, 33F23L0933, 33F24E0271, 33F24G0166, 33F24J0086, 33F24L0064, 33F24M0224, 33F25C0652, 33F25D0052, 33F25D0700, 33F25E1081, 33F25F0015, 33F25F0388, 33F25G0702, 33F25H0785; CS-15192-VFIE/10801902199659/33F23D0853, 33F23E0773, 33F23G0044, 33F23G0532, 33F23H0611, 33F23K0169,33F23K1105,33F23L0934, 33F24A0912, 33F24A0913, 33F24C0058, 33F24D1001, 33F24G0167,33F24G0187, 33F24J0030, 33F24J0032, 33F24J0339, 33F24J0381, 33F24K0659, 33F24L0058, 33F24L0511, 33F24M0155, 33F24M0215, 33F24M0265, 33F25A0143, 33F25A0407, 33F25B0259, 33F25C0037, 33F25D0285, 33F25D0738, 33F25F0060, 33F25G0635; CS-15232-VFI/10801902194463/33F23C0864, 33F23E0578, 33F23E0832, 33F23G0535, 33F23G0840, 33F23H0612, 33F23K0144, 33F24A0914, 33F24C0079, 33F24E0269, 33F24J0042, 33F25B0256, 33F25C0014, 33F25C0709, 33F25C0650, 33F25E1085, 33F25E1130, 33F25F0009, 33F25G0023, 33F25G0450, 33F25H0341, 33F25J1014; CS-15232-VFIE/10801902195149/33F23D0855, 33F23E0774, 33F23G0047, 33F23G0048, 33F23G0049, 33F23K0145, 33F23K0175, 33F23L0938, 33F24A0915, 33F24C0069, 33F24G0169, 33F24J0026, 33F24J0027, 33F24J0028, 33F24J0084, 33F24K0700, 33F24L0178, 33F24M0005, 33F24M0214, 33F24M0219, 33F25C0646, 33F25C0665, 33F25D0097, 33F25E0358, 33F25E0434, 33F25F0012, 33F25F0275, 33F25F0328, 33F25G0069, 33F25H0293, 33F25H0822, 33F25K0235; CS-15272-VFI/10801902193640, 10801902127362/33F23E0871, 33F23F0742, 33F23H0981, 33F23K0181, 33F24A0306, 33F24C0084, 33F24J0062, 33F25D0098, 33F25E0307, 33F25E0332, 33F25E0354, 33F25F0058, 33F25F0245, 33F25J0659; CS-15272-VFIE/10801902195255/33F23E0886, 33F23G0537, 33F23H0982, 33F23K0180, 33F23L0946, 33F24A0922, 33F24C0065, 33F24D1011, 33F24E0686, 33F24E0805, 33F24K0508, 33F24M0223, 33F25A0410, 33F25C0009, 33F25G0717; CS-15312-VFI/10801902197778/33F23G0543, 33F23L0953, 33F24D1007, 33F24E0810, 33F24J0048, 33F25C0039, 33F25D0218, 33F25E0470, 33F25J0021; CS-15312-VFIE/10801902195491/33F23K0183, 33F23L0954, 33F24A0923, 33F24D1013, 33F25A0403, 33F25F0534, 33F25G0722; CS-15422-VFI/10801902193664/33F23G0549, 33F24E0815, 33F25E1074; CS-15422-VFIE/10801902197440/33F23G0550, 33F23K0178, 33F23L0958, 33F24A0919, 33F24C0073, 33F24E0816, 33F25F0303; CS-15552-VFI/10801902193671/33F23K0184, 33F24J0076, 33F25E1075; CS-15552-VFIE/10801902195163/33F23E0865, 33F23F0743, 33F24D0972, 33F24E0819, 33F24G0098, 33F24K0656, 33F25A0032; CS-15192-VFIM/10801902193589/33F24E0792, 33F25C0676, 33F25L0035; CS-15232-VFIM/10801902193619/33F23C0879, 33F23L0939, 33F24A0304, 33F24E0798, 33F24J0047; CS-15272-VFIM/10801902197761/33F23H1027; ACS-15192-VF/10801902126693/33F24G0637; ACS-15232-VF/10801902126716/33F23H1016; ACS-15272-VF/10801902126730/33F23H1024; ACS-15552-VF/10801902126792/33F23H1021; CS-15192-VF/20801902193593/33F23K0186, 33F23L0931, 33F24C0082, 33F24E0788, 33F24J0054, 33F24M0162, 33F24M0230, 33F25D0271; CS-15192-VFE/10801902195460/33F23E0776, 33F23F0728, 33F23G0531, 33F24A0917, 33F24C0063, 33F24D1003, 33F24E0789, 33F24J0039, 33F24L0069, 33F24M0156, 33F24M0159, 33F25C0683, 33F25D0107, 33F25D0220, 33F25E0343, 33F25F0273, 33F25F0462, 33F25G0444, 33F25H0820, 33F25K0384; CS-15232-VF/10801902193626/33F23C0873, 33F23J0546, 33F24A0294, 33F24C0071, 33R24G0168, 33F24J0044, 33F25D0089, 33F25E0333, 33F25E0427, 33F25E1095, 33F25F0404, 33F25H0294, 33F25J1009; CS-15232-VFE/10801902195132/33F23E0775, 33F23F0720, 33F23K0176, 33F23K0194, 33F23L0937, 33F24A0927, 33F24C0059, 33F24D1010, 33F24E0270, 33F24E0796, 33F24G0045, 33F24J0035, 33F24J0083, 33F24L0171, 33F24M0216, 33F25A0004, 33F25A0083, 33F25C0023, 33F25C0659, 33F25D0106, 33F25D0219, 33F25D0726, 33F25E0478, 33F25E1105, 33F25F0298, 33F25J1056, 33F25K0335, 33F25L0011; CS-15272-VF/10801902193657/33F23C0880, 33F23F0740, 33F23L0944, 33F24C0081, 33F24E0804, 33F24J0051, 33F24J0686, 33F24M0228, 33F25C0668, 33F25E0337, 33F25F0403, 33F25J0590; CS-15272-VFE/10801902195248/33F23E0777, 33F23F0732, 33F23H0980, 33F23K0172, 33F23L0945, 33F24A0918, 33F24C0064, 33F24H0044, 33F24H0255, 33F24M0237, 33F25C0049, 33F25E0349, 33F25E1132, 33F25G0637; CS-15312-VF/10801902127447/33F24G0060, 33F25D0216; CS-15312-VFE/10801902195484/33F23F0734, 33F23G0542, 33F23L0952, 33F24A0925, 33F24C0076, 33F24J0053, 33F24M0225, 33F25A0033, 33F25C0667, 33F25E0320, 33F25E0469, 33F25G0603; CS-15422-VF/10801902128666/33F23H1020, 33F25G0734; CS-15422-VFE/10801902197341/33F23G0548, 33F23H0986, 33F23L0957, 33F24A0929, 33F24J0483, 33F24M0229, 33F25C0681, 33F25E0440, 33F25F0250, 33F25G0484; CS-15552-VF/10801902128703/33F23H1012, 33F25C0674, 33F25J0588; CS-15552-VFE/10801902195156/33F23D0868, 33F23G0261, 33F23G0551, 33F23K0173, 33F24A0928, 33F24D1014, 33F24E0818, 33F24J0059, 33F24K0511, 33F25C0670, 33F25E0471, 33F25F0455, 33F25G0447; CS-15192-VFM/10801902193602/33F23K0189, 33F24C0078, 33F24J0049, 33F24M0243, 33F25C0672, 33F25E1077, 33F25F0418; CS-15232-VFM/10801902193633/33F23J0547, 33F24A0289, 33F24C0077, 33F24E0799, 33F24J0045, 33F24J0093, 33F25A0026, 33F25C0050, 33F25E0348, 33F25K0348; CS-15272-VFM/10801902127393/33F25C0687", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2157-2026%22", "url": "https://recallledger.net/recalls/device-z-2157-2026-arrow-clark-vectorflow-antegrade-chronic-hemodialysis-catheter-ref-a/"}, {"id": "fda-device-z-2156-2026", "source": "FDA", "category": "device", "recall_number": "Z-2156-2026", "title": "Arrow Edge Hemodialysis Catheterization Product recall (ARROW INTERNATIONAL, LLC)", "product": "Arrow Edge Hemodialysis Catheterization Product, REF: CS-15242-I, CS-15282-I, CS-15322-I", "reason": "16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets. Sheath introducer may not split as intended, and may result in withdrawal resistance, prolonged procedure time, pain, bleeding, hematoma, tissue injury, vessel wall injury.", "hazard_level": "Class I", "company": "ARROW INTERNATIONAL, LLC", "company_location": "Morrisville, NC, United States", "date": "2026-04-10", "report_date": "2026-05-20", "status": "Ongoing", "distribution": "Worldwide distribution: US nationwide and countries of: AE, AL, AR, AT, AU, BE, BG, BS, BR, BW, CA, CH, CL, CN, CO, CZ, DE, EC, EE, ES, FR, GB, GR, GT, HU, ID, IE, IN, IT, JP, KW, KZ, LB, LT, LU, MN, MZ, NA, NL, NO, NP, NZ, PA, PE, PF, PH, PL, PT, QA, RO, RS, RU, SA, SG, SL, SK, SZ, TH, TN, TR, TT, UA, VN, ZA, ZM, and ZW", "states": ["AL", "AR", "CA", "MN", "TN"], "nationwide": true, "quantity": "285", "codes": "REF/UDI-DI/Lot: CS-15242-I/ 30801902195280/33F23G0536; CS-15282-I/30801902195532/33F23C0877, 33F24A0281, 33F24H0041; CS-15322-I/30801902197451/33F23G0545", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2156-2026%22", "url": "https://recallledger.net/recalls/device-z-2156-2026-arrow-edge-hemodialysis-catheterization-product-ref-cs-15242-i-cs-1/"}, {"id": "fda-device-z-2066-2026", "source": "FDA", "category": "device", "recall_number": "Z-2066-2026", "title": "Custom Convenience Kit containing recalled Medline Namic Angiographic Control Syringes... recall (Windstone Medical Packaging, Inc.)", "product": "Custom Convenience Kit containing recalled Medline Namic Angiographic Control Syringes with Rotating Adapter (Namic RA Syringes) Angio Pack Part numbers AMS6908E, AMS6908F", "reason": "Affected kits contain Medline Namic RA Syringes, which are recalled by their manufacturer due to risk of syringe rotating adapter unwinding during use, which may result in a loose connection or full disconnection between syringe and manifold. If unwinding occurs, there is a potential for biohazard exposure, blood loss, infection. or air embolism.", "hazard_level": "Class I", "company": "Windstone Medical Packaging, Inc.", "company_location": "Billings, MT, United States", "date": "2026-04-02", "report_date": "2026-05-20", "status": "Ongoing", "distribution": "US Nationwide distribution in the state of Arizona.", "states": ["AZ"], "nationwide": true, "quantity": "150 kits (US only)", "codes": "Pack AMS6908E UDI-DI B098AMS6908E0 Lot 214875 Pack AMS6908F UDI-DI B098AMS6908F0 Lots 215436, 225001, 226706, 234088", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2066-2026%22", "url": "https://recallledger.net/recalls/device-z-2066-2026-custom-convenience-kit-containing-recalled-medline-namic-angiographic/"}, {"id": "fda-food-h-0837-2026", "source": "FDA", "category": "food", "recall_number": "H-0837-2026", "title": "Bulk WN-976-782-1 Seasoning for Cheese Sauce recall (Givaudan Flavors Corp)", "product": "Bulk WN-976-782-1 Seasoning for Cheese Sauce, Net Wt. 43.50 lbs., in a brown kraft bag", "reason": "Product has the potential to be contaminated with Salmonella.", "hazard_level": "Class I", "company": "Givaudan Flavors Corp", "company_location": "Cincinnati, OH, United States", "date": "2026-04-22", "report_date": "2026-05-13", "status": "Terminated", "distribution": "1 manufacturer in MO", "states": [], "nationwide": false, "quantity": "24,012 lbs.", "codes": "Batch: CS00140785; Expiry Date: 26 SEP 2026", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0837-2026%22", "url": "https://recallledger.net/recalls/food-h-0837-2026-bulk-wn-976-782-1-seasoning-for-cheese-sauce-net-wt-43-50-lbs-in-a/"}, {"id": "fda-food-h-0776-2026", "source": "FDA", "category": "food", "recall_number": "H-0776-2026", "title": "Publix Bran Flakes recall (Post Consumer Brands, LLC)", "product": "Publix Bran Flakes, Wheat Cereal. Net Wt 18oz (1 lb 2 oz) 510g. UPC 0 41415-24305 7. Distributed by Publix Super Markets, Inc. Lakeland, FL 33802.", "reason": "Foreign Material (plastic)", "hazard_level": "Class II", "company": "Post Consumer Brands, LLC", "company_location": "Lakeville, MN, United States", "date": "2026-04-16", "report_date": "2026-05-13", "status": "Terminated", "distribution": "AL, FL, GA, NC", "states": ["AL", "FL", "GA", "NC"], "nationwide": false, "quantity": "13,824 units", "codes": "SKU 4141524305 Item Number 47026 Lot Code OCT0526RBA (all time stamps)", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0776-2026%22", "url": "https://recallledger.net/recalls/food-h-0776-2026-publix-bran-flakes-wheat-cereal-net-wt-18oz-1-lb-2-oz-510g-upc/"}, {"id": "fda-food-h-0767-2026", "source": "FDA", "category": "food", "recall_number": "H-0767-2026", "title": "LUNDBERG FAMILY FAMRS WHITE RICE JASMINE recall (Wehah Farms)", "product": "LUNDBERG FAMILY FAMRS WHITE RICE JASMINE NET WT 32 OZ (2 lb) 907 g Manufactured and Distributed by: Lundberg Family Farms Richvale, CA 95974 UPC: 073416040281", "reason": "Potential contamination with foreign materials.", "hazard_level": "Class II", "company": "Wehah Farms", "company_location": "Richvale, CA, United States", "date": "2026-04-03", "report_date": "2026-05-13", "status": "Terminated", "distribution": "U.S. States: CA, CT, FL, IL, NC, NH, NY, PA, TN, VT, WA, WI. Foreign distribution: None", "states": ["CA", "CT", "FL", "IL", "NC", "NH", "NY", "PA", "TN", "VT", "WA", "WI"], "nationwide": false, "quantity": "27,324 packages (6 packages/case; 4,554 cases)", "codes": "Lot, Best Before: 260201MA, 01FEB2027; 260202MA, 02FEB2027.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0767-2026%22", "url": "https://recallledger.net/recalls/food-h-0767-2026-lundberg-family-famrs-white-rice-jasmine-net-wt-32-oz-2-lb-907-g-ma/"}, {"id": "fda-food-h-0766-2026", "source": "FDA", "category": "food", "recall_number": "H-0766-2026", "title": "RAW FARM ORIGINAL RAW CHEDDAR 80 OZ [BULK ITEM] recall (Raw Farm LLC)", "product": "RAW FARM ORIGINAL RAW CHEDDAR 80 OZ [BULK ITEM] UPC: 835204001160", "reason": "Multi-state outbreak of E. coli O157:H7.", "hazard_level": "Class I", "company": "Raw Farm LLC", "company_location": "Fresno, CA, United States", "date": "2026-04-02", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "U.S. distribution: AZ, CA, CO, FL, GA, IL, IN, MD, NV, TX. Foreign distribution: None.", "states": ["AZ", "CA", "CO", "FL", "GA", "IL", "IN", "MD", "NV", "TX"], "nationwide": false, "quantity": "Not provided", "codes": "80 oz - BATCH: 20251015-4, BEST BY: 8/11/2026 and all prior batches/dates.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0766-2026%22", "url": "https://recallledger.net/recalls/food-h-0766-2026-raw-farm-original-raw-cheddar-80-oz-bulk-item-upc-835204001160/"}, {"id": "fda-food-h-0765-2026", "source": "FDA", "category": "food", "recall_number": "H-0765-2026", "title": "RAW FARM SHREDDED RAW CHEDDAR 80 OZ [BULK ITEM] recall (Raw Farm LLC)", "product": "RAW FARM SHREDDED RAW CHEDDAR 80 OZ [BULK ITEM] UPC: 835204000194", "reason": "Multi-state outbreak of E. coli O157:H7.", "hazard_level": "Class I", "company": "Raw Farm LLC", "company_location": "Fresno, CA, United States", "date": "2026-04-02", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "U.S. distribution: AZ, CA, CO, FL, GA, IL, IN, MD, NV, TX. Foreign distribution: None.", "states": ["AZ", "CA", "CO", "FL", "GA", "IL", "IN", "MD", "NV", "TX"], "nationwide": false, "quantity": "Not provided", "codes": "80 oz - BATCH: 2026020, BEST BY: 5/6/2026 and all prior batches/dates.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0765-2026%22", "url": "https://recallledger.net/recalls/food-h-0765-2026-raw-farm-shredded-raw-cheddar-80-oz-bulk-item-upc-835204000194/"}, {"id": "fda-food-h-0764-2026", "source": "FDA", "category": "food", "recall_number": "H-0764-2026", "title": "RAW FARM RAW CHEDDAR SIMPLY SHREDDED Original MADE WITH: WHOLE RAW MILK TRULY RAW -... recall (Raw Farm LLC)", "product": "RAW FARM RAW CHEDDAR SIMPLY SHREDDED Original MADE WITH: WHOLE RAW MILK TRULY RAW - NEVER WARMED ABOVE 102F MADE IN THE USA KEEP REFRIGERATED INGREDIENTS: WHOLE RAW MILK, VEGETABLE RENNET, CULTURES, KOSHER SEA SALT Produced By: RAW FARM, LLC www.rawfarmusa.com 8 oz (227g) UPC: 835204001184", "reason": "Multi-state outbreak of E. coli O157:H7.", "hazard_level": "Class I", "company": "Raw Farm LLC", "company_location": "Fresno, CA, United States", "date": "2026-04-02", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "U.S. distribution: AZ, CA, CO, FL, GA, IL, IN, MD, NV, TX. Foreign distribution: None.", "states": ["AZ", "CA", "CO", "FL", "GA", "IL", "IN", "MD", "NV", "TX"], "nationwide": false, "quantity": "Not provided", "codes": "8 oz - BATCH: 20260212, BEST BY: 5/13/2026 and all prior batches/dates.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0764-2026%22", "url": "https://recallledger.net/recalls/food-h-0764-2026-raw-farm-raw-cheddar-simply-shredded-original-made-with-whole-raw-mil/"}, {"id": "fda-food-h-0763-2026", "source": "FDA", "category": "food", "recall_number": "H-0763-2026", "title": "RAW FARM RAW CHEDDAR Jalapeno NEVER WARMED ABOVE 102F recall (Raw Farm LLC)", "product": "RAW FARM RAW CHEDDAR Jalapeno NEVER WARMED ABOVE 102F (TRULY RAW) MADE WITH WHOLE RAW MILK MADE IN USA KEEP REFRIGERATED INGREDIENTS: whole raw milk, vegetable rennet, cultures, kosher sea salt, 100% organic chili powder jalapeno, air dried green jalapeno peppers Produced By: RAW FARM, LLC www.rawfarmusa.com 8 oz (227g) UPC: 835204000330 16 oz (454g) UPC: 835204000354", "reason": "Multi-state outbreak of E. coli O157:H7.", "hazard_level": "Class I", "company": "Raw Farm LLC", "company_location": "Fresno, CA, United States", "date": "2026-04-02", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "U.S. distribution: AZ, CA, CO, FL, GA, IL, IN, MD, NV, TX. Foreign distribution: None.", "states": ["AZ", "CA", "CO", "FL", "GA", "IL", "IN", "MD", "NV", "TX"], "nationwide": false, "quantity": "Not provided", "codes": "8 oz - BATCH: 20251128-2J, BEST BY: 9/24/2026 and all prior batches/dates. 16 oz - BATCH: 20251128-1J, BEST BY: 9/24/2026 and all prior batches/dates.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0763-2026%22", "url": "https://recallledger.net/recalls/food-h-0763-2026-raw-farm-raw-cheddar-jalapeno-never-warmed-above-102f-truly-raw-made/"}, {"id": "fda-food-h-0762-2026", "source": "FDA", "category": "food", "recall_number": "H-0762-2026", "title": "RAW FARM RAW CHEDDAR Original NEVER WARMED ABOVE 102F recall (Raw Farm LLC)", "product": "RAW FARM RAW CHEDDAR Original NEVER WARMED ABOVE 102F (TRULY RAW) MADE WITH WHOLE RAW MILK MADE IN USA KEEP REFRIGERATED INGREDIENTS: whole raw milk, vegetable rennet, cultures, kosher sea salt Produced By: RAW FARM, LLC www.rawfarmusa.com 8 oz (227g) UPC: 835204001177 16 oz (454g) UPC: 835204000156", "reason": "Multi-state outbreak of E. coli O157:H7.", "hazard_level": "Class I", "company": "Raw Farm LLC", "company_location": "Fresno, CA, United States", "date": "2026-04-02", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "U.S. distribution: AZ, CA, CO, FL, GA, IL, IN, MD, NV, TX. Foreign distribution: None.", "states": ["AZ", "CA", "CO", "FL", "GA", "IL", "IN", "MD", "NV", "TX"], "nationwide": false, "quantity": "Not provided", "codes": "8 oz - BATCH: 20260212, BEST BY: 5/13/2026 and all prior batches/dates. 16 oz - BATCH: 20251027-4, BEST BY: 8/23/2026 and all prior batches/dates.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0762-2026%22", "url": "https://recallledger.net/recalls/food-h-0762-2026-raw-farm-raw-cheddar-original-never-warmed-above-102f-truly-raw-made/"}, {"id": "fda-food-h-0761-2026", "source": "FDA", "category": "food", "recall_number": "H-0761-2026", "title": "Good & Gather Fresh from Our Deli. Sesame Teriyaki Chicken with Rice. Net Wt 18.0 oz recall (Target Corporation)", "product": "Good & Gather Fresh from Our Deli. Sesame Teriyaki Chicken with Rice. Net Wt 18.0 oz (1.125lb). Keep Refrigerated. DPCI # 878-02-0227. UPC (01) 00250086000009 (3922) 00999. Distributed by SuperTarget Mpls, MN 55403.", "reason": "Undeclared allergens (sesame and soy)", "hazard_level": "Class II", "company": "Target Corporation", "company_location": "Minneapolis, MN, United States", "date": "2026-04-24", "report_date": "2026-05-13", "status": "Terminated", "distribution": "AL, AZ, CA, CO, FL, GA, IA, IL, IN, KS, LA, MN, MO, NC, ND, NE, OK, TN, TX, UT, VA, WI", "states": ["AL", "AZ", "CA", "CO", "FL", "GA", "IA", "IL", "IN", "KS", "LA", "MN", "MO", "NC", "ND", "NE", "OK", "TN", "TX", "UT", "VA", "WI"], "nationwide": false, "quantity": "558 units", "codes": "Use or Freeze By: 4/15/26 through 4/27/26", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0761-2026%22", "url": "https://recallledger.net/recalls/food-h-0761-2026-good-gather-fresh-from-our-deli-sesame-teriyaki-chicken-with-rice/"}, {"id": "fda-food-h-0760-2026", "source": "FDA", "category": "food", "recall_number": "H-0760-2026", "title": "Chocolate Showers Ice Cream - 32 oz recall (Silver Moon LP dba Loard's Ice Cream)", "product": "Chocolate Showers Ice Cream - 32 oz (5 labels: Mollie Stone's; Dehoff's; Farmer Joe's, Piazza's Fine Foods, and Berkeley Bowl) UPC: 8-12017-00918", "reason": "Undeclared Soy (with mitigating circumstances)", "hazard_level": "Class II", "company": "Silver Moon LP dba Loard's Ice Cream", "company_location": "San Leandro, CA, United States", "date": "2026-04-15", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Loard's brand distributed to Loard's Ice Cream parlors located in Northern California. Private labels distributed to grocery stores located in Northern California.", "states": ["CA"], "nationwide": false, "quantity": "1396 TOTAL units (32 oz/unit)", "codes": "UPC: 8-12017-00918", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0760-2026%22", "url": "https://recallledger.net/recalls/food-h-0760-2026-chocolate-showers-ice-cream-32-oz-5-labels-mollie-stone-s-dehoff/"}, {"id": "fda-food-h-0759-2026", "source": "FDA", "category": "food", "recall_number": "H-0759-2026", "title": "Peppermint Ice Cream - 32 oz recall (Silver Moon LP dba Loard's Ice Cream)", "product": "Peppermint Ice Cream - 32 oz (4 labels: Mollie Stone's; Dehoff's; Farmer Joe's, Piazza's Fine Foods) UPC: 8-12017-00933", "reason": "Undeclared Red #40", "hazard_level": "Class III", "company": "Silver Moon LP dba Loard's Ice Cream", "company_location": "San Leandro, CA, United States", "date": "2026-04-15", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Loard's brand distributed to Loard's Ice Cream parlors located in Northern California. Private labels distributed to grocery stores located in Northern California.", "states": ["CA"], "nationwide": false, "quantity": "1076 TOTAL units (32 oz/unit)", "codes": "UPC: 8-12017-00933", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0759-2026%22", "url": "https://recallledger.net/recalls/food-h-0759-2026-peppermint-ice-cream-32-oz-4-labels-mollie-stone-s-dehoff-s-farm/"}, {"id": "fda-food-h-0758-2026", "source": "FDA", "category": "food", "recall_number": "H-0758-2026", "title": "Chocolate Mint Ice Cream - 32 oz recall (Silver Moon LP dba Loard's Ice Cream)", "product": "Chocolate Mint Ice Cream - 32 oz (4 labels: Mollie Stone's; Dehoff's; Farmer Joe's, Piazza's Fine Foods) UPC: 8-12017-00917", "reason": "Undeclared Soy (with mitigating circumstances), Yellow #5, Blue #1", "hazard_level": "Class II", "company": "Silver Moon LP dba Loard's Ice Cream", "company_location": "San Leandro, CA, United States", "date": "2026-04-15", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Loard's brand distributed to Loard's Ice Cream parlors located in Northern California. Private labels distributed to grocery stores located in Northern California.", "states": ["CA"], "nationwide": false, "quantity": "1464 TOTAL units (32 oz/unit)", "codes": "UPC: 8-12017-00917", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0758-2026%22", "url": "https://recallledger.net/recalls/food-h-0758-2026-chocolate-mint-ice-cream-32-oz-4-labels-mollie-stone-s-dehoff-s/"}, {"id": "fda-food-h-0757-2026", "source": "FDA", "category": "food", "recall_number": "H-0757-2026", "title": "Burgundy Cherry Ice Cream - 32 oz recall (Silver Moon LP dba Loard's Ice Cream)", "product": "Burgundy Cherry Ice Cream - 32 oz (4 labels: Mollie Stone's; Dehoff's; Farmer Joe's, Piazza's Fine Foods) UPC: 8-12017-00909", "reason": "Undeclared Red #40, Blue #1, Blue #2", "hazard_level": "Class III", "company": "Silver Moon LP dba Loard's Ice Cream", "company_location": "San Leandro, CA, United States", "date": "2026-04-15", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Loard's brand distributed to Loard's Ice Cream parlors located in Northern California. Private labels distributed to grocery stores located in Northern California.", "states": ["CA"], "nationwide": false, "quantity": "888 TOTAL units (32 oz/unit)", "codes": "UPC: 8-12017-00909", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0757-2026%22", "url": "https://recallledger.net/recalls/food-h-0757-2026-burgundy-cherry-ice-cream-32-oz-4-labels-mollie-stone-s-dehoff-s/"}, {"id": "fda-food-h-0756-2026", "source": "FDA", "category": "food", "recall_number": "H-0756-2026", "title": "Banana Ice Cream - 32 oz recall (Silver Moon LP dba Loard's Ice Cream)", "product": "Banana Ice Cream - 32 oz (4 labels: Mollie Stone's; Dehoff's; Farmer Joe's, Piazza's Fine Foods) UPC: 8-12017-00903", "reason": "Undeclared Yellow #5", "hazard_level": "Class II", "company": "Silver Moon LP dba Loard's Ice Cream", "company_location": "San Leandro, CA, United States", "date": "2026-04-15", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Loard's brand distributed to Loard's Ice Cream parlors located in Northern California. Private labels distributed to grocery stores located in Northern California.", "states": ["CA"], "nationwide": false, "quantity": "664 TOTAL units (32 oz/unit)", "codes": "UPC: 8-12017-00903", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0756-2026%22", "url": "https://recallledger.net/recalls/food-h-0756-2026-banana-ice-cream-32-oz-4-labels-mollie-stone-s-dehoff-s-farmer-j/"}, {"id": "fda-food-h-0755-2026", "source": "FDA", "category": "food", "recall_number": "H-0755-2026", "title": "Loard's Vanilla Ice Cream - 32 oz recall (Silver Moon LP dba Loard's Ice Cream)", "product": "Loard's Vanilla Ice Cream - 32 oz; 56 oz", "reason": "Undeclared Milk.", "hazard_level": "Class II", "company": "Silver Moon LP dba Loard's Ice Cream", "company_location": "San Leandro, CA, United States", "date": "2026-04-15", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Loard's brand distributed to Loard's Ice Cream parlors located in Northern California. Private labels distributed to grocery stores located in Northern California.", "states": ["CA"], "nationwide": false, "quantity": "2008 units (32 oz/unit); 676 units (56 oz/unit)", "codes": "None", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0755-2026%22", "url": "https://recallledger.net/recalls/food-h-0755-2026-loard-s-vanilla-ice-cream-32-oz-56-oz/"}, {"id": "fda-food-h-0754-2026", "source": "FDA", "category": "food", "recall_number": "H-0754-2026", "title": "Loard's Ube Ice Cream - 32 oz recall (Silver Moon LP dba Loard's Ice Cream)", "product": "Loard's Ube Ice Cream - 32 oz", "reason": "Undeclared Milk, Red #3, Red #40, Blue #1, Blue #2.", "hazard_level": "Class II", "company": "Silver Moon LP dba Loard's Ice Cream", "company_location": "San Leandro, CA, United States", "date": "2026-04-15", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Loard's brand distributed to Loard's Ice Cream parlors located in Northern California. Private labels distributed to grocery stores located in Northern California.", "states": ["CA"], "nationwide": false, "quantity": "1568 units (32 oz/unit)", "codes": "None", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0754-2026%22", "url": "https://recallledger.net/recalls/food-h-0754-2026-loard-s-ube-ice-cream-32-oz/"}, {"id": "fda-food-h-0753-2026", "source": "FDA", "category": "food", "recall_number": "H-0753-2026", "title": "Loard's Toasted Almond Ice Cream - 32 oz recall (Silver Moon LP dba Loard's Ice Cream)", "product": "Loard's Toasted Almond Ice Cream - 32 oz", "reason": "Undeclared Milk, Almonds.", "hazard_level": "Class II", "company": "Silver Moon LP dba Loard's Ice Cream", "company_location": "San Leandro, CA, United States", "date": "2026-04-15", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Loard's brand distributed to Loard's Ice Cream parlors located in Northern California. Private labels distributed to grocery stores located in Northern California.", "states": ["CA"], "nationwide": false, "quantity": "656 units (32 oz/unit)", "codes": "None", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0753-2026%22", "url": "https://recallledger.net/recalls/food-h-0753-2026-loard-s-toasted-almond-ice-cream-32-oz/"}, {"id": "fda-food-h-0752-2026", "source": "FDA", "category": "food", "recall_number": "H-0752-2026", "title": "Loard's Strawberry Ice Cream - 32 oz recall (Silver Moon LP dba Loard's Ice Cream)", "product": "Loard's Strawberry Ice Cream - 32 oz; 56 oz", "reason": "Undeclared Milk, Red #40.", "hazard_level": "Class II", "company": "Silver Moon LP dba Loard's Ice Cream", "company_location": "San Leandro, CA, United States", "date": "2026-04-15", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Loard's brand distributed to Loard's Ice Cream parlors located in Northern California. Private labels distributed to grocery stores located in Northern California.", "states": ["CA"], "nationwide": false, "quantity": "910 units (32 oz/unit); 292 units (56 oz/unit)", "codes": "None", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0752-2026%22", "url": "https://recallledger.net/recalls/food-h-0752-2026-loard-s-strawberry-ice-cream-32-oz-56-oz/"}, {"id": "fda-food-h-0751-2026", "source": "FDA", "category": "food", "recall_number": "H-0751-2026", "title": "Loard's Sea Salt Caramel Ice Cream - 32 oz recall (Silver Moon LP dba Loard's Ice Cream)", "product": "Loard's Sea Salt Caramel Ice Cream - 32 oz", "reason": "Undeclared Milk, Soy, Sulfites.", "hazard_level": "Class II", "company": "Silver Moon LP dba Loard's Ice Cream", "company_location": "San Leandro, CA, United States", "date": "2026-04-15", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Loard's brand distributed to Loard's Ice Cream parlors located in Northern California. Private labels distributed to grocery stores located in Northern California.", "states": ["CA"], "nationwide": false, "quantity": "1064 units (32 oz/unit)", "codes": "None", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0751-2026%22", "url": "https://recallledger.net/recalls/food-h-0751-2026-loard-s-sea-salt-caramel-ice-cream-32-oz/"}, {"id": "fda-food-h-0750-2026", "source": "FDA", "category": "food", "recall_number": "H-0750-2026", "title": "Loard's Rocky Road Ice Cream - 56 oz recall (Silver Moon LP dba Loard's Ice Cream)", "product": "Loard's Rocky Road Ice Cream - 56 oz", "reason": "Undeclared Milk, Walnuts, Eggs.", "hazard_level": "Class II", "company": "Silver Moon LP dba Loard's Ice Cream", "company_location": "San Leandro, CA, United States", "date": "2026-04-15", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Loard's brand distributed to Loard's Ice Cream parlors located in Northern California. Private labels distributed to grocery stores located in Northern California.", "states": ["CA"], "nationwide": false, "quantity": "516 units (56 oz/unit)", "codes": "None", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0750-2026%22", "url": "https://recallledger.net/recalls/food-h-0750-2026-loard-s-rocky-road-ice-cream-56-oz/"}, {"id": "fda-food-h-0749-2026", "source": "FDA", "category": "food", "recall_number": "H-0749-2026", "title": "Loard's Raspberry Sherbert - 32 oz recall (Silver Moon LP dba Loard's Ice Cream)", "product": "Loard's Raspberry Sherbert - 32 oz", "reason": "Undeclared Milk, Red #40.", "hazard_level": "Class II", "company": "Silver Moon LP dba Loard's Ice Cream", "company_location": "San Leandro, CA, United States", "date": "2026-04-15", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Loard's brand distributed to Loard's Ice Cream parlors located in Northern California. Private labels distributed to grocery stores located in Northern California.", "states": ["CA"], "nationwide": false, "quantity": "132 units (32 oz/unit)", "codes": "None", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0749-2026%22", "url": "https://recallledger.net/recalls/food-h-0749-2026-loard-s-raspberry-sherbert-32-oz/"}, {"id": "fda-food-h-0748-2026", "source": "FDA", "category": "food", "recall_number": "H-0748-2026", "title": "Loard's Rainbow Sherbert - 32 oz recall (Silver Moon LP dba Loard's Ice Cream)", "product": "Loard's Rainbow Sherbert - 32 oz", "reason": "Undeclared Milk, Soy, Yellow #5, Red #40, Green #3.", "hazard_level": "Class II", "company": "Silver Moon LP dba Loard's Ice Cream", "company_location": "San Leandro, CA, United States", "date": "2026-04-15", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Loard's brand distributed to Loard's Ice Cream parlors located in Northern California. Private labels distributed to grocery stores located in Northern California.", "states": ["CA"], "nationwide": false, "quantity": "252 units (32 oz/unit)", "codes": "None", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0748-2026%22", "url": "https://recallledger.net/recalls/food-h-0748-2026-loard-s-rainbow-sherbert-32-oz/"}, {"id": "fda-food-h-0747-2026", "source": "FDA", "category": "food", "recall_number": "H-0747-2026", "title": "Loard's Pumpkin Ice Cream - 32 oz recall (Silver Moon LP dba Loard's Ice Cream)", "product": "Loard's Pumpkin Ice Cream - 32 oz", "reason": "Undeclared Milk, Yellow #6.", "hazard_level": "Class II", "company": "Silver Moon LP dba Loard's Ice Cream", "company_location": "San Leandro, CA, United States", "date": "2026-04-15", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Loard's brand distributed to Loard's Ice Cream parlors located in Northern California. Private labels distributed to grocery stores located in Northern California.", "states": ["CA"], "nationwide": false, "quantity": "294 units (32 oz/unit)", "codes": "None", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0747-2026%22", "url": "https://recallledger.net/recalls/food-h-0747-2026-loard-s-pumpkin-ice-cream-32-oz/"}, {"id": "fda-food-h-0746-2026", "source": "FDA", "category": "food", "recall_number": "H-0746-2026", "title": "Loard's Pistachio Ice Cream - 32 oz recall (Silver Moon LP dba Loard's Ice Cream)", "product": "Loard's Pistachio Ice Cream - 32 oz", "reason": "Undeclared Milk, Pistachios, Yellow #5, Blue #1.", "hazard_level": "Class II", "company": "Silver Moon LP dba Loard's Ice Cream", "company_location": "San Leandro, CA, United States", "date": "2026-04-15", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Loard's brand distributed to Loard's Ice Cream parlors located in Northern California. 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Private labels distributed to grocery stores located in Northern California.", "states": ["CA"], "nationwide": false, "quantity": "188 units (32 oz/unit)", "codes": "None", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0724-2026%22", "url": "https://recallledger.net/recalls/food-h-0724-2026-loard-s-champagne-sherbert-32-oz/"}, {"id": "fda-food-h-0723-2026", "source": "FDA", "category": "food", "recall_number": "H-0723-2026", "title": "Loard's Caramel Cashew Ice Cream - 32 oz recall (Silver Moon LP dba Loard's Ice Cream)", "product": "Loard's Caramel Cashew Ice Cream - 32 oz", "reason": "Undeclared Milk, Cashews, Soy, Sulfites.", "hazard_level": "Class II", "company": "Silver Moon LP dba Loard's Ice Cream", "company_location": "San Leandro, CA, United States", "date": "2026-04-15", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Loard's brand distributed to Loard's Ice Cream parlors located in Northern California. Private labels distributed to grocery stores located in Northern California.", "states": ["CA"], "nationwide": false, "quantity": "332 units (32 oz/unit)", "codes": "None", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0723-2026%22", "url": "https://recallledger.net/recalls/food-h-0723-2026-loard-s-caramel-cashew-ice-cream-32-oz/"}, {"id": "fda-food-h-0722-2026", "source": "FDA", "category": "food", "recall_number": "H-0722-2026", "title": "Loard's Butterscotch Marble Ice Cream - 32 oz recall (Silver Moon LP dba Loard's Ice Cream)", "product": "Loard's Butterscotch Marble Ice Cream - 32 oz", "reason": "Undeclared Milk.", "hazard_level": "Class II", "company": "Silver Moon LP dba Loard's Ice Cream", "company_location": "San Leandro, CA, United States", "date": "2026-04-15", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Loard's brand distributed to Loard's Ice Cream parlors located in Northern California. Private labels distributed to grocery stores located in Northern California.", "states": ["CA"], "nationwide": false, "quantity": "422 units (32 oz/unit)", "codes": "None", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0722-2026%22", "url": "https://recallledger.net/recalls/food-h-0722-2026-loard-s-butterscotch-marble-ice-cream-32-oz/"}, {"id": "fda-food-h-0721-2026", "source": "FDA", "category": "food", "recall_number": "H-0721-2026", "title": "Loard's Butter Brickle Ice Cream - 32 oz recall (Silver Moon LP dba Loard's Ice Cream)", "product": "Loard's Butter Brickle Ice Cream - 32 oz", "reason": "Undeclared Milk, Almonds, Soy.", "hazard_level": "Class II", "company": "Silver Moon LP dba Loard's Ice Cream", "company_location": "San Leandro, CA, United States", "date": "2026-04-15", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Loard's brand distributed to Loard's Ice Cream parlors located in Northern California. Private labels distributed to grocery stores located in Northern California.", "states": ["CA"], "nationwide": false, "quantity": "556 units (32 oz/unit)", "codes": "None", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0721-2026%22", "url": "https://recallledger.net/recalls/food-h-0721-2026-loard-s-butter-brickle-ice-cream-32-oz/"}, {"id": "fda-food-h-0720-2026", "source": "FDA", "category": "food", "recall_number": "H-0720-2026", "title": "Loard's Burgundy Cherry Ice Cream - 32 oz recall (Silver Moon LP dba Loard's Ice Cream)", "product": "Loard's Burgundy Cherry Ice Cream - 32 oz", "reason": "Undeclared Milk, Red #40, Blue #1, Blue #2.", "hazard_level": "Class II", "company": "Silver Moon LP dba Loard's Ice Cream", "company_location": "San Leandro, CA, United States", "date": "2026-04-15", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Loard's brand distributed to Loard's Ice Cream parlors located in Northern California. Private labels distributed to grocery stores located in Northern California.", "states": ["CA"], "nationwide": false, "quantity": "618 units (32 oz/unit)", "codes": "None", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0720-2026%22", "url": "https://recallledger.net/recalls/food-h-0720-2026-loard-s-burgundy-cherry-ice-cream-32-oz/"}, {"id": "fda-food-h-0719-2026", "source": "FDA", "category": "food", "recall_number": "H-0719-2026", "title": "Loard's Brownie Nut Fudge Ice Cream - 32 oz recall (Silver Moon LP dba Loard's Ice Cream)", "product": "Loard's Brownie Nut Fudge Ice Cream - 32 oz", "reason": "Undeclared Milk, Walnuts, Eggs, Wheat, Soy.", "hazard_level": "Class II", "company": "Silver Moon LP dba Loard's Ice Cream", "company_location": "San Leandro, CA, United States", "date": "2026-04-15", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Loard's brand distributed to Loard's Ice Cream parlors located in Northern California. Private labels distributed to grocery stores located in Northern California.", "states": ["CA"], "nationwide": false, "quantity": "78 units (32 oz/unit)", "codes": "None", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0719-2026%22", "url": "https://recallledger.net/recalls/food-h-0719-2026-loard-s-brownie-nut-fudge-ice-cream-32-oz/"}, {"id": "fda-food-h-0718-2026", "source": "FDA", "category": "food", "recall_number": "H-0718-2026", "title": "Loard's Blueberry Cheesecake Ice Cream - 32 oz recall (Silver Moon LP dba Loard's Ice Cream)", "product": "Loard's Blueberry Cheesecake Ice Cream - 32 oz", "reason": "Undeclared Milk, Red #40, Blue #1.", "hazard_level": "Class II", "company": "Silver Moon LP dba Loard's Ice Cream", "company_location": "San Leandro, CA, United States", "date": "2026-04-15", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Loard's brand distributed to Loard's Ice Cream parlors located in Northern California. Private labels distributed to grocery stores located in Northern California.", "states": ["CA"], "nationwide": false, "quantity": "200 units (32 oz/unit)", "codes": "None", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0718-2026%22", "url": "https://recallledger.net/recalls/food-h-0718-2026-loard-s-blueberry-cheesecake-ice-cream-32-oz/"}, {"id": "fda-food-h-0717-2026", "source": "FDA", "category": "food", "recall_number": "H-0717-2026", "title": "Loard's Black Walnut Ice Cream - 32 oz recall (Silver Moon LP dba Loard's Ice Cream)", "product": "Loard's Black Walnut Ice Cream - 32 oz; 56 oz", "reason": "Undeclared Milk, Walnuts.", "hazard_level": "Class II", "company": "Silver Moon LP dba Loard's Ice Cream", "company_location": "San Leandro, CA, United States", "date": "2026-04-15", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Loard's brand distributed to Loard's Ice Cream parlors located in Northern California. Private labels distributed to grocery stores located in Northern California.", "states": ["CA"], "nationwide": false, "quantity": "302 units (32 oz/unit); 70 units (56 oz/unit)", "codes": "None", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0717-2026%22", "url": "https://recallledger.net/recalls/food-h-0717-2026-loard-s-black-walnut-ice-cream-32-oz-56-oz/"}, {"id": "fda-food-h-0716-2026", "source": "FDA", "category": "food", "recall_number": "H-0716-2026", "title": "Loard's Black Raspberry Ice Cream - 32 oz recall (Silver Moon LP dba Loard's Ice Cream)", "product": "Loard's Black Raspberry Ice Cream - 32 oz", "reason": "Undeclared Milk, Red #40, Blue #1.", "hazard_level": "Class II", "company": "Silver Moon LP dba Loard's Ice Cream", "company_location": "San Leandro, CA, United States", "date": "2026-04-15", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Loard's brand distributed to Loard's Ice Cream parlors located in Northern California. Private labels distributed to grocery stores located in Northern California.", "states": ["CA"], "nationwide": false, "quantity": "446 units (32 oz/unit)", "codes": "None", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0716-2026%22", "url": "https://recallledger.net/recalls/food-h-0716-2026-loard-s-black-raspberry-ice-cream-32-oz/"}, {"id": "fda-food-h-0715-2026", "source": "FDA", "category": "food", "recall_number": "H-0715-2026", "title": "Loard's Black Raspberry Marble Ice Cream - 32 oz recall (Silver Moon LP dba Loard's Ice Cream)", "product": "Loard's Black Raspberry Marble Ice Cream - 32 oz", "reason": "Undeclared Milk, Red #40, Blue #1.", "hazard_level": "Class II", "company": "Silver Moon LP dba Loard's Ice Cream", "company_location": "San Leandro, CA, United States", "date": "2026-04-15", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Loard's brand distributed to Loard's Ice Cream parlors located in Northern California. Private labels distributed to grocery stores located in Northern California.", "states": ["CA"], "nationwide": false, "quantity": "362 units (32 oz/unit)", "codes": "None", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0715-2026%22", "url": "https://recallledger.net/recalls/food-h-0715-2026-loard-s-black-raspberry-marble-ice-cream-32-oz/"}, {"id": "fda-food-h-0714-2026", "source": "FDA", "category": "food", "recall_number": "H-0714-2026", "title": "Loard's Banana Ice Cream - 32 oz recall (Silver Moon LP dba Loard's Ice Cream)", "product": "Loard's Banana Ice Cream - 32 oz; 56 oz", "reason": "Undeclared Milk, Yellow #5.", "hazard_level": "Class II", "company": "Silver Moon LP dba Loard's Ice Cream", "company_location": "San Leandro, CA, United States", "date": "2026-04-15", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Loard's brand distributed to Loard's Ice Cream parlors located in Northern California. Private labels distributed to grocery stores located in Northern California.", "states": ["CA"], "nationwide": false, "quantity": "510 units (32 oz/unit); 164 units (56 oz/unit)", "codes": "None", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0714-2026%22", "url": "https://recallledger.net/recalls/food-h-0714-2026-loard-s-banana-ice-cream-32-oz-56-oz/"}, {"id": "fda-food-h-0713-2026", "source": "FDA", "category": "food", "recall_number": "H-0713-2026", "title": "Loard's Almond Joy Ice Cream - 32 oz recall (Silver Moon LP dba Loard's Ice Cream)", "product": "Loard's Almond Joy Ice Cream - 32 oz", "reason": "Undeclared Milk, Almonds, Soy, Sulfites.", "hazard_level": "Class II", "company": "Silver Moon LP dba Loard's Ice Cream", "company_location": "San Leandro, CA, United States", "date": "2026-04-15", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Loard's brand distributed to Loard's Ice Cream parlors located in Northern California. Private labels distributed to grocery stores located in Northern California.", "states": ["CA"], "nationwide": false, "quantity": "100 units (32 oz/unit)", "codes": "None", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0713-2026%22", "url": "https://recallledger.net/recalls/food-h-0713-2026-loard-s-almond-joy-ice-cream-32-oz/"}, {"id": "fda-food-h-0712-2026", "source": "FDA", "category": "food", "recall_number": "H-0712-2026", "title": "french broad CHOCOLATE bette's bake sale recall (French Broad Chocolate Factory)", "product": "french broad CHOCOLATE bette's bake sale (a multi-flavor bonbon assortment). 6-piece NET WT. 2.5 OZ (70.75G); 12-piece NET WT. 5 OZ (141.75G); and 24-piece NET WT. 10 OZ (283.5G), French Broad Chocolate Crafted in Asheville, NC 28801, USA", "reason": "Undeclared nut allergen (walnut) due to mislabeling. The product's printed tasting guide incorrectly identifies the Walnut Fudge and Peach Cobbler flavor chocolates (bonbons). Consumers relying on the printed materials could mistakenly consume a nut-containing bonbon.", "hazard_level": "Class I", "company": "French Broad Chocolate Factory", "company_location": "Asheville, NC, United States", "date": "2026-04-23", "report_date": "2026-05-13", "status": "Terminated", "distribution": "Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DC, FL, GA, IA, IL, IN, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, VT, WA, WI & WV.", "states": ["AL", "AR", "AZ", "CA", "CO", "CT", "DC", "FL", "GA", "IA", "IL", "IN", "KY", "LA", "MA", "MD", "MI", "MN", "MO", "MS", "MT", "NC", "NE", "NH", "NJ", "NM", "NY", "OH", "OK", "OR", "PA", "SC", "SD", "TN", "TX", "UT", "VA", "VT", "WA", "WI", "WV"], "nationwide": false, "quantity": "34/2.5oz boxes, 400/5oz boxes, 53/10oz boxes", "codes": "6-piece: Batch 260414 Best By Jun. 29 2026 & Batch 260417 Best By Jun. 30 2026 12-piece: Batch 260414 Best By Jun. 22 2026 & Batch 260417 Best By Jun. 30 2026 24-piece: Batch 260414 Best By Jun. 29 2026 & Batch 260417 Best By Jun. 30 2026", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0712-2026%22", "url": "https://recallledger.net/recalls/food-h-0712-2026-french-broad-chocolate-bette-s-bake-sale-a-multi-flavor-bonbon-assort/"}, {"id": "fda-food-h-0710-2026", "source": "FDA", "category": "food", "recall_number": "H-0710-2026", "title": "Hatch Green Chile Creamed Honey 671333101339 * These product labels may also say ... recall (Walker Honey Co)", "product": "Hatch Green Chile Creamed Honey 671333101339 * These product labels may also say Whipped Honey instead of Creamed Honey as labels and size were changed in this timeline from 14 oz Creamed Honey to 11 oz Whipped Honey. The UPC codes remained the same. Packaged in Glass jars UPC Code: 671333101339", "reason": "Creamed honey products may contain stainless steel dust/flakes and/or small particles or shreds of plastic.", "hazard_level": "Class II", "company": "Walker Honey Co", "company_location": "Rogers, TX, United States", "date": "2026-04-03", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Texas", "states": ["TX"], "nationwide": false, "quantity": "2,650 units (Total)", "codes": "packed after 12/1/2025", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0710-2026%22", "url": "https://recallledger.net/recalls/food-h-0710-2026-hatch-green-chile-creamed-honey-671333101339-these-product-labels-ma/"}, {"id": "fda-food-h-0709-2026", "source": "FDA", "category": "food", "recall_number": "H-0709-2026", "title": "Darkside of the Hive Creamed Honey/Salted Chocolate Creamed Honey 671333101414 *These... recall (Walker Honey Co)", "product": "Darkside of the Hive Creamed Honey/Salted Chocolate Creamed Honey 671333101414 *These product labels may also say Whipped Honey instead of Creamed Honey as labels and size were changed in this timeline from 14 oz Creamed Honey to 11 oz Whipped Honey. The UPC codes remained the same. Packaged in Glass jars UPC Code: 671333101414", "reason": "Creamed honey products may contain stainless steel dust/flakes and/or small particles or shreds of plastic.", "hazard_level": "Class II", "company": "Walker Honey Co", "company_location": "Rogers, TX, United States", "date": "2026-04-03", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Texas", "states": ["TX"], "nationwide": false, "quantity": "2,650 units (Total)", "codes": "packed after 12/1/2025", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0709-2026%22", "url": "https://recallledger.net/recalls/food-h-0709-2026-darkside-of-the-hive-creamed-honey-salted-chocolate-creamed-honey-6713/"}, {"id": "fda-food-h-0708-2026", "source": "FDA", "category": "food", "recall_number": "H-0708-2026", "title": "Natural Creamed Honey recall (Walker Honey Co)", "product": "Natural Creamed Honey, 671333101377 *These product labels may also say Whipped Honey instead of Creamed Honey as labels and size were changed in this timeline from 14 oz Creamed Honey to 11 oz Whipped Honey. The UPC codes remained the same. Packaged in Glass jars UPC Code: 671333101377", "reason": "Creamed honey products may contain stainless steel dust/flakes and/or small particles or shreds of plastic.", "hazard_level": "Class II", "company": "Walker Honey Co", "company_location": "Rogers, TX, United States", "date": "2026-04-03", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Texas", "states": ["TX"], "nationwide": false, "quantity": "2,650 units (Total)", "codes": "packed after 12/1/2025", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0708-2026%22", "url": "https://recallledger.net/recalls/food-h-0708-2026-natural-creamed-honey-671333101377-these-product-labels-may-also-say/"}, {"id": "fda-food-h-0707-2026", "source": "FDA", "category": "food", "recall_number": "H-0707-2026", "title": "Lemon Creamed Honey recall (Walker Honey Co)", "product": "Lemon Creamed Honey, 671333101353 *These product labels may also say Whipped Honey instead of Creamed Honey as labels and size were changed in this timeline from 14 oz Creamed Honey to 11 oz Whipped Honey. The UPC codes remained the same. Packaged in Glass jars UPC Code: 671333101353", "reason": "Creamed honey products may contain stainless steel dust/flakes and/or small particles or shreds of plastic.", "hazard_level": "Class II", "company": "Walker Honey Co", "company_location": "Rogers, TX, United States", "date": "2026-04-03", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Texas", "states": ["TX"], "nationwide": false, "quantity": "2,650 units (Total)", "codes": "packed after 12/1/2025", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0707-2026%22", "url": "https://recallledger.net/recalls/food-h-0707-2026-lemon-creamed-honey-671333101353-these-product-labels-may-also-say/"}, {"id": "fda-food-h-0706-2026", "source": "FDA", "category": "food", "recall_number": "H-0706-2026", "title": "Hatch Creamed Honey 671333101339 * These product labels may also say Whipped Honey ... recall (Walker Honey Co)", "product": "Hatch Creamed Honey 671333101339 * These product labels may also say Whipped Honey instead of Creamed Honey as labels and size were changed in this timeline from 14 oz Creamed Honey to 11 oz Whipped Honey. The UPC codes remained the same. Packaged in Glass jars UPC Code: 671333101339", "reason": "Creamed honey products may contain stainless steel dust/flakes and/or small particles or shreds of plastic.", "hazard_level": "Class II", "company": "Walker Honey Co", "company_location": "Rogers, TX, United States", "date": "2026-04-03", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Texas", "states": ["TX"], "nationwide": false, "quantity": "2,650 units (Total)", "codes": "packed after 12/1/2025", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0706-2026%22", "url": "https://recallledger.net/recalls/food-h-0706-2026-hatch-creamed-honey-671333101339-these-product-labels-may-also-say/"}, {"id": "fda-food-h-0705-2026", "source": "FDA", "category": "food", "recall_number": "H-0705-2026", "title": "Dark Pecan Creamed Honey/Pecan Creamed Honey 671333101407 * These product labels may... recall (Walker Honey Co)", "product": "Dark Pecan Creamed Honey/Pecan Creamed Honey 671333101407 * These product labels may also say Whipped Honey instead of Creamed Honey as labels and size were changed in this timeline from 14 oz Creamed Honey to 11 oz Whipped Honey. The UPC codes remained the same. Packaged in Glass jars UPC Code: 671333101407", "reason": "Creamed honey products may contain stainless steel dust/flakes and/or small particles or shreds of plastic.", "hazard_level": "Class II", "company": "Walker Honey Co", "company_location": "Rogers, TX, United States", "date": "2026-04-03", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Texas", "states": ["TX"], "nationwide": false, "quantity": "2,650 units (Total)", "codes": "packed after 12/1/2025", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0705-2026%22", "url": "https://recallledger.net/recalls/food-h-0705-2026-dark-pecan-creamed-honey-pecan-creamed-honey-671333101407-these-prod/"}, {"id": "fda-food-h-0704-2026", "source": "FDA", "category": "food", "recall_number": "H-0704-2026", "title": "Cinnamon Creamed Honey 671333101360 * These product labels may also say Whipped Honey... recall (Walker Honey Co)", "product": "Cinnamon Creamed Honey 671333101360 * These product labels may also say Whipped Honey instead of Creamed Honey as labels and size were changed in this timeline from 14 oz Creamed Honey to 11 oz Whipped Honey. The UPC codes remained the same. Packaged in Glass jars UPC: 671333101360", "reason": "Creamed honey products may contain stainless steel dust/flakes and/or small particles or shreds of plastic.", "hazard_level": "Class II", "company": "Walker Honey Co", "company_location": "Rogers, TX, United States", "date": "2026-04-03", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Texas", "states": ["TX"], "nationwide": false, "quantity": "2,650 units (Total)", "codes": "packed after 12/1/2025", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0704-2026%22", "url": "https://recallledger.net/recalls/food-h-0704-2026-cinnamon-creamed-honey-671333101360-these-product-labels-may-also-sa/"}, {"id": "fda-food-h-0703-2026", "source": "FDA", "category": "food", "recall_number": "H-0703-2026", "title": "Blackberry Creamed Honey 671333101308 * These product labels may also say Whipped... recall (Walker Honey Co)", "product": "Blackberry Creamed Honey 671333101308 * These product labels may also say Whipped Honey instead of Creamed Honey as labels and size were changed in this timeline from 14 oz Creamed Honey to 11 oz Whipped Honey.The UPC codes remained the same. Packaged in Glass jars UPC Code: 671333101308", "reason": "Creamed honey products may contain stainless steel dust/flakes and/or small particles or shreds of plastic.", "hazard_level": "Class II", "company": "Walker Honey Co", "company_location": "Rogers, TX, United States", "date": "2026-04-03", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Texas", "states": ["TX"], "nationwide": false, "quantity": "2,650 units (Total)", "codes": "packed after 12/1/2025", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0703-2026%22", "url": "https://recallledger.net/recalls/food-h-0703-2026-blackberry-creamed-honey-671333101308-these-product-labels-may-also/"}, {"id": "fda-food-h-0702-2026", "source": "FDA", "category": "food", "recall_number": "H-0702-2026", "title": "Raspberry Creamed Honey 671333101322 ¿\tThese product labels may also say Whipped... recall (Walker Honey Co)", "product": "Raspberry Creamed Honey 671333101322 ¿\tThese product labels may also say Whipped Honey instead of Creamed Honey as labels and size were changed in this timeline from 14 oz Creamed Honey to 11 oz Whipped Honey, UPC Code: 671333101322", "reason": "Creamed honey products may contain stainless steel dust/flakes and/or small particles or shreds of plastic.", "hazard_level": "Class II", "company": "Walker Honey Co", "company_location": "Rogers, TX, United States", "date": "2026-04-03", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Texas", "states": ["TX"], "nationwide": false, "quantity": "2,650 units (Total)", "codes": "packed after 12/1/2025", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0702-2026%22", "url": "https://recallledger.net/recalls/food-h-0702-2026-raspberry-creamed-honey-671333101322-these-product-labels-may-also-s/"}, {"id": "fda-food-h-0701-2026", "source": "FDA", "category": "food", "recall_number": "H-0701-2026", "title": "Fain s Blackberry Honey Spread recall (Walker Honey Co)", "product": "Fain s Blackberry Honey Spread, 12oz net wt., UPC 01832213862", "reason": "Creamed honey products may contain stainless steel dust/flakes and/or small particles or shreds of plastic.", "hazard_level": "Class II", "company": "Walker Honey Co", "company_location": "Rogers, TX, United States", "date": "2026-04-03", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Texas", "states": ["TX"], "nationwide": false, "quantity": "2,650 units (Total)", "codes": "Packed after 12/1/2025", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0701-2026%22", "url": "https://recallledger.net/recalls/food-h-0701-2026-fain-s-blackberry-honey-spread-12oz-net-wt-upc-01832213862/"}, {"id": "fda-food-h-0700-2026", "source": "FDA", "category": "food", "recall_number": "H-0700-2026", "title": "Buttermilk Powder - paper bags 25 kg. recall (California Dairies Inc.)", "product": "Buttermilk Powder - paper bags 25 kg. (packed under 1 label: BMP Extra Grade Standard)", "reason": "Potential contamination with Salmonella.", "hazard_level": "Class I", "company": "California Dairies Inc.", "company_location": "Visalia, CA, United States", "date": "2026-04-20", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "U.S. Distribution: Unknown and to be determined during RAC assignment. Domestic consignees pick-up product from CDI. Foreign Distribution: Mexico, Philippines, Dominican Republic.", "states": [], "nationwide": false, "quantity": "19,841 lbs.", "codes": "Batch Codes for recalled product all start with A or B full list below. Batch Codes and Production Date: A22525-08-A 8/13/2025; A22525-08-B 8/13/2025; A22525-08-C 8/13/2025; A22525-08-D 8/13/2025; A22525-08-E 8/13/2025; A22525-08-F 8/13/2025; A22525-08-G 8/13/2025; A22525-08-H 8/13/2025.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0700-2026%22", "url": "https://recallledger.net/recalls/food-h-0700-2026-buttermilk-powder-paper-bags-25-kg-packed-under-1-label-bmp-extr/"}, {"id": "fda-food-h-0699-2026", "source": "FDA", "category": "food", "recall_number": "H-0699-2026", "title": "Low Heat Non-Fat Dried Milk Powder - paper bags 25 kg. recall (California Dairies Inc.)", "product": "Low Heat Non-Fat Dried Milk Powder - paper bags 25 kg. (packed under 5 labels: Off Grade NFDM Variable; Extra Grade NFDM Standard rBST Free; Grade A NFDM LH Basic; Grade A NFDM LH Standard rBST Free; Grade A NFDM LH Tier 1 rBST Free)", "reason": "Potential contamination with Salmonella.", "hazard_level": "Class I", "company": "California Dairies Inc.", "company_location": "Visalia, CA, United States", "date": "2026-04-20", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "U.S. Distribution: Unknown and to be determined during RAC assignment. Domestic consignees pick-up product from CDI. Foreign Distribution: Mexico, Philippines, Dominican Republic.", "states": [], "nationwide": false, "quantity": "1,568,793 lbs.", "codes": "Batch Codes for recalled product all start with A or B full list below. Batch Codes and Production Date: B22725-01-A 8/15/2025; B22725-01-B 8/15/2025; B22725-01-C 8/15/2025; B22725-01-D 8/15/2025; B22725-01-E 8/15/2025; B22725-01-F 8/15/2025; B22725-01-G 8/15/2025; B22725-01-H 8/15/2025; B22825-01-A 8/16/2025; B22825-01-B 8/16/2025; B22825-02-A 8/16/2025; B22825-02-B 8/16/2025; B22825-02-C 8/16/2025; B22825-02-D 8/16/2025; B22825-02-E 8/16/2025; B22825-02-F 8/16/2025; B22825-02-G 8/16/2025; B22825-02-H 8/16/2025; B22825-03-A 8/16/2025; B22825-03-B 8/16/2025; B22825-03-C 8/16/2025; B22825-03-D 8/16/2025; B22825-03-E 8/16/2025; B22825-03-F 8/16/2025; B22825-03-G 8/16/2025; B22825-03-H 8/16/2025; B22825-04-A 8/16/2025; B22825-04-B 8/16/2025; B22825-04-C 8/16/2025; B22825-04-D 8/16/2025; B22825-04-E 8/16/2025; B22825-04-F 8/16/2025; B22825-04-G 8/16/2025; B22825-04-H 8/16/2025; B22825-05-A 8/16/2025; B22825-05-B 8/16/2025; B22825-05-C 8/16/2025; B22825-05-D 8/16/2025; B22825-05-E 8/16/2025; B22825-05-F 8/16/2025; B22825-05-G 8/16/2025; B22825-05-H 8/16/2025; B22925-05-A 8/17/2025; B22925-05-B 8/17/2025; B22925-05-C 8/17/2025; B22925-05-D 8/17/2025; B22925-05-E 8/17/2025; B22925-05-F 8/17/2025; B22925-05-G 8/17/2025; B22925-05-H 8/17/2025; B22925-06-A 8/17/2025; B22925-06-B 8/17/2025; B22925-06-C 8/17/2025; B22925-06-D 8/17/2025; B22925-06-E 8/17/2025; B22925-06-F 8/17/2025; B22925-06-G 8/17/2025; B22925-06-H 8/17/2025; B23025-01-A 8/18/2025; B23025-01-B 8/18/2025; B23025-01-C 8/18/2025; B23025-01-D 8/18/2025; B23025-01-E 8/18/2025; B23025-01-F 8/18/2025; B23025-01-G 8/18/2025; B23025-01-H 8/18/2025; B23025-02-A 8/18/2025; B23025-02-B 8/18/2025; B23025-02-C 8/18/2025; B23025-02-D 8/18/2025; B23025-02-E 8/18/2025; B23025-02-F 8/18/2025; B23025-02-G 8/18/2025; B23025-02-H 8/18/2025; B23025-03-A 8/18/2025; B23025-03-B 8/18/2025; B23025-03-C 8/18/2025; B23025-03-D 8/18/2025; B23025-03-E 8/18/2025; B23025-03-F 8/18/2025; B23025-03-G 8/18/2025; B23025-03-H 8/18/2025; B23025-04-A 8/18/2025; B23025-04-B 8/18/2025; B23025-04-C 8/18/2025; B23025-04-D 8/18/2025; B23025-04-E 8/18/2025; B23025-04-F 8/18/2025; B23025-04-G 8/18/2025; B23025-04-H 8/18/2025; B23125-10-A 8/19/2025; B23125-10-B 8/19/2025; B23125-10-C 8/19/2025; B23125-10-D 8/19/2025; B23125-10-E 8/19/2025; B23125-10-F 8/19/2025; B23125-10-G 8/19/2025; B23125-10-H 8/19/2025; B23425-02-A 8/22/2025; B23425-02-B 8/22/2025; B23425-02-C 8/22/2025; B23425-02-D 8/22/2025; B23425-02-E 8/22/2025; B23425-02-F 8/22/2025; B23425-02-G 8/22/2025; B23425-02-H 8/22/2025; B23425-03-A 8/22/2025; B23425-03-B 8/22/2025; B23425-03-C 8/22/2025; B23425-03-D 8/22/2025; B23425-03-E 8/22/2025; B23425-03-F 8/22/2025; B23425-03-G 8/22/2025; B23425-03-H 8/22/2025; B23625-01-A 8/24/2025; B23625-01-B 8/24/2025; B23625-01-C 8/24/2025; B23625-01-D 8/24/2025; B23625-01-E 8/24/2025; B23625-01-F 8/24/2025; B23625-01-G 8/24/2025; B23625-01-H 8/24/2025; B23625-02-A 8/24/2025; B23625-02-B 8/24/2025; B23625-02-C 8/24/2025; B23625-02-D 8/24/2025; B23625-02-E 8/24/2025; B23625-02-F 8/24/2025; B23625-02-G 8/24/2025; B23625-02-H 8/24/2025; B23925-05-A 8/27/2025; B23925-05-B 8/27/2025; B23925-05-C 8/27/2025; B23925-05-D 8/27/2025; B23925-05-E 8/27/2025; B23925-05-F 8/27/2025; B23925-05-G 8/27/2025; B23925-05-H 8/27/2025; B23925-06-A 8/27/2025; B23925-06-B 8/27/2025; B23925-06-C 8/27/2025; B23925-06-D 8/27/2025; B23925-06-E 8/27/2025; B23925-06-F 8/27/2025; B23925-06-G 8/27/2025; B23925-06-H 8/27/2025; B24025-06-A 8/28/2025; B24025-06-B 8/28/2025; B24025-06-C 8/28/2025; B24025-06-D 8/28/2025; B24025-06-E 8/28/2025; B24025-06-F 8/28/2025; B24025-06-G 8/28/2025; B24025-06-H 8/28/2025; B24025-07-A 8/28/2025; B24025-07-B 8/28/2025; B24025-07-C 8/28/2025; B24025-07-D 8/28/2025; B24025-07-E 8/28/2025; B24025-07-F 8/28/2025; B24025-07-G 8/28/2025; B24025-07-H 8/28/2025; B24125-01-A 8/29/2025; B24125-01-B 8/29/2025; B24125-01-C 8/29/2025; B24125-01-D 8/29/2025; B24125-01-E 8/29/2025; B24125-01-F 8/29/2025; B24125-01-G 8/29/2025; B24125-01-H 8/29/2025; B24125-02-A 8/29/2025; B24125-02-B 8/29/2025; B24125-02-C 8/29/2025; B24125-02-D 8/29/2025; B24125-02-E 8/29/2025; B24125-02-F 8/29/2025; B24125-02-G 8/29/2025; B24125-02-H 8/29/2025; B24125-03-A 8/29/2025; B24125-03-B 8/29/2025; B24125-03-C 8/29/2025; B24125-03-D 8/29/2025; B24125-03-E 8/29/2025; B24125-03-F 8/29/2025; B24125-03-G 8/29/2025; B24125-03-H 8/29/2025; B24125-04-A 8/29/2025; B24125-04-B 8/29/2025; B24125-04-C 8/29/2025; B24125-04-D 8/29/2025; B24125-04-E 8/29/2025; B24125-04-F 8/29/2025; B24125-04-G 8/29/2025; B24125-04-H 8/29/2025; B24125-05-A 8/29/2025; B24125-05-B 8/29/2025; B24125-05-C 8/29/2025; B24125-05-D 8/29/2025; B24125-05-E 8/29/2025; B24125-05-F 8/29/2025; B24125-05-G 8/29/2025; B24125-05-H 8/29/2025; B24125-06-A 8/29/2025; B24125-06-B 8/29/2025; B24125-06-C 8/29/2025; B24125-06-D 8/29/2025; B24125-06-E 8/29/2025; B24125-06-F 8/29/2025; B24125-06-G 8/29/2025; B24125-06-H 8/29/2025; B24125-07-A 8/29/2025; B24125-07-B 8/29/2025; B24125-07-C 8/29/2025; B24125-07-D 8/29/2025; B24125-07-E 8/29/2025; B24125-07-F 8/29/2025; B24125-07-G 8/29/2025; B24125-07-H 8/29/2025; B24125-08-A 8/29/2025; B24125-08-B 8/29/2025; B24125-08-C 8/29/2025; B24125-08-D 8/29/2025; B24125-08-E 8/29/2025; B24125-08-F 8/29/2025; B24125-08-G 8/29/2025; B24125-08-H 8/29/2025; B24125-09-A 8/29/2025; B24125-09-B 8/29/2025; B24125-09-C 8/29/2025; B24125-09-D 8/29/2025; B24125-09-E 8/29/2025; B24125-09-F 8/29/2025; B24125-09-G 8/29/2025; B24125-09-H 8/29/2025; B24125-10-A 8/29/2025; B24125-10-B 8/29/2025; B24125-10-C 8/29/2025; B24125-10-D 8/29/2025; B24125-10-E 8/29/2025; B24125-10-F 8/29/2025; B24125-10-G 8/29/2025; B24125-10-H 8/29/2025; B32125-01-A 11/17/2025; B32125-01-B 11/17/2025; B32125-01-C 11/17/2025; B32125-01-D 11/17/2025; B32125-01-E 11/17/2025; B32125-01-F 11/17/2025; B32125-01-G 11/17/2025; B32125-01-H 11/17/2025; B32125-02-A 11/17/2025; B32125-02-B 11/17/2025; B32125-02-C 11/17/2025; B32125-02-D 11/17/2025; B32125-02-E 11/17/2025; B32125-02-F 11/17/2025; B32125-02-G 11/17/2025; B32125-02-H 11/17/2025; B32125-03-A 11/17/2025; B32125-03-B 11/17/2025; B32125-03-C 11/17/2025; B32125-03-D 11/17/2025; B32125-03-E 11/17/2025; B32125-03-F 11/17/2025; B32125-03-G 11/17/2025; B32125-03-H 11/17/2025; B32125-04-A 11/17/2025; B32125-04-B 11/17/2025; B32125-04-C 11/17/2025; B32125-04-D 11/17/2025; B32125-04-E 11/17/2025; B32125-04-F 11/17/2025; B32125-04-G 11/17/2025; B32125-04-H 11/17/2025; B32125-05-A 11/17/2025; B32125-05-B 11/17/2025; B32125-05-C 11/17/2025; B32125-05-D 11/17/2025; B32125-05-E 11/17/2025; B32125-05-F 11/17/2025; B32125-05-G 11/17/2025; B32125-05-H 11/17/2025; B32125-06-A 11/17/2025; B32125-06-B 11/17/2025; B32125-06-C 11/17/2025; B32125-06-D 11/17/2025; B32125-06-E 11/17/2025; B32125-06-F 11/17/2025; B32125-06-G 11/17/2025; B32125-06-H 11/17/2025; B32125-07-A 11/17/2025; B32125-07-B 11/17/2025; B32125-07-C 11/17/2025; B32125-07-D 11/17/2025; B32125-07-E 11/17/2025; B32125-07-F 11/17/2025; B32125-07-G 11/17/2025; B32125-07-H 11/17/2025; B32125-08-A 11/17/2025; B32125-08-B 11/17/2025; B32125-08-C 11/17/2025; B32125-08-D 11/17/2025; B32125-08-E 11/17/2025; B32125-08-F 11/17/2025; B32125-08-G 11/17/2025; B32125-08-H 11/17/2025; B32125-09-A 11/17/2025; B32125-09-B 11/17/2025; B32125-09-C 11/17/2025; B32125-09-D 11/17/2025; B32125-09-E 11/17/2025; B32125-09-F 11/17/2025; B32125-09-G 11/17/2025; B32125-09-H 11/17/2025; B32125-10-A 11/17/2025; B32125-10-B 11/17/2025; B32125-10-C 11/17/2025; B32125-10-D 11/17/2025; B32125-10-E 11/17/2025; B32125-10-F 11/17/2025; B32125-10-G 11/17/2025; B32125-10-H 11/17/2025; B32125-11-A 11/17/2025; B32125-11-B 11/17/2025; B32125-11-C 11/17/2025; B32125-11-D 11/17/2025; B32125-11-E 11/17/2025; B32125-11-F 11/17/2025; B32125-11-G 11/17/2025; B32125-11-H 11/17/2025; B32125-12-A 11/17/2025; B32125-12-B 11/17/2025; B32125-12-C 11/17/2025; B32125-12-D 11/17/2025; B32125-12-E 11/17/2025; B32125-12-F 11/17/2025; B32125-12-G 11/17/2025; B32125-12-H 11/17/2025; B32125-13-A 11/17/2025; B32125-13-B 11/17/2025; B32125-13-C 11/17/2025; B32125-13-D 11/17/2025; B32225-01-A 11/18/2025; B32225-01-B 11/18/2025; B32225-01-C 11/18/2025; B32225-01-D 11/18/2025; B32225-01-E 11/18/2025; B32225-01-F 11/18/2025; B32225-01-G 11/18/2025; B32225-01-H 11/18/2025; B32225-02-A 11/18/2025; B32225-02-B 11/18/2025; B32225-02-C 11/18/2025; B32225-02-D 11/18/2025; B32225-02-E 11/18/2025; B32225-02-F 11/18/2025; B32225-02-G 11/18/2025; B32225-02-H 11/18/2025; B32225-03-A 11/18/2025; B32225-03-B 11/18/2025; B32225-03-C 11/18/2025; B32225-03-D 11/18/2025; B32225-03-E 11/18/2025; B32225-03-F 11/18/2025; B32225-03-G 11/18/2025; B32225-03-H 11/18/2025; B32225-04-A 11/18/2025; B32225-04-B 11/18/2025; B32225-04-C 11/18/2025; B32225-04-D 11/18/2025; B32225-04-E 11/18/2025; B32225-04-F 11/18/2025; B32225-04-G 11/18/2025; B32225-04-H 11/18/2025; B32225-05-A 11/18/2025; B32225-05-B 11/18/2025; B32225-05-C 11/18/2025; B32225-05-D 11/18/2025; B32225-05-E 11/18/2025; B32225-05-F 11/18/2025; B32225-05-G 11/18/2025; B32225-05-H 11/18/2025; B32225-06-A 11/18/2025; B32225-06-B 11/18/2025; B32225-06-C 11/18/2025; B32225-06-D 11/18/2025; B32225-06-E 11/18/2025; B32225-06-F 11/18/2025; B32225-06-G 11/18/2025; B32225-06-H 11/18/2025; B32225-07-A 11/18/2025; B32225-07-B 11/18/2025; B32225-07-C 11/18/2025; B32225-07-D 11/18/2025; B32225-07-E 11/18/2025; B32225-07-F 11/18/2025; B32225-07-G 11/18/2025; B32225-07-H 11/18/2025; B32225-08-A 11/18/2025; B32225-08-B 11/18/2025; B32225-08-C 11/18/2025; B32225-08-D 11/18/2025; B32225-08-E 11/18/2025; B32225-08-F 11/18/2025; B32325-04-A 11/19/2025; B32325-04-B 11/19/2025; B32325-04-C 11/19/2025; B32325-04-D 11/19/2025; B32325-04-E 11/19/2025; B32325-04-F 11/19/2025; B32325-04-G 11/19/2025; B32325-04-H 11/19/2025; B32325-05-A 11/19/2025; B32325-05-B 11/19/2025; B32325-05-C 11/19/2025; B32325-05-D 11/19/2025; B32325-05-E 11/19/2025; B32325-05-F 11/19/2025; B32325-05-G 11/19/2025; B32325-05-H 11/19/2025; B32325-06-A 11/19/2025; B32325-06-B 11/19/2025; B32325-06-C 11/19/2025; B32325-06-D 11/19/2025; B32325-06-E 11/19/2025; B32325-06-F 11/19/2025; B32325-06-G 11/19/2025; B32325-06-H 11/19/2025; B32325-07-A 11/19/2025; B32325-07-B 11/19/2025; B32325-07-C 11/19/2025; B32325-07-D 11/19/2025; B32325-07-E 11/19/2025; B32325-07-F 11/19/2025; B32325-07-G 11/19/2025; B32325-07-H 11/19/2025; B32325-08-A 11/19/2025; B32325-08-B 11/19/2025; B32325-08-C 11/19/2025; B32325-08-D 11/19/2025; B32325-08-E 11/19/2025; B32325-08-F 11/19/2025; B32325-08-G 11/19/2025; B32325-08-H 11/19/2025; B32325-09-A 11/19/2025; B32325-09-B 11/19/2025; B32325-09-C 11/19/2025; B32325-09-D 11/19/2025; B32325-09-E 11/19/2025; B32325-09-F 11/19/2025; B32325-09-G 11/19/2025; B32325-09-H 11/19/2025; B32325-10-A 11/19/2025; B32325-10-B 11/19/2025; B32325-10-C 11/19/2025; B32325-10-D 11/19/2025; B32325-10-E 11/19/2025; B32325-10-F 11/19/2025; B32325-10-G 11/19/2025; B32325-10-H 11/19/2025; B32325-11-A 11/19/2025; B32325-11-B 11/19/2025; B32325-11-C 11/19/2025; B32325-11-D 11/19/2025; B32325-11-E 11/19/2025; B32325-11-F 11/19/2025; B32325-11-G 11/19/2025; B32325-11-H 11/19/2025; B32325-12-A 11/19/2025; B32325-12-B 11/19/2025; B32325-12-C 11/19/2025; B32325-12-D 11/19/2025; B32325-12-E 11/19/2025; B32325-12-F 11/19/2025; B32325-12-G 11/19/2025; B32325-12-H 11/19/2025; B32325-13-A 11/19/2025; B32325-13-B 11/19/2025; B32325-13-C 11/19/2025; B32325-13-D 11/19/2025; B32325-13-E 11/19/2025; B32325-13-F 11/19/2025; B32325-13-G 11/19/2025; B32325-13-H 11/19/2025; B32325-14-A 11/19/2025; B32325-14-B 11/19/2025; B32325-14-C 11/19/2025; B32325-14-D 11/19/2025; B32325-14-E 11/19/2025; B32325-14-F 11/19/2025; B32425-01-A 11/20/2025; B32425-01-B 11/20/2025; B32425-01-C 11/20/2025; B32425-01-D 11/20/2025; B32425-01-E 11/20/2025; B32425-01-F 11/20/2025; B32425-01-G 11/20/2025; B32425-01-H 11/20/2025; B32425-02-A 11/20/2025; B32425-02-B 11/20/2025; B32425-02-C 11/20/2025; B32425-02-D 11/20/2025; B32425-02-E 11/20/2025; B32425-02-F 11/20/2025; B32425-02-G 11/20/2025; B32425-02-H 11/20/2025; B32425-03-A 11/20/2025; B32425-03-B 11/20/2025; B32425-03-C 11/20/2025; B32425-03-D 11/20/2025; B32425-03-E 11/20/2025; B32425-03-F 11/20/2025; B32425-03-G 11/20/2025; B32425-03-H 11/20/2025; B32425-04-A 11/20/2025; B32425-04-B 11/20/2025; B32425-04-C 11/20/2025; B32425-04-D 11/20/2025; B32425-04-E 11/20/2025; B32425-04-F 11/20/2025; B32425-04-G 11/20/2025; B32425-04-H 11/20/2025; B32425-05-A 11/20/2025; B32425-05-B 11/20/2025; B32425-05-C 11/20/2025; B32425-05-D 11/20/2025; B32425-05-E 11/20/2025; B32425-05-F 11/20/2025; B32425-05-G 11/20/2025; B32425-05-H 11/20/2025; B32425-06-A 11/20/2025; B32425-06-B 11/20/2025; B32425-06-C 11/20/2025; B32425-06-D 11/20/2025; B32425-06-E 11/20/2025; B32425-06-F 11/20/2025; B32425-06-G 11/20/2025; B32425-06-H 11/20/2025; B32425-07-A 11/20/2025; B32425-07-B 11/20/2025; B32425-07-C 11/20/2025; B32425-07-D 11/20/2025; B32425-07-E 11/20/2025; B32425-07-F 11/20/2025; B32425-07-G 11/20/2025; B32425-07-H 11/20/2025; B32425-08-A 11/20/2025; B32425-08-B 11/20/2025; B32425-08-C 11/20/2025; B32425-08-D 11/20/2025; B32425-08-E 11/20/2025; B32425-08-F 11/20/2025; B32425-08-G 11/20/2025; B32425-08-H 11/20/2025; B32425-09-A 11/20/2025; B32425-09-B 11/20/2025; B32425-09-C 11/20/2025; B32425-09-D 11/20/2025; B32425-09-E 11/20/2025; B32425-09-F 11/20/2025; B32425-09-G 11/20/2025; B32425-09-H 11/20/2025; B32425-10-A 11/20/2025; B32425-10-B 11/20/2025; B32425-10-C 11/20/2025; B32425-10-D 11/20/2025; B32425-10-E 11/20/2025; B32425-10-F 11/20/2025; B32425-10-G 11/20/2025; B32425-10-H 11/20/2025; B32425-11-A 11/20/2025; B32425-11-B 11/20/2025; B32425-11-C 11/20/2025; B32425-11-D 11/20/2025; B32425-11-E 11/20/2025; B32425-11-F 11/20/2025; B32425-11-G 11/20/2025; B32425-11-H 11/20/2025; B32425-12-A 11/20/2025; B32425-12-B 11/20/2025; B32425-12-C 11/20/2025; B32425-12-D 11/20/2025; B32425-12-E 11/20/2025; B32425-12-F 11/20/2025; B32425-12-G 11/20/2025; B32425-12-H 11/20/2025; B32425-13-A 11/20/2025; B32425-13-B 11/20/2025; B32425-13-C 11/20/2025; B32425-13-D 11/20/2025; B32425-13-E 11/20/2025; B32425-13-F 11/20/2025; B32425-13-G 11/20/2025; B32425-13-H 11/20/2025; B32425-14-A 11/20/2025; B32425-14-B 11/20/2025; B32425-14-C 11/20/2025; B32625-10-A 11/22/2025; B32625-10-B 11/22/2025; B32625-10-C 11/22/2025; B32625-10-D 11/22/2025; B32625-10-E 11/22/2025; B32625-10-F 11/22/2025; B32625-10-G 11/22/2025; B32625-10-H 11/22/2025; B32625-11-A 11/22/2025; B32625-11-B 11/22/2025; B32625-11-C 11/22/2025; B32625-11-D 11/22/2025; B32625-11-E 11/22/2025; B32625-11-F 11/22/2025; B32625-11-G 11/22/2025; B32625-11-H 11/22/2025; B32625-12-A 11/22/2025; B32625-12-B 11/22/2025; B32625-12-C 11/22/2025; B32625-12-D 11/22/2025; B32625-12-E 11/22/2025; B32625-12-F 11/22/2025; B32625-12-G 11/22/2025; B32625-12-H 11/22/2025; B24925-01-A 9/6/2025; B24925-01-B 9/6/2025; B24925-01-C 9/6/2025; B24925-01-D 9/6/2025; B24925-01-E 9/6/2025; B24925-01-F 9/6/2025; B24925-01-G 9/6/2025; B22925-01-A 8/17/2025; B22925-01-B 8/17/2025; B22925-01-C 8/17/2025; B22925-01-D 8/17/2025; B22925-04-A 8/17/2025.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0699-2026%22", "url": "https://recallledger.net/recalls/food-h-0699-2026-low-heat-non-fat-dried-milk-powder-paper-bags-25-kg-packed-under/"}, {"id": "fda-food-h-0698-2026", "source": "FDA", "category": "food", "recall_number": "H-0698-2026", "title": "Low Heat Non-Fat Dried Milk Powder - plastic totes recall (California Dairies Inc.)", "product": "Low Heat Non-Fat Dried Milk Powder - plastic totes (NTE) 2200 lbs. (packed under 5 labels: Off Grade NFDM Variable; Grade A NFDM LH Basic; Grade A NFDM LH Green Loop rBST Free; Grade A NFDM LH Standard NC rBST Free; NFDM LH Variable Standard)", "reason": "Potential contamination with Salmonella.", "hazard_level": "Class I", "company": "California Dairies Inc.", "company_location": "Visalia, CA, United States", "date": "2026-04-20", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "U.S. Distribution: Unknown and to be determined during RAC assignment. Domestic consignees pick-up product from CDI. Foreign Distribution: Mexico, Philippines, Dominican Republic.", "states": [], "nationwide": false, "quantity": "1,110,564 lbs.", "codes": "Batch Codes for recalled product all start with A or B full list below. Batch Code and Production Date: B22625-01-1 8/14/2025; B22625-01-2 8/14/2025; B22625-01-3 8/14/2025; B22625-01-4 8/14/2025; B22625-01-5 8/14/2025; B22625-01-6 8/14/2025; B22625-01-7 8/14/2025; B22625-01-8 8/14/2025; B22625-02-1 8/14/2025; B22625-02-2 8/14/2025; B22625-02-3 8/14/2025; B22625-02-4 8/14/2025; B22625-02-5 8/14/2025; B22625-02-6 8/14/2025; B22625-02-7 8/14/2025; B22625-02-8 8/14/2025; B22625-03-1 8/14/2025; B22625-03-2 8/14/2025; B22625-03-3 8/14/2025; B22625-03-4 8/14/2025; B22625-03-5 8/14/2025; B22625-03-6 8/14/2025; B22625-03-7 8/14/2025; B22625-03-8 8/14/2025; B22625-04-1 8/14/2025; B22625-04-2 8/14/2025; B22625-04-3 8/14/2025; B22625-04-4 8/14/2025; B22625-04-5 8/14/2025; B22625-04-6 8/14/2025; B22625-04-7 8/14/2025; B22625-04-8 8/14/2025; B22625-05-1 8/14/2025; B22625-05-2 8/14/2025; B22625-05-3 8/14/2025; B22625-05-4 8/14/2025; B22625-05-5 8/14/2025; B22625-05-6 8/14/2025; B22625-05-7 8/14/2025; B22625-05-8 8/14/2025; B22625-06-1 8/14/2025; B22625-06-2 8/14/2025; B22625-06-3 8/14/2025; B22625-06-4 8/14/2025; B22625-06-5 8/14/2025; B22625-06-6 8/14/2025; B22625-06-7 8/14/2025; B22625-06-8 8/14/2025; B22625-07-1 8/14/2025; B22625-07-2 8/14/2025; B22625-07-3 8/14/2025; B22625-07-4 8/14/2025; B22625-07-5 8/14/2025; B22625-07-6 8/14/2025; B22625-07-7 8/14/2025; B22625-07-8 8/14/2025; B22625-08-1 8/14/2025; B22625-08-2 8/14/2025; B22625-08-3 8/14/2025; B22625-08-4 8/14/2025; B22625-08-5 8/14/2025; B22625-08-6 8/14/2025; B22625-08-7 8/14/2025; B22625-08-8 8/14/2025; B22625-09-1 8/14/2025; B22625-09-2 8/14/2025; B22625-09-3 8/14/2025; B22625-09-4 8/14/2025; B22625-09-5 8/14/2025; B22625-09-6 8/14/2025; B22625-09-7 8/14/2025; B22625-10-1 8/14/2025; B22625-10-2 8/14/2025; B22625-10-3 8/14/2025; B22625-10-4 8/14/2025; B22625-10-5 8/14/2025; B22625-10-6 8/14/2025; B22625-10-7 8/14/2025; B22625-10-8 8/14/2025; B22625-11-1 8/14/2025; B22625-11-2 8/14/2025; B22625-11-3 8/14/2025; B22625-11-4 8/14/2025; B22625-11-5 8/14/2025; B22625-11-6 8/14/2025; B22625-11-7 8/14/2025; B22625-11-8 8/14/2025; B22625-12-1 8/14/2025; B22625-12-2 8/14/2025; B22625-12-3 8/14/2025; B22625-12-4 8/14/2025; B22625-12-5 8/14/2025; B22625-12-6 8/14/2025; B22625-12-7 8/14/2025; B22625-12-8 8/14/2025; B22625-13-1 8/14/2025; B22625-13-2 8/14/2025; B22625-13-3 8/14/2025; B22625-13-4 8/14/2025; B22625-13-5 8/14/2025; B22625-13-6 8/14/2025; B22625-13-7 8/14/2025; B22625-13-8 8/14/2025; B22725-02-1 8/15/2025; B22725-02-2 8/15/2025; B22725-02-3 8/15/2025; B22725-02-4 8/15/2025; B22725-02-5 8/15/2025; B22725-02-6 8/15/2025; B22725-02-7 8/15/2025; B22725-02-8 8/15/2025; B22725-03-1 8/15/2025; B22725-03-2 8/15/2025; B22725-03-3 8/15/2025; B22725-03-4 8/15/2025; B22725-03-5 8/15/2025; B22725-03-6 8/15/2025; B22725-03-7 8/15/2025; B22725-03-8 8/15/2025; B22725-04-1 8/15/2025; B22725-04-2 8/15/2025; B22725-04-3 8/15/2025; B22725-04-4 8/15/2025; B22725-04-5 8/15/2025; B22725-04-6 8/15/2025; B22725-04-7 8/15/2025; B22725-04-8 8/15/2025; B22725-05-1 8/15/2025; B22725-05-2 8/15/2025; B22725-05-3 8/15/2025; B22725-05-4 8/15/2025; B22725-05-5 8/15/2025; B22725-05-6 8/15/2025; B22725-05-7 8/15/2025; B22725-05-8 8/15/2025; B22725-06-1 8/15/2025; B22725-06-2 8/15/2025; B22725-06-3 8/15/2025; B22725-06-4 8/15/2025; B22725-06-5 8/15/2025; B22725-06-6 8/15/2025; B22725-06-7 8/15/2025; B22725-06-8 8/15/2025; B22725-07-1 8/15/2025; B22725-07-2 8/15/2025; B22725-07-6 8/15/2025; B22725-07-7 8/15/2025; B22725-07-8 8/15/2025; B22725-08-1 8/15/2025; B22725-08-2 8/15/2025; B22725-08-3 8/15/2025; B22725-08-4 8/15/2025; B22725-08-5 8/15/2025; B22725-08-6 8/15/2025; B22725-08-7 8/15/2025; B22725-08-8 8/15/2025; B22725-09-1 8/15/2025; B22725-09-2 8/15/2025; B22725-09-3 8/15/2025; B22725-09-4 8/15/2025; B22725-09-5 8/15/2025; B22725-09-6 8/15/2025; B22725-09-7 8/15/2025; B22725-09-8 8/15/2025; B22825-01-1 8/16/2025; B22825-01-2 8/16/2025; B22825-01-3 8/16/2025; B22825-01-4 8/16/2025; B22825-01-5 8/16/2025; B22825-01-6 8/16/2025; B22825-01-7 8/16/2025; B22825-01-8 8/16/2025; B22825-02-1 8/16/2025; B22825-02-2 8/16/2025; B22825-02-3 8/16/2025; B22825-02-4 8/16/2025; B22825-02-5 8/16/2025; B22825-02-6 8/16/2025; B22825-02-7 8/16/2025; B22825-02-8 8/16/2025; B22825-03-1 8/16/2025; B22825-03-2 8/16/2025; B22825-03-3 8/16/2025; B22825-03-4 8/16/2025; B22825-03-5 8/16/2025; B22825-03-6 8/16/2025; B22825-03-7 8/16/2025; B22825-03-8 8/16/2025; B22825-04-1 8/16/2025; B22825-04-2 8/16/2025; B22825-04-3 8/16/2025; B22825-04-4 8/16/2025; B22825-04-5 8/16/2025; B22825-04-6 8/16/2025; B22825-04-7 8/16/2025; B22825-04-8 8/16/2025; B22825-05-1 8/16/2025; B22825-05-2 8/16/2025; B22825-05-3 8/16/2025; B22825-05-4 8/16/2025; B22825-05-5 8/16/2025; B22825-05-6 8/16/2025; B22825-05-7 8/16/2025; B22825-05-8 8/16/2025; B22825-06-1 8/16/2025; B22825-06-2 8/16/2025; B22825-06-3 8/16/2025; B22825-06-4 8/16/2025; B22825-06-5 8/16/2025; B22825-06-6 8/16/2025; B22825-06-7 8/16/2025; B22825-06-8 8/16/2025; B22825-07-1 8/16/2025; B22825-07-2 8/16/2025; B22825-07-3 8/16/2025; B22825-07-4 8/16/2025; B22825-07-5 8/16/2025; B22825-07-6 8/16/2025; B22825-07-7 8/16/2025; 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UPC:0-4256300780-5 Lot Code: 20425GOLY with Best by: 07/23/2027 Lot Code: 20525GOLY with Best by: 07/24/2027 Lot Code: 32025GOLY with Best by: 11/16/2027 Woodstock Organic Shelled Edamame 3 lbs. UPC: 0-4256301242-7 Lot Code: 20425GOLY with Best by: 07/23/2027", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0694-2026%22", "url": "https://recallledger.net/recalls/food-h-0694-2026-woodstock-organic-shelled-edamame-10-oz-and-48-oz/"}, {"id": "fda-drug-d-0540-2026", "source": "FDA", "category": "drug", "recall_number": "D-0540-2026", "title": "Lactated Ringer's Injection USP recall (B BRAUN MEDICAL INC)", "product": "Lactated Ringer's Injection USP, 1000 mL container, Rx only, B. Braun Medical, Inc., Bethlehem, PA 18018-3524 USA, NDC 0264-7750-07.", "reason": "Presence of Particulate Matter.", "hazard_level": "Class I", "company": "B BRAUN MEDICAL INC", "company_location": "Allentown, PA, United States", "date": "2026-04-28", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "U.S.A. Nationwide", "states": [], "nationwide": true, "quantity": "95,412 containers", "codes": "Lot #:J4P756, J4S843, Exp 5/31/2027", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0540-2026%22", "url": "https://recallledger.net/recalls/drug-d-0540-2026-lactated-ringer-s-injection-usp-1000-ml-container-rx-only-b-braun/"}, {"id": "fda-drug-d-0523-2026", "source": "FDA", "category": "drug", "recall_number": "D-0523-2026", "title": "NAPROXEN ORAL SUSPENSION recall (Acella Pharmaceuticals, LLC)", "product": "NAPROXEN ORAL SUSPENSION, USP, 125 mg/5mL, Rx only, 16fl oz (473 mL) bottles, Distributed by: Acella Pharmaceuticals, LLC, Alpharetta, GA 30005, Made in Canada NDC 42192-619-16", "reason": "Chemical contamination; presence of lead and lithium above specification", "hazard_level": "Class II", "company": "Acella Pharmaceuticals, LLC", "company_location": "Alpharetta, GA, United States", "date": "2026-04-20", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Nationwide", "states": [], "nationwide": true, "quantity": "6,336 bottles", "codes": "Lot: 23F02, Expires: 05/2026; 25A37, Expires: 01/2028.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0523-2026%22", "url": "https://recallledger.net/recalls/drug-d-0523-2026-naproxen-oral-suspension-usp-125-mg-5ml-rx-only-16fl-oz-473-ml-b/"}, {"id": "fda-drug-d-0522-2026", "source": "FDA", "category": "drug", "recall_number": "D-0522-2026", "title": "Duloxetine Delayed-Release Capsules USP recall (Breckenridge Pharmaceutical, Inc.)", "product": "Duloxetine Delayed-Release Capsules USP, 60mg, Rx Only, 90-count bottle, Mfr. by Towa Pharmaceutical Eurpoe S.L., Martorelles, (Barcelona), Spain, Dist. by. Breckenridge Pharmaceutical, Inc., Berkely Heights, NJ 07922, NDC 51991-748-90.", "reason": "CGMP Deviations; presence of N-nitroso-duloxetine impurity above the FDA recommended limit", "hazard_level": "Class II", "company": "Breckenridge Pharmaceutical, Inc.", "company_location": "Berkeley Heights, NJ, United States", "date": "2026-04-21", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Nationwide in the USA", "states": [], "nationwide": true, "quantity": "165,761 90-count bottles", "codes": "Lot: 241069C, Exp 05/31/2027", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0522-2026%22", "url": "https://recallledger.net/recalls/drug-d-0522-2026-duloxetine-delayed-release-capsules-usp-60mg-rx-only-90-count-bott/"}, {"id": "fda-drug-d-0520-2026", "source": "FDA", "category": "drug", "recall_number": "D-0520-2026", "title": "Enalapril Maleate Tablets recall (JB Chemicals and Pharmaceuticals Ltd)", "product": "Enalapril Maleate Tablets, USP, 20 mg, 1,000-count bottle, Rx only, Manufactured by: Unique Pharmaceutical Laboratories (A Div. of J.B. Chemicals & Pharmaceuticals Ltd.), Mumbai 400 030, India, Distributed by: Rising Pharma Holdings, Inc., East Brunswick, NJ 08816, NDC 64980-688-10.", "reason": "Failed Impurities/Degradation Specifications:Out of specification result occurred in Organic Impurities Test", "hazard_level": "Class II", "company": "JB Chemicals and Pharmaceuticals Ltd", "company_location": "Mumbai, India", "date": "2026-04-23", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Nationwide in the USA", "states": [], "nationwide": true, "quantity": "675 bottles", "codes": "Lot #: GEH25023, Expires: 6/30/2027", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0520-2026%22", "url": "https://recallledger.net/recalls/drug-d-0520-2026-enalapril-maleate-tablets-usp-20-mg-1-000-count-bottle-rx-only-ma/"}, {"id": "fda-drug-d-0519-2026", "source": "FDA", "category": "drug", "recall_number": "D-0519-2026", "title": "Octreotide Acetate for Injectable Suspension recall (Teva Pharmaceuticals USA, Inc)", "product": "Octreotide Acetate for Injectable Suspension, for gluteal intramuscular use, 30 mg, In Single-Dose kits containing: 8-mL vial of 30 mg strength, a pre-filled syringe containing 2 mL of diluent, one vial adapter, and one sterile 1¿ 19-gauge safety injection needle, Rx only, Manufactured in Greece BY: Pharmathen International S.A, Rodopi, 69300 Greece, Manufactured For: TEVA Pharmaceuticals, Parsippany, NJ 07054. NDC Kit Carton: 0480-9262-08; Vial Label: 0480-9260-01; Tray Label: 0480-9262-08; Diluent Label: 0480-9263-21.", "reason": "Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.", "hazard_level": "Class II", "company": "Teva Pharmaceuticals USA, Inc", "company_location": "Parsippany, NJ, United States", "date": "2026-04-24", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Nationwide in the USA", "states": [], "nationwide": true, "quantity": "2,200 kits", "codes": "Lot: 45011002, Exp. 03/31/2027", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0519-2026%22", "url": "https://recallledger.net/recalls/drug-d-0519-2026-octreotide-acetate-for-injectable-suspension-for-gluteal-intramuscula/"}, {"id": "fda-drug-d-0518-2026", "source": "FDA", "category": "drug", "recall_number": "D-0518-2026", "title": "BD PurPrep recall (CareFusion 213, LLC)", "product": "BD PurPrep, Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl alcohol 72.5% w/w Sterile Solution, 0.36 fl. oz. (10.5 mL) x 25 applicators per box. Carefusion 213, LLC, El Paso, TX 79912, subsidary of Becton Dickinson and Co. NDC 54365-014-41", "reason": "Lack of assurance of Sterility: potential product contamination", "hazard_level": "Class II", "company": "CareFusion 213, LLC", "company_location": "El Paso, TX, United States", "date": "2026-04-22", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Nationwide in the USA", "states": [], "nationwide": true, "quantity": "", "codes": "Lots# 4263873, Exp. Date 08-31-2026, 4320590, Exp. Date 09-30-2026, 4320591, Exp. Date 10-31-2026.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0518-2026%22", "url": "https://recallledger.net/recalls/drug-d-0518-2026-bd-purprep-povidone-iodine-8-3-w-w-0-83-available-iodine-with-iso/"}, {"id": "fda-drug-d-0517-2026", "source": "FDA", "category": "drug", "recall_number": "D-0517-2026", "title": "BD PurPrep recall (CareFusion 213, LLC)", "product": "BD PurPrep, Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl alcohol 72.5% w/w Sterile Solution, 25x26mL Applicators per carton. Carefusion 213 LLC, El Paso, TX 79912, NDC 54365-014-42.", "reason": "Lack of assurance of Sterility: potential product contamination", "hazard_level": "Class II", "company": "CareFusion 213, LLC", "company_location": "El Paso, TX, United States", "date": "2026-04-22", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Nationwide in the USA", "states": [], "nationwide": true, "quantity": "", "codes": "Lot# 4258309, 4260329, 4256875, Exp. Date, 08-31-2026; 4296453, 4317319, 4290654, Exp. Date 09-30-2026; 4322449, 4323861, 4318679, Exp Date 10-31- Exp.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0517-2026%22", "url": "https://recallledger.net/recalls/drug-d-0517-2026-bd-purprep-povidone-iodine-8-3-w-w-0-83-available-iodine-with-iso/"}, {"id": "fda-drug-d-0516-2026", "source": "FDA", "category": "drug", "recall_number": "D-0516-2026", "title": "Duloxetine Delayed-Release Capsules recall (Ajanta Pharma Ltd.)", "product": "Duloxetine Delayed-Release Capsules, 20 mg, Rx Only, 60 capsules, Marketed by: Ajanta Pharma USA Inc., Bridgewater, NJ 08807, Made in India, NDC 27241-097-06.", "reason": "CGMP Deviations: Presence of N-nitroso-Duloxetine impurity above FDA recommended limit of 0.83 ppm, identified at the 12-month and 18-month long-term stability intervals.", "hazard_level": "Class II", "company": "Ajanta Pharma Ltd.", "company_location": "Aurangabad, India", "date": "2026-04-29", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Nationwide within U.S", "states": [], "nationwide": true, "quantity": "117,168 packs", "codes": "Lot#: PA10734, Exp. Jun 2026.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0516-2026%22", "url": "https://recallledger.net/recalls/drug-d-0516-2026-duloxetine-delayed-release-capsules-20-mg-rx-only-60-capsules-mark/"}, {"id": "fda-drug-d-0515-2026", "source": "FDA", "category": "drug", "recall_number": "D-0515-2026", "title": "Duloxetine Delayed-Release Capsules recall (Ajanta Pharma Ltd.)", "product": "Duloxetine Delayed-Release Capsules, 60 mg, Rx Only, 30 capsules, Marketed by: Ajanta Pharma USA Inc., Bridgewater, NJ 08807, Made in India, NDC 27241-099-03", "reason": "CGMP Deviations: Presence of N-nitroso-Duloxetine impurity above FDA recommended limit of 0.83 ppm, identified at the 12-month and 18-month long-term stability intervals.", "hazard_level": "Class II", "company": "Ajanta Pharma Ltd.", "company_location": "Aurangabad, India", "date": "2026-04-29", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Nationwide within U.S", "states": [], "nationwide": true, "quantity": "77,376 packs.", "codes": "Lot#: PA07434, Exp. May 2026.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0515-2026%22", "url": "https://recallledger.net/recalls/drug-d-0515-2026-duloxetine-delayed-release-capsules-60-mg-rx-only-30-capsules-mark/"}, {"id": "fda-drug-d-0514-2026", "source": "FDA", "category": "drug", "recall_number": "D-0514-2026", "title": "Duloxetine Delayed-Release Capsules recall (Ajanta Pharma Ltd.)", "product": "Duloxetine Delayed-Release Capsules, 30 mg, Rx Only, a) 90 Capsules, NDC 27241-098-09, b) 30 capsules, NDC 27241-098-03, c) 1000 Capsules, NDC 27241-098-10, Marketed by: Ajanta Pharma USA Inc., Bridgewater, NJ 08807, Made in India", "reason": "CGMP Deviations: Presence of N-nitroso-Duloxetine impurity above FDA recommended limit of 0.83 ppm, identified at the 12-month and 18-month long-term stability intervals.", "hazard_level": "Class II", "company": "Ajanta Pharma Ltd.", "company_location": "Aurangabad, India", "date": "2026-04-29", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Nationwide within U.S", "states": [], "nationwide": true, "quantity": "312,894 packs", "codes": "Lot#: a) PA10774, Exp. May 2026; b) PA10794, PA12174, Exp. Jun 2026; c) PA10804, Exp. Jun-26.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0514-2026%22", "url": "https://recallledger.net/recalls/drug-d-0514-2026-duloxetine-delayed-release-capsules-30-mg-rx-only-a-90-capsules-n/"}, {"id": "fda-drug-d-0513-2026", "source": "FDA", "category": "drug", "recall_number": "D-0513-2026", "title": "DELFLEX recall (Fresenius Medical Care Holdings, Inc.)", "product": "DELFLEX, Dextrose Peritoneal Dialysis Solution with attached stay-safe Exchange Set for Intraperitoneal Dialysis Only, 2.5% DEX. LM/LC, 2L 5PK, Part Number 054-20222, Fresenius Medical Care North America, 920 Winter Street, Waltham, MA 02451.", "reason": "Lack of Assurance of Sterility: Potential leaks from perforations in bags.", "hazard_level": "Class II", "company": "Fresenius Medical Care Holdings, Inc.", "company_location": "Waltham, MA, United States", "date": "2026-04-06", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Nationwide in the USA", "states": [], "nationwide": true, "quantity": "43,225 bags", "codes": "Lots 25CU02002, 25CU02011, 25CU02012, 25CU02013", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0513-2026%22", "url": "https://recallledger.net/recalls/drug-d-0513-2026-delflex-dextrose-peritoneal-dialysis-solution-with-attached-stay-safe/"}, {"id": "fda-drug-d-0512-2026", "source": "FDA", "category": "drug", "recall_number": "D-0512-2026", "title": "DELFLEX recall (Fresenius Medical Care Holdings, Inc.)", "product": "DELFLEX, Dextrose Peritoneal Dialysis Solution with attached stay-safe Exchange Set for Intraperitoneal Dialysis Only, 1.5% DEX. LM/LC, 2L 5PK, Part Number 054-20221, Fresenius Medical Care North America, 920 Winter Street, Waltham, MA 02451.", "reason": "Lack of Assurance of Sterility: Potential leaks from perforations in bags.", "hazard_level": "Class II", "company": "Fresenius Medical Care Holdings, Inc.", "company_location": "Waltham, MA, United States", "date": "2026-04-06", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Nationwide in the USA", "states": [], "nationwide": true, "quantity": "37,215 bags", "codes": "Lot #: 25CU02007, 25CU02008, 25CU02009", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0512-2026%22", "url": "https://recallledger.net/recalls/drug-d-0512-2026-delflex-dextrose-peritoneal-dialysis-solution-with-attached-stay-safe/"}, {"id": "fda-drug-d-0511-2026", "source": "FDA", "category": "drug", "recall_number": "D-0511-2026", "title": "busPIRone Hydrochloride Tablets recall (Unichem Pharmaceuticals USA Inc.)", "product": "busPIRone Hydrochloride Tablets, USP, 5 mg, 500-count bottle, Rx Only, Manufactured by Unichem Laboratories LTD., Ind, Area, Meerut Road, Ghazibad - 201 003, India Manufactured for: Unichem Pharmaceuticals (USA), Inc. East Brunswick, NJ 08816, NDC 29300-244-05.", "reason": "Subpotent drug", "hazard_level": "Class III", "company": "Unichem Pharmaceuticals USA Inc.", "company_location": "East Brunswick, NJ, United States", "date": "2026-04-13", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "USA Nationwide", "states": [], "nationwide": true, "quantity": "10,875 Bottles", "codes": "Lot: ZBUL25001, Exp 12/31/2027", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0511-2026%22", "url": "https://recallledger.net/recalls/drug-d-0511-2026-buspirone-hydrochloride-tablets-usp-5-mg-500-count-bottle-rx-only/"}, {"id": "fda-device-z-2088-2026", "source": "FDA", "category": "device", "recall_number": "Z-2088-2026", "title": "One Step P in vitro diagnostic test REF: 8194 recall (DFI Co., Ltd.)", "product": "One Step P in vitro diagnostic test REF: 8194", "reason": "The devices were distributed without required 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"reason": "The devices were distributed without required FDA premarket clearance or approval.", "hazard_level": "Class II", "company": "DFI Co., Ltd.", "company_location": "Gimhae, Korea (the Republic of)", "date": "2026-04-02", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Worldwide - US Nationwide distribution in the states of FL, PA and the country of England.", "states": ["FL", "PA"], "nationwide": true, "quantity": "59815 units", "codes": "UDI: 08806141303077/ Lot: 241023, 250415, 250509, 250617, 250905", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2086-2026%22", "url": "https://recallledger.net/recalls/device-z-2086-2026-uric-acid-in-vitro-diagnostic-test-ref-31h0p/"}, {"id": "fda-device-z-2085-2026", "source": "FDA", "category": "device", "recall_number": "Z-2085-2026", "title": "QUCARE Total Cholesterol in vitro diagnostic test REF: 6407 recall (DFI Co., Ltd.)", "product": "QUCARE Total Cholesterol in vitro diagnostic test REF: 6407", "reason": "The devices were distributed without required FDA premarket clearance or approval.", "hazard_level": "Class II", "company": "DFI Co., Ltd.", "company_location": "Gimhae, Korea (the Republic of)", "date": "2026-04-02", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Worldwide - US Nationwide distribution in the states of FL, PA and the country of England.", "states": ["FL", "PA"], "nationwide": true, "quantity": "6398 units", "codes": "UDI: 08806141303060/ Lot: BS032501, BS042502, BS062501, BS062502, BS082501", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2085-2026%22", "url": "https://recallledger.net/recalls/device-z-2085-2026-qucare-total-cholesterol-in-vitro-diagnostic-test-ref-6407/"}, {"id": "fda-device-z-2084-2026", "source": "FDA", "category": "device", "recall_number": "Z-2084-2026", "title": "One Step pH in vitro diagnostic test REF: 31I4P recall (DFI Co., Ltd.)", "product": "One Step pH in vitro diagnostic test REF: 31I4P", "reason": "The devices were distributed without required FDA premarket clearance or approval.", "hazard_level": "Class II", "company": "DFI Co., Ltd.", "company_location": "Gimhae, Korea (the Republic of)", "date": "2026-04-02", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Worldwide - US Nationwide distribution in the states of FL, PA and the country of England.", "states": ["FL", "PA"], "nationwide": true, "quantity": "7860 units", "codes": "UDI: 08806141303060/ Lot: 250305, 250415, 250509, 250625, 250905", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2084-2026%22", "url": "https://recallledger.net/recalls/device-z-2084-2026-one-step-ph-in-vitro-diagnostic-test-ref-31i4p/"}, {"id": "fda-device-z-2083-2026", "source": "FDA", "category": "device", "recall_number": "Z-2083-2026", "title": "One Step UTI in vitro diagnostic test REF: 3374 recall (DFI Co., Ltd.)", "product": "One Step UTI in vitro diagnostic test REF: 3374", "reason": "The devices were distributed without required FDA premarket clearance or approval.", "hazard_level": "Class II", "company": "DFI Co., Ltd.", "company_location": "Gimhae, Korea (the Republic of)", "date": "2026-04-02", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Worldwide - US Nationwide distribution in the states of FL, PA and the country of England.", "states": ["FL", "PA"], "nationwide": true, "quantity": "2423 units", "codes": "UDI: 08806141303480/ Lot: 241023, 250625, 250905", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2083-2026%22", "url": "https://recallledger.net/recalls/device-z-2083-2026-one-step-uti-in-vitro-diagnostic-test-ref-3374/"}, {"id": "fda-device-z-2082-2026", "source": "FDA", "category": "device", "recall_number": "Z-2082-2026", "title": "One Step 10A in vitro diagnostic test recall (DFI Co., Ltd.)", "product": "One Step 10A in vitro diagnostic test", "reason": "The devices were distributed without required FDA premarket clearance or approval.", "hazard_level": "Class II", "company": "DFI Co., Ltd.", "company_location": "Gimhae, Korea (the Republic of)", "date": "2026-04-02", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Worldwide - US Nationwide distribution in the states of FL, PA and the country of England.", "states": ["FL", "PA"], "nationwide": true, "quantity": "6533 units", "codes": "UDI: 08806141303497/ Lot: 241023, 250305, 250415, 250527, 250625, 250905", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2082-2026%22", "url": "https://recallledger.net/recalls/device-z-2082-2026-one-step-10a-in-vitro-diagnostic-test/"}, {"id": "fda-device-z-2081-2026", "source": "FDA", "category": "device", "recall_number": "Z-2081-2026", "title": "Biofire Spotfire Respiratory/Sore Throat Panel REF: 423485 recall (BioFire Diagnostics, LLC)", "product": "Biofire Spotfire Respiratory/Sore Throat Panel REF: 423485", "reason": "Respiratory/sore throat panel test may result in false negative results and control failures.", "hazard_level": "Class II", "company": "BioFire Diagnostics, LLC", "company_location": "Salt Lake City, UT, United States", "date": "2026-04-01", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "US Nationwide distribution in the states of MS, TX MN, VA.", "states": ["MN", "MS", "TX", "VA"], "nationwide": true, "quantity": "2400 pouches", "codes": "Lot Number: 2215125/UDI: 00815381020390", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2081-2026%22", "url": "https://recallledger.net/recalls/device-z-2081-2026-biofire-spotfire-respiratory-sore-throat-panel-ref-423485/"}, {"id": "fda-device-z-2067-2026", "source": "FDA", "category": "device", "recall_number": "Z-2067-2026", "title": "BioFire Joint Infection recall (BioFire Diagnostics, LLC)", "product": "BioFire Joint Infection (JI) Panel REF: RFIT-ASY-0138, 30 test Kit.", "reason": "Contamination to in-vitro diagnostic test may result in false positives.", "hazard_level": "Class II", "company": "BioFire Diagnostics, LLC", "company_location": "Salt Lake City, UT, United States", "date": "2026-04-22", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Worldwide - US Nationwide distribution in the states of TX, NC, UT, MD and the countries of France, Italy, Germany, Spain, Belgium, Switzerland, United Kingdom, Netherlands, Poland, Austria, India, Finland, Czech Republic, Egypt, Lebanon, Morocco, Slovenia, Romania, \tDominican Republic, Serbia.", "states": ["MD", "NC", "TX", "UT"], "nationwide": true, "quantity": "106 kits (3,180 test)", "codes": "Lot #s:0883425,0878825/DI: 00815381020192", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2067-2026%22", "url": "https://recallledger.net/recalls/device-z-2067-2026-biofire-joint-infection-ji-panel-ref-rfit-asy-0138-30-test-kit/"}, {"id": "fda-device-z-2065-2026", "source": "FDA", "category": "device", "recall_number": "Z-2065-2026", "title": "LIFEPAK 15 recall (Physio-Control, Inc.)", "product": "LIFEPAK 15, REF: 99577-000025, 99577-000047, 99577-001256, 99577-001217, 99577-001241, 99577-001255, 99577-001219, 99577-001957, 99577-001935, 99577-001964, 99577-001955, 99577-001956, 99577-001588, 99577-001958, 99577-001950, 99577-001962, 99577-002178, 99577-001372, 99577-001938, 99577-000045; LIFEPAK 1000, REF: 99425-000025, 99425-000023, 99425-000096; LIFEPAK 35, REF: 99335-000013, 99335-000031; LIFEPAK 20e, REF: 99507-000122", "reason": "Some defibrillators serviced between July 2023 through November 2025 were serviced without objective evidence that a Performance Inspection Procedure (PIP) was conducted, and the inability to perform the device's intended use may result in potential harms such as delays or inability to provide therapy.", "hazard_level": "Class II", "company": "Physio-Control, Inc.", "company_location": "Redmond, WA, United States", "date": "2026-04-13", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "US Nationwide distribution in the states of MI, WA, KY, IN, FL, NC, TX, LA, VA, NY, MA, CO, PA, OH, SC, OK, MN, WV, NJ, WI.", "states": ["CO", "FL", "IN", "KY", "LA", "MA", "MI", "MN", "NC", "NJ", "NY", "OH", "OK", "PA", "SC", "TX", "VA", "WA", "WI", "WV"], "nationwide": true, "quantity": "206", "codes": "Device/UDI/Serial Number: LIFEPAK 15/0088387391164815011543166573, 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0088387387708118121947855371, 0088387387169018122047857172, 0088387387169018122047858660, 0088387387171318122847872868, 0088387387171319031248018370, 0088387387169019061248247559, 0088387387168319062748298704, 0088387387169019100848453060, 0088387387171319101448455890, 0088387387171319121848586351, 0088387387171319121948586599, 0088387387168320012848651507, 0088387387171320030548701689, 0088387387708120042848784975, 0088387387171320071648887706, 0088387387168320081748921846, 0088387387169020092448981398, 0088387387169020102649032288, 0088387387169020102649050140, 0088387387162120110249055931, 0088387387168320122949156402, 0088387387169021011149162067, 0088387387169021011149167463, 0088387387169021013049212578, 0088387387169021020949225869, 0088387387169021020949226060, 0088387387176821021949240566, 0088387387168321033149345530, 0088387387169021042149378981, 0088387387169021042649381781, 0088387387169021042749381576, 0088387387168321081849559854, 0088387387168321081949560127, 0088387387164521091649607224, 0088387387171321102149662806, 0088387377697122070750045009, 0088387387169022090150136719, 0088387387171322090850152289, 0088387387708122091350158293, 0088387387169022101950223934, 0088387387708122112150288760, 0088387387171322120150307353, 0088387387169023062850629377, 0088387387169023072450653772, 0088387387169023072450667197, 0088387387708123072850669746, 0088387387708123082850714419, 0088387387171323082950720588, 0088387387169023112150850129, 0088387387708123122050883524, 0088387388434824052251092313, 0088387387170624121151422867, 0088387387170624122351440213, 0088387387170624122351444039, 0088387388434824052251092313, 0088387387169019100848453060, 0088387387201715090843839264, 0088387387171318121847850793/ 38523489, 39736196, 40465345, 40717931, 40765749, 41130420, 41139184, 41420681, 41446039, 41446693, 41704583, 42221131, 42920956, 42921954, 43166573, 43394891, 43524360, 43914574, 43915122, 44187447, 44252611, 44262721, 44277082, 44282280, 44574340, 44896329, 44962804, 45447229, 45743786, 45834209, 45998142, 46103043, 46303288, 46303092, 46587130, 46602003, 46608783, 46614788, 46813507, 46966267, 47337396, 47401928, 47611441, 47784931, 47786317, 47847661, 47848950, 47845317, 47855371, 47857172, 47858660, 47872868, 48018370, 48247559, 48298704, 48453060, 48455890, 48586351, 48586599, 48651507, 48701689, 48784975, 48887706, 48921846, 48981398, 49032288, 49050140, 49055931, 49156402, 49162067, 49167463, 49212578, 49225869, 49226060, 49240566, 49345530, 49378981, 49381781, 49381576, 49559854, 49560127, 49607224, 49662806, 50045009, 50136719, 50152289, 50158293, 50223934, 50288760, 50307353, 50629377, 50653772, 50667197, 50669746, 50714419, 50720588, 50850129, 50883524, 51092313, 51422867, 51440213, 51444039, 51092313, 48453060, 43839264, 47850793, 38369584. LIFEPAK 1000/0088507469887815020943235807, 0088507469895315031343346860, 0088507469887815111944068667, 0088507469887815111944068669, 0088507469895316011844239775, 0088507469887816041444539726, 0088507469887817061745966118, 0088507469887817061745966121, 0088507469887817061745966122, 0088507469887817061745966126, 0088507469887817061945966131, 0088507469887817062945994506, 0088507469887817062946004311, 0088507469887817063046012479, 0088507469887818060547291148, 0088387381546519080648366102, 0088387381545820092948987376, 0088387381545821011249174469, 0088387381545821081349544565, 0088387381545821090249586700, 0088387381546521122249752235, 0088387381545822012649794992, 0088387381545822032949882696, 0088387381545822032949882698, 0088387381545822032949882819/ 34933095, 35096556, 35184465, 36153943, 36199099, 36560529, 36560531, 37119097, 37226402, 37330295, 38074718, 38074722, 38074727, 38074737, 38074741, 38074744, 38074745, 38074747, 38074748, 38074749, 38077938, 38077939, 38077940, 38077941, 38077944, 38378802, 38513659, 38656117, 38656121, 38656122, 38957375, 38957392, 38957397, 38957399, 38957402, 38972629, 38972677, 39775405, 39775406, 39775407, 39775415, 39964908, 40323073, 40412729, 40541187, 40584085, 40594714, 40707896, 40725568, 40725569, 40725571, 40725572, 40725575, 40725584, 40725582, 40725583, 41306695, 41692754, 41863786, 42504017, 42520778, 42803174, 42921847, 43235807, 43346860, 44068667, 44068669, 44239775, 44539726, 45966118, 45966121, 45966122, 45966126, 45966131, 45994506, 46004311, 46012479, 47291148, 48366102, 48987376, 49174469, 49544565, 49586700, 49752235, 49794992, 49882696, 49882698, 49882819. LIFEPAK 35/0088387377265224042251041190, 0088387377265224041851042010, 0088387377265224042251044581, 0088387376560924071151156570, 0088387376560924071151157072, 0088387376560924071151157449, 0088387376560924080651182632, 0088387376560924091251263526, 0088387376560924121051417585, 0088387376560925020451496956/ 51041190, 51042010, 51044581, 51156570, 51157072, 51157449, 51182632, 51263526, 51417585, 51496956. LIFEPAK 20e/0088387385386320082448935344, 0088387385386320082448935408, 0088387385386321080249537075/ 48935344, 48935408, 49537075", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2065-2026%22", "url": "https://recallledger.net/recalls/device-z-2065-2026-lifepak-15-ref-99577-000025-99577-000047-99577-001256-99577-00121/"}, {"id": "fda-device-z-2046-2026", "source": "FDA", "category": "device", "recall_number": "Z-2046-2026", "title": "Brand Name: Da Vinci X and Da Vinci Xi Product Name: da Vinci X recall (Intuitive Surgical, Inc.)", "product": "Brand Name: Da Vinci X and Da Vinci Xi Product Name: da Vinci X, Xi Surgical System Model/Catalog Number: IS4000; IS4200 Software Version: N/A Product Description: he da Vinci Xi, X Surgical systems each consist of three main components: the Surgeon Console (SC), the Vision Cart (VC), and the Patient Cart (PC). The PC is the operative component of the system, and its primary function is to support the instrument arms and camera arm. Each system have four Universal Surgical Manipulators (USMs) also known as arms, which allow the surgeon to control up to three instruments and an endoscope simultaneously to perform surgical tasks (e.g. cutting, suturing, tissue approximation) in a variety of procedures. As the surgeon moves the hand controls within the console, the PC moves the robotic instruments within the patient in a corresponding manner. The da Vinci system and its software are designed such that instruments motion precisely tracks the motion inputs from the hand controls during surgery. Component: The affected part based on this recall, 380647-xx, USM, is a sub component of da Vinci Surgical Instrument", "reason": "Due to manipulator containing screws with in the arm sub-assembly that my be susceptible to breaking.", "hazard_level": "Class II", "company": "Intuitive Surgical, Inc.", "company_location": "Sunnyvale, CA, United States", "date": "2026-04-02", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "Worldwide - U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, WA, WI, WV, and WY. The countries of Argentina, Australia, Austria, Belgium, Brazil, Canada, China, Croatia, Cyprus, Czech Republic, Denmark, Ecuador, Finland, France, Germany, Greece, Hong Kong, Hungary, India, Ireland, Israel, Italy, Japan, Luxembourg, Malaysia, Malta, Mexico, Netherlands, Norway, Poland, Portugal, Qatar, Romania, Saudi Arabia, Singapore, Slovakia, Slovenia, South Africa, South Korea, Spain, Sweden, Switzerland, Taiwan, Turkey, United Arab Emirates, and United Kingdom.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "CT", "DC", "DE", "FL", "GA", "HI", "IA", "ID", "IL", "IN", "KS", "KY", "LA", "MA", "MD", "ME", "MI", "MN", "MO", "MS", "MT", "NC", "ND", "NE", "NH", "NJ", "NM", "NV", "NY", "OH", "OK", "OR", "PA", "SC", "SD", "TN", "TX", "UT", "VA", "WA", "WI", "WV", "WY"], "nationwide": true, "quantity": "2781", "codes": "Lot Code: UDI: 00886874114216 FDA Medical Device Listing Number: D531324 See attachment Affected Product List UDI: 00886874114216 FDA Medical Device Listing Number: D295931 See attachment Affected Product List", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2046-2026%22", "url": "https://recallledger.net/recalls/device-z-2046-2026-brand-name-da-vinci-x-and-da-vinci-xi-product-name-da-vinci-x-xi/"}, {"id": "fda-device-z-1936-2026", "source": "FDA", "category": "device", "recall_number": "Z-1936-2026", "title": "Beacon Tip Centimeter Sizing Catheter RPN/GPN NR5.0-35-70-P-10S-0-CSC-20 G31213 ... recall (Cook Incorporated)", "product": "Beacon Tip Centimeter Sizing Catheter RPN/GPN NR5.0-35-70-P-10S-0-CSC-20 G31213 NR5.0-35-100-P-10S-0-CSC-20 G31214 NR5.0-35-100-P-10S-PIG-CSC-20 G31216 NR5.0-35-70-P-10S-VCF-CSC-20 G31220 NR5.0-35-100-P-10S-VCF-CSC-20 G31221 Sizing catheters are single-use, sterile catheters with gold marker bands. These catheters are for use in angiographic procedures and available in a variety of lengths (70 and 100 cm) and tip configurations (straight, PIG, and VCF).", "reason": "Marker bands may be at an increased risk of cracking/breakage. Potential adverse events that may result include increased procedural time, harms associated with device fragmentation/separation, and vessel injury. In a worst-case scenario, device fragmentation and separation may cause life-threatening harm or death.", "hazard_level": "Class I", "company": "Cook Incorporated", "company_location": "Bloomington, IN, United States", "date": "2026-04-02", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "US distribution nationwide. OUS distribution to Brunei, Brazil, Canda, China, Colombia, Costa Rica, Hong Kong, Israel, India, Japan, South Korea, Macau, New Zealand, Singapore, El Salvador, Taiwan, Uruguay", "states": [], "nationwide": true, "quantity": "4,245", "codes": "G31213 UDI-DI 00827002312135 Lot 16805456 G31214 UDI-DI 00827002312142 Lots 16886459 16874181 16855513 16867505 16815763 16796665 16802282 16766437 16734169 16695772 G31216 UDI-DI 00827002312166 Lots 16886460 16891299 16912494 16831676 16836358 16836359 16836360 16864534 16864652 16881655 16882508 16912493 16872559 16878260 16824312 16831675 16874182 16855514 16868889 16859732 16858079 16878261 16806270 16804619 16805454 16804399 16815762 16803920 16803921 16802096 16802097 16814369 16814370 16806333 16804620 16831528 16822289 16822290 16782945 16782946 16795733 16796300 16779437 16795734 16800424 16802632 16824313 16764526 16763024 16800730 16802633 16802133 16800731 16821105 16824314 16711110 16717839 16730326 16720153 16736740 16739291 16693653 16690051 16673569 16680240 16704378 G31220 UDI-DI 00827002312203 Lots 16881657 16872241 16827163 16852999 16805455 16804400 16802132 16779438 16730325 16739292 16700199 16690050 16661312 16674400 G31221 UDI-DI 00827002312210 Lots 16839296 16879977 16814371 16821104", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1936-2026%22", "url": "https://recallledger.net/recalls/device-z-1936-2026-beacon-tip-centimeter-sizing-catheter-rpn-gpn-nr5-0-35-70-p-10s-0-cs/"}, {"id": "fda-device-z-1935-2026", "source": "FDA", "category": "device", "recall_number": "Z-1935-2026", "title": "Aurous Centimeter Sizing Catheter RPN N5.0-35-100-P-10S-PIG-CSC-20-01 GPN G47308 ... recall (Cook Incorporated)", "product": "Aurous Centimeter Sizing Catheter RPN N5.0-35-100-P-10S-PIG-CSC-20-01 GPN G47308 Sizing catheters are single-use, sterile catheters with gold marker bands. These catheters are for use in angiographic procedures and available in a variety of lengths (70 and 100 cm) and tip configurations (straight, PIG, and VCF).", "reason": "Marker bands may be at an increased risk of cracking/breakage. Potential adverse events that may result include increased procedural time, harms associated with device fragmentation/separation, and vessel injury. In a worst-case scenario, device fragmentation and separation may cause life-threatening harm or death.", "hazard_level": "Class I", "company": "Cook Incorporated", "company_location": "Bloomington, IN, United States", "date": "2026-04-02", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "US distribution nationwide. OUS distribution to Brunei, Brazil, Canda, China, Colombia, Costa Rica, Hong Kong, Israel, India, Japan, South Korea, Macau, New Zealand, Singapore, El Salvador, Taiwan, Uruguay", "states": [], "nationwide": true, "quantity": "271", "codes": "UDI-DI 00827002473089 Lots 16858459 16869145 16857138 16763324 16750208 16752733 16821053 16713191", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1935-2026%22", "url": "https://recallledger.net/recalls/device-z-1935-2026-aurous-centimeter-sizing-catheter-rpn-n5-0-35-100-p-10s-pig-csc-20-01/"}, {"id": "fda-device-z-1934-2026", "source": "FDA", "category": "device", "recall_number": "Z-1934-2026", "title": "Centimeter Sizing Catheter RPN N5.0-35-100-P-10S-PIG-CSC-20 GPN G11916 Catheters... recall (Cook Incorporated)", "product": "Centimeter Sizing Catheter RPN N5.0-35-100-P-10S-PIG-CSC-20 GPN G11916 Catheters for use in angiographic procedures are available in a variety of French sizes, endhole sizes, lengths, materials and designs (e.g., polyethylene or nylon, non-braided or braided with 1:1 torque). The choice of catheter material for different angiographic procedures should be based on the physician s experience.", "reason": "Marker bands may be at an increased risk of cracking/breakage. Potential adverse events that may result include increased procedural time, harms associated with device fragmentation/separation, and vessel injury. In a worst-case scenario, device fragmentation and separation may cause life-threatening harm or death.", "hazard_level": "Class I", "company": "Cook Incorporated", "company_location": "Bloomington, IN, United States", "date": "2026-04-02", "report_date": "2026-05-13", "status": "Ongoing", "distribution": "US distribution nationwide. OUS distribution to Brunei, Brazil, Canda, China, Colombia, Costa Rica, Hong Kong, Israel, India, Japan, South Korea, Macau, New Zealand, Singapore, El Salvador, Taiwan, Uruguay", "states": [], "nationwide": true, "quantity": "11,253", "codes": "UDI-DI 00827002119161 Lots 16905390 16905390X 16888263 NS16888264 16905391 16905391X 16909577 16918137 16924645 16924646 16928311 16928311X 16928312 16928313 16947353 16899656 16899655 16894976 16879299 16890985 16903201 16885859 16890986 16890982 16888268 16904428 16899658 16903202 16903203 16903204 16905389 16888267 16890983 16888269 16890981 16879296 16864346 16879301 16888261 16864344 16864351 16846774 16869144 16879300 16864350 16869143 16869143X NS16861721 16879297 16861735 16864347 16864347X 16882666 16899657 16890984 16899659 16888266 16861729 16857145 16858460 16857141 16861730 16861724 16858463 16852206 16855698 16858458 16858461 16858462 16858462X 16861726 16861727 16861728 16852209 16855686 16855696 16857146 16859718 16861720 16861723 16861725 16857137 16857142 16857139 16857140 16877835 16864345 16882665 16864353 16864348 16865462 16865462X 16879302 16843256 16833320 16843258 16845235 16845236 16839886 16845242 16845244 16845223 16845223X 16845226 16846777 16845230 16845227 16833315 16845218 16845246 16845233 16846778 16845229 16845240 16846779 16845241 16855694 16851384 16855695 16852208 16855693 16855697 16852207 16851381 16861733 16852711 16855688 16849691 NS16845220 NS16845220X 16846771 16846776 16845231 16851379 16851378 16851374 16846775 16851376 16855690 16849688 16846770 16846773 16861731 16861731X 16861732 16864352 16864354 NS16861722 16857144 16855691 16855692 16846772 16851380 16861734 16861734X 16864349 16851382 16857143 16857143X 16833228 16833298 16833292 16833321 16845239 16836838 16839887 16823055 16807168 16816808 16823045 16833290 16833299 16836839 16836839X 16833316 16833314 16833310 16823062 16823062X 16825484 16833229 16833230 16833231 16833232 16833289 16833307 16833308 16833309 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"https://recallledger.net/recalls/device-z-1934-2026-centimeter-sizing-catheter-rpn-n5-0-35-100-p-10s-pig-csc-20-gpn-g119/"}, {"id": "fda-food-h-0686-2026", "source": "FDA", "category": "food", "recall_number": "H-0686-2026", "title": "Black label with blue lettering. FOOD Korean Food recall (HEMU TRADING INC)", "product": "Black label with blue lettering. FOOD Korean Food, ENOKI MUSHROOM, 150g clear plastic package; Product of Korea, Keep Refrigerated. Distributed by Hemu Trading Inc. UPC: 8801234567893", "reason": "product tested positive for Listeria Monocytogenes.", "hazard_level": "Class I", "company": "HEMU TRADING INC", "company_location": "Los Angeles, CA, United States", "date": "2026-04-02", "report_date": "2026-05-06", "status": "Ongoing", "distribution": "5 direct account consignees located in CA, FL and MD.", "states": ["CA", "FL", "MD"], "nationwide": false, "quantity": "1056 cases (34 packs/case)", "codes": "Lot code:215", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0686-2026%22", "url": "https://recallledger.net/recalls/food-h-0686-2026-black-label-with-blue-lettering-food-korean-food-enoki-mushroom-150/"}, {"id": "fda-food-h-0685-2026", "source": "FDA", "category": "food", "recall_number": "H-0685-2026", "title": "Calypso Tropic Tango Lemonade. 16 FL oz recall (King Juice Company, Inc.)", "product": "Calypso Tropic Tango Lemonade. 16 FL oz (1PT) (473 ML). UPC 0 79581-18709 7. Keep Refrigerated After Opening. King Juice Company, Inc., Milwaukee, Wisconsin 53221.", "reason": "Product contains undeclared Yellow No. 5.", "hazard_level": "Class II", "company": "King Juice Company, Inc.", "company_location": "Milwaukee, WI, United States", "date": "2026-04-23", "report_date": "2026-05-06", "status": "Terminated", "distribution": "Nationwide. Outside the US to Australia, New Zealand, Singapore, and Trinidad and Tobago", "states": [], "nationwide": true, "quantity": "299,779 cases (12 bottles per case)", "codes": "All Lot Codes including and prior to 01APR2027", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0685-2026%22", "url": "https://recallledger.net/recalls/food-h-0685-2026-calypso-tropic-tango-lemonade-16-fl-oz-1pt-473-ml-upc-0-79581/"}, {"id": "fda-food-h-0684-2026", "source": "FDA", "category": "food", "recall_number": "H-0684-2026", "title": "My Mochi Strawberry flavored Non-Dairy Frozen Dessert recall (The Mochi Ice Cream Company, LLC)", "product": "My Mochi Strawberry flavored Non-Dairy Frozen Dessert; 7.5 oz; 6 pieces per container. UPC# 0-70934-99645-8", "reason": "Foreign object found inside retail container.", "hazard_level": "Class II", "company": "The Mochi Ice Cream Company, LLC", "company_location": "Vernon, CA, United States", "date": "2026-04-20", "report_date": "2026-05-06", "status": "Terminated", "distribution": "Product was distributed to 6 retail consignees with several locations nationwide.", "states": [], "nationwide": true, "quantity": "1270 cases", "codes": "Lot# 041-26 BEST BUY 2/20/2027", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0684-2026%22", "url": "https://recallledger.net/recalls/food-h-0684-2026-my-mochi-strawberry-flavored-non-dairy-frozen-dessert-7-5-oz-6-piece/"}, {"id": "fda-food-h-0680-2026", "source": "FDA", "category": "food", "recall_number": "H-0680-2026", "title": "Specially SELECTED brand Vanilla Creme Brulee recall (LACTALIS CANADA, INC)", "product": "Specially SELECTED brand Vanilla Creme Brulee; NET WT 3.6oz (103g); INGREDIENTS: CREAM (MILK, CREAM), FROZEN YOLK MIX (EGG YOLK, SUGAR) SUGAR, NATURAL VANILLA FLAVOR, TAPIOCA STARCH, CARRAGEENAN; TOPPING INGREDIENTS: CARAMEL FLAKES (SUGAR, GLUCOSE SYRUP); CONTAINS: MILK, EGGS. MAY CONTAIN: WHEAT, SOY; DIST.SOLD EXCLUSIVELY BY: ALDI BATAVIA, IL; packaged in glass jars", "reason": "Product may contain foreign objects, specifically glass.", "hazard_level": "Class II", "company": "LACTALIS CANADA, INC", "company_location": "Toronto, Quebec, Canada", "date": "2026-04-14", "report_date": "2026-05-06", "status": "Terminated", "distribution": "NY, IN, FL, IL, VA, MD, and MI", "states": ["FL", "IL", "IN", "MD", "MI", "NY", "VA"], "nationwide": false, "quantity": "2,869 cases", "codes": "Best Before/Use By Date: 5/9/2026 Product Number: 710298-4099100342826 Barcode: 4099100342826", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0680-2026%22", "url": "https://recallledger.net/recalls/food-h-0680-2026-specially-selected-brand-vanilla-creme-brulee-net-wt-3-6oz-103g-in/"}, {"id": "fda-food-h-0679-2026", "source": "FDA", "category": "food", "recall_number": "H-0679-2026", "title": "Negita Cracker- Shrimp 2.8oz recall (Hadson (Toko) Trading Co. Inc.)", "product": "Negita Cracker- Shrimp 2.8oz", "reason": "Contains undeclared FD&C Yellow 6", "hazard_level": "Class II", "company": "Hadson (Toko) Trading Co. Inc.", "company_location": "Maspeth, NY, United States", "date": "2026-04-16", "report_date": "2026-05-06", "status": "Ongoing", "distribution": "CT, GA, IL, MA, MD, NJ, NY, OH, PA, TX, UT, VA", "states": ["CT", "GA", "IL", "MA", "MD", "NJ", "NY", "OH", "PA", "TX", "UT", "VA"], "nationwide": false, "quantity": "142 units", "codes": "UPC code: 4975934313310 Best by: 1/6/2027", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0679-2026%22", "url": "https://recallledger.net/recalls/food-h-0679-2026-negita-cracker-shrimp-2-8oz/"}, {"id": "fda-food-h-0678-2026", "source": "FDA", "category": "food", "recall_number": "H-0678-2026", "title": "52USA brand POPPING BOBA recall (Guangdong Zonegoing Food Co., LTD)", "product": "52USA brand POPPING BOBA; MANGO FLAVOR; Net wt: 7 lb (3.2kg); Ingredients Drinking water, fructose syrup, food additives (hydroxypropyl distarch phosphate (E1442), calcium lactate (E327), DL-malic acid (E296), sodium alginate (E401), citric acid (E330), carrageenan (EE407), potassium chloride (E508), potassium sorbate (E202), guar gum (E412), trisodium citrate (E331), beta-carotene (E160a). sucralose (E955), tartrazine (E102), sunset yellow (E110)), food flavors.; CONTAINS NO JUICE; Shelf Life: 18 months; Distributed for Felicific Inc., Queens, NY 11435; PRODUCT OF CHINA; UPC 8 1018 42124 4", "reason": "Products contain unapproved colors, specifically tartrazine (FD&C Yellow 5), sunset yellow (FD&C Yellow 6), and allura red (FD&C Red 40).", "hazard_level": "Class II", "company": "Guangdong Zonegoing Food Co., LTD", "company_location": "Huizhou, China", "date": "2026-04-13", "report_date": "2026-05-06", "status": "Ongoing", "distribution": "NY", "states": ["NY"], "nationwide": false, "quantity": "5,196 units (total)", "codes": "Lot Numbers: 20250813 Expiration Date: Feb 8, 2027", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0678-2026%22", "url": "https://recallledger.net/recalls/food-h-0678-2026-52usa-brand-popping-boba-mango-flavor-net-wt-7-lb-3-2kg-ingredie/"}, {"id": "fda-food-h-0677-2026", "source": "FDA", "category": "food", "recall_number": "H-0677-2026", "title": "52USA brand POPPING BOBA recall (Guangdong Zonegoing Food Co., LTD)", "product": "52USA brand POPPING BOBA; PASSION FRUIT FLAVOR; Net wt: 7 lb (3.2kg); Ingredients Drinking water, fructose syrup, food additives (hydroxypropyl distarch phosphate (E1442), calcium lactate (E327), DL-malic acid (E296), sodium alginate (E401), citric acid (E330), carrageenan (EE407), potassium chloride (E508), potassium sorbate (E202), guar gum (E412), trisodium citrate (E331), beta-carotene (E160a). sucralose (E955), tartrazine (E102), sunset yellow (E110)), food flavors.; CONTAINS NO JUICE; Shelf Life: 18 months; Distributed for Felicific Inc., Queens, NY 11435; PRODUCT OF CHINA; UPC 8 1018 42125 1", "reason": "Products contain unapproved colors, specifically tartrazine (FD&C Yellow 5), sunset yellow (FD&C Yellow 6), and allura red (FD&C Red 40).", "hazard_level": "Class II", "company": "Guangdong Zonegoing Food Co., LTD", "company_location": "Huizhou, China", "date": "2026-04-13", "report_date": "2026-05-06", "status": "Ongoing", "distribution": "NY", "states": ["NY"], "nationwide": false, "quantity": "5,196 units (total)", "codes": "Lot Numbers: 20250813 Expiration Date: Feb 8, 2027", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0677-2026%22", "url": "https://recallledger.net/recalls/food-h-0677-2026-52usa-brand-popping-boba-passion-fruit-flavor-net-wt-7-lb-3-2kg/"}, {"id": "fda-food-h-0676-2026", "source": "FDA", "category": "food", "recall_number": "H-0676-2026", "title": "52USA brand POPPING BOBA recall (Guangdong Zonegoing Food Co., LTD)", "product": "52USA brand POPPING BOBA; STRAWBERRY FLAVOR; Net wt: 7 lb (3.2kg); Ingredients Drinking water, fructose syrup, food additives (hydroxypropyl distarch phosphate (E1442), calcium lactate (E327), DL-malic acid (E296), sodium alginate (E401), citric acid (E330), carageenan (EE407), potassium chloride (E508), potassium sorbate (E202), guar gum (E412), trisodium citrate (E331), sucralose (E955), allura red (E129), food flavors.; CONTAINS NO JUICE; Shelf Life: 18 months; Distributed for Felicific Inc., Queens, NY 11435; PRODUCT OF CHINA; UPC 8 10185 42123 7", "reason": "Products contain unapproved colors, specifically tartrazine (FD&C Yellow 5), sunset yellow (FD&C Yellow 6), and allura red (FD&C Red 40).", "hazard_level": "Class II", "company": "Guangdong Zonegoing Food Co., LTD", "company_location": "Huizhou, China", "date": "2026-04-13", "report_date": "2026-05-06", "status": "Ongoing", "distribution": "NY", "states": ["NY"], "nationwide": false, "quantity": "5,196 units (total)", "codes": "Lot Numbers: 20250813 Expiration Date: Feb 8, 2027", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0676-2026%22", "url": "https://recallledger.net/recalls/food-h-0676-2026-52usa-brand-popping-boba-strawberry-flavor-net-wt-7-lb-3-2kg-ing/"}, {"id": "fda-drug-d-0526-2026", "source": "FDA", "category": "drug", "recall_number": "D-0526-2026", "title": "Alendronate Sodium Oral Solution recall (Hikma Pharmaceuticals USA INC)", "product": "Alendronate Sodium Oral Solution, 70 mg/75 mL, 75 mL, Rx only, 4 x 75 mL Single Dose Bottles, Distr. by: Hikma Pharmaceuticals USA Inc., Berkeley Heights, NJ 07922, NDC 0054-0282-59.", "reason": "This recall is being conducted due to out of specification assay results in a limited number of bottles that were stored on side.", "hazard_level": "Class II", "company": "Hikma Pharmaceuticals USA INC", "company_location": "Columbus, OH, United States", "date": "2026-04-07", "report_date": "2026-05-06", "status": "Ongoing", "distribution": "US Nationwide.", "states": [], "nationwide": true, "quantity": "4 single dose 75 ml bottles", "codes": "Lot # AC2040A, Exp Date: 04/2026", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0526-2026%22", "url": "https://recallledger.net/recalls/drug-d-0526-2026-alendronate-sodium-oral-solution-70-mg-75-ml-75-ml-rx-only-4-x-75/"}, {"id": "fda-drug-d-0509-2026", "source": "FDA", "category": "drug", "recall_number": "D-0509-2026", "title": "Lidocaine Wound Gel recall (Water-Jel Technologies, LLC)", "product": "Lidocaine Wound Gel (Benzalkonium Chloride, 0.13% and Lidocaine Hydrochloride, 2%), NET WT 0.5 OZ (14 g), Distributed by: CVS PHarmacy, INc., One CVS Drive, Woonsocket, RI 02895. NDC 59898-950", "reason": "Failed PH Specifications", "hazard_level": "Class III", "company": "Water-Jel Technologies, LLC", "company_location": "Huntersville, NC, United States", "date": "2026-04-07", "report_date": "2026-05-06", "status": "Ongoing", "distribution": "Nationwide in the USA", "states": [], "nationwide": true, "quantity": "31,488 tubes", "codes": "Lots: A5014, A5018, A5019", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0509-2026%22", "url": "https://recallledger.net/recalls/drug-d-0509-2026-lidocaine-wound-gel-benzalkonium-chloride-0-13-and-lidocaine-hydroc/"}, {"id": "fda-drug-d-0508-2026", "source": "FDA", "category": "drug", "recall_number": "D-0508-2026", "title": "fentaNYL Citrate Injectable Solution in 0.9% Sodium Chloride recall (Wells Pharma of Houston LLC)", "product": "fentaNYL Citrate Injectable Solution in 0.9% Sodium Chloride, 50 mcg/5mL)(10 mcg per mL), wells pharma, NDC 73702-202-15.", "reason": "cGMP deviations.", "hazard_level": "Class II", "company": "Wells Pharma of Houston LLC", "company_location": "Houston, TX, United States", "date": "2026-04-01", "report_date": "2026-05-06", "status": "Ongoing", "distribution": "U.S. Nationwide.", "states": [], "nationwide": true, "quantity": "50 syringes", "codes": "Lot 020226202150202, Exp Date 05/05/2026.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0508-2026%22", "url": "https://recallledger.net/recalls/drug-d-0508-2026-fentanyl-citrate-injectable-solution-in-0-9-sodium-chloride-50-mcg-5/"}, {"id": "fda-drug-d-0507-2026", "source": "FDA", "category": "drug", "recall_number": "D-0507-2026", "title": "Ketamine Hydrochloride Injectable Solution recall (Wells Pharma of Houston LLC)", "product": "Ketamine Hydrochloride Injectable Solution, 50mg/ml, (50 mg per mL) Volume: 1 mL, 5265 Kitty Drive, Houston, TX 77054, NDC 73702-302-31.", "reason": "cGMP deviations.", "hazard_level": "Class II", "company": "Wells Pharma of Houston LLC", "company_location": "Houston, TX, United States", "date": "2026-04-01", "report_date": "2026-05-06", "status": "Ongoing", "distribution": "U.S. Nationwide.", "states": [], "nationwide": true, "quantity": "4975 syringes", "codes": "120925302312764, Exp Date 04/09/2026, 123125302312879 Exp Date, 05/05/2026, 123125302312880, Exp Date 05/05/2026, 010226302310003, Exp Date 05/06/2026, 010626302310007, Exp Date 05/08/2026, 010626302310008, Exp Date 05/08/2026 020426302310243, Exp Date 06/06/2026.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0507-2026%22", "url": "https://recallledger.net/recalls/drug-d-0507-2026-ketamine-hydrochloride-injectable-solution-50mg-ml-50-mg-per-ml-vo/"}, {"id": "fda-drug-d-0506-2026", "source": "FDA", "category": "drug", "recall_number": "D-0506-2026", "title": "fentaNYL Citrate Injectable Solution in 0.9% Sodium Chloride recall (Wells Pharma of Houston LLC)", "product": "fentaNYL Citrate Injectable Solution in 0.9% Sodium Chloride, 1000 mcg/50mL (20 mcg per mL), well pharma of Houston, NDC 73702-203-65.", "reason": "cGMP deviations.", "hazard_level": "Class II", "company": "Wells Pharma of Houston LLC", "company_location": "Houston, TX, United States", "date": "2026-04-01", "report_date": "2026-05-06", "status": "Ongoing", "distribution": "U.S. Nationwide.", "states": [], "nationwide": true, "quantity": "150 syringes", "codes": "Lot 022326203650432; 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Cork, Ireland", "date": "2026-04-03", "report_date": "2026-05-06", "status": "Ongoing", "distribution": "US Nationwide distribution in the states of MN, NC, TX.", "states": ["MN", "NC", "TX"], "nationwide": true, "quantity": "3 units", "codes": "Part Number: 150450105. UDI-DI: 10603295533122. Lot Number: AF1007829. Expiration Date: 12/31/2035.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1986-2026%22", "url": "https://recallledger.net/recalls/device-z-1986-2026-depuy-synthes-attune-revision-hinge-femoral-lt-sz-5-cem-part-number/"}, {"id": "fda-device-z-1985-2026", "source": "FDA", "category": "device", "recall_number": "Z-1985-2026", "title": "Depuy Synthes recall (DEPUY (IRELAND))", "product": "Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 4 CEM. Part Number: 150450104.", "reason": "The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.", "hazard_level": "Class II", "company": "DEPUY (IRELAND)", "company_location": "Co. Cork, Ireland", "date": "2026-04-03", "report_date": "2026-05-06", "status": "Ongoing", "distribution": "US Nationwide distribution in the states of MN, NC, TX.", "states": ["MN", "NC", "TX"], "nationwide": true, "quantity": "3 units", "codes": "Part Number: 150450104. UDI-DI: 10603295533115. Lot Number: 1007844. Expiration Date: 11/30/2035", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1985-2026%22", "url": "https://recallledger.net/recalls/device-z-1985-2026-depuy-synthes-attune-revision-hinge-femoral-lt-sz-4-cem-part-number/"}, {"id": "fda-device-z-1983-2026", "source": "FDA", "category": "device", "recall_number": "Z-1983-2026", "title": "BD GasPak EZ Campy Pouch System. Catalog Number: 260685. for microbiologic use recall (Becton Dickinson & Co.)", "product": "BD GasPak EZ Campy Pouch System. Catalog Number: 260685. for microbiologic use", "reason": "BD identified an issue affecting certain lots of BD GasPak EZ CO2 and BD GasPak EZ Campy Gas Generating Pouch Systems, where gas generating sachets may produce carbon dioxide levels below specification.", "hazard_level": "Class II", "company": "Becton Dickinson & Co.", "company_location": "Sparks, MD, United States", "date": "2026-04-07", "report_date": "2026-05-06", "status": "Ongoing", "distribution": "Worldwide distribution - US Nationwide and the country of Hong Kong.", "states": [], "nationwide": true, "quantity": "2,200 units", "codes": "Catalog Number: 260685; UDI-DI: 30382902606858; Lot Number: 5329863.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1983-2026%22", "url": "https://recallledger.net/recalls/device-z-1983-2026-bd-gaspak-ez-campy-pouch-system-catalog-number-260685-for-microbiol/"}, {"id": "fda-device-z-1982-2026", "source": "FDA", "category": "device", "recall_number": "Z-1982-2026", "title": "BD GasPak EZ CO2 Pouch System. Catalog Number: 260684. for microbiologic use recall (Becton Dickinson & Co.)", "product": "BD GasPak EZ CO2 Pouch System. Catalog Number: 260684. for microbiologic use", "reason": "BD identified an issue affecting certain lots of BD GasPak EZ CO2 and BD GasPak EZ Campy Gas Generating Pouch Systems, where gas generating sachets may produce carbon dioxide levels below specification.", "hazard_level": "Class II", "company": "Becton Dickinson & Co.", "company_location": "Sparks, MD, United States", "date": "2026-04-07", "report_date": "2026-05-06", "status": "Ongoing", "distribution": "Worldwide distribution - US Nationwide and the country of Hong Kong.", "states": [], "nationwide": true, "quantity": "25,760 units", "codes": "Catalog Nunber: 260684; UDI-DI: 30382902606841; Lot Numbers: 5303157, 5329857, 5329860.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1982-2026%22", "url": "https://recallledger.net/recalls/device-z-1982-2026-bd-gaspak-ez-co2-pouch-system-catalog-number-260684-for-microbiolog/"}, {"id": "fda-device-z-1969-2026", "source": "FDA", "category": "device", "recall_number": "Z-1969-2026", "title": "Philips Upgrade to MR 7700 with MR Elastography recall (Philips North America)", "product": "Philips Upgrade to MR 7700 with MR Elastography (MRE). 1. Model Number (REF): 782130.", "reason": "The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.", "hazard_level": "Class II", "company": "Philips North America", "company_location": "Cambridge, MA, United States", "date": "2026-04-14", "report_date": "2026-05-06", "status": "Ongoing", "distribution": "Worldwide - US Nationwide and the countries of Argentina, Australia, Bangladesh, Belgium, Brazil, Canada, Chile, Cuba, Cyprus, Denmark, Ecuador, Egypt, France, Germany, Greece, Hong Kong, India, Indonesia, Iran, Iraq, Israel, Italy, Japan, Kenya, Lebanon, Lithuania, Malta, Mexico, Myanmar, Netherlands, Pakistan, Palestine, Peru, Poland, Portugal, Russian Fed., Singapore, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, United Kingdom.", "states": [], "nationwide": true, "quantity": "15 units", "codes": "1. Model Number (REF): 782130. UDI: (01)00884838104402(21)45052, (01)00884838104402(21)42030, (01)00884838104402(21)42151, (01)00884838104402(21)71279, (01)00884838104402(21)71565, (01)00884838104402(21)42104, (01)00884838104402(21)42163, (01)00884838104402(21)42376, (01)00884838104402(21)45179, (01)00884838104402(21)45236, (01)00884838104402(21)45263, (01)00884838104402(21)71532, (01)00884838104402(21)85394, (01)00884838104402(21)85643, (01)00884838104402(21)85644. Serial Numbers: 45052, 42030, 42151, 71279, 71565, 42104, 42163, 42376, 45179, 45236, 45263, 71532, 85394, 85643, 85644.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1969-2026%22", "url": "https://recallledger.net/recalls/device-z-1969-2026-philips-upgrade-to-mr-7700-with-mr-elastography-mre-1-model-nu/"}, {"id": "fda-device-z-1968-2026", "source": "FDA", "category": "device", "recall_number": "Z-1968-2026", "title": "Philips SmartPath to Ingenia Elition X with MR Elastography recall (Philips North America)", "product": "Philips SmartPath to Ingenia Elition X with MR Elastography (MRE). 1. Model Number (REF): 782118. 2. Model Number (REF): 782144. 3. Model Number (REF): 782163.", "reason": "The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.", "hazard_level": "Class II", "company": "Philips North America", "company_location": "Cambridge, MA, United States", "date": "2026-04-14", "report_date": "2026-05-06", "status": "Ongoing", "distribution": "Worldwide - US Nationwide and the countries of Argentina, Australia, Bangladesh, Belgium, Brazil, Canada, Chile, Cuba, Cyprus, Denmark, Ecuador, Egypt, France, Germany, Greece, Hong Kong, India, Indonesia, Iran, Iraq, Israel, Italy, Japan, Kenya, Lebanon, Lithuania, Malta, Mexico, Myanmar, Netherlands, Pakistan, Palestine, Peru, Poland, Portugal, Russian Fed., Singapore, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, United Kingdom.", "states": [], "nationwide": true, "quantity": "3 units", "codes": "1. Model Number (REF): 782118. UDI: (01)00884838099746(21)85655. Serial Numbers: 85655. 2. Model Number (REF): 782144. UDI: (01)00884838108677(21)71087. Serial Numbers: 71087. 3. Model Number (REF): 782163. UDI: (01)00884838115743(21)42299. Serial Numbers: 42299.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1968-2026%22", "url": "https://recallledger.net/recalls/device-z-1968-2026-philips-smartpath-to-ingenia-elition-x-with-mr-elastography-mre/"}, {"id": "fda-device-z-1967-2026", "source": "FDA", "category": "device", "recall_number": "Z-1967-2026", "title": "Philips SmartPath to dStream for XR and 3.0T with MR Elastography recall (Philips North America)", "product": "Philips SmartPath to dStream for XR and 3.0T with MR Elastography (MRE). 1. Model Number (REF): 781270. 2. Model Number (REF): 782113.", "reason": "The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.", "hazard_level": "Class II", "company": "Philips North America", "company_location": "Cambridge, MA, United States", "date": "2026-04-14", "report_date": "2026-05-06", "status": "Ongoing", "distribution": "Worldwide - US Nationwide and the countries of Argentina, Australia, Bangladesh, Belgium, Brazil, Canada, Chile, Cuba, Cyprus, Denmark, Ecuador, Egypt, France, Germany, Greece, Hong Kong, India, Indonesia, Iran, Iraq, Israel, Italy, Japan, Kenya, Lebanon, Lithuania, Malta, Mexico, Myanmar, Netherlands, Pakistan, Palestine, Peru, Poland, Portugal, Russian Fed., Singapore, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, United Kingdom.", "states": [], "nationwide": true, "quantity": "14 units", "codes": "1. Model Number (REF): 781270. UDI: (01)00884838095083(21)38109, (01)00884838095083(21)17386, (01)00884838095083(21)38356, (01)00884838095083(21)34211, (01)00884838095083(21)38113, (01)00884838095083(21)17356, (01)00884838095083(21)38111, (01)00884838095083(21)74011, (01)00884838095083(21)24058, (01)00884838095083(21)24066, (01)00884838095083(21)34223. Serial Numbers: 38109, 17386, 38356, 34211, 38113, 17356, 38111, 74011, 24058, 24066, 34223. 2. Model Number (REF): 782113. UDI: (01)00884838098909(21)38066, (01)00884838098909(21)38117, (01)00884838098909(21)17384. Serial Numbers: 38066, 38117, 17384.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1967-2026%22", "url": "https://recallledger.net/recalls/device-z-1967-2026-philips-smartpath-to-dstream-for-xr-and-3-0t-with-mr-elastography-mre/"}, {"id": "fda-device-z-1966-2026", "source": "FDA", "category": "device", "recall_number": "Z-1966-2026", "title": "Philips SmartPath to dStream for 3.0T with MR Elastography recall (Philips North America)", "product": "Philips SmartPath to dStream for 3.0T with MR Elastography (MRE). 1. Model Number (REF): 782145.", "reason": "The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.", "hazard_level": "Class II", "company": "Philips North America", "company_location": "Cambridge, MA, United States", "date": "2026-04-14", "report_date": "2026-05-06", "status": "Ongoing", "distribution": "Worldwide - US Nationwide and the countries of Argentina, Australia, Bangladesh, Belgium, Brazil, Canada, Chile, Cuba, Cyprus, Denmark, Ecuador, Egypt, France, Germany, Greece, Hong Kong, India, Indonesia, Iran, Iraq, Israel, Italy, Japan, Kenya, Lebanon, Lithuania, Malta, Mexico, Myanmar, Netherlands, Pakistan, Palestine, Peru, Poland, Portugal, Russian Fed., Singapore, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, United Kingdom.", "states": [], "nationwide": true, "quantity": "1 unit", "codes": "1. Model Number (REF): 782145. UDI: (01)00884838108684(21)17385. Serial Numbers: 17385.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1966-2026%22", "url": "https://recallledger.net/recalls/device-z-1966-2026-philips-smartpath-to-dstream-for-3-0t-with-mr-elastography-mre/"}, {"id": "fda-device-z-1965-2026", "source": "FDA", "category": "device", "recall_number": "Z-1965-2026", "title": "Philips SmartPath to dStream for 1.5T with MR Elastography recall (Philips North America)", "product": "Philips SmartPath to dStream for 1.5T with MR Elastography (MRE). 1. Model Number (REF): 781260. 2. Model Number (REF): 782112.", "reason": "The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.", "hazard_level": "Class II", "company": "Philips North America", "company_location": "Cambridge, MA, United States", "date": "2026-04-14", "report_date": "2026-05-06", "status": "Ongoing", "distribution": "Worldwide - US Nationwide and the countries of Argentina, Australia, Bangladesh, Belgium, Brazil, Canada, Chile, Cuba, Cyprus, Denmark, Ecuador, Egypt, France, Germany, Greece, Hong Kong, India, Indonesia, Iran, Iraq, Israel, Italy, Japan, Kenya, Lebanon, Lithuania, Malta, Mexico, Myanmar, Netherlands, Pakistan, Palestine, Peru, Poland, Portugal, Russian Fed., Singapore, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, United Kingdom.", "states": [], "nationwide": true, "quantity": "6 units", "codes": "1. Model Number (REF): 781260. UDI: (01)00884838095076(21)21554, (01)00884838095076(21)13018, (01)00884838095076(21)12033. Serial Numbers: 21554, 13018, 12033. 2. Model Number (REF): 782112. UDI: (01)00884838098886(21)30143, (01)00884838098886(21)22051, (01)00884838098886(21)32156. Serial Numbers: 30143, 22051, 32156.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1965-2026%22", "url": "https://recallledger.net/recalls/device-z-1965-2026-philips-smartpath-to-dstream-for-1-5t-with-mr-elastography-mre/"}, {"id": "fda-device-z-1964-2026", "source": "FDA", "category": "device", "recall_number": "Z-1964-2026", "title": "Philips MR 7700 with MR Elastography recall (Philips North America)", "product": "Philips MR 7700 with MR Elastography (MRE). 1. Model Number (REF): 782120. 2. Model Number (REF): 782153.", "reason": "The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.", "hazard_level": "Class II", "company": "Philips North America", "company_location": "Cambridge, MA, United States", "date": "2026-04-14", "report_date": "2026-05-06", "status": "Ongoing", "distribution": "Worldwide - US Nationwide and the countries of Argentina, Australia, Bangladesh, Belgium, Brazil, Canada, Chile, Cuba, Cyprus, Denmark, Ecuador, Egypt, France, Germany, Greece, Hong Kong, India, Indonesia, Iran, Iraq, Israel, Italy, Japan, Kenya, Lebanon, Lithuania, Malta, Mexico, Myanmar, Netherlands, Pakistan, Palestine, Peru, Poland, Portugal, Russian Fed., Singapore, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, United Kingdom.", "states": [], "nationwide": true, "quantity": "25 untis", "codes": "1. Model Number (REF): 782120. UDI: (01)00884838104112(21)65019, (01)00884838104112(21)65004, (01)00884838104112(21)65028, (01)00884838104112(21)65031, (01)00884838104112(21)65039, (01)00884838104112(21)65056, (01)00884838104112(21)65066, (01)00884838104112(21)65065, (01)00884838104112(21)65038, (01)00884838104112(21)65005, (01)00884838104112(21)65043, (01)00884838104112(21)65049, (01)00884838104112(21)65051, (01)00884838104112(21)65060. Serial Numbers: 65019, 65004, 65028, 65031, 65039, 65056, 65066, 65065, 65038, 65005, 65043, 65049, 65051, 65060. 2. Model Number (REF): 782153. UDI: (01)00884838112858(21)68034, (01)00884838112858(21)68042, (01)00884838112858(21)68014, (01)00884838112858(21)68001, (01)00884838112858(21)68007, (01)00884838112858(21)68008, (01)00884838112858(21)68017, (01)00884838112858(21)68025, (01)00884838112858(21)68037, (01)00884838112858(21)68041, (01)00884838112858(21)68019. Serial Numbers: 68034, 68042, 68014, 68001, 68007, 68008, 68017, 68025, 68037, 68041, 68019.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1964-2026%22", "url": "https://recallledger.net/recalls/device-z-1964-2026-philips-mr-7700-with-mr-elastography-mre-1-model-number-ref/"}, {"id": "fda-device-z-1963-2026", "source": "FDA", "category": "device", "recall_number": "Z-1963-2026", "title": "Philips Ingenia Elition X with MR Elastography recall (Philips North America)", "product": "Philips Ingenia Elition X with MR Elastography (MRE). 1. Model Number (REF): 781358. 2. Model Number (REF): 782107. 3. Model Number (REF): 782136. 510(k) Numbers: K213516, K223458, K230972, K232030, K251397, K251808", "reason": "The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.", "hazard_level": "Class II", "company": "Philips North America", "company_location": "Cambridge, MA, United States", "date": "2026-04-14", "report_date": "2026-05-06", "status": "Ongoing", "distribution": "Worldwide - US Nationwide and the countries of Argentina, Australia, Bangladesh, Belgium, Brazil, Canada, Chile, Cuba, Cyprus, Denmark, Ecuador, Egypt, France, Germany, Greece, Hong Kong, India, Indonesia, Iran, Iraq, Israel, Italy, Japan, Kenya, Lebanon, Lithuania, Malta, Mexico, Myanmar, Netherlands, Pakistan, Palestine, Peru, Poland, Portugal, Russian Fed., Singapore, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, United Kingdom.", "states": [], "nationwide": true, "quantity": "103 units", "codes": "1. Model Number (REF): 781358. UDI: (01)00884838088115(21)45121, (01)00884838088115(21)45148, (01)00884838088115(21)45160, (01)00884838088115(21)45438, (01)00884838088115(21)45034, (01)00884838088115(21)45049, (01)00884838088115(21)45066, (01)00884838088115(21)45090, (01)00884838088115(21)45141, (01)00884838088115(21)45149, (01)00884838088115(21)45170, (01)00884838088115(21)45250, (01)00884838088115(21)45290, (01)00884838088115(21)45085, (01)00884838088115(21)45312, (01)00884838088115(21)45376, (01)00884838088115(21)45122, (01)00884838088115(21)45169, (01)00884838088115(21)45191, (01)00884838088115(21)45192, (01)00884838088115(21)45203, (01)00884838088115(21)45204, (01)00884838088115(21)45207, (01)00884838088115(21)45220, (01)00884838088115(21)45228, (01)00884838088115(21)45229, (01)00884838088115(21)45249, (01)00884838088115(21)45278, (01)00884838088115(21)45279, (01)00884838088115(21)45320, (01)00884838088115(21)45028, (01)00884838088115(21)45195, (01)00884838088115(21)45174, (01)00884838088115(21)45165, (01)00884838088115(21)45382, (01)00884838088115(21)45011, (01)00884838088115(21)45055, (01)00884838088115(21)45075, (01)00884838088115(21)45113, (01)00884838088115(21)45147, (01)00884838088115(21)45152, (01)00884838088115(21)45235, (01)00884838088115(21)45237, (01)00884838088115(21)45245, (01)00884838088115(21)45264, (01)00884838088115(21)45269, (01)00884838088115(21)45277, (01)00884838088115(21)45316, (01)00884838088115(21)45322, (01)00884838088115(21)45337, (01)00884838088115(21)45338, (01)00884838088115(21)45353, (01)00884838088115(21)45398, (01)00884838088115(21)45414, (01)00884838088115(21)45429, (01)00884838088115(21)45051. Serial Numbers: 45121, 45148, 45160, 45438, 45034, 45049, 45066, 45090, 45141, 45149, 45170, 45250, 45290, 45085, 45312, 45376, 45122, 45169, 45191, 45192, 45203, 45204, 45207, 45220, 45228, 45229, 45249, 45278, 45279, 45320, 45028, 45195, 45174, 45165, 45382, 45011, 45055, 45075, 45113, 45147, 45152, 45235, 45237, 45245, 45264, 45269, 45277, 45316, 45322, 45337, 45338, 45353, 45398, 45414, 45429, 45051. 2. Model Number (REF): 782107. UDI: (01)00884838098336(21)45590, (01)00884838098336(21)62158, (01)00884838098336(21)62180, (01)00884838098336(21)62044, (01)00884838098336(21)45567, (01)00884838098336(21)62031, (01)00884838098336(21)62166, (01)00884838098336(21)62184, (01)00884838098336(21)62190, (01)00884838098336(21)62240, (01)00884838098336(21)45519, (01)00884838098336(21)45533, (01)00884838098336(21)62024, (01)00884838098336(21)62047, (01)00884838098336(21)62048, (01)00884838098336(21)62051, (01)00884838098336(21)62052, (01)00884838098336(21)45554, (01)00884838098336(21)62145, (01)00884838098336(21)62146, (01)00884838098336(21)62148, (01)00884838098336(21)45500, (01)00884838098336(21)45501, (01)00884838098336(21)45510, (01)00884838098336(21)45511, (01)00884838098336(21)45514, (01)00884838098336(21)45516, (01)00884838098336(21)45518, (01)00884838098336(21)45589, (01)00884838098336(21)62017, (01)00884838098336(21)62039, (01)00884838098336(21)62073, (01)00884838098336(21)62081, (01)00884838098336(21)62088, (01)00884838098336(21)45521, (01)00884838098336(21)45600, (01)00884838098336(21)45563, (01)00884838098336(21)45570, (01)00884838098336(21)62153, (01)00884838098336(21)62181, (01)00884838098336(21)62182, (01)00884838098336(21)62183. Serial Numbers: 45590, 62158, 62180, 62044, 45567, 62031, 62166, 62184, 62190, 62240, 45519, 45533, 62024, 62047, 62048, 62051, 62052, 45554, 62145, 62146, 62148, 45500, 45501, 45510, 45511, 45514, 45516, 45518, 45589, 62017, 62039, 62073, 62081, 62088, 45521, 45600, 45563, 45570, 62153, 62181, 62182, 62183. 3. Model Number (REF): 782136. UDI: (01)00884838108608(21)28568, (01)00884838108608(21)28503, (01)00884838108608(21)28515, (01)00884838108608(21)28528, (01)00884838108608(21)28577. Serial Numbers: 28568, 28503, 28515, 28528, 28577.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1963-2026%22", "url": "https://recallledger.net/recalls/device-z-1963-2026-philips-ingenia-elition-x-with-mr-elastography-mre-1-model-num/"}, {"id": "fda-device-z-1962-2026", "source": "FDA", "category": "device", "recall_number": "Z-1962-2026", "title": "Philips Ingenia Elition S with MR Elastography recall (Philips North America)", "product": "Philips Ingenia Elition S with MR Elastography (MRE). 1. Model Number (REF): 781357. 2. Model Number (REF): 782106. 3. Model Number (REF): 782137.", "reason": "The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.", "hazard_level": "Class II", "company": "Philips North America", "company_location": "Cambridge, MA, United States", "date": "2026-04-14", "report_date": "2026-05-06", "status": "Ongoing", "distribution": "Worldwide - US Nationwide and the countries of Argentina, Australia, Bangladesh, Belgium, Brazil, Canada, Chile, Cuba, Cyprus, Denmark, Ecuador, Egypt, France, Germany, Greece, Hong Kong, India, Indonesia, Iran, Iraq, Israel, Italy, Japan, Kenya, Lebanon, Lithuania, Malta, Mexico, Myanmar, Netherlands, Pakistan, Palestine, Peru, Poland, Portugal, Russian Fed., Singapore, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, United Kingdom.", "states": [], "nationwide": true, "quantity": "6 units", "codes": "1. Model Number (REF): 781357. UDI: (01)00884838088108(21)46002. Serial Numbers: 46002. 2. Model Number (REF): 782106. UDI: (01)00884838098329(21)46243, (01)00884838098329(21)46292, (01)00884838098329(21)46317. Serial Numbers: 46243, 46292, 46317. 3. Model Number (REF): 782137. UDI: (01)00884838108615(21)64034, (01)00884838108615(21)64045. Serial Numbers: 64034, 64045.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1962-2026%22", "url": "https://recallledger.net/recalls/device-z-1962-2026-philips-ingenia-elition-s-with-mr-elastography-mre-1-model-num/"}, {"id": "fda-device-z-1961-2026", "source": "FDA", "category": "device", "recall_number": "Z-1961-2026", "title": "Philips Ingenia Ambition X with MR Elastography recall (Philips North America)", "product": "Philips Ingenia Ambition X with MR Elastography (MRE). 1. Model Number (REF): 781356. 2. Model Number (REF): 782109. 3. Model Number (REF): 782138. 4. Model Number (REF): 782160.", "reason": "The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.", "hazard_level": "Class II", "company": "Philips North America", "company_location": "Cambridge, MA, United States", "date": "2026-04-14", "report_date": "2026-05-06", "status": "Ongoing", "distribution": "Worldwide - US Nationwide and the countries of Argentina, Australia, Bangladesh, Belgium, Brazil, Canada, Chile, Cuba, Cyprus, Denmark, Ecuador, Egypt, France, Germany, Greece, Hong Kong, India, Indonesia, Iran, Iraq, Israel, Italy, Japan, Kenya, Lebanon, Lithuania, Malta, Mexico, Myanmar, Netherlands, Pakistan, Palestine, Peru, Poland, Portugal, Russian Fed., Singapore, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, United Kingdom.", "states": [], "nationwide": true, "quantity": "86 units", "codes": "1. Model Number (REF): 781356. UDI: (01)00884838090040(21)47056, (01)00884838090040(21)47272, (01)00884838090040(21)47189, (01)00884838090040(21)47310, (01)00884838090040(21)47006, (01)00884838090040(21)47029, (01)00884838090040(21)47044, (01)00884838090040(21)47068, (01)00884838090040(21)47196, (01)00884838090040(21)47206, (01)00884838090040(21)47208, (01)00884838090040(21)47237, (01)00884838090040(21)47260, (01)00884838090040(21)47289, (01)00884838090040(21)47291, (01)00884838090040(21)47294, (01)00884838090040(21)47303, (01)00884838090040(21)47305, (01)00884838090040(21)47322, (01)00884838090040(21)47325, (01)00884838090040(21)47330, (01)00884838090040(21)47339, (01)00884838090040(21)47380, (01)00884838090040(21)47387. Serial Numbers: 47056, 47272, 47189, 47310, 47006, 47029, 47044, 47068, 47196, 47206, 47208, 47237, 47260, 47289, 47291, 47294, 47303, 47305, 47322, 47325, 47330, 47339, 47380, 47387. 2. Model Number (REF): 782109. UDI: (01)00884838098350(21)47869, (01)00884838098350(21)47565, (01)00884838098350(21)47644, (01)00884838098350(21)47881, (01)00884838098350(21)47509, (01)00884838098350(21)47919, (01)00884838098350(21)47634, (01)00884838098350(21)47681, (01)00884838098350(21)47706, (01)00884838098350(21)47907, (01)00884838098350(21)47867, (01)00884838098350(21)47550, (01)00884838098350(21)47804, (01)00884838098350(21)47549, (01)00884838098350(21)47635, (01)00884838098350(21)47788, (01)00884838098350(21)47617, (01)00884838098350(21)47566, (01)00884838098350(21)47597, (01)00884838098350(21)47892, (01)00884838098350(21)47893, (01)00884838098350(21)47894, (01)00884838098350(21)47534, (01)00884838098350(21)47538, (01)00884838098350(21)47554, (01)00884838098350(21)47590, (01)00884838098350(21)47642, (01)00884838098350(21)47659, (01)00884838098350(21)47726, (01)00884838098350(21)47760, (01)00884838098350(21)47761, (01)00884838098350(21)47767, (01)00884838098350(21)47771, (01)00884838098350(21)47789, (01)00884838098350(21)47799, (01)00884838098350(21)47814, (01)00884838098350(21)47835, (01)00884838098350(21)47849, (01)00884838098350(21)47862, (01)00884838098350(21)47888, (01)00884838098350(21)47929, (01)00884838098350(21)47931, (01)00884838098350(21)47950, (01)00884838098350(21)47962. Serial Numbers: 47869, 47565, 47644, 47881, 47509, 47919, 47634, 47681, 47706, 47907, 47867, 47550, 47804, 47549, 47635, 47788, 47617, 47566, 47597, 47892, 47893, 47894, 47534, 47538, 47554, 47590, 47642, 47659, 47726, 47760, 47761, 47767, 47771, 47789, 47799, 47814, 47835, 47849, 47862, 47888, 47929, 47931, 47950, 47962. 3. Model Number (REF): 782138. UDI: (01)00884838108622(21)49004, (01)00884838108622(21)49251, (01)00884838108622(21)49045, (01)00884838108622(21)49058, (01)00884838108622(21)49129, (01)00884838108622(21)49153, (01)00884838108622(21)49165, (01)00884838108622(21)49161, (01)00884838108622(21)49205, (01)00884838108622(21)49228, (01)00884838108622(21)49206, (01)00884838108622(21)49057, (01)00884838108622(21)49100, (01)00884838108622(21)49172, (01)00884838108622(21)49210, (01)00884838108622(21)49215, (01)00884838108622(21)49231. Serial Numbers: 49004, 49251, 49045, 49058, 49129, 49153, 49165, 49161, 49205, 49228, 49206, 49057, 49100, 49172, 49210, 49215, 49231. 4. Model Number (REF): 782160. UDI: (01)00884838115712(21)92039. Serial Numbers: 92039.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1961-2026%22", "url": "https://recallledger.net/recalls/device-z-1961-2026-philips-ingenia-ambition-x-with-mr-elastography-mre-1-model-nu/"}, {"id": "fda-device-z-1960-2026", "source": "FDA", "category": "device", "recall_number": "Z-1960-2026", "title": "Philips Ingenia Ambition S with MR Elastography recall (Philips North America)", "product": "Philips Ingenia Ambition S with MR Elastography (MRE). 1. Model Number (REF): 781359. 2. Model Number (REF): 782108. 3. Model Number (REF): 782139.", "reason": "The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.", "hazard_level": "Class II", "company": "Philips North America", "company_location": "Cambridge, MA, United States", "date": "2026-04-14", "report_date": "2026-05-06", "status": "Ongoing", "distribution": "Worldwide - US Nationwide and the countries of Argentina, Australia, Bangladesh, Belgium, Brazil, Canada, Chile, Cuba, Cyprus, Denmark, Ecuador, Egypt, France, Germany, Greece, Hong Kong, India, Indonesia, Iran, Iraq, Israel, Italy, Japan, Kenya, Lebanon, Lithuania, Malta, Mexico, Myanmar, Netherlands, Pakistan, Palestine, Peru, Poland, Portugal, Russian Fed., Singapore, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, United Kingdom.", "states": [], "nationwide": true, "quantity": "7 units", "codes": "1. Model Number (REF): 781359. UDI: (01)00884838090057(21)48218, (01)00884838090057(21)48233. Serial Numbers: 48218, 48233. 2. Model Number (REF): 782108. UDI: (01)00884838098343(21)48652, (01)00884838098343(21)48551, (01)00884838098343(21)48669. Serial Numbers: 48652, 48551, 48669. 3. Model Number (REF): 782139. UDI: (01)00884838108639(21)29076, (01)00884838108639(21)29079. Serial Numbers: 29076, 29079.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1960-2026%22", "url": "https://recallledger.net/recalls/device-z-1960-2026-philips-ingenia-ambition-s-with-mr-elastography-mre-1-model-nu/"}, {"id": "fda-device-z-1959-2026", "source": "FDA", "category": "device", "recall_number": "Z-1959-2026", "title": "Philips Ingenia 3.0T CX with MR Elastography recall (Philips North America)", "product": "Philips Ingenia 3.0T CX with MR Elastography (MRE). 1. Model Number (REF): 781271. 2. Model Number (REF): 782105. 510(k) Numbers: K173079, K183063, K193215, K213583, K223458, K251397, K251808.", "reason": "The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.", "hazard_level": "Class II", "company": "Philips North America", "company_location": "Cambridge, MA, United States", "date": "2026-04-14", "report_date": "2026-05-06", "status": "Ongoing", "distribution": "Worldwide - US Nationwide and the countries of Argentina, Australia, Bangladesh, Belgium, Brazil, Canada, Chile, Cuba, Cyprus, Denmark, Ecuador, Egypt, France, Germany, Greece, Hong Kong, India, Indonesia, Iran, Iraq, Israel, Italy, Japan, Kenya, Lebanon, Lithuania, Malta, Mexico, Myanmar, Netherlands, Pakistan, Palestine, Peru, Poland, Portugal, Russian Fed., Singapore, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, United Kingdom.", "states": [], "nationwide": true, "quantity": "22 units", "codes": "1. Model Number (REF): 781271. UDI: (01)00884838068452(21)78017, (01)00884838068452(21)78013, (01)00884838068452(21)78014, (01)00884838068452(21)78034, (01)00884838068452(21)78058, (01)00884838068452(21)78073, (01)00884838068452(21)78075, (01)00884838068452(21)78092, (01)00884838068452(21)78112, (01)00884838068452(21)78123, (01)00884838068452(21)78201, (01)00884838068452(21)78202, (01)00884838068452(21)78215, (01)00884838068452(21)78217, (01)00884838068452(21)78239, (01)00884838068452(21)78247, (01)00884838068452(21)78260,(01)00884838068452(21)78286, (01)00884838068452(21)78287, (01)00884838068452(21)78026. Serial Numbers: 78017, 78013, 78014, 78034, 78058, 78073, 78075, 78092, 78112, 78123, 78201, 78202, 78215, 78217, 78239, 78247, 78260, 78286, 78287, 78026. 2. Model Number (REF): 782105. UDI: (01)00884838098312(21)78532, (01)00884838098312(21)78576. Serial Numbers: 78532, 78576.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1959-2026%22", "url": "https://recallledger.net/recalls/device-z-1959-2026-philips-ingenia-3-0t-cx-with-mr-elastography-mre-1-model-numbe/"}, {"id": "fda-device-z-1958-2026", "source": "FDA", "category": "device", "recall_number": "Z-1958-2026", "title": "Philips Ingenia 3.0T with MR Elastography recall (Philips North America)", "product": "Philips Ingenia 3.0T with MR Elastography (MRE). 1. Model Number (REF): 781342. 2. Model Number (REF): 781377. 3. Model Number (REF): 782103. 510(k) Numbers: K163116, K173079, K183063, K193215, K213516, K213583, K223458, K251397, K251808", "reason": "The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.", "hazard_level": "Class II", "company": "Philips North America", "company_location": "Cambridge, MA, United States", "date": "2026-04-14", "report_date": "2026-05-06", "status": "Ongoing", "distribution": "Worldwide - US Nationwide and the countries of Argentina, Australia, Bangladesh, Belgium, Brazil, Canada, Chile, Cuba, Cyprus, Denmark, Ecuador, Egypt, France, Germany, Greece, Hong Kong, India, Indonesia, Iran, Iraq, Israel, Italy, Japan, Kenya, Lebanon, Lithuania, Malta, Mexico, Myanmar, Netherlands, Pakistan, Palestine, Peru, Poland, Portugal, Russian Fed., Singapore, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, United Kingdom.", "states": [], "nationwide": true, "quantity": "64 units", "codes": "1. Model Number (REF): 781342. UDI: (01)00884838055339(21)71693, (01)00884838055339(21)71581, (01)00884838055339(21)71582, (01)00884838055339(21)71607, (01)00884838055339(21)85216, (01)00884838055339(21)71106, (01)00884838055339(21)71477, (01)00884838055339(21)71512, (01)00884838055339(21)71966, (01)00884838055339(21)71967, (01)00884838055339(21)85147, (01)00884838055339(21)85224, (01)00884838055339(21)85318, (01)00884838055339(21)71462, (01)00884838055339(21)71619, (01)00884838055339(21)85250, (01)00884838055339(21)71002, (01)00884838055339(21)71037, (01)00884838055339(21)71269, (01)00884838055339(21)71841, (01)00884838055339(21)71885, (01)00884838055339(21)71897, (01)00884838055339(21)85126, (01)00884838055339(21)85109, (01)00884838055339(21)71296, (01)00884838055339(21)71188, (01)00884838055339(21)71088, (01)00884838055339(21)71387, (01)00884838055339(21)71799, (01)00884838055339(21)71040, (01)00884838055339(21)71344, (01)00884838055339(21)71583, (01)00884838055339(21)71916, (01)00884838055339(21)71368, (01)00884838055339(21)71756, (01)00884838055339(21)71822, (01)00884838055339(21)71459, (01)00884838055339(21)71022, (01)00884838055339(21)71185, (01)00884838055339(21)71286, (01)00884838055339(21)71378, (01)00884838055339(21)71646, (01)00884838055339(21)71732, (01)00884838055339(21)71612, (01)00884838055339(21)71340, (01)00884838055339(21)71336. Serial Numbers: 71693, 71581, 71582, 71607, 85216, 71106, 71477, 71512, 71966, 71967, 85147, 85224, 85318, 71462, 71619, 85250, 71002, 71037, 71269, 71841, 71885, 71897, 85126, 85109, 71296, 71188, 71088, 71387, 71799, 71040, 71344, 71583, 71916, 71368, 71756, 71822, 71459, 71022, 71185, 71286, 71378, 71646, 71732, 71612, 71340, 71336. 2. Model Number (REF): 781377. UDI: (01)00884838009813(21)42305, (01)00884838009813(21)42097, (01)00884838009813(21)42364, (01)00884838009813(21)42136, (01)00884838009813(21)42237, (01)00884838009813(21)42455, (01)00884838009813(21)42087, (01)00884838009813(21)42401, (01)00884838009813(21)42321, (01)00884838009813(21)42001, (01)00884838009813(21)42036, (01)00884838009813(21)42053, (01)00884838009813(21)42126, (01)00884838009813(21)42400. Serial Numbers: 42305, 42097, 42364, 42136, 42237, 42455, 42087, 42401, 42321, 42001, 42036, 42053, 42126, 42400. 3. Model Number (REF): 782103. UDI: (01)00884838098299(21)85672, (01)00884838098299(21)85673, (01)00884838098299(21)85674, (01)00884838098299(21)85646. Serial Numbers: 85672, 85673, 85674, 85646.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1958-2026%22", "url": "https://recallledger.net/recalls/device-z-1958-2026-philips-ingenia-3-0t-with-mr-elastography-mre-1-model-number/"}, {"id": "fda-device-z-1957-2026", "source": "FDA", "category": "device", "recall_number": "Z-1957-2026", "title": "Philips Ingenia 1.5T CX with MR Elastography recall (Philips North America)", "product": "Philips Ingenia 1.5T CX with MR Elastography (MRE). 1. Model Number (REF): 781262.", "reason": "The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.", "hazard_level": "Class II", "company": "Philips North America", "company_location": "Cambridge, MA, United States", "date": "2026-04-14", "report_date": "2026-05-06", "status": "Ongoing", "distribution": "Worldwide - US Nationwide and the countries of Argentina, Australia, Bangladesh, Belgium, Brazil, Canada, Chile, Cuba, Cyprus, Denmark, Ecuador, Egypt, France, Germany, Greece, Hong Kong, India, Indonesia, Iran, Iraq, Israel, Italy, Japan, Kenya, Lebanon, Lithuania, Malta, Mexico, Myanmar, Netherlands, Pakistan, Palestine, Peru, Poland, Portugal, Russian Fed., Singapore, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, United Kingdom.", "states": [], "nationwide": true, "quantity": "1 unit", "codes": "1. Model Number (REF): 781262. UDI: (01)00884838068445(21)77144. Serial Numbers: 77144.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1957-2026%22", "url": "https://recallledger.net/recalls/device-z-1957-2026-philips-ingenia-1-5t-cx-with-mr-elastography-mre-1-model-numbe/"}, {"id": "fda-device-z-1956-2026", "source": "FDA", "category": "device", "recall_number": "Z-1956-2026", "title": "Philips Ingenia 1.5T with MR Elastography recall (Philips North America)", "product": "Philips Ingenia 1.5T with MR Elastography (MRE). 1. Model Number (REF): 781315. 2. Model Number (REF): 781341. 3. Model Number (REF): 781396. 4. Model Number (REF): 782115. 510(k) Numbers: K163116, K173079, K183063, K193215, K213583, K223458, K251397, K251808", "reason": "The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.", "hazard_level": "Class II", "company": "Philips North America", "company_location": "Cambridge, MA, United States", "date": "2026-04-14", "report_date": "2026-05-06", "status": "Ongoing", "distribution": "Worldwide - US Nationwide and the countries of Argentina, Australia, Bangladesh, Belgium, Brazil, Canada, Chile, Cuba, Cyprus, Denmark, Ecuador, Egypt, France, Germany, Greece, Hong Kong, India, Indonesia, Iran, Iraq, Israel, Italy, Japan, Kenya, Lebanon, Lithuania, Malta, Mexico, Myanmar, Netherlands, Pakistan, Palestine, Peru, Poland, Portugal, Russian Fed., Singapore, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, United Kingdom.", "states": [], "nationwide": true, "quantity": "54 units", "codes": "1. Model Number (REF): 781315. UDI: (01)00884838099715(21)61067, (01)00884838099715(21)61058, (01)00884838099715(21)61056. Serial Numbers: 61067 61058, 61056. 2. Model Number (REF): 781341. UDI: (01)00884838055322(21)70229, (01)00884838055322(21)84667, (01)00884838055322(21)70311, (01)00884838055322(21)70668, (01)00884838055322(21)70845, (01)00884838055322(21)70851, (01)00884838055322(21)87151, (01)00884838055322(21)87112, (01)00884838055322(21)84322, (01)00884838055322(21)84323, (01)00884838055322(21)84228, (01)00884838055322(21)84789, (01)00884838055322(21)84261, (01)00884838055322(21)84500, (01)00884838055322(21)84556, (01)00884838055322(21)87187, (01)00884838055322(21)84840, (01)00884838055322(21)70685, (01)00884838055322(21)84661, (01)00884838055322(21)70787, (01)00884838055322(21)70063, (01)00884838055322(21)70621, (01)00884838055322(21)70743, (01)00884838055322(21)70911, (01)00884838055322(21)84049, (01)00884838055322(21)84088, (01)00884838055322(21)84147, (01)00884838055322(21)84254, (01)00884838055322(21)84283, (01)00884838055322(21)84403, (01)00884838055322(21)84433, (01)00884838055322(21)84460, (01)00884838055322(21)84462, (01)00884838055322(21)84467, (01)00884838055322(21)84475, (01)00884838055322(21)84734, (01)00884838055322(21)84538. Serial Numbers: 70229, 84667, 70311, 70668, 70845, 70851, 87151, 87112, 84322, 84323, 84228, 84789, 84261, 84500, 84556, 87187, 84840, 70685, 84661, 70787, 70063, 70621, 70743, 70911, 84049, 84088, 84147, 84254, 84283, 84403, 84433, 84460, 84462, 84467, 84475, 84498, 84538. 3. Model Number (REF): 781396. UDI: (01)00884838009820(21)41175, (01)00884838009820(21)41108, (01)00884838009820(21)41395, (01)00884838009820(21)41037, (01)00884838009820(21)41066, (01)00884838009820(21)41098, (01)00884838009820(21)41194, (01)00884838009820(21)41208, (01)00884838009820(21)41354, (01)00884838009820(21)41356, (01)00884838009820(21)41370, (01)00884838009820(21)41552. Serial Numbers: 41175, 41108, 41395, 41037, 41066, 41098, 41194, 41208, 41354, 41356, 41370, 41552. 4. Model Number (REF): 782115. UDI: (01)00884838099043(21)61214, (01)00884838099043(21)61221. Serial Numbers: 61214, 61221.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1956-2026%22", "url": "https://recallledger.net/recalls/device-z-1956-2026-philips-ingenia-1-5t-with-mr-elastography-mre-1-model-number/"}, {"id": "fda-device-z-1955-2026", "source": "FDA", "category": "device", "recall_number": "Z-1955-2026", "title": "Philips Evolution upgrade 3.0T with MR Elastography recall (Philips North America)", "product": "Philips Evolution upgrade 3.0T with MR Elastography (MRE). 1. Model Number (REF): 782143. 2. Model Number (REF): 782162.", "reason": "The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.", "hazard_level": "Class II", "company": "Philips North America", "company_location": "Cambridge, MA, United States", "date": "2026-04-14", "report_date": "2026-05-06", "status": "Ongoing", "distribution": "Worldwide - US Nationwide and the countries of Argentina, Australia, Bangladesh, Belgium, Brazil, Canada, Chile, Cuba, Cyprus, Denmark, Ecuador, Egypt, France, Germany, Greece, Hong Kong, India, Indonesia, Iran, Iraq, Israel, Italy, Japan, Kenya, Lebanon, Lithuania, Malta, Mexico, Myanmar, Netherlands, Pakistan, Palestine, Peru, Poland, Portugal, Russian Fed., Singapore, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, United Kingdom.", "states": [], "nationwide": true, "quantity": "3 units", "codes": "1. Model Number (REF): 782143. UDI: (01)00884838108660(21)42218, (01)00884838108660(21)42225. Serial Numbers: 42218, 42225. 2. Model Number (REF): 782162. UDI: (01)00884838115736(21)71403. Serial Numbers: 71403.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1955-2026%22", "url": "https://recallledger.net/recalls/device-z-1955-2026-philips-evolution-upgrade-3-0t-with-mr-elastography-mre-1-mode/"}, {"id": "fda-device-z-1954-2026", "source": "FDA", "category": "device", "recall_number": "Z-1954-2026", "title": "Philips Evolution Upgrade 1.5T with MR Elastography recall (Philips North America)", "product": "Philips Evolution Upgrade 1.5T with MR Elastography (MRE). 1. Model Number (REF): 782116 2. Model Number (REF): 782148. 3. Model Number (REF): 782166.", "reason": "The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.", "hazard_level": "Class II", "company": "Philips North America", "company_location": "Cambridge, MA, United States", "date": "2026-04-14", "report_date": "2026-05-06", "status": "Ongoing", "distribution": "Worldwide - US Nationwide and the countries of Argentina, Australia, Bangladesh, Belgium, Brazil, Canada, Chile, Cuba, Cyprus, Denmark, Ecuador, Egypt, France, Germany, Greece, Hong Kong, India, Indonesia, Iran, Iraq, Israel, Italy, Japan, Kenya, Lebanon, Lithuania, Malta, Mexico, Myanmar, Netherlands, Pakistan, Palestine, Peru, Poland, Portugal, Russian Fed., Singapore, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, United Kingdom.", "states": [], "nationwide": true, "quantity": "8 units", "codes": "1. Model Number (REF): 782116. UDI: (01)00884838099722(21)41527, (01)00884838099722(21)70949, (01)00884838099722(21)84741. Serial Numbers: 41527, 70949, 84741. 2. Model Number (REF): 782148. UDI: (01)00884838108714(21)84560, (01)00884838108714(21)41277, (01)00884838108714(21)70769, (01)00884838108714(21)70983. Serial Numbers: 84560, 41277, 70769, 70983. 3. Model Number (REF): 782166. UDI: (01)00884838115774(21)70042. Serial Numbers: 70042.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1954-2026%22", "url": "https://recallledger.net/recalls/device-z-1954-2026-philips-evolution-upgrade-1-5t-with-mr-elastography-mre-1-mode/"}, {"id": "fda-device-z-1953-2026", "source": "FDA", "category": "device", "recall_number": "Z-1953-2026", "title": "Philips Achieva 3.0T with MR Elastography recall (Philips North America)", "product": "Philips Achieva 3.0T with MR Elastography (MRE). 1. Model Number (REF): 781278.", "reason": "The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.", "hazard_level": "Class II", "company": "Philips North America", "company_location": "Cambridge, MA, United States", "date": "2026-04-14", "report_date": "2026-05-06", "status": "Ongoing", "distribution": "Worldwide - US Nationwide and the countries of Argentina, Australia, Bangladesh, Belgium, Brazil, Canada, Chile, Cuba, Cyprus, Denmark, Ecuador, Egypt, France, Germany, Greece, Hong Kong, India, Indonesia, Iran, Iraq, Israel, Italy, Japan, Kenya, Lebanon, Lithuania, Malta, Mexico, Myanmar, Netherlands, Pakistan, Palestine, Peru, Poland, Portugal, Russian Fed., Singapore, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, United Kingdom.", "states": [], "nationwide": true, "quantity": "1 unit", "codes": "1. Model Number (REF): 781278. UDI: (01)00884838004139(21)38103. Serial Numbers: 38103.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1953-2026%22", "url": "https://recallledger.net/recalls/device-z-1953-2026-philips-achieva-3-0t-with-mr-elastography-mre-1-model-number/"}, {"id": "fda-device-z-1952-2026", "source": "FDA", "category": "device", "recall_number": "Z-1952-2026", "title": "Philips Achieva 1.5T Initial system with MR Elastography recall (Philips North America)", "product": "Philips Achieva 1.5T Initial system with MR Elastography (MRE). 1. Model Number (REF): 781178.", "reason": "The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.", "hazard_level": "Class II", "company": "Philips North America", "company_location": "Cambridge, MA, United States", "date": "2026-04-14", "report_date": "2026-05-06", "status": "Ongoing", "distribution": "Worldwide - US Nationwide and the countries of Argentina, Australia, Bangladesh, Belgium, Brazil, Canada, Chile, Cuba, Cyprus, Denmark, Ecuador, Egypt, France, Germany, Greece, Hong Kong, India, Indonesia, Iran, Iraq, Israel, Italy, Japan, Kenya, Lebanon, Lithuania, Malta, Mexico, Myanmar, Netherlands, Pakistan, Palestine, Peru, Poland, Portugal, Russian Fed., Singapore, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, United Kingdom.", "states": [], "nationwide": true, "quantity": "1 unit", "codes": "1. Model Number (REF): 781178. UDI: None. Serial Numbers: 20088.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1952-2026%22", "url": "https://recallledger.net/recalls/device-z-1952-2026-philips-achieva-1-5t-initial-system-with-mr-elastography-mre-1/"}, {"id": "fda-device-z-1951-2026", "source": "FDA", "category": "device", "recall_number": "Z-1951-2026", "title": "Philips Achieva 1.5T with MR Elastography recall (Philips North America)", "product": "Philips Achieva 1.5T with MR Elastography (MRE). 1. Model Number (REF): 781196. 2. Model Number (REF): 781296.", "reason": "The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.", "hazard_level": "Class II", "company": "Philips North America", "company_location": "Cambridge, MA, United States", "date": "2026-04-14", "report_date": "2026-05-06", "status": "Ongoing", "distribution": "Worldwide - US Nationwide and the countries of Argentina, Australia, Bangladesh, Belgium, Brazil, Canada, Chile, Cuba, Cyprus, Denmark, Ecuador, Egypt, France, Germany, Greece, Hong Kong, India, Indonesia, Iran, Iraq, Israel, Italy, Japan, Kenya, Lebanon, Lithuania, Malta, Mexico, Myanmar, Netherlands, Pakistan, Palestine, Peru, Poland, Portugal, Russian Fed., Singapore, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, United Kingdom.", "states": [], "nationwide": true, "quantity": "3 units", "codes": "1. Model Number (REF): 781196. UDI: None. Serial Numbers: 21957. 2. Model Number (REF): 781296. UDI: (01)00884838004108(21)32039, (01)00884838004108(21)32095. Serial Numbers: 32039, 32095.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1951-2026%22", "url": "https://recallledger.net/recalls/device-z-1951-2026-philips-achieva-1-5t-with-mr-elastography-mre-1-model-number/"}, {"id": "cpsc-26458", "source": "CPSC", "category": "consumer-product", "recall_number": "26458", "title": "American Honda Motor Recalls Off-Road Motorcycles Due to Risk of Serious Injury or Death Due to Crash Hazard", "product": "Model Year 2025-2026 CRF250R/RX/RWE and CRF450R/RX/RWE Off-Road Motorcycles", "reason": "The handlebar's clamp can unexpectedly cause the handlebar to rotate, posing a risk of serious injury or death due to a crash hazard.", "hazard_level": null, "company": "American Honda Motor Co. Inc, of Torrance, California", "company_location": "Japan", "date": "2026-04-30", "report_date": "2026-05-01", "status": "Announced", "distribution": "Sold in the United States at Authorized Honda Powersports dealers nationwide from June 2024 through March 2026 for between $8,900 and $13,200.", "states": [], "nationwide": true, "quantity": "About 12,600 (In addition, about six were sold in Canada)", "codes": "", "remedy": "Consumers should stop using the recalled off-road motorcycles immediately and contact an authorized Honda Powersports dealer to schedule an appointment for a free inspection and if necessary, a replacement of the handlebar's clamp at the dealer's location. Repair Replace", "retailers": ["Authorized Honda Powersports dealers nationwide from June 2024 through March 2026 for between $8,900 and $13,200."], "injuries": "The firm has received one report of a crash. No injuries have been reported.", "source_url": "https://www.cpsc.gov/Recalls/2026/American-Honda-Motor-Recalls-Off-Road-Motorcycles-Due-to-Risk-of-Serious-Injury-or-Death-Due-to-Crash-Hazard", "url": "https://recallledger.net/recalls/product-26458-american-honda-motor-recalls-off-road-motorcycles-due-to-risk-of-serio/"}, {"id": "cpsc-26457", "source": "CPSC", "category": "consumer-product", "recall_number": "26457", "title": "Build-A-Bear Workshop Recalls Heartwarming Hugs Bears Due to Risk of Serious Injury or Death from Choking Hazard to Children", "product": "Build-A-Bear Workshop Heartwarming Hugs Bears", "reason": "The zipper slider on the side pouch can detach, posing a risk of serious injury or death from choking hazard to children.", "hazard_level": null, "company": "Build-A-Bear Workshop, Inc., of St Louis, Missouri", "company_location": "China", "date": "2026-04-30", "report_date": "2026-05-01", "status": "Announced", "distribution": "Sold in the United States at Build-A-Bear Workshop stores and online at www.buildabear.com from January 2026 through March 2026 for about $48.", "states": [], "nationwide": true, "quantity": "About 36,000 (In addition 520 were sold in Canada)", "codes": "", "remedy": "Consumers should immediately stop using the recalled Heartwarming Hugs Bear and return it to a local Build-A-Bear Workshop store to receive a refund in the form of original payment or a gift card for the original purchase price redeemable toward any available Make-Your-Own furry friend and any other available merchandise. If a consumer is unable to return their Heartwarming Hugs Bear to a local store, they can visit www.buildabear.com/recalls for more information or call Build-A-Bear to receive a free return shipping label to return the recalled bear and to receive a refund check in the form of original payment or in the form of a digital gift card to use on the firm's website. Refund Replace", "retailers": ["Build-A-Bear Workshop stores and online at www.buildabear.com from January 2026 through March 2026 for about $48."], "injuries": "There has been one consumer report in the United Kingdom of the zipper slider detaching while in use, and no reports in the United States. No injuries have been reported.", "source_url": "https://www.cpsc.gov/Recalls/2026/Build-A-Bear-Workshop-Recalls-Heartwarming-Hugs-Bears-Due-to-Risk-of-Serious-Injury-or-Death-from-Choking-Hazard-to-Children", "url": "https://recallledger.net/recalls/product-26457-build-a-bear-workshop-recalls-heartwarming-hugs-bears-due-to-risk-of-s/"}, {"id": "cpsc-26456", "source": "CPSC", "category": "consumer-product", "recall_number": "26456", "title": "CBC Group Recalls Stephan Baby Boo Bunnie and Friends Children's Toys Due to Risk of Serious Injury from Choking and Laceration Hazards", "product": "Stephan Baby Boo Bunnie and Friends Children's Toys", "reason": "The toys' plastic cube can break into small parts or sharp edges, posing a risk of serious injury from choking and laceration hazards.", "hazard_level": null, "company": "CBC Group, Inc., of Phoenix, Arizona", "company_location": "China", "date": "2026-04-30", "report_date": "2026-05-01", "status": "Announced", "distribution": "Sold in the United States at Independent stores nationwide and online at Stephanbaby.com, Amazon.com, Walmart.com, Target.com and other websites from August 2017 through January 2026 for between $9 and $2.", "states": [], "nationwide": true, "quantity": "About 227,500 (In addition, about 1,400 were sold in Canada)", "codes": "", "remedy": "Consumers should immediately stop using the recalled toys' plastic cube and take it away from children. Consumers should contact Stephan Baby for a refund or store credit. Consumers with proof of purchase will receive a full refund. Consumers without proof of purchase will receive a $10 refund in the form of a check or a $20 stephanbaby.com store credit. Consumers will be asked to write in permanent marker \"Recalled\" on the indented area of the cube and upload a photo of the toy and the marked cube to https://recall.stephanbaby.com/ to receive a pre-paid shipping return label for the cube. Refund", "retailers": ["Independent stores nationwide and online at Stephanbaby.com, Amazon.com, Walmart.com, Target.com and other websites from August 2017 through January 2026 for between $9 and $2."], "injuries": "CPSC has received 20 reports of the toys' cube cracking or breaking into small parts, including one that resulted in a child swallowing sharp pieces.", "source_url": "https://www.cpsc.gov/Recalls/2026/CBC-Group-Recalls-Stephan-Baby-Boo-Bunnie-and-Friends-Childrens-Toys-Due-to-Risk-of-Serious-Injury-from-Choking-and-Laceration-Hazards", "url": "https://recallledger.net/recalls/product-26456-cbc-group-recalls-stephan-baby-boo-bunnie-and-friends-children-s-toys/"}, {"id": "cpsc-26455", "source": "CPSC", "category": "consumer-product", "recall_number": "26455", "title": "Bayer Recalls 6 mL Size Afrin Original Nasal Spray Bottles Due to Risk of Serious Injury or Illness from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging", "product": "Travel Size Afrin® Original Nasal Spray 6 mL Bottles", "reason": "The 6 mL nasal sprays contain an imidazoline, which must be in child-resistant packaging or meet the labeling requirements for non-complying packaging, as required by the Poison Prevention Packaging Act. The 6 mL nasal spray's packaging is not child-resistant nor bears the required labeling statement, posing a risk of serious injury or illness from poisoning, if the contents are swallowed by young children.", "hazard_level": null, "company": "Bayer HealthCare LLC, of Whippany, New Jersey", "company_location": "Germany", "date": "2026-04-30", "report_date": "2026-05-01", "status": "Announced", "distribution": "Sold in the United States at Retailers such as convenience stores and travel hubs including airports from September 2024 to April 2026 for about $7 to $9.", "states": [], "nationwide": true, "quantity": "About 786,100", "codes": "", "remedy": "Consumers should immediately secure the recalled bottles out of sight and reach of children and go to the webform posted on www.livewell.bayer.com/afrin-original-spray-recall to begin a request for a refund. Consumers will be asked to take and submit a photo of the product before disposing of it in order to receive a refund. Refund", "retailers": ["Retailers such as convenience stores and travel hubs including airports from September 2024 to April 2026 for about $7 to $9."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/Bayer-Recalls-6-mL-Size-Afrin-Original-Nasal-Spray-Bottles-Due-to-Risk-of-Serious-Injury-or-Illness-from-Child-Poisoning-Violates-Mandatory-Standard-for-Child-Resistant-Packaging", "url": "https://recallledger.net/recalls/product-26455-bayer-recalls-6-ml-size-afrin-original-nasal-spray-bottles-due-to-risk/"}, {"id": "cpsc-26454", "source": "CPSC", "category": "consumer-product", "recall_number": "26454", "title": "Qumeney Bicycle Light Sets Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Button Cell Batteries; Sold on Amazon by Smfanlus", "product": "Qumeney Bicycle Light Sets", "reason": "The recalled bicycle lights violate the mandatory standard for consumer products with button cell and coin batteries because they contain button cell batteries that can be accessed easily by children, posing an ingestion hazard. Additionally, the bicycle lights do not have the warnings required under Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns, and death.", "hazard_level": null, "company": "Xiamen Fanlu Technology Co., Ltd., doing business as Smfanlus, of China", "company_location": "China", "date": "2026-04-30", "report_date": "2026-05-01", "status": "Announced", "distribution": "Sold in the United States at Online at Amazon.com from March 2024 through February 2026 for between $7 and $10 (6-pack) and between $15 and $18 (24-pack).", "states": [], "nationwide": true, "quantity": "About 2,800", "codes": "", "remedy": "Consumers should stop using the recalled bicycle lights immediately and contact Smfanlus for a full refund. Consumers will be asked to remove and properly dispose of the batteries and send a photo of the destroyed pieces of the light components to qumeneybicyclelightsrecall@outlook.com to receive a full refund. Note: Button cell batteries are hazardous. Batteries should be disposed of or recycled by following local hazardous waste procedures. Refund", "retailers": ["Online at Amazon.com from March 2024 through February 2026 for between $7 and $10 (6-pack) and between $15 and $18 (24-pack)."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/Qumeney-Bicycle-Light-Sets-Recalled-Due-to-Risk-of-Serious-Injury-or-Death-from-Battery-Ingestion-Violates-Mandatory-Standard-for-Consumer-Products-with-Button-Cell-Batteries-Sold-on-Amazon-by-Smfanlus", "url": "https://recallledger.net/recalls/product-26454-qumeney-bicycle-light-sets-recalled-due-to-risk-of-serious-injury-or-d/"}, {"id": "cpsc-26453", "source": "CPSC", "category": "consumer-product", "recall_number": "26453", "title": "Acer America Corporation Recalls Two-Wheeled Folding Electric Due to Risk of Injury from Fall Hazard", "product": "Acer AES015 Two-Wheeled Folding Electric Scooters", "reason": "A loose screw can cause the front tube to fold down unexpectedly, posing a risk of injury from a fall hazard.", "hazard_level": null, "company": "Acer America Corporation, of Irvine, California", "company_location": "China", "date": "2026-04-30", "report_date": "2026-05-01", "status": "Announced", "distribution": "Sold in the United States at Online at Acer.com, Amazon.com and in stores at BrandMart from between June 2023 and February 2026 for between $245 and $70.", "states": [], "nationwide": true, "quantity": "About 510 (In addition, about 311 were sold in Canada and about 150 were sold in Mexico)", "codes": "", "remedy": "Consumers should stop using the recalled folding electric scooter immediately and contact Acer at https://www.acer.com/us-en/support/alerts-recalls for instructions on how to tighten the screw. Free repair tools will be available to consumers upon request. Repair", "retailers": ["Online at Acer.com, Amazon.com and in stores at BrandMart from between June 2023 and February 2026 for between $245 and $70."], "injuries": "None reported in the United States (and one report of the tube folding down resulting in a fall and minor abrasions internationally).", "source_url": "https://www.cpsc.gov/Recalls/2026/Acer-America-Corporation-Recalls-Two-Wheeled-Folding-Electric-Scooters-Due-to-Risk-of-Injury-from-Fall-Hazard", "url": "https://recallledger.net/recalls/product-26453-acer-america-corporation-recalls-two-wheeled-folding-electric-due-to-r/"}, {"id": "cpsc-26452", "source": "CPSC", "category": "consumer-product", "recall_number": "26452", "title": "Pressure Washers Recalled Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards; Imported by DGIVOVO US", "product": "DGIVOVO US Electric Pressure Washers", "reason": "The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI), posing a serious risk of injury or death from shock and electrocution hazards.", "hazard_level": null, "company": "Ningbopingyao E-Commerce Ltd., dba DGIVOVO US, of China", "company_location": "China", "date": "2026-04-30", "report_date": "2026-05-01", "status": "Announced", "distribution": "Sold in the United States at Online at Amazon.com from October 2025 through January 2026 for about $90.", "states": [], "nationwide": true, "quantity": "50", "codes": "", "remedy": "Consumers should immediately stop using the recalled pressure washers and contact DGIVOVO US for a free replacement pressure washer of at least equal value to the recalled pressure washer, including shipping. Consumers will be asked to destroy the pressure washer by unplugging it and cutting the power cord in half and send a photo of the destroyed power washer to dgivovo@163.com. Consumers should then dispose of the destroyed recalled product. Replace", "retailers": ["Online at Amazon.com from October 2025 through January 2026 for about $90."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/Pressure-Washers-Recalled-Due-to-Serious-Risk-of-Injury-or-Death-from-Shock-and-Electrocution-Hazards-Imported-by-DGIVOVO-US", "url": "https://recallledger.net/recalls/product-26452-pressure-washers-recalled-due-to-serious-risk-of-injury-or-death-from/"}, {"id": "cpsc-26451", "source": "CPSC", "category": "consumer-product", "recall_number": "26451", "title": "Earthtec Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violates Virginia Graeme Baker Pool & Spa Safety Act; Manufactured by Tonyidea", "product": "Earthtec 7 3/8 Inch Pool Drain Covers", "reason": "The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing entrapment and drowning hazards to swimmers and bathers.", "hazard_level": null, "company": "Shenzhen Qiangonghui Technology Co., Ltd., dba Tonyidea", "company_location": "China", "date": "2026-04-30", "report_date": "2026-05-01", "status": "Announced", "distribution": "Sold in the United States at Online at Amazon.com from October 2025 through April 2026 for about $15.", "states": [], "nationwide": true, "quantity": "About 211", "codes": "", "remedy": "Pool owners, pool operators and consumers should stop using pools with the recalled pool drain covers immediately. To receive a refund, consumers should remove the drain cover from the pool, and destroy it, take a photo of the removed cover, and send it to Tonyidea by email at earthtecrecall@outlook.com. Ensure all pools and spas have VGBA-compliant drain covers and teach children to stay away from drains. Refund", "retailers": ["Online at Amazon.com from October 2025 through April 2026 for about $15."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/Earthtec-Pool-Drain-Covers-Recalled-Due-to-Risk-of-Serious-Injury-or-Death-from-Entrapment-and-Drowning-Hazards-Violates-Virginia-Graeme-Baker-Pool-Spa-Safety-Act-Manufactured-by-Tonyidea", "url": "https://recallledger.net/recalls/product-26451-earthtec-pool-drain-covers-recalled-due-to-risk-of-serious-injury-or-d/"}, {"id": "cpsc-26450", "source": "CPSC", "category": "consumer-product", "recall_number": "26450", "title": "Residential Elevators Recalls Elevator StrikeLock Hoistway Door Locking Device Due to Risk of Serious Injury or Death from Fall and Injury Hazards", "product": "Residential Elevators StrikeLock Hoistway Door Locking Device", "reason": "The elevator's StrikeLock hoistway door locking device can allow the elevator cab to move with a landing door open, posing a risk of serious injury or death due to fall and injury hazards.", "hazard_level": null, "company": "Residential Elevators, Inc., of Crawfordville, Florida", "company_location": "United States", "date": "2026-04-30", "report_date": "2026-05-01", "status": "Announced", "distribution": "Sold in the United States at Residential Elevators and authorized elevator dealers nationwide from April 2024 through March 2026 for about $1,000.", "states": [], "nationwide": true, "quantity": "About 450", "codes": "", "remedy": "Consumers should immediately stop using the residential elevator systems where StrikeLock hoistway door locking devices are installed and contact Residential Elevators or the local elevator dealer that installed their residential elevator system to schedule a free repair of their StrikeLock hoistway door locking devices. Consumers should contact Residential Elevators or the local elevator dealer that installed their residential elevator system if they are uncertain whether their residential elevator has a StrikeLock hoistway door locking device installed. Repair", "retailers": ["Residential Elevators and authorized elevator dealers nationwide from April 2024 through March 2026 for about $1,000."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/Residential-Elevators-Recalls-Elevator-StrikeLock-Hoistway-Door-Locking-Device-Due-to-Risk-of-Serious-Injury-or-Death-from-Fall-and-Injury-Hazards", "url": "https://recallledger.net/recalls/product-26450-residential-elevators-recalls-elevator-strikelock-hoistway-door-lockin/"}, {"id": "cpsc-26449", "source": "CPSC", "category": "consumer-product", "recall_number": "26449", "title": "Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails; Imported by Hepo Care Medical Equipment Online", "product": "Hepo Adult Portable Bed Rails", "reason": "The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. The bed rails also do not meet structural stability or retention strap requirements, posing a fall hazard. The bed rails' push pins and push pin holes are incorrectly sized, posing a laceration hazard. In addition, the bed rails do not bear the required hazard warning labels.", "hazard_level": null, "company": "Mobility Source Medical Technology Co., Ltd. of China", "company_location": "China", "date": "2026-04-30", "report_date": "2026-05-01", "status": "Announced", "distribution": "Sold in the United States at Online at Walmart.com from November 2025 through January 2026 for about $100 Amazon.com from June 2025 through January 2026 for between $35 and $40.", "states": [], "nationwide": true, "quantity": "About 2,200", "codes": "", "remedy": "Consumers should stop using the recalled adult portable bed rails immediately and contact Hepo Care Medical Equipment Online for a full refund. Consumers will be asked to destroy the bed rails by dismantling the bed rails, cutting off the storage bag and writing \"RECALLED\" on the upper and lower rails with permanent marker, take a photo of the destroyed rails and upload the photo to www.hepolife.com/bed-rail-safety-recall or email the photo to manager@lqxmedical.com. Refund", "retailers": ["Online at Walmart.com from November 2025 through January 2026 for about $100 Amazon.com from June 2025 through January 2026 for between $35 and $40."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/Adult-Portable-Bed-Rails-Recalled-Due-to-Risk-of-Serious-Injury-or-Death-from-Entrapment-and-Asphyxiation-Violate-Mandatory-Standard-for-Adult-Portable-Bed-Rails-Imported-by-Hepo-Care-Medical-Equipment-Online", "url": "https://recallledger.net/recalls/product-26449-adult-portable-bed-rails-recalled-due-to-risk-of-serious-injury-or-dea/"}, {"id": "cpsc-26448", "source": "CPSC", "category": "consumer-product", "recall_number": "26448", "title": "5-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory Standard for Clothing Storage Units; Imported by UHOMEPRO", "product": "UHOMEPRO 5-Drawer Dressers", "reason": "The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or death to children. The dressers violate the mandatory safety standard as required by the STURDY Act.", "hazard_level": null, "company": "UHOMEPRO Inc., of China", "company_location": "China", "date": "2026-04-30", "report_date": "2026-05-01", "status": "Announced", "distribution": "Sold in the United States at Online at Walmart.com from November 2025 through January 2026 for about $100.", "states": [], "nationwide": true, "quantity": "About 5,190", "codes": "", "remedy": "Consumers should immediately stop using the recalled dressers if they are not anchored to the wall and place them in an area that children cannot access. Contact UHOMEPRO for instructions on how to identify affected units and dispose of the dressers to receive a full refund. Consumers will be asked to write the word \"recalled\" on the top and all sides of the dresser with a permanent marker and to submit a photo to uhomeprorecall@outlook.com demonstrating disposal of the product. Refund", "retailers": ["Online at Walmart.com from November 2025 through January 2026 for about $100."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/5-Drawer-Dressers-Recalled-Due-to-Risk-of-Serious-Injury-or-Death-from-Tip-Over-and-Entrapment-Hazards-Violates-Mandatory-Standard-for-Clothing-Storage-Units-Imported-by-UHOMEPRO", "url": "https://recallledger.net/recalls/product-26448-5-drawer-dressers-recalled-due-to-risk-of-serious-injury-or-death-from/"}, {"id": "cpsc-26447", "source": "CPSC", "category": "consumer-product", "recall_number": "26447", "title": "Malker Bicycle Light Sets Recalled Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violates Mandatory Standard for Consumer Products with Button Cell Batteries; Sold on Amazon by MalkerDirect", "product": "Malker Bicycle Light Sets", "reason": "The recalled bicycle lights violate the mandatory standard for consumer products with button cell and coin batteries because they contain button cell batteries that can be accessed easily by children, posing an ingestion hazard. Additionally, the bicycle lights do not have the warnings required under Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.", "hazard_level": null, "company": "Shenzhen Maikeer Industrial Co., Ltd., doing business as MalkerDirect, of China", "company_location": "China", "date": "2026-04-30", "report_date": "2026-05-01", "status": "Announced", "distribution": "Sold in the United States at Online at Amazon.com from October 2025 through November 2025 for between $7 and $10.", "states": [], "nationwide": true, "quantity": "About 7,000", "codes": "", "remedy": "Consumers should stop using the recalled bicycle lights immediately and contact MalkerDirect for a full refund. Consumers should throw the bicycle lights away and send a photo of the product in the trash to USMalkerCustomerservice@outlook.com. Note: Button cell batteries are hazardous. Batteries should be disposed of or recycled by following local hazardous waste procedures. Refund", "retailers": ["Online at Amazon.com from October 2025 through November 2025 for between $7 and $10."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/Malker-Bicycle-Light-Sets-Recalled-Due-to-Risk-of-Serious-Injury-or-Death-from-Battery-Ingestion-Hazard-Violates-Mandatory-Standard-for-Consumer-Products-with-Button-Cell-Batteries-Sold-on-Amazon-by-MalkerDirect", "url": "https://recallledger.net/recalls/product-26447-malker-bicycle-light-sets-recalled-due-to-risk-of-serious-injury-or-de/"}, {"id": "cpsc-26446", "source": "CPSC", "category": "consumer-product", "recall_number": "26446", "title": "Segmart 4-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment; Violate Mandatory Standard for Clothing Storage Units; Sold on Walmart.com by SOFT", "product": "Segmart 4-Drawer Dressers", "reason": "The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or death to children. The dressers violate the mandatory safety standard as required by the STURDY Act.", "hazard_level": null, "company": "SOFT INC., of Denver, Colorado", "company_location": "China, United Arab Emirates", "date": "2026-04-30", "report_date": "2026-05-01", "status": "Announced", "distribution": "Sold in the United States at Online at Walmart from January 2025 through March 2026 for about $80.", "states": [], "nationwide": true, "quantity": "About 16,440", "codes": "", "remedy": "Consumers should immediately stop using the recalled dressers if they are not anchored to the wall and place them in an area that children cannot access. Contact SOFT for instructions on how to identify affected units and dispose of the dressers to receive a full refund. Consumers will be asked to submit a photo to segmartdresserecall@outlook.com demonstrating disposal of the product. Refund", "retailers": ["Online at Walmart from January 2025 through March 2026 for about $80."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/Segmart-4-Drawer-Dressers-Recalled-Due-to-Risk-of-Serious-Injury-or-Death-from-Tip-Over-and-Entrapment-Violate-Mandatory-Standard-for-Clothing-Storage-Units-Sold-on-Walmart-com-by-SOFT", "url": "https://recallledger.net/recalls/product-26446-segmart-4-drawer-dressers-recalled-due-to-risk-of-serious-injury-or-de/"}, {"id": "cpsc-26445", "source": "CPSC", "category": "consumer-product", "recall_number": "26445", "title": "Alliance Chemical Recalls 1-K Kerosene Heater Fluid Containers Due to Risk of Serious Injury or Death from Flash Fire, Burn and Child Poisoning; Violates Mandatory Standards for Portable Fuel Containers", "product": "1-K Kerosene Heater Fluid Portable Fuel Containers", "reason": "The pre-filled fuel containers violate the mandatory safety standards for portable fuel containers because they lack flame mitigation devices required under the Portable Fuel Container Safety Act, posing a deadly risk of flash fire. In addition, the Children's Gasoline Burn Prevention Act requires all closures on portable kerosene fuel containers to be child-resistant. The container is not child-resistant, posing a risk of burn and poisoning to children.", "hazard_level": null, "company": "Alliance Chemical, of Taylor, Texas", "company_location": "United States", "date": "2026-04-30", "report_date": "2026-05-01", "status": "Announced", "distribution": "Sold in the United States at Online at Amazon.com and AllianceChemical.com from January 2023 through March 2026 for between $18 and $102 depending on the size.", "states": [], "nationwide": true, "quantity": "About 30,155", "codes": "", "remedy": "Consumers should stop using the recalled fuel containers immediately, place them out of reach of children and contact Alliance Chemical for a full refund. Consumers will be asked to provide a dated photo of the product and dispose of the fuel following local hazardous waste procedures. Note: Kerosene fuel is hazardous. Fuel containers should be disposed of or recycled by following local hazardous waste procedures. Refund", "retailers": ["Online at Amazon.com and AllianceChemical.com from January 2023 through March 2026 for between $18 and $102 depending on the size."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/Alliance-Chemical-Recalls-1-K-Kerosene-Heater-Fluid-Containers-Due-to-Risk-of-Serious-Injury-or-Death-from-Flash-Fire-Burn-and-Child-Poisoning-Violates-Mandatory-Standards-for-Portable-Fuel-Containers", "url": "https://recallledger.net/recalls/product-26445-alliance-chemical-recalls-1-k-kerosene-heater-fluid-containers-due-to/"}, {"id": "cpsc-26444", "source": "CPSC", "category": "consumer-product", "recall_number": "26444", "title": "Thermos Recalls 8.2 Million Stainless King Food Jars and Bottles Due to Serious Impact Injury and Laceration Hazards", "product": "Thermos Stainless King 3000 and 3020 Food Jars and Thermos Sportsman 3010 Food & Beverage Bottles", "reason": "If perishable food or beverages are stored in the container for an extended period of time, the stopper can forcefully eject when opened, which can result in serious impact injury and laceration hazards to the consumer.", "hazard_level": null, "company": "Thermos L.L.C., of Schaumburg, Illinois", "company_location": "China, Malaysia", "date": "2026-04-30", "report_date": "2026-05-01", "status": "Announced", "distribution": "Sold in the United States at Target, Walmart and other stores nationwide and online at Amazon.com, Walmart.com, Target.com and Thermos.com between around March 2008 and July 2024 for about $30.", "states": [], "nationwide": true, "quantity": "About 5.8 million Stainless King Food Jars and about 2.3 million Sportsman Food & Beverage Bottles", "codes": "", "remedy": "Consumers should stop using the recalled Food Jars and Bottles immediately and contact Thermos to receive a free replacement pressure relief stopper or replacement Bottle, depending on the model. For recalled 3000 and 3020 Food Jars, consumers will be asked to throw away the stopper and send a photo of the disposed stopper to Thermos. For recalled 3010 Bottles, consumers will be asked to return their recalled Bottle to Thermos using a prepaid shipping label. Replace", "retailers": ["Target, Walmart and other stores nationwide and online at Amazon.com, Walmart.com, Target.com and Thermos.com between around March 2008 and July 2024 for about $30."], "injuries": "Thermos has received 27 reports of consumers who were struck by a stopper that forcefully ejected from these containers upon opening, including complaints of impact and laceration injuries requiring medical attention. Three consumers suffered permanent vision loss after being struck in the eye.", "source_url": "https://www.cpsc.gov/Recalls/2026/Thermos-Recalls-8-2-Million-Stainless-King-Food-Jars-and-Bottles-Due-to-Serious-Impact-Injury-and-Laceration-Hazards", "url": "https://recallledger.net/recalls/product-26444-thermos-recalls-8-2-million-stainless-king-food-jars-and-bottles-due-t/"}, {"id": "fda-food-h-0682-2026", "source": "FDA", "category": "food", "recall_number": "H-0682-2026", "title": "Kirkland Signature Traditional Madeleines 12 Count/net wt. 18oz. recall (Costco Wholesale Corporation)", "product": "Kirkland Signature Traditional Madeleines 12 Count/net wt. 18oz., Item #2000012, UPC 000020000127. Plastic clamshell container is packed with 9 pieces of Filled Heart Madeleines. Distributed by Costco Wholesale Corp. Seattle, WA. Label of recalled package is read in part: TRADITIONAL MADELEINES***INGREDIENTS: WHEAT FLOUR **EGGS, BUTTER (CREAM) ***ALLERGEN INFORMATION: CONTAINS WHEAT, EGG, MILK*** PRODUCED ON EQUIPMENT THAT ALSO PROCESSES PEANUTS, TREE NUTS AND SESAME***.", "reason": "Undeclared hazelnut and soy lecithin.", "hazard_level": "Class I", "company": "Costco Wholesale Corporation", "company_location": "Issaquah, WA, United States", "date": "2026-04-06", "report_date": "2026-04-29", "status": "Terminated", "distribution": "Distributed in CA, CO, FL, IL, MT, VA, WA, WI, and in Puerto Rico.", "states": ["CA", "CO", "FL", "IL", "MT", "PR", "VA", "WA", "WI"], "nationwide": false, "quantity": "92 units", "codes": "Pack Date: 3/30/26 to 4/6/26 Sell By: 04/2/26 to 4/9/26", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0682-2026%22", "url": "https://recallledger.net/recalls/food-h-0682-2026-kirkland-signature-traditional-madeleines-12-count-net-wt-18oz-item/"}, {"id": "fda-food-h-0674-2026", "source": "FDA", "category": "food", "recall_number": "H-0674-2026", "title": "EL MEXICANO agua fresca de horchata Instant Horchata Drink recall (Marquez Brothers International, Inc.)", "product": "EL MEXICANO agua fresca de horchata Instant Horchata Drink NET WT 12oz (340g) INGREDIENTS: *** MILK SUBSTITUTE (WHEY *** LACTOSE *** DISTRIBUTED BY MARQUEZ BROTHERS INTERNATIONAL, INC. San Jose CA 95138 UPC: 042743190204 Item: 102279", "reason": "Undeclared milk.", "hazard_level": "Class II", "company": "Marquez Brothers International, Inc.", "company_location": "Fresno, CA, United States", "date": "2026-04-07", "report_date": "2026-04-29", "status": "Ongoing", "distribution": "Domestic distribution: AK, AL, AR, AZ, CA, CO, FL, IA, ID, IL, IN, KS, LA, MI, MN, MO, MT, NE, NM, NV, OH, OK, OR, TN, TX, UT, VA, WA, WI. Foreign distribution: Canada, Japan.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "FL", "IA", "ID", "IL", "IN", "KS", "LA", "MI", "MN", "MO", "MT", "NE", "NM", "NV", "OH", "OK", "OR", "TN", "TX", "UT", "VA", "WA", "WI"], "nationwide": false, "quantity": "405,136 packages (16 packages/case; 25,321 cases)", "codes": "Lot, Expiration: HR02324, 01/26/26; HR02324, 01/29/26; HR06424, 03/07/26; HR09924, 04/09/26; HR10024, 04/10/26; HR12924, 05/09/26; HR13024, 05/13/26; HR13024, 05/14/26; HR16424, 06/13/26; HR17824, 06/27/26; HR17824, 06/28/26; HR21124, 07/30/26; HR21224, 07/31/26; HR23524, 08/26/26; HR23624, 08/27/26; HR26724, 09/25/26; HR29724, 10/24/26; HR29824, 10/25/26; HR29924, 11/19/26; HR32424, 11/20/26; HR02225, 01/23/27; HR02225, 01/24/27; HR05825, 03/05/27; HR05925, 03/06/27; HR08625, 03/28/27; HR08625, 03/31/27; HR08725, 04/01/27; HR15725, 06/09/27; HR16025, 06/10/27; HR16225, 06/12/27; HR16325, 06/13/27; HR19125, 07/11/27; HR19225, 07/15/27; HR23325, 08/22/27; HR23225, 08/21/27; HR27925, 10/08/27; HR28225, 10/13/27; HR34425, 12/15/27; HR34525, 12/16/27.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0674-2026%22", "url": "https://recallledger.net/recalls/food-h-0674-2026-el-mexicano-agua-fresca-de-horchata-instant-horchata-drink-net-wt-12oz/"}, {"id": "fda-food-h-0673-2026", "source": "FDA", "category": "food", "recall_number": "H-0673-2026", "title": "EL MEXICANO horchata casera Instant Horchata Drink recall (Marquez Brothers International, Inc.)", "product": "EL MEXICANO horchata casera Instant Horchata Drink NET WT 14oz (396g) INGREDIENTS: *** MILK SUBSTITUTE (WHEY *** LACTOSE *** DISTRIBUTED BY MARQUEZ BROTHERS INTERNATIONAL, INC. San Jose CA 95138 UPC: 042743190266 Item: 102284", "reason": "Undeclared milk.", "hazard_level": "Class II", "company": "Marquez Brothers International, Inc.", "company_location": "Fresno, CA, United States", "date": "2026-04-07", "report_date": "2026-04-29", "status": "Ongoing", "distribution": "Domestic distribution: AK, AL, AR, AZ, CA, CO, FL, IA, ID, IL, IN, KS, LA, MI, MN, MO, MT, NE, NM, NV, OH, OK, OR, TN, TX, UT, VA, WA, WI. Foreign distribution: Canada, Japan.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "FL", "IA", "ID", "IL", "IN", "KS", "LA", "MI", "MN", "MO", "MT", "NE", "NM", "NV", "OH", "OK", "OR", "TN", "TX", "UT", "VA", "WA", "WI"], "nationwide": false, "quantity": "40,032 packages (16 packages/case; 2,502 cases)", "codes": "Lot, Expiration: HC10124, 04/11/26; HC16524, 06/14/26; HC21324, 08/01/26; HC29924, 10/28/26; HC06625, 03/06/27; HC06625, 03/07/27; HC16325, 06/13/27; HC19525, 07/15/27; HC28325, 10/13/27; HC28325, 10/14/27.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0673-2026%22", "url": "https://recallledger.net/recalls/food-h-0673-2026-el-mexicano-horchata-casera-instant-horchata-drink-net-wt-14oz-396g/"}, {"id": "fda-food-h-0672-2026", "source": "FDA", "category": "food", "recall_number": "H-0672-2026", "title": "Bulk Horchata Powder 3951 recall (Marquez Brothers International, Inc.)", "product": "Bulk Horchata Powder 3951 (100547) 1/25 HORCHATA UPC: 042743-19015-0 Item: 100547", "reason": "Undeclared milk.", "hazard_level": "Class II", "company": "Marquez Brothers International, Inc.", "company_location": "Fresno, CA, United States", "date": "2026-04-07", "report_date": "2026-04-29", "status": "Ongoing", "distribution": "Domestic distribution: AK, AL, AR, AZ, CA, CO, FL, IA, ID, IL, IN, KS, LA, MI, MN, MO, MT, NE, NM, NV, OH, OK, OR, TN, TX, UT, VA, WA, WI. Foreign distribution: Canada, Japan.", "states": ["AK", "AL", "AR", "AZ", "CA", "CO", "FL", "IA", "ID", "IL", "IN", "KS", "LA", "MI", "MN", "MO", "MT", "NE", "NM", "NV", "OH", "OK", "OR", "TN", "TX", "UT", "VA", "WA", "WI"], "nationwide": false, "quantity": "2,494 cases (25 lbs/case)", "codes": "Lot, Expiration: HR02224, 01/23/26; HR06124, 03/05/26; HR16524, 06/14/26; HR23624, 08/27/26; HR34124, 12/11/26; HR07125, 03/13/27; HR09025, 04/03/27; HR23425, 08/27/27; HR34425, 12/15/27; HR01926, 01/28/28.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0672-2026%22", "url": "https://recallledger.net/recalls/food-h-0672-2026-bulk-horchata-powder-3951-100547-1-25-horchata-upc-042743-19015-0/"}, {"id": "fda-drug-d-0521-2026", "source": "FDA", "category": "drug", "recall_number": "D-0521-2026", "title": "Claravis recall (Teva Pharmaceuticals USA, Inc)", "product": "Claravis (isotretinoin capsule, USP), 10 mg, Packaged as a) 100-count carton, NDC 0555-1054-56, with 10x10 blister packs NDC 0555-1054-60; b) 30-count carton, NDC 0555-1054-86, with 3X10 blister pack NDC 0555-1054-60; Rx only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454.", "reason": "Failed Impurities/Degradation Specifications: Out of specification for specific impurity Tretinoin", "hazard_level": "Class II", "company": "Teva Pharmaceuticals USA, Inc", "company_location": "Parsippany, NJ, United States", "date": "2026-04-06", "report_date": "2026-04-29", "status": "Ongoing", "distribution": "Nationwide in the USA, Puerto Rico and Virgin Islands", "states": ["PR"], "nationwide": true, "quantity": "5,101 cartons", "codes": "Lots#: 100067507, 100067508, Exp 07/31/2026", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0521-2026%22", "url": "https://recallledger.net/recalls/drug-d-0521-2026-claravis-isotretinoin-capsule-usp-10-mg-packaged-as-a-100-count/"}, {"id": "fda-drug-d-0498-2026", "source": "FDA", "category": "drug", "recall_number": "D-0498-2026", "title": "LACTATED RINGER'S IRRIGATION recall (B BRAUN MEDICAL INC)", "product": "LACTATED RINGER'S IRRIGATION, 3000 mL bags, Sterile, Ex only, B. Braun Medical Inc., Bethlehem, PA 18018-3524, USA, NDC: 0264-7389-60.", "reason": "Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed.", "hazard_level": "Class II", "company": "B BRAUN MEDICAL INC", "company_location": "Allentown, PA, United States", "date": "2026-04-02", "report_date": "2026-04-29", "status": "Ongoing", "distribution": "US Nationwide.", "states": [], "nationwide": true, "quantity": "54,540 bags", "codes": "Lot # J5E234, J5E236, Exp Date: 30APR2028; Lot # J5H158, J5H159, J5H160, J5H161, J5H162, J5H163, J5H174, J5H175, Exp Date: 31MAY2028.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0498-2026%22", "url": "https://recallledger.net/recalls/drug-d-0498-2026-lactated-ringer-s-irrigation-3000-ml-bags-sterile-ex-only-b-braun/"}, {"id": "fda-drug-d-0497-2026", "source": "FDA", "category": "drug", "recall_number": "D-0497-2026", "title": "0.9 % SODIUM CHLORIDE IRRIGATION recall (B BRAUN MEDICAL INC)", "product": "0.9 % SODIUM CHLORIDE IRRIGATION, USP, 3000 mL bags, Rx only, Sterile, B. Braun Medical Inc., Bethlehem, PA 18018-3524, USA, NDC: 0264-7388-60.", "reason": "Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed.", "hazard_level": "Class II", "company": "B BRAUN MEDICAL INC", "company_location": "Allentown, PA, United States", "date": "2026-04-02", "report_date": "2026-04-29", "status": "Ongoing", "distribution": "US Nationwide.", "states": [], "nationwide": true, "quantity": "124,244 bags", "codes": "Lot # J5E226, J5E227, J5E228, J5E229, J5E230, J5E231, J5E232, J5E233, J5E238, J5E239, Exp Date: 30Apr2028, Lot # J5E240, J5E241, J5E242, J5E243, J5E244, J5E245, J5E247, J5E248, Exp Date: 30Apr2028, Lot # J5H151, J5H152, J5H153, J5H154, J5H155, Exp Date: 31 May2028.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0497-2026%22", "url": "https://recallledger.net/recalls/drug-d-0497-2026-0-9-sodium-chloride-irrigation-usp-3000-ml-bags-rx-only-sterile/"}, {"id": "fda-drug-d-0496-2026", "source": "FDA", "category": "drug", "recall_number": "D-0496-2026", "title": "DEXTROSE INJECTION USP recall (B BRAUN MEDICAL INC)", "product": "DEXTROSE INJECTION USP, 70%, 2000 mL bags, Rx only, Sterile, B. Braun Medical Inc., Bethlehem, PA 18018-3524, USA, NDC: 0264-7387-50.", "reason": "Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed.", "hazard_level": "Class II", "company": "B BRAUN MEDICAL INC", "company_location": "Allentown, PA, United States", "date": "2026-04-02", "report_date": "2026-04-29", "status": "Ongoing", "distribution": "US Nationwide.", "states": [], "nationwide": true, "quantity": "17,124 bags", "codes": "Lot # J5H166, J5H167, Exp Date: 30NOV2026.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0496-2026%22", "url": "https://recallledger.net/recalls/drug-d-0496-2026-dextrose-injection-usp-70-2000-ml-bags-rx-only-sterile-b-braun/"}, {"id": "fda-drug-d-0495-2026", "source": "FDA", "category": "drug", "recall_number": "D-0495-2026", "title": "Sterile Water for Injection USP recall (B BRAUN MEDICAL INC)", "product": "Sterile Water for Injection USP, 3000 mL bags, Rx only, Pharmacy Bulk Package, B. Braun Medical Inc., Bethlehem, PA 18018-3524, NDC: 0264-7385-60.", "reason": "Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed.", "hazard_level": "Class II", "company": "B BRAUN MEDICAL INC", "company_location": "Allentown, PA, United States", "date": "2026-04-02", "report_date": "2026-04-29", "status": "Ongoing", "distribution": "US Nationwide.", "states": [], "nationwide": true, "quantity": "24,928 bags", "codes": "Lot # J5H165, Exp Date: 31 May2028; Lot # J5E237, Exp Date: 30APR2028.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0495-2026%22", "url": "https://recallledger.net/recalls/drug-d-0495-2026-sterile-water-for-injection-usp-3000-ml-bags-rx-only-pharmacy-bulk/"}, {"id": "fda-drug-d-0493-2026", "source": "FDA", "category": "drug", "recall_number": "D-0493-2026", "title": "Omega-3-Acid recall (The Harvard Drug Group LLC)", "product": "Omega-3-Acid, Ethyl Esters, Capsules, USP, 1 gram, 50 capsules (5 x 10 unit dose blister cards) per carton, Rx only, Packaged and Distributed by: Major Pharmaceuticals, Indianapolis, IN 46288. NDC: 0904-7495-06", "reason": "Failed Capsule Specifications: Out of specification results obtained during routine stability testing for Loss on Drying of Capsule Shells.", "hazard_level": "Class II", "company": "The Harvard Drug Group LLC", "company_location": "Dublin, OH, United States", "date": "2026-04-09", "report_date": "2026-04-29", "status": "Ongoing", "distribution": "Nationwide in the USA", "states": [], "nationwide": true, "quantity": "2,238 5 x 10 unit dose cartons", "codes": "Lot#: Lot N02406, Exp 10/31/2026; Lot N02845, Exp 12/31/2026", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0493-2026%22", "url": "https://recallledger.net/recalls/drug-d-0493-2026-omega-3-acid-ethyl-esters-capsules-usp-1-gram-50-capsules-5-x-10/"}, {"id": "fda-drug-d-0490-2026", "source": "FDA", "category": "drug", "recall_number": "D-0490-2026", "title": "Premier recall (Premier Dental Products Co)", "product": "Premier, Monsel's, Ferric Subsulfate Solution, 8 mL bottles, Rx only, Manufacturer: Premier Medical Products, 1710 Romano Drive, Plymouth Meeting, PA 19462, NDC 48783-112-08.", "reason": "Labeling: Incorrect or Missing Lot and/or Exp Date:The expiration date has an extra digit and is printed as 2709114 instead of the correct 270914 (2027-09-14). It is important to note that this error is limited to the vial itself; the saleable unit of the box of 12 bottles has the correct expiration date printed.", "hazard_level": "Class III", "company": "Premier Dental Products Co", "company_location": "Plymouth Meeting, PA, United States", "date": "2026-04-14", "report_date": "2026-04-29", "status": "Ongoing", "distribution": "Nationwide within the United States", "states": [], "nationwide": true, "quantity": "573 cartons", "codes": "Lot #: 640911253, Exp Date. 09/14/2027.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0490-2026%22", "url": "https://recallledger.net/recalls/drug-d-0490-2026-premier-monsel-s-ferric-subsulfate-solution-8-ml-bottles-rx-only/"}, {"id": "fda-drug-d-0489-2026", "source": "FDA", "category": "drug", "recall_number": "D-0489-2026", "title": "FRESHKOTE LUBRICANT EYEDROPS recall (Harrow Eye LLC)", "product": "FRESHKOTE LUBRICANT EYEDROPS, Sterile, 0.33 FL OZ (10mL), Harrow Eye LLC, Nashville, TN USA.", "reason": "Lack of Assurance of Sterility", "hazard_level": "Class II", "company": "Harrow Eye LLC", "company_location": "Nashville, TN, United States", "date": "2026-04-17", "report_date": "2026-04-29", "status": "Ongoing", "distribution": "Nationwide within the United States", "states": [], "nationwide": true, "quantity": "50,900 units", "codes": "Lot #: 1X68, 1X69, Exp. Date 05/31/2027.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0489-2026%22", "url": "https://recallledger.net/recalls/drug-d-0489-2026-freshkote-lubricant-eyedrops-sterile-0-33-fl-oz-10ml-harrow-eye-l/"}, {"id": "cpsc-26440", "source": "CPSC", "category": "consumer-product", "recall_number": "26440", "title": "KMUYSL Big Red Barn Farm Animal Playsets Recalled Due to Risk of Serious Injury or Death from Choking; Violates Small Parts Ban; Sold on Amazon by MISSJUNE", "product": "KMUYSL Big Red Barn Farm Animal Playsets", "reason": "The recalled children's toys violate the small parts ban because the toy is intended for children under three years of age and the fence handles can detach from the toy, posing a deadly choking hazard.", "hazard_level": null, "company": "Shenzhen Leye E-commerce Co., Ltd., dba MISSJUNE, of China", "company_location": "China", "date": "2026-04-23", "report_date": "2026-04-24", "status": "Announced", "distribution": "Sold in the United States at Online at Amazon.com from July 2023 through June 2025 for about $20.", "states": [], "nationwide": true, "quantity": "3000", "codes": "", "remedy": "Consumers should stop using the recalled toys immediately, take them away from children and contact MISSJUNE for a full refund. Consumers will be asked to remove and properly dispose of the fence handles into the trash and send a photo of the disposed product to kmuyslfarmanimalrecall@gmail.com to receive a full refund. Refund", "retailers": ["Online at Amazon.com from July 2023 through June 2025 for about $20."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/KMUYSL-Big-Red-Barn-Farm-Animal-Playsets-Recalled-Due-to-Risk-of-Serious-Injury-or-Death-from-Choking-Violates-Small-Parts-Ban-Sold-on-Amazon-by-MISSJUNE", "url": "https://recallledger.net/recalls/product-26440-kmuysl-big-red-barn-farm-animal-playsets-recalled-due-to-risk-of-serio/"}, {"id": "cpsc-26438", "source": "CPSC", "category": "consumer-product", "recall_number": "26438", "title": "Cpzzkq Baby Loungers Recalled Due to Risk of Serious Injury or Death from Suffocation Hazard; Violates Mandatory Standard for Infant Support Cushions; Sold on Amazon by CetoPMax", "product": "Cpzzkq Baby Loungers", "reason": "The recalled baby loungers violate the mandatory safety standard for infant support cushions because the padding can obstruct an infant's breathing, posing a serious risk of injury or deadly suffocation hazard.", "hazard_level": null, "company": "Guangzhou Dida Electronic Commerce Co., Ltd. dba CetoPMax, of China", "company_location": "China", "date": "2026-04-23", "report_date": "2026-04-24", "status": "Announced", "distribution": "Sold in the United States at Online at Amazon.com from October 2025 through November 2025 for about $50.", "states": [], "nationwide": true, "quantity": "About 2,100", "codes": "", "remedy": "Consumers should stop using the baby loungers immediately and contact CetoPMax for a refund. Consumers will be asked to remove the foam and pad from the baby lounger's cover and cut the cover, foam and pad in half. Consumers will then email photos of the destroyed pieces to?CetoPMaxRecall@outlook.com?to receive a refund. Refund", "retailers": ["Online at Amazon.com from October 2025 through November 2025 for about $50."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/Cpzzkq-Baby-Loungers-Recalled-Due-to-Risk-of-Serious-Injury-or-Death-from-Suffocation-Hazard-Violates-Mandatory-Standard-for-Infant-Support-Cushions-Sold-on-Amazon-by-CetoPMax", "url": "https://recallledger.net/recalls/product-26438-cpzzkq-baby-loungers-recalled-due-to-risk-of-serious-injury-or-death-f/"}, {"id": "cpsc-26437", "source": "CPSC", "category": "consumer-product", "recall_number": "26437", "title": "HappyGira Recalls Sweetie Baby and Style Life Eleven Baby Loungers Due to Risk of Serious Injury or Death from Suffocation and Fall Hazards; Violates Mandatory Standard for Infant Sleep Products", "product": "Sweetie Baby and Style Life Eleven Baby Loungers", "reason": "The baby loungers violate the mandatory standard for infant sleep products because the sides are shorter than the minimum side height limit to secure the infant and they do not have a stand, posing a fall hazard. Additionally, an infant can fall out of the enclosed opening at the foot of the lounger or become entrapped. Furthermore, the sleeping pad's thickness exceeds the maximum limit, posing a suffocation hazard. These violations create an unsafe sleeping environment for infants, posing a risk of serious injury or death.", "hazard_level": null, "company": "Caw Group Inc., dba HappyGira, of Beaverton, Oregon", "company_location": "China", "date": "2026-04-23", "report_date": "2026-04-24", "status": "Announced", "distribution": "Sold in the United States at Online at HappyGira.com from September 2025 through February 2026 for between $70 and $100.", "states": [], "nationwide": true, "quantity": "About 70", "codes": "", "remedy": "Consumers should stop using the baby loungers immediately and contact HappyGira for a full refund. Consumers will be asked to destroy the loungers by removing the sleeping pad and bumpers covers, cutting the bumpers, sleeping pad and the covers in half, and send a photo of the destroyed pieces to?support@happygira.com. Consumers should then dispose of the destroyed product. Refund", "retailers": ["Online at HappyGira.com from September 2025 through February 2026 for between $70 and $100."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/HappyGira-Recalls-Sweetie-Baby-and-Style-Life-Eleven-Baby-Loungers-Due-to-Risk-of-Serious-Injury-or-Death-from-Suffocation-and-Fall-Hazards-Violates-Mandatory-Standard-for-Infant-Sleep-Products", "url": "https://recallledger.net/recalls/product-26437-happygira-recalls-sweetie-baby-and-style-life-eleven-baby-loungers-due/"}, {"id": "cpsc-26436", "source": "CPSC", "category": "consumer-product", "recall_number": "26436", "title": "Magnetic Stick Figure Sets Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys; Sold on Walmart by BlissfulDestiny", "product": "BlissfulDestiny Magnetic Stick Figure Sets", "reason": "The magnetic stick figures violate the mandatory standard for toys because they contain loose magnets posing an ingestion hazard to children. When high-powered magnets are swallowed, the ingested magnets can attract each other, or other metal objects and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning and death.", "hazard_level": null, "company": "Yiwu Shijie E-Commerce Co., Ltd., dba BlissfulDestiny, of China", "company_location": "China", "date": "2026-04-23", "report_date": "2026-04-24", "status": "Announced", "distribution": "Sold in the United States at Online at Walmart.com from May 2025 to October 2025 for about $13.", "states": [], "nationwide": true, "quantity": "About 140", "codes": "", "remedy": "Consumers should stop using the recalled magnetic stick figures immediately and take them away from children. Contact BlissfulDestiny for information on how to receive a full refund. Consumers will be asked to throw the recalled magnetic stick figures away and email a photo of the disposed product to Blissful_Destiny@outlook.com. Refund", "retailers": ["Online at Walmart.com from May 2025 to October 2025 for about $13."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/Magnetic-Stick-Figure-Sets-Recalled-Due-to-Risk-of-Serious-Injury-or-Death-from-Magnet-Ingestion-Violate-Mandatory-Standard-for-Toys-Sold-on-Walmart-by-BlissfulDestiny", "url": "https://recallledger.net/recalls/product-26436-magnetic-stick-figure-sets-recalled-due-to-risk-of-serious-injury-or-d/"}, {"id": "cpsc-26435", "source": "CPSC", "category": "consumer-product", "recall_number": "26435", "title": "32 Degrees Recalls Heated Socks Due to Burn Hazard", "product": "32 Degrees Heated Socks", "reason": "When worn during high-intensity activities that generate a combination of heat, excessive friction, moisture and pressure, the socks can pose an injury hazard including burns.", "hazard_level": null, "company": "David Peyser Sportswear d/b/a 32 Degrees, of New York, New York", "company_location": "China", "date": "2026-04-23", "report_date": "2026-04-24", "status": "Announced", "distribution": "Sold in the United States at Costco stores and online at Costco.com from August 2025 through March 2026 for between $30 and $46.", "states": [], "nationwide": true, "quantity": "About 207,806", "codes": "", "remedy": "Consumers should immediately stop using the heated socks and return them to Costco for a full refund. Refund", "retailers": ["Costco stores and online at Costco.com from August 2025 through March 2026 for between $30 and $46."], "injuries": "14 heat-related incidents have been reported, with 13 involving first- or second-degree burns.", "source_url": "https://www.cpsc.gov/Recalls/2026/32-Degrees-Recalls-Heated-Socks-Due-to-Burn-Hazard", "url": "https://recallledger.net/recalls/product-26435-32-degrees-recalls-heated-socks-due-to-burn-hazard/"}, {"id": "cpsc-26434", "source": "CPSC", "category": "consumer-product", "recall_number": "26434", "title": "Autobrush Recalls Sonic Pro Children's Toothbrush Boxes Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Coin Batteries", "product": "Autobrush Sonic Pro Kids Toothbrush Boxes", "reason": "The recalled delivery boxes violate the mandatory standard for consumer products containing button cell and coin batteries because they contain a lithium coin battery that can be easily accessed by children, posing an ingestion hazard. The packaging also does not bear the required warning labels for products containing such batteries as required by Reese's Law. If button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, including internal chemical burns, and death.", "hazard_level": null, "company": "Lander Enterprises LLC, dba Autobrush, of Miami, Florida", "company_location": "China", "date": "2026-04-23", "report_date": "2026-04-24", "status": "Announced", "distribution": "Sold in the United States at Online at TryAutobrush.com from March 2023 through December 2025 for between $85 and $90.", "states": [], "nationwide": true, "quantity": "About 48,000", "codes": "", "remedy": "Consumers should stop using the boxes for the toothbrushes immediately, take them away from children and contact Autobrush for a $5 refund in the form of store credit. Consumers will be asked to write \"Recalled\" with permanent marker on the box and send a photo of the marked box to recall-support@autobrush.com. Consumers should then dispose of the box. Note: Button cell batteries are hazardous. Batteries should be disposed of or recycled by following local hazardous waste procedures. Refund", "retailers": ["Online at TryAutobrush.com from March 2023 through December 2025 for between $85 and $90."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/Autobrush-Recalls-Sonic-Pro-Childrens-Toothbrush-Boxes-Due-to-Risk-of-Serious-Injury-or-Death-from-Battery-Ingestion-Violates-Mandatory-Standard-for-Consumer-Products-with-Coin-Batteries", "url": "https://recallledger.net/recalls/product-26434-autobrush-recalls-sonic-pro-children-s-toothbrush-boxes-due-to-risk-of/"}, {"id": "cpsc-26433", "source": "CPSC", "category": "consumer-product", "recall_number": "26433", "title": "Children's Tower Stools Recalled Due to Risk of Serious Injury and Death from Entrapment and Fall Hazards; Imported by AMZCMJ DGD", "product": "AMZCMJ DGD Children's Tower Stools", "reason": "The recalled tower stools can collapse or tip over while in use and a child's torso can fit through the openings on the tower's sides, posing a risk of serious injury and death due to tip over, fall and entrapment hazards.", "hazard_level": null, "company": "SiPaiSaiErDianZiShangWu (ShenZhen) YouXianGongSi, dba AMZCMJ DGD, of China", "company_location": "China", "date": "2026-04-23", "report_date": "2026-04-24", "status": "Announced", "distribution": "Sold in the United States at Online at Amazon.com from February 2025 through March 2026 for between $85 and $100.", "states": [], "nationwide": true, "quantity": "About 130", "codes": "", "remedy": "Consumers should stop using the recalled tower stools immediately and contact AMZCMJ DGD for a full refund. Consumers will be asked to destroy the stool by writing \"recalled\" in permanent marker on all sides, disassembling it and sending a photo of the destroyed stool to dgdtoddlertowerrecall@dchskj.cn. Consumers should then dispose of the destroyed product. Refund", "retailers": ["Online at Amazon.com from February 2025 through March 2026 for between $85 and $100."], "injuries": "The firm is aware of seven incidents of children falling from the stool or becoming entrapped, resulting in four injuries such as contusions, splinters and scrapes.", "source_url": "https://www.cpsc.gov/Recalls/2026/Childrens-Tower-Stools-Recalled-Due-to-Risk-of-Serious-Injury-and-Death-from-Entrapment-and-Fall-Hazards-Imported-by-AMZCMJ-DGD", "url": "https://recallledger.net/recalls/product-26433-children-s-tower-stools-recalled-due-to-risk-of-serious-injury-and-dea/"}, {"id": "cpsc-26432", "source": "CPSC", "category": "consumer-product", "recall_number": "26432", "title": "Children's Tower Stools Recalled Due to Risk of Serious Injury and Death from Entrapment and Fall Hazards; Imported by TOETOL HOME", "product": "TOETOL Tower Stools", "reason": "The recalled tower stools can collapse or tip over while in use and a child's torso can fit through the openings on the tower's sides, posing a risk of serious injury and death due to tip over, fall and entrapment hazards.", "hazard_level": null, "company": "Dali Fortune Trade CO., dba TOETOL HOME, of China", "company_location": "China", "date": "2026-04-23", "report_date": "2026-04-24", "status": "Announced", "distribution": "Sold in the United States at Online at Amazon.com from October 2024 through March 2026 for about $130.", "states": [], "nationwide": true, "quantity": "About 3,000", "codes": "", "remedy": "Consumers should immediately stop using the recalled tower stools and contact TOETOL HOME for a full refund. Consumers will be asked to destroy the stool by disassembling it and send a photo of the destroyed stool to TOETOLHOMEStepStoolsrecall@outlook.com. Consumers should then dispose of the destroyed product. Refund", "retailers": ["Online at Amazon.com from October 2024 through March 2026 for about $130."], "injuries": "The firm has received 18 reports of the stools collapsing, resulting in eleven injuries including contusions, cuts and scrapes.", "source_url": "https://www.cpsc.gov/Recalls/2026/Childrens-Tower-Stools-Recalled-Due-to-Risk-of-Serious-Injury-and-Death-from-Entrapment-and-Fall-Hazards-Imported-by-TOETOL-HOME", "url": "https://recallledger.net/recalls/product-26432-children-s-tower-stools-recalled-due-to-risk-of-serious-injury-and-dea/"}, {"id": "cpsc-26431", "source": "CPSC", "category": "consumer-product", "recall_number": "26431", "title": "Tzumi Electronics Recalls FitRx SmartBell Quick-Select Adjustable Dumbbells Due to Serious Injury from Impact Hazard", "product": "FitRx SmartBell Quick-Select 5-52.5lbs Adjustable Dumbbells", "reason": "Weight plates can dislodge from the handle during use, posing a risk of serious injury due to impact hazard.", "hazard_level": null, "company": "Tzumi Electronics Inc. of New York, New York", "company_location": "China", "date": "2026-04-23", "report_date": "2026-04-24", "status": "Announced", "distribution": "Sold in the United States at Walmart stores nationwide and online at Walmart.com from January 2024 through November 2024 for about $100.", "states": [], "nationwide": true, "quantity": "About 50,000", "codes": "", "remedy": "Consumers should immediately stop using the adjustable dumbbell and contact Tzumi Electronics for a free replacement of the dumbbell and tray. Consumers should write the word \"Recalled\" across the dumbbell tray using permanent spray paint or marker, register at https://myfitrx.com/recall-52-lbs/ and dispose of the product after registration is confirmed. Replace", "retailers": ["Walmart stores nationwide and online at Walmart.com from January 2024 through November 2024 for about $100."], "injuries": "There have been more than 115 reports of weight plates dislodging during use, with at least six injuries, including broken toes, bruises, contusions and lacerations.", "source_url": "https://www.cpsc.gov/Recalls/2026/Tzumi-Electronics-Recalls-FitRx-SmartBell-Quick-Select-Adjustable-Dumbbells-Due-to-Serious-Injury-from-Impact-Hazard", "url": "https://recallledger.net/recalls/product-26431-tzumi-electronics-recalls-fitrx-smartbell-quick-select-adjustable-dumb/"}, {"id": "cpsc-26430", "source": "CPSC", "category": "consumer-product", "recall_number": "26430", "title": "Wiifo Children's Tower Stools Recalled Due to Risk of Serious Injury and Death from Entrapment and Fall Hazards; Imported by Wiifo", "product": "Wiifo Children's Tower Stools", "reason": "The recalled tower stools can collapse or tip over while in use, and a child's torso can fit through the openings on the tower's sides, posing a risk of serious injury and death due to tip over, fall and entrapment hazards.", "hazard_level": null, "company": "Hangzhou Xinyanchuangxin Technology Co Ltd., dba Wiifo, of China", "company_location": "China", "date": "2026-04-23", "report_date": "2026-04-24", "status": "Announced", "distribution": "Sold in the United States at Online at Amazon.com from June 2022 through March of 2026 for about $60.", "states": [], "nationwide": true, "quantity": "About 9,700", "codes": "", "remedy": "Consumers should stop using the recalled tower stools immediately and contact Wiifo for a full refund. Consumers will be asked to destroy the stool by disassembling it and send a photo of the destroyed stool to support@wiifo.net. Consumers should then dispose of the destroyed product. Refund", "retailers": ["Online at Amazon.com from June 2022 through March of 2026 for about $60."], "injuries": "The firm is aware of 22 incidents of stools collapsing, resulting in six injuries such as contusions and scrapes.", "source_url": "https://www.cpsc.gov/Recalls/2026/Wiifo-Childrens-Tower-Stools-Recalled-Due-to-Risk-of-Serious-Injury-and-Death-from-Entrapment-and-Fall-Hazards-Imported-by-Wiifo", "url": "https://recallledger.net/recalls/product-26430-wiifo-children-s-tower-stools-recalled-due-to-risk-of-serious-injury-a/"}, {"id": "cpsc-26429", "source": "CPSC", "category": "consumer-product", "recall_number": "26429", "title": "mGanna Sodium Hydroxide Pellet Bags Recalled Due to Risk of Serious Injury or Death from Chemical Burns and Irritation to the Skin and Eyes; Violate Mandatory Standard for Child-Resistant Packaging; Sold on Amazon by Archie Xpress", "product": "mGanna Sodium Hydroxide (lye) Pellet Bags", "reason": "The recalled products contain sodium hydroxide (lye), which must be in child-resistant packaging as required by the Poison Prevention Packaging Act (PPPA). The packaging is not child-resistant, posing a risk of chemical burns and irritation to the skin and eyes. The products also violate the labeling requirements for hazardous substances under the Federal Hazardous Substances Act (FHSA).", "hazard_level": null, "company": "Dhanlaxmi Ashish Ganna, dba Archie Xpress, of India", "company_location": "India", "date": "2026-04-23", "report_date": "2026-04-24", "status": "Announced", "distribution": "Sold in the United States at Online at Amazon.com from November 2024 through March 2026 for about $10.", "states": [], "nationwide": true, "quantity": "About 3,240", "codes": "", "remedy": "Consumers should stop using and secure the recalled sodium hydroxide product out of sight and reach of children immediately and contact Archie Xpress for a full refund. Consumers will be asked to write \"RECALLED\" on the back of the zip-top pouch and send a photo of the marked pouch to support@archieenterprise.in. Consumers should then dispose of the pellets in accordance with local and state regulations. Note: Consumers should follow local household hazardous waste (HHW) guidance for corrosive solids. Contact your city, county, or state HHW program for instructions, as requirements may differ by location. Recommend safe approach: Keep the product in its package, clearly label it \"DO NOT USE\" and bring it to a local HHW drop-off facility. Refund", "retailers": ["Online at Amazon.com from November 2024 through March 2026 for about $10."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/mGanna-Sodium-Hydroxide-Pellet-Bags-Recalled-Due-to-Risk-of-Serious-Injury-or-Death-from-Chemical-Burns-and-Irritation-to-the-Skin-and-Eyes-Violate-Mandatory-Standard-for-Child-Resistant-Packaging-Sold-on-Amazon-by-Archie-Xpress", "url": "https://recallledger.net/recalls/product-26429-mganna-sodium-hydroxide-pellet-bags-recalled-due-to-risk-of-serious-in/"}, {"id": "fda-food-h-0681-2026", "source": "FDA", "category": "food", "recall_number": "H-0681-2026", "title": "Label is predominantly green with white lettering in a clear plastic clamshell... recall (PURE PALM C/O DVD)", "product": "Label is predominantly green with white lettering in a clear plastic clamshell container. Pure Palm dates- Medjool Dates Net Wt. 16OZ UPC: 852160007005", "reason": "mislabeled Coconut Date Bites. (product is coconut covered, label is for regular date bites)", "hazard_level": "Class II", "company": "PURE PALM C/O DVD", "company_location": "Coachella, CA, United States", "date": "2026-04-01", "report_date": "2026-04-22", "status": "Terminated", "distribution": "Product was distributed to a single Direct Account with multiple locations across several East Coast states including (Delaware, Pennsylvania, New Jersey, Maryland, New York)", "states": ["DE", "MD", "NJ", "NY", "PA"], "nationwide": false, "quantity": "50 cases", "codes": "LOT CODE PP0576D1 BEST BY:02/26/2027", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0681-2026%22", "url": "https://recallledger.net/recalls/food-h-0681-2026-label-is-predominantly-green-with-white-lettering-in-a-clear-plastic-c/"}, {"id": "fda-drug-d-0532-2026", "source": "FDA", "category": "drug", "recall_number": "D-0532-2026", "title": "Lidocaine HCl Injection recall (Huons Co., Ltd.)", "product": "Lidocaine HCl Injection, USP, 2%, 100 mg/5mL (20 mg/mL), 5 mL Single-Dose Vials, Rx only, Manufactured by: Huons Co., Ltd., 100 Bio valley-ro, Jecheon-si, Chungchengbuk-do, Korea, NDC 73293-0003-1 (vial), NDC 73293-0003-2 (10 count carton); Distributed by: Brookefield Pharmaceuticals, LLC, Brookefield, WI, NDC 71351-023-05 (vials), NDC 71351-023-10 (10 count cartons), NDC 71351-023-25 (25 count cartons); Manufactured for: Precision Dose Inc, South Beloit IL NDC 68094-081-01 (vial), NDC 68094-081-25 (25 count carton); Distributed by Novagenix Labs LLC, Morrisville, NC NDC 84769-0002-1 (vials), NDC 84769-0002-2 (10 count carton)", "reason": "Lack of Assurance of Sterility", "hazard_level": "Class II", "company": "Huons Co., Ltd.", "company_location": "Jecheon, N/A, Korea (the Republic of)", "date": "2026-04-02", "report_date": "2026-04-22", "status": "Ongoing", "distribution": "USA Nationwide.", "states": [], "nationwide": true, "quantity": "N/A", "codes": "All lots within expiry", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0532-2026%22", "url": "https://recallledger.net/recalls/drug-d-0532-2026-lidocaine-hcl-injection-usp-2-100-mg-5ml-20-mg-ml-5-ml-single-d/"}, {"id": "fda-drug-d-0531-2026", "source": "FDA", "category": "drug", "recall_number": "D-0531-2026", "title": "0.9% Sodium Chloride Injection recall (Huons Co., Ltd.)", "product": "0.9% Sodium Chloride Injection, USP, 10 mL Ampules, Rx only, Single Dose, Preservative Free, Manufactured for: Spectra Medical Devices, LLC, Wilmington, MA, 01887, By: Houns Co., Ltd, Jecheon, Korea, 27159, NDC 65282-1510-1.", "reason": "Lack of Assurance of Sterility", "hazard_level": "Class II", "company": "Huons Co., Ltd.", "company_location": "Jecheon, N/A, Korea (the Republic of)", "date": "2026-04-02", "report_date": "2026-04-22", "status": "Ongoing", "distribution": "USA Nationwide.", "states": [], "nationwide": true, "quantity": "7,120,750 ampules", "codes": "All lots within expiry", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0531-2026%22", "url": "https://recallledger.net/recalls/drug-d-0531-2026-0-9-sodium-chloride-injection-usp-10-ml-ampules-rx-only-single-do/"}, {"id": "fda-drug-d-0530-2026", "source": "FDA", "category": "drug", "recall_number": "D-0530-2026", "title": "Bupivacaine Hydrochloride 0.75% in 8.25% Dextrose Injection recall (Huons Co., Ltd.)", "product": "Bupivacaine Hydrochloride 0.75% in 8.25% Dextrose Injection, USP (15 mg/2 mL) (7.5 mg/mL) ampules, Rx only, Manufactured by: Houns Co., Ltd, 100, Bio valley, Je-cheor-Si, Chungcheongbuk-dc, Korea, NDC 73293-0002-1 (2 mL ampule), NDC 73293-0002-2 (50 x 2 Single-dose ampules); Distributed: Brookfield Pharmaceuticals, LLC, Brookfield, WI 53005, Made in S. Korea, NDC 71351-022-02 (ampule), NDC 71351-022-10 (10 count ampules), NDC 71351-022-50 (50 count ampules)", "reason": "Lack of Assurance of Sterility", "hazard_level": "Class II", "company": "Huons Co., Ltd.", "company_location": "Jecheon, N/A, Korea (the Republic of)", "date": "2026-04-02", "report_date": "2026-04-22", "status": "Ongoing", "distribution": "USA Nationwide.", "states": [], "nationwide": true, "quantity": "3,260,170 ampules", "codes": "All lots within expiry", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0530-2026%22", "url": "https://recallledger.net/recalls/drug-d-0530-2026-bupivacaine-hydrochloride-0-75-in-8-25-dextrose-injection-usp-15-m/"}, {"id": "fda-drug-d-0529-2026", "source": "FDA", "category": "drug", "recall_number": "D-0529-2026", "title": "Lidocaine HCl injection recall (Huons Co., Ltd.)", "product": "Lidocaine HCl injection, USP, 1% 50mg/5mL (10 mg/mL), 5 mL Single Dose Vials, Rx only, Manufactured by: Huons Co, Ltd, Chungcheongbuk-do, Korea NDC 73293-0001-1 (vial), NDC 73293-0001-2 (10 count carton); Distributed by: McKesson Corporation, dba Sky Packaging, NDC 63739-170-13 (vials), NDC 63739-170-24 (10 count cartons) and NDC 63739-170-27 (25 count cartons); Distributed by: Brookefield Pharmaceuticals, LLC, Brookefield, WI, Manufactured by: Huons Co., Ltd., 100 Bio valley-ro, Jecheon-si, Chungchengbuk-do, Korea, NDC 71351-021-05 (vials), NDC 71351-021-10 (10 count cartons), NDC 71351-021-25 (25 count cartons); Distributed by Novagenix Labs LLC, Morrisville, NC NDC 84769-0001-1 (vials), NDC 84769-0001-2 (10 count carton)", "reason": "Lack of Assurance of Sterility", "hazard_level": "Class II", "company": "Huons Co., Ltd.", "company_location": "Jecheon, N/A, Korea (the Republic of)", "date": "2026-04-02", "report_date": "2026-04-22", "status": "Ongoing", "distribution": "USA Nationwide.", "states": [], "nationwide": true, "quantity": "33,599,925 ampules and 23658125 vials", "codes": "All lots within expiry", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0529-2026%22", "url": "https://recallledger.net/recalls/drug-d-0529-2026-lidocaine-hcl-injection-usp-1-50mg-5ml-10-mg-ml-5-ml-single-dose/"}, {"id": "fda-drug-d-0510-2026", "source": "FDA", "category": "drug", "recall_number": "D-0510-2026", "title": "Desmopressin Nasal Spray recall (Apotex Corp.)", "product": "Desmopressin Nasal Spray, USP, 10 mcg/0.1 mL, 5 mL bottle (50 doses), Rx only, Mfg by: Apotek inc., Toronto, Ontario, Canada, M9L 1T9, Mfg for: Apotek Corp., Weston, FL 33326, NDC 60505-0815-0", "reason": "Defective container: defect in a batch of bottle caps, specifically involving dislodged or missing cap liners.", "hazard_level": "Class II", "company": "Apotex Corp.", "company_location": "Weston, FL, United States", "date": "2026-04-08", "report_date": "2026-04-22", "status": "Ongoing", "distribution": "U.S.A. Nationwide", "states": [], "nationwide": true, "quantity": "N/A", "codes": "Lot #: VM4231, Exp 06/30/2027", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0510-2026%22", "url": "https://recallledger.net/recalls/drug-d-0510-2026-desmopressin-nasal-spray-usp-10-mcg-0-1-ml-5-ml-bottle-50-doses/"}, {"id": "fda-drug-d-0487-2026", "source": "FDA", "category": "drug", "recall_number": "D-0487-2026", "title": "Blemish Spot Treatment recall (Island Kinetics, Inc. d.b.a. CoValence Laboratories)", "product": "Blemish Spot Treatment (Salicylic Acid) 1%, .5 fl oz (15 ml) bottles, Skin Script, Chandler, AZ 85226, UPC 6 10563 13873 9.", "reason": "Failed Stability Specifications", "hazard_level": "Class II", "company": "Island Kinetics, Inc. d.b.a. CoValence Laboratories", "company_location": "Chandler, AZ, United States", "date": "2026-04-01", "report_date": "2026-04-22", "status": "Ongoing", "distribution": "U.S. Nationwide", "states": [], "nationwide": true, "quantity": "28,163 bottles", "codes": "Lot#: 4228D2, 4229D1, Exp.: 07/31/2026 Lot#: 5147D2, Exp.: 04/30/2027", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0487-2026%22", "url": "https://recallledger.net/recalls/drug-d-0487-2026-blemish-spot-treatment-salicylic-acid-1-5-fl-oz-15-ml-bottles/"}, {"id": "fda-drug-d-0483-2026", "source": "FDA", "category": "drug", "recall_number": "D-0483-2026", "title": "EPINEPHRINE Injection recall (International Medication Systems Ltd.)", "product": "EPINEPHRINE Injection, USP, 1 mg/10mL (0.1 mg/mL), Rx only, INTERNATIONAL MEDICATION SYSTEMS, LIMITED, So. EL Monte, CA 91733, An Amphastar Pharmaceutical Company, NDC 76329-3318-1", "reason": "Lack of Assurance of Sterility", "hazard_level": "Class II", "company": "International Medication Systems Ltd.", "company_location": "South El Monte, CA, United States", "date": "2026-04-01", "report_date": "2026-04-22", "status": "Ongoing", "distribution": "U.S. Nationwide", "states": [], "nationwide": true, "quantity": "81,520 units", "codes": "Lot Number: EA038A5, Expiration Date: 08/2026.", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0483-2026%22", "url": "https://recallledger.net/recalls/drug-d-0483-2026-epinephrine-injection-usp-1-mg-10ml-0-1-mg-ml-rx-only-internatio/"}, {"id": "cpsc-26428", "source": "CPSC", "category": "consumer-product", "recall_number": "26428", "title": "JC Sales Recalls Lil' Buddies Pet Laser Toys Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violates Mandatory Standard for Consumer Products with Button Cell Batteries", "product": "Lil' Buddies Pet Laser Toy", "reason": "The Montessori toy sets contain an airplane shaped teething toy that has tentacle ends that can pose a choking hazard to young children. The toys also violate the teething toy provision of the mandatory standard for children's toys.", "hazard_level": null, "company": "Shims Bargain, Inc., dba JC Sales, of Los Angeles, California", "company_location": "China", "date": "2026-04-16", "report_date": "2026-04-17", "status": "Announced", "distribution": "Sold in the United States at VR Wholesale (Arizona), Viva Bargain (California), and various discount stores nationwide and online at jcsalesweb.com from February 2023 through November 2025 for about $1.", "states": [], "nationwide": true, "quantity": "About 51,160", "codes": "UPCs: 885490244963", "remedy": "Consumers should stop using the recalled pet toys, place them in an area that children cannot access and properly dispose of the batteries. Contact JC Sales for a full refund. Customers will be asked to email a photograph of the disposed items to Recall@jcsales.net. Note: Button cell batteries are hazardous. Batteries should be disposed of or recycled by following local hazardous waste procedures. Refund", "retailers": ["VR Wholesale (Arizona), Viva Bargain (California), and various discount stores nationwide and online at jcsalesweb.com from February 2023 through November 2025 for about $1."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/JC-Sales-Recalls-Lil-Buddies-Pet-Laser-Toys-Due-to-Risk-of-Serious-Injury-or-Death-from-Battery-Ingestion-Hazard-Violates-Mandatory-Standard-for-Consumer-Products-with-Button-Cell-Batteries", "url": "https://recallledger.net/recalls/product-26428-jc-sales-recalls-lil-buddies-pet-laser-toys-due-to-risk-of-serious-in/"}, {"id": "cpsc-26427", "source": "CPSC", "category": "consumer-product", "recall_number": "26427", "title": "Montessori Toy Sets Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Violate Mandatory Standard for Teething Toys; Sold on Amazon by SpringFlower", "product": "SpringFlower 5-in-1 Montessori Toy Set", "reason": "The Montessori toy sets contain an airplane shaped teething toy that has tentacle ends that can pose a choking hazard to young children. The toys also violate the teething toy provision of the mandatory standard for children's toys.", "hazard_level": null, "company": "Shantou Ai Xing Trading Co., Ltd., dba SpringFlower, of China", "company_location": "China", "date": "2026-04-16", "report_date": "2026-04-17", "status": "Announced", "distribution": "Sold in the United States at Online at Amazon.com from October 2023 through November 2025 for about $30.", "states": [], "nationwide": true, "quantity": "About 21,900", "codes": "", "remedy": "Consumers should stop using the Montessori toy sets immediately and take them away from children and contact SpringFlower for a free replacement part or a refund. Consumers will be asked to cut off all the tentacles from the airplane shaped teething toy, write the date and customer's initials in permanent marker on its base, and submit photos of the destroyed and marked airplane shaped toy to springflower.com.cn/product-recall. Consumers can then dispose of the airplane shaped toy. Refund Replace", "retailers": ["Online at Amazon.com from October 2023 through November 2025 for about $30."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/Montessori-Toy-Sets-Recalled-Due-to-Risk-of-Serious-Injury-or-Death-from-Choking-Hazard-Violate-Mandatory-Standard-for-Teething-Toys-Sold-on-Amazon-by-SpringFlower", "url": "https://recallledger.net/recalls/product-26427-montessori-toy-sets-recalled-due-to-risk-of-serious-injury-or-death-fr/"}, {"id": "cpsc-26426", "source": "CPSC", "category": "consumer-product", "recall_number": "26426", "title": "Apex Gaming PCs Recalls Manik and Apex-branded ATX Computer Power Supplies Due to Risk of Serious Injury or Death from Electrical Shock and Electrocution Hazards", "product": "Manik and Apex-branded ATX Computer Power Supplies (PSU)", "reason": "The units lack a permanent, on-product warning label identifying potential electrical shock and electrocution hazards, posing a risk of serious injury or death if the unit is opened or disassembled.", "hazard_level": null, "company": "Apex Gaming PCs Inc., of Houston, Texas", "company_location": "China", "date": "2026-04-16", "report_date": "2026-04-17", "status": "Announced", "distribution": "Sold in the United States at Online at www.ApexGamingPCs.com from December 2021 through February 2026, for between $70 and $150.", "states": [], "nationwide": true, "quantity": "About 17,730 (In addition, about 500 were sold in Canada)", "codes": "", "remedy": "Consumers should stop using the recalled computer power supplies immediately and contact Apex Gaming PCs Inc. for a free repair in the form of one permanent, UL-recognized, heat-resistant adhesive safety label containing an ANSI-compliant \"Danger/Warning\" shock hazard and \"No User-Serviceable Parts\" label sticker to be mailed to the consumer via U.S. Mail. Consumers who are uncomfortable adding the UL-recognized safety label can request a free replacement unit. Replacement units will be sent free of charge, and the original unit must be returned using the same box and provided shipping label that is sent with the replacement unit. Consumers should not, under any circumstances, attempt to open, disassemble, or service the power supply unit. Repair Replace", "retailers": ["Online at www.ApexGamingPCs.com from December 2021 through February 2026, for between $70 and $150."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/Apex-Gaming-PCs-Recalls-Manik-and-Apex-branded-ATX-Computer-Power-Supplies-Due-to-Risk-of-Serious-Injury-or-Death-from-Electrical-Shock-and-Electrocution-Hazards", "url": "https://recallledger.net/recalls/product-26426-apex-gaming-pcs-recalls-manik-and-apex-branded-atx-computer-power-supp/"}, {"id": "cpsc-26425", "source": "CPSC", "category": "consumer-product", "recall_number": "26425", "title": "Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violates Mandatory Standard for Adult Portable Bed Rails; Sold on Amazon by ZOLIQUEX", "product": "ZOLIQUEX Adult Portable Bed Rails", "reason": "The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. In addition, the bed rails do not bear the required hazard warning labels.", "hazard_level": null, "company": "ZOLIQUEX, of China", "company_location": "China", "date": "2026-04-16", "report_date": "2026-04-17", "status": "Announced", "distribution": "Sold in the United States at Online at Amazon.com from August 2023 through February 2026 for about $43.", "states": [], "nationwide": true, "quantity": "About 16,000", "codes": "", "remedy": "Consumers should stop using the recalled adult portable bed rails immediately and contact ZOLIQUEX for a full refund. Consumers should cut the black safety strap in half and write \"RECALLED\" on the upper and lower bed rails with a permanent marker, take a photo of the marked bed rail with the buyer's name on a piece of paper and email the photo to ZEXnaturemedical@outlook.com. Refund", "retailers": ["Online at Amazon.com from August 2023 through February 2026 for about $43."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/Adult-Portable-Bed-Rails-Recalled-Due-to-Risk-of-Serious-Injury-or-Death-from-Entrapment-and-Asphyxiation-Violates-Mandatory-Standard-for-Adult-Portable-Bed-Rails-Sold-on-Amazon-by-ZOLIQUEX", "url": "https://recallledger.net/recalls/product-26425-adult-portable-bed-rails-recalled-due-to-risk-of-serious-injury-or-dea/"}, {"id": "cpsc-26424", "source": "CPSC", "category": "consumer-product", "recall_number": "26424", "title": "ZMC Group Recalls LED Finger Beam Lights Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys", "product": "LED Finger Beam Lights", "reason": "The recalled toys violate the mandatory safety standard for children's toys because the toy contains button cell batteries that can be easily accessed by children. If button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, including internal chemical burns, and death.", "hazard_level": null, "company": "ZMC Group, Inc. of Los Angeles, California", "company_location": "China", "date": "2026-04-16", "report_date": "2026-04-17", "status": "Announced", "distribution": "Sold in the United States at Various discount stores nationwide from August 2025 through March 2026 for about $1.", "states": [], "nationwide": true, "quantity": "About 14,400", "codes": "", "remedy": "Consumers should take the LED Finger Beam Lights away from children, stop using them immediately and contact ZMC Group for full refund or a replacement product. Consumers should remove the batteries, break each component in half and submit a photo of the destroyed pieces to recallzmctoy@gmail.com. Note: Button cell batteries are hazardous. Batteries should be disposed of or recycled by following local hazardous waste procedures. Refund Replace", "retailers": ["Various discount stores nationwide from August 2025 through March 2026 for about $1."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/ZMC-Group-Recalls-LED-Finger-Beam-Lights-Due-to-Risk-of-Serious-Injury-or-Death-from-Battery-Ingestion-Violates-Mandatory-Standard-for-Toys", "url": "https://recallledger.net/recalls/product-26424-zmc-group-recalls-led-finger-beam-lights-due-to-risk-of-serious-injury/"}, {"id": "cpsc-26423", "source": "CPSC", "category": "consumer-product", "recall_number": "26423", "title": "Sweetcrispy Recalls Pressure Washers Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards", "product": "Sweetcrispy Electric Pressure Washers", "reason": "The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI), posing a serious risk of injury or death from shock and electrocution hazards.", "hazard_level": null, "company": "Zhejiang Hengjian Home Furnishing Co Ltd., dba Sweetcrispy, of China", "company_location": "China", "date": "2026-04-16", "report_date": "2026-04-17", "status": "Announced", "distribution": "Sold in the United States at Online at Amazon.com from July 2025 through January 2026 for between $60 and $130.", "states": [], "nationwide": true, "quantity": "2300", "codes": "", "remedy": "Consumers should stop using the recalled pressure washers immediately and contact Sweetcrispy for a full refund. Consumers will be asked to destroy the pressure washer by cutting the unplugged power cord and send a photo of the destroyed power washer to LR023784@outlook.com. Consumers should then dispose of the destroyed recalled product. Refund", "retailers": ["Online at Amazon.com from July 2025 through January 2026 for between $60 and $130."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/Sweetcrispy-Recalls-Pressure-Washers-Due-to-Serious-Risk-of-Injury-or-Death-from-Shock-and-Electrocution-Hazards", "url": "https://recallledger.net/recalls/product-26423-sweetcrispy-recalls-pressure-washers-due-to-serious-risk-of-injury-or/"}, {"id": "cpsc-26422", "source": "CPSC", "category": "consumer-product", "recall_number": "26422", "title": "Le Hao Tool Recalls Pressure Washers Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards", "product": "Le Hao Tool Electric Pressure Washers", "reason": "The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI), posing a serious risk of injury or death from shock and electrocution hazards.", "hazard_level": null, "company": "Ningbofenghuaxinlehaodianziyouxiangongsi, dba Le Hao Tool, of China", "company_location": "China", "date": "2026-04-16", "report_date": "2026-04-17", "status": "Announced", "distribution": "Sold in the United States at Online at Amazon.com from November 2023 through January 2026 for between $60 and $130.", "states": [], "nationwide": true, "quantity": "3100", "codes": "", "remedy": "Consumers should stop using the recalled pressure washers immediately and contact Le Hao Tool for a full refund. Consumers will be asked to destroy the pressure washer by cutting the unplugged power cord in half and send a photo of the destroyed power washer to LeHaoService2026@outlook.com. Consumers should then dispose of the destroyed recalled product. Refund", "retailers": ["Online at Amazon.com from November 2023 through January 2026 for between $60 and $130."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/Le-Hao-Tool-Recalls-Pressure-Washers-Due-to-Serious-Risk-of-Injury-or-Death-from-Shock-and-Electrocution-Hazards", "url": "https://recallledger.net/recalls/product-26422-le-hao-tool-recalls-pressure-washers-due-to-serious-risk-of-injury-or/"}, {"id": "cpsc-26421", "source": "CPSC", "category": "consumer-product", "recall_number": "26421", "title": "Fengrong Tool Recalls Pressure Washers Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards", "product": "Fengrong Tool Electric Pressure Washers", "reason": "The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI), posing a serious risk of injury or death from shock and electrocution hazards.", "hazard_level": null, "company": "Ningboaonadianzishangwuyouxiangongsi., dba Fengrong Tool, of China", "company_location": "China", "date": "2026-04-16", "report_date": "2026-04-17", "status": "Announced", "distribution": "Sold in the United States at Online at Amazon.com from October 2025 through January 2026 for between $80 and $130.", "states": [], "nationwide": true, "quantity": "About 500", "codes": "", "remedy": "Consumers should stop using the recalled pressure washers immediately and contact Fengrong Tool for a full refund. Consumers will be asked to destroy the pressure washer by cutting the unplugged power cord and send a photo of the destroyed power washer to fengrongservice@163.com. Consumers should then dispose of the destroyed recalled product. Refund", "retailers": ["Online at Amazon.com from October 2025 through January 2026 for between $80 and $130."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/Fengrong-Tool-Recalls-Pressure-Washers-Due-to-Serious-Risk-of-Injury-or-Death-from-Shock-and-Electrocution-Hazards", "url": "https://recallledger.net/recalls/product-26421-fengrong-tool-recalls-pressure-washers-due-to-serious-risk-of-injury-o/"}, {"id": "cpsc-26420", "source": "CPSC", "category": "consumer-product", "recall_number": "26420", "title": "Agiiman Recalls Pressure Washers Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards", "product": "Agiiman Electric Pressure Washers", "reason": "The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI), posing a serious risk of injury or death from shock and electrocution.", "hazard_level": null, "company": "Jiangxi Runfuyuan Biotechnology Co., Ltd dba Agiiman, of China", "company_location": "China", "date": "2026-04-16", "report_date": "2026-04-17", "status": "Announced", "distribution": "Sold in the United States at Online at Amazon.com from October 2025 through November 2025 for about $90.", "states": [], "nationwide": true, "quantity": "80", "codes": "", "remedy": "Consumers should stop using the recalled pressure washers immediately and contact Agiiman for a full refund. Consumers will be asked to cut the power cord in half to destroy the pressure washer and send a photo of the destroyed pressure washer to agiimanservice@163.com. Consumers should then dispose of the destroyed recalled product. Refund", "retailers": ["Online at Amazon.com from October 2025 through November 2025 for about $90."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/Agiiman-Recalls-Pressure-Washers-Due-to-Serious-Risk-of-Injury-or-Death-from-Shock-and-Electrocution-Hazards", "url": "https://recallledger.net/recalls/product-26420-agiiman-recalls-pressure-washers-due-to-serious-risk-of-injury-or-deat/"}, {"id": "cpsc-26419", "source": "CPSC", "category": "consumer-product", "recall_number": "26419", "title": "Free-Standing Professional Gas Ranges Recalled Due to Risk of Burn Hazard; Manufactured by Fisher & Paykel", "product": "Fisher & Paykel Gas Ranges", "reason": "The ovens in the ranges can experience a delayed ignition, causing gas to accumulate and the oven door to open from combustion, posing a burn hazard to users.", "hazard_level": null, "company": "Fisher & Paykel Appliances (Thailand) Co., Ltd, of Thailand", "company_location": "Thailand", "date": "2026-04-16", "report_date": "2026-04-17", "status": "Announced", "distribution": "Sold in the United States at Factory Builder Stores, Albert Lee Inc and other appliance retail stores nationwide from June 2025 through March 2026 for between $6,200 and $14,000.", "states": [], "nationwide": true, "quantity": "About 433 (In addition, about 70 were sold in Canada)", "codes": "UPCs: 822843828494, 822843828500, 822843820030, 822843820047, 822843820054, 822843823833, 822843823840, 822843829736, 822843829743, 822843829750, 822843829767, 191127003606, 191127003613, 191127003804", "remedy": "Consumers should stop using the ovens in the recalled gas ranges immediately and contact Fisher & Paykel for a free inspection and repair. Fisher & Paykel will provide professional in-home repair of the oven's ignitor. Consumers can continue to use the cooktop burners on the range. Repair", "retailers": ["Factory Builder Stores, Albert Lee Inc and other appliance retail stores nationwide from June 2025 through March 2026 for between $6,200 and $14,000."], "injuries": "The firm has received 18 reports of gas ranges with delayed ignition and one report of a minor burn injury.", "source_url": "https://www.cpsc.gov/Recalls/2026/Free-Standing-Professional-Gas-Ranges-Recalled-Due-to-Risk-of-Burn-Hazard-Manufactured-by-Fisher-and-Paykel", "url": "https://recallledger.net/recalls/product-26419-free-standing-professional-gas-ranges-recalled-due-to-risk-of-burn-haz/"}, {"id": "cpsc-26417", "source": "CPSC", "category": "consumer-product", "recall_number": "26417", "title": "Pressure Washers Recalled Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards; Imported by Patoolio Direct", "product": "Patoolio Direct Electric Pressure Washers", "reason": "The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI), posing a serious risk of injury or death from shock and electrocution hazards.", "hazard_level": null, "company": "Shenzhen Xingyashang Technology Co., Ltd., dba Patoolio Direct, of China", "company_location": "China", "date": "2026-04-16", "report_date": "2026-04-17", "status": "Announced", "distribution": "Sold in the United States at Online at Amazon.com from October 2025 through January 2026 for between $45 and $150.", "states": [], "nationwide": true, "quantity": "2066", "codes": "", "remedy": "Consumers should stop using the recalled pressure washers immediately and contact Patoolio Direct for a full refund. Consumers will be asked to destroy the pressure washer by cutting the power cord in half and send a photo of the destroyed power washer to PatoolioPressureWasherrecall@outlook.com. Consumers should then dispose of the destroyed recalled product. Refund", "retailers": ["Online at Amazon.com from October 2025 through January 2026 for between $45 and $150."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/Pressure-Washers-Recalled-Due-to-Serious-Risk-of-Injury-or-Death-from-Shock-and-Electrocution-Hazards-Imported-by-Patoolio-Direct", "url": "https://recallledger.net/recalls/product-26417-pressure-washers-recalled-due-to-serious-risk-of-injury-or-death-from/"}, {"id": "cpsc-26414", "source": "CPSC", "category": "consumer-product", "recall_number": "26414", "title": "Mini Round Toddler Trampolines Recalled Due to Strangulation Hazard; Risk of Serious Injury or Death; Manufactured by SEGMART", "product": "SEGMART 55\" Indoor/Outdoor Mini Round Toddler Trampolines with Enclosure Nets and Accessory Kits", "reason": "Young children can become entangled in the straps of the hammock, punching bag and hand ring accessories, posing a strangulation hazard, which can result in serious injury or death.", "hazard_level": null, "company": "Shenzhen Segmart Technology Electronics Co., Ltd., of China", "company_location": "China", "date": "2026-04-16", "report_date": "2026-04-17", "status": "Announced", "distribution": "Sold in the United States at Online at Walmart.com and TikTok Shop from December 2025 through February 2026 for about $140.", "states": [], "nationwide": true, "quantity": "About 1,200", "codes": "", "remedy": "Consumers should remove the hammock, punching bag, hand ring and basketball board accessories immediately before continuing to use the trampoline. SEGMART will provide a $30 refund to consumers who remove and destroy the hammock, punching bag, hand ring and basketball board accessories. Consumers will be asked to cut the straps on the accessories and submit photos of the cut accessories to the firm. Instructions can be found at www.segmart.com. Refund", "retailers": ["Online at Walmart.com and TikTok Shop from December 2025 through February 2026 for about $140."], "injuries": "The firm has received one report of an incident in which a child's neck became entangled in the hammock straps, resulting in a rope burn injury around the child's neck.", "source_url": "https://www.cpsc.gov/Recalls/2026/Mini-Round-Toddler-Trampolines-Recalled-Due-to-Strangulation-Hazard-Risk-of-Serious-Injury-or-Death-Manufactured-by-SEGMART", "url": "https://recallledger.net/recalls/product-26414-mini-round-toddler-trampolines-recalled-due-to-strangulation-hazard-r/"}, {"id": "cpsc-26413", "source": "CPSC", "category": "consumer-product", "recall_number": "26413", "title": "Fun and Function Recalls Children's Metal Multi-Point Swing Frames Due to Risk of Injury from Fall Hazard", "product": "Multi-Point Swing Frames", "reason": "The swing frames can crack or break during use, posing a fall hazard, which can result in injury.", "hazard_level": null, "company": "Fun and Function, of Narberth, Pennsylvania", "company_location": "China", "date": "2026-04-16", "report_date": "2026-04-17", "status": "Announced", "distribution": "Sold in the United States at Online at Funandfunction.com from May 2022 through February 2026 for between $200 and $250.", "states": [], "nationwide": true, "quantity": "About 1,300", "codes": "", "remedy": "Consumers should immediately stop using the recalled multi-point suspension swing frame and contact Fun and Function for a full refund. Consumers should register at https://funandfunction.com/pages/swing-recall and disassemble and dispose of the product, according to the directions provided on the registration page. Refund", "retailers": ["Online at Funandfunction.com from May 2022 through February 2026 for between $200 and $250."], "injuries": "The firm received 10 reports of the swing frame cracking or breaking and children falling, resulting in two children sustaining contusions.", "source_url": "https://www.cpsc.gov/Recalls/2026/Fun-and-Function-Recalls-Childrens-Metal-Multi-Point-Swing-Frames-Due-to-Risk-of-Injury-from-Fall-Hazard", "url": "https://recallledger.net/recalls/product-26413-fun-and-function-recalls-children-s-metal-multi-point-swing-frames-due/"}, {"id": "cpsc-26412", "source": "CPSC", "category": "consumer-product", "recall_number": "26412", "title": "Macy's Recalls Arch Studio Tea Kettles Due to Risk of Serious Injury from Burn Hazard", "product": "Arch Studio Tea Kettle", "reason": "The tea kettles' handle can detach during use when heated, posing a risk of serious injury from burn hazard.", "hazard_level": null, "company": "Macy's Merchandising Group, Inc., of New York", "company_location": "China", "date": "2026-04-16", "report_date": "2026-04-17", "status": "Announced", "distribution": "Sold in the United States at Macy's stores nationwide and online at macys.com from August 2025 through February 2026 for about $50.", "states": [], "nationwide": true, "quantity": "About 4,600", "codes": "", "remedy": "Consumers should stop using the recalled tea kettles immediately and contact Macy's for a full refund in the form of a check for the purchase price. Consumers will be asked to complete a recall form at https://www.recallrtr.com/teakettle for a prepaid shipping label to return the product. No purchase receipt will be required. Refund", "retailers": ["Macy's stores nationwide and online at macys.com from August 2025 through February 2026 for about $50."], "injuries": "The firm has received three reports of the handle detaching. No injuries have been reported.", "source_url": "https://www.cpsc.gov/Recalls/2026/Macys-Recalls-Arch-Studio-Tea-Kettles-Due-to-Risk-of-Serious-Injury-from-Burn-Hazard", "url": "https://recallledger.net/recalls/product-26412-macy-s-recalls-arch-studio-tea-kettles-due-to-risk-of-serious-injury-f/"}, {"id": "cpsc-26411", "source": "CPSC", "category": "consumer-product", "recall_number": "26411", "title": "ATOYUS Children's Activity Cubes Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Violate Small Parts Ban and Mandatory Standard for Toys; Sold on Amazon by Melofaver US", "product": "ATOYUS Children's Activity Cubes", "reason": "The recalled toys violate the small parts ban because the toys are intended for children under three and the toys' xylophone screws and clock hands can detach. In addition, the toys violate the mandatory safety standard for children's toys because the mallets have spherical ends, posing a choking hazard.", "hazard_level": null, "company": "Shen Zhen Zhuoyuechaoqun Electronic Commerce Co., Ltd., dba Melofaver US, of China", "company_location": "China", "date": "2026-04-16", "report_date": "2026-04-17", "status": "Announced", "distribution": "Sold in the United States at Online at Amazon.com from January 2026 through February 2026 for about $26.", "states": [], "nationwide": true, "quantity": "About 70", "codes": "", "remedy": "Consumers should immediately stop using the recalled toys, take them away from children and contact Melofaver US for a full refund. Consumers will be asked to destroy the toy by writing \"recalled\" on all sides of the multi-sided wooden cube and cutting the playmat in half and email a photo of the destroyed toy to ATOYUSActivityCubeRecall@outlook.com. Consumers should then dispose of the recalled product. Refund", "retailers": ["Online at Amazon.com from January 2026 through February 2026 for about $26."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/ATOYUS-Childrens-Activity-Cubes-Recalled-Due-to-Risk-of-Serious-Injury-or-Death-from-Choking-Hazard-Violate-Small-Parts-Ban-and-Mandatory-Standard-for-Toys-Sold-on-Amazon-by-Melofaver-US", "url": "https://recallledger.net/recalls/product-26411-atoyus-children-s-activity-cubes-recalled-due-to-risk-of-serious-injur/"}, {"id": "cpsc-26409", "source": "CPSC", "category": "consumer-product", "recall_number": "26409", "title": "nvyue Magic Pocket Staffs Recalled Due to Projectile and Laceration Hazards; Imported by Xingwenfeng", "product": "nvyue Magic Pocket Staffs", "reason": "The protective pin mechanism on the Magic Pocket Staffs can fail to prevent unintentional expansion, posing serious projectile and laceration hazards. Even when engaged, the expansion occurs too rapidly for consumers to react, leaving virtually no opportunity for protection.", "hazard_level": null, "company": "Xingwenfeng, of China", "company_location": "China", "date": "2026-04-16", "report_date": "2026-04-17", "status": "Announced", "distribution": "Sold in the United States at Online at Amazon.com from September 2020 through March 2026 for between $8 and $26.", "states": [], "nationwide": true, "quantity": "About 25,000", "codes": "", "remedy": "Consumers should stop using the Magic Pocket Staff immediately and contact Xingwenfeng for a full refund. Consumers will be asked to write their initials and the current date with permanent marker on the Magic Pocket Staff and send a photo of the marked Magic Pocket Staff to nvyue_recall@163.com. Consumers will be instructed to safely expand the Magic Pocket Staff before disposal. Consumers should then dispose of the recalled product. Do not sell or give away these hazardous products. Refund", "retailers": ["Online at Amazon.com from September 2020 through March 2026 for between $8 and $26."], "injuries": "CPSC has received 163 reports of incidents involving injuries to the eyes, face and hands. Reported injuries include corneal lacerations, temporary vision loss and injuries requiring stitches, many involving children as young as nine years old.", "source_url": "https://www.cpsc.gov/Recalls/2026/nvyue-Magic-Pocket-Staffs-Recalled-Due-to-Projectile-and-Laceration-Hazards-Imported-by-Xingwenfeng", "url": "https://recallledger.net/recalls/product-26409-nvyue-magic-pocket-staffs-recalled-due-to-projectile-and-laceration-ha/"}, {"id": "cpsc-26408", "source": "CPSC", "category": "consumer-product", "recall_number": "26408", "title": "Sanlebi Pet Vet Playsets Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys; Sold on Amazon by Letokids", "product": "Sanlebi Pet Vet Playsets", "reason": "The Pet Vet Playset violates the mandatory standard for toys because the button cell batteries in the nail grinder and otoscope can be easily accessed by children.", "hazard_level": null, "company": "Guangzhou Letao Keji Youxiangongsi, doing business as Letokids, of China", "company_location": "China", "date": "2026-04-16", "report_date": "2026-04-17", "status": "Announced", "distribution": "Sold in the United States at Online at Amazon.com from June 2025 through January 2026 for between $20 and $26.", "states": [], "nationwide": true, "quantity": "About 4,650", "codes": "", "remedy": "Consumers should take away the nail grinder and otoscope from children immediately, stop using them and remove and properly dispose of the batteries. Consumers will be asked to throw the nail grinder and otoscope components away and send a photo of the disposed components to letorecall@outlook.com to receive a $5 refund or replacement nail grinder and otoscope. Note: Button cell batteries are hazardous. Batteries should be disposed of or recycled by following local hazardous waste procedures. Refund Replace", "retailers": ["Online at Amazon.com from June 2025 through January 2026 for between $20 and $26."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/Sanlebi-Pet-Vet-Playsets-Recalled-Due-to-Risk-of-Serious-Injury-or-Death-from-Battery-Ingestion-Violates-Mandatory-Standard-for-Toys-Sold-on-Amazon-by-Letokids", "url": "https://recallledger.net/recalls/product-26408-sanlebi-pet-vet-playsets-recalled-due-to-risk-of-serious-injury-or-dea/"}, {"id": "cpsc-26407", "source": "CPSC", "category": "consumer-product", "recall_number": "26407", "title": "Generac Power Systems Recalls Portable Generators Due to Risk of Serious Injury or Death from Burn and Fire Hazards", "product": "Generac Portable Generators", "reason": "When first filling the recalled generator with gasoline, fuel can leak from the carburetor, posing a risk of serious injury or death from fire or burn hazard. Consumers with generators that have previously been filled with enough gasoline to move the gauge off \"E,\" or have been used without any gasoline leakage, can continue to be used.", "hazard_level": null, "company": "", "company_location": "Vietnam", "date": "2026-04-16", "report_date": "2026-04-17", "status": "Announced", "distribution": "Sold in the United States at Home Depot, Lowe's and other home improvement and hardware stores nationwide and online from May 2025 through February 2026 for between $600 and $1,300.", "states": [], "nationwide": true, "quantity": "About 149,400 (In addition, about 260 were sold in Canada)", "codes": "", "remedy": "Consumers should immediately stop using the recalled Generac portable generator and go to https://www.generac.com/about/recalls/GP-Carburetor to check to see if your model and serial number are included in this recall. If your unit is included in the recall and has either not yet been filled with fuel or exhibited leakage after fueling as described above, please contact your dealer to arrange for free repair at the dealer's location. Repair", "retailers": ["Home Depot, Lowe's and other home improvement and hardware stores nationwide and online from May 2025 through February 2026 for between $600 and $1,300."], "injuries": "The firm has received 114 reports of generator fuel leaks. No injuries have been reported.", "source_url": "https://www.cpsc.gov/Recalls/2026/Generac-Power-Systems-Recalls-Portable-Generators-Due-to-Risk-of-Serious-Injury-or-Death-from-Burn-and-Fire-Hazards", "url": "https://recallledger.net/recalls/product-26407-generac-power-systems-recalls-portable-generators-due-to-risk-of-serio/"}, {"id": "cpsc-26406", "source": "CPSC", "category": "consumer-product", "recall_number": "26406", "title": "Pressure Washers Recalled Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards; Imported by BAYOTAK USA", "product": "BAYOTAK USA Electric Pressure Washers", "reason": "The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI), posing a serious risk of injury or death from shock and electrocution hazards.", "hazard_level": null, "company": "NingboRuiyaodianzishangwuyouxiangongsi, dba BAYOTAK USA, of China", "company_location": "China", "date": "2026-04-16", "report_date": "2026-04-17", "status": "Announced", "distribution": "Sold in the United States at Online at Amazon.com from October 2025 through January of 2026 for about $110.", "states": [], "nationwide": true, "quantity": "360", "codes": "", "remedy": "Consumers should immediately stop using the recalled pressure washers and contact BATOYAK USA for a free replacement pressure washer of at least equal value to the recalled pressure washer, including shipping. Consumers will be asked to destroy the pressure washer by unplugging it and cutting the power cord in half and send a photo of the destroyed power washer to bayotakservice@163.com. Consumers should then dispose of the destroyed recalled product. Replace", "retailers": ["Online at Amazon.com from October 2025 through January of 2026 for about $110."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/Pressure-Washers-Recalled-Due-to-Serious-Risk-of-Injury-or-Death-from-Shock-and-Electrocution-Hazards-Imported-by-BAYOTAK-USA", "url": "https://recallledger.net/recalls/product-26406-pressure-washers-recalled-due-to-serious-risk-of-injury-or-death-from/"}, {"id": "fda-food-h-0659-2026", "source": "FDA", "category": "food", "recall_number": "H-0659-2026", "title": "ReadyMeals Turkey Bacon & Cheddar Pretzel Duo Sandwich recall (F&S Fresh Foods, Inc.)", "product": "ReadyMeals Turkey Bacon & Cheddar Pretzel Duo Sandwich, perishable, Keep Refrigerated, plastic clamshell, net wt. 10 oz, UPC 8 26766 25036 3. Distributed By F&S Fresh Foods Vineland, NJ 08360. Label declares CONTAINS EGG, MILK, SOY, WHEAT.", "reason": "Undeclared sesame. Sandwich contains visible sesame but label does not declare sesame.", "hazard_level": "Class II", "company": "F&S Fresh Foods, Inc.", "company_location": "Vineland, NJ, United States", "date": "2026-04-02", "report_date": "2026-04-15", "status": "Terminated", "distribution": "distributed in OR", "states": [], "nationwide": false, "quantity": "325 units distributed (only 27 units were mis-labeled)", "codes": "Best if Used By: 04/06/26 Lot: FSNW 089 Manufacturing location (Clackamas, OR) Julian Date", "remedy": null, "retailers": [], "injuries": null, "source_url": "https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0659-2026%22", "url": "https://recallledger.net/recalls/food-h-0659-2026-readymeals-turkey-bacon-cheddar-pretzel-duo-sandwich-perishable-ke/"}, {"id": "cpsc-26405", "source": "CPSC", "category": "consumer-product", "recall_number": "26405", "title": "Muscccm Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violates Virginia Graeme Baker Pool & Spa Safety Act; Sold on Amazon by SZ Hengxun", "product": "Muscccm Pool Drain Covers", "reason": "The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing entrapment and drowning hazards to swimmers and bathers.", "hazard_level": null, "company": "Qingyuan Fenle Sauna & Pool Equipment Co., Ltd., of China", "company_location": "China", "date": "2026-04-09", "report_date": "2026-04-10", "status": "Announced", "distribution": "Sold in the United States at Online at Amazon.com from February 2026 through March 2026 for about $19.", "states": [], "nationwide": true, "quantity": "About 480", "codes": "", "remedy": "Pool owners, pool operators and consumers should immediately stop using pools with the recalled pool drain covers. To receive a refund, consumers should remove the drain cover from the pool, take a photo of the removed cover, and send it to SZ Hengxun by email at MuscccmRecall@126.com. Ensure all pools and spas have VGBA-compliant drain covers and teach children to stay away from drains. Refund", "retailers": ["Online at Amazon.com from February 2026 through March 2026 for about $19."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/Muscccm-Pool-Drain-Covers-Recalled-Due-to-Risk-of-Serious-Injury-or-Death-from-Entrapment-and-Drowning-Hazards-Violates-Virginia-Graeme-Baker-Pool-Spa-Safety-Act-Sold-on-Amazon-by-SZ-Hengxun", "url": "https://recallledger.net/recalls/product-26405-muscccm-pool-drain-covers-recalled-due-to-risk-of-serious-injury-or-de/"}, {"id": "cpsc-26404", "source": "CPSC", "category": "consumer-product", "recall_number": "26404", "title": "Prestige Import Group Recalls Supernova and Typhoon Lighters Due to Risk of Serious Injury or Death from Fire and Burn Hazards; Violates Mandatory Standard for Cigarette Lighters", "product": "Supernova and Typhoon Lighters", "reason": "The recalled lighters violate the mandatory standard for cigarette lighters because they do not have the required child-resistant mechanism, posing a risk of serious injury or death from fire and burn hazards. In addition, the lighters failed to meet the pre-market lighter submission requirement needed to demonstrate that the lighters feature child-resistant mechanisms and ensuring their safety and compliance with U.S. regulations.", "hazard_level": null, "company": "Prestige Import Group, of Deerfield, Florida", "company_location": "China", "date": "2026-04-09", "report_date": "2026-04-10", "status": "Announced", "distribution": "Sold in the United States at Small independent stores nationwide and online at prestigeimportgroup.com from October 2023 through March 2026 for between $7 and $10.", "states": [], "nationwide": true, "quantity": "About 4,300", "codes": "", "remedy": "Consumers should stop using the recalled lighters immediately and contact Prestige Import Group for a full refund or store credit. Consumers will be asked to write \"Recalled\" in permanent marker and send a photo of the marked lighter to salesdept2@prestigeimportgroup.com. Consumers should then dispose of the recalled product in accordance with state and local waste disposal procedures. Refund", "retailers": ["Small independent stores nationwide and online at prestigeimportgroup.com from October 2023 through March 2026 for between $7 and $10."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/Prestige-Import-Group-Recalls-Supernova-and-Typhoon-Lighters-Due-to-Risk-of-Serious-Injury-or-Death-from-Fire-and-Burn-Hazards-Violates-Mandatory-Standard-for-Cigarette-Lighters", "url": "https://recallledger.net/recalls/product-26404-prestige-import-group-recalls-supernova-and-typhoon-lighters-due-to-ri/"}, {"id": "cpsc-26403", "source": "CPSC", "category": "consumer-product", "recall_number": "26403", "title": "LED Lights Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Coin Batteries; Sold on Amazon by Happiness Light", "product": "Happiness Light LED Lights", "reason": "The recalled LED lights violate the mandatory standard for consumer products containing button cell or coin batteries because they contain lithium coin batteries that can be accessed easily by children, posing an ingestion hazard. Additionally, the LED lights do not have the warnings as required by Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.", "hazard_level": null, "company": "J U Kai Technology Co., LTD, dba Happiness Light, of China", "company_location": "China", "date": "2026-04-09", "report_date": "2026-04-10", "status": "Announced", "distribution": "Sold in the United States at Online at Amazon.com from March 2024 through February 2026 for about $20.", "states": [], "nationwide": true, "quantity": "About 2,800", "codes": "", "remedy": "Consumers should stop using the recalled LED lights immediately and place them in an area where children cannot access them. Consumers will be asked to disassemble the lights and submerge all of the components in water. To receive a full refund, email a photo showing the submerged product to usa@happinesslight.com. Note: Button cell and coin batteries are hazardous. Batteries should be disposed of or recycled by following local hazardous waste procedures. Refund", "retailers": ["Online at Amazon.com from March 2024 through February 2026 for about $20."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/LED-Lights-Recalled-Due-to-Risk-of-Serious-Injury-or-Death-from-Battery-Ingestion-Violates-Mandatory-Standard-for-Consumer-Products-with-Coin-Batteries-Sold-on-Amazon-by-Happiness-Light", "url": "https://recallledger.net/recalls/product-26403-led-lights-recalled-due-to-risk-of-serious-injury-or-death-from-batter/"}, {"id": "cpsc-26401", "source": "CPSC", "category": "consumer-product", "recall_number": "26401", "title": "Shenzhen Shijingjie Network Technology Male-to-Male Extension Cords Recalled Due to Risk of Serious Injury and Death from Electrocution and Carbon Monoxide Poisoning Hazards; Sold on Walmart", "product": "Male-to-Male Extension Cords", "reason": "The recalled male-to-male extension cords violate safety requirements because their exposed prongs can become energized when one end is plugged into a generator or other power source, posing a risk of serious injury and death from electrocution. In addition, using the cords to supply power from a generator to a residential electrical system (backfeeding) poses a risk of electrocution and fire. The cords' short length encourages the use of generators close to homes or enclosed spaces, posing a risk of carbon monoxide (CO) poisoning.", "hazard_level": null, "company": "Shenzhen Shijingjie Network Technology Co., Ltd., of China", "company_location": "China", "date": "2026-04-09", "report_date": "2026-04-10", "status": "Announced", "distribution": "Sold in the United States at Online at Walmart.com from April 2025 through November 2025 for between $18 and $26.", "states": [], "nationwide": true, "quantity": "About 200", "codes": "", "remedy": "Consumers should stop using the recalled extension cords immediately, taking care not to touch the live end of the cord when unplugging, and contact Shenzhen Shijingjie Network Technology for a full refund. Refund", "retailers": ["Online at Walmart.com from April 2025 through November 2025 for between $18 and $26."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/Shenzhen-Shijingjie-Network-Technology-Male-to-Male-Extension-Cords-Recalled-Due-to-Risk-of-Serious-Injury-and-Death-from-Electrocution-and-Carbon-Monoxide-Poisoning-Hazards-Sold-on-Walmart", "url": "https://recallledger.net/recalls/product-26401-shenzhen-shijingjie-network-technology-male-to-male-extension-cords-re/"}, {"id": "cpsc-26399", "source": "CPSC", "category": "consumer-product", "recall_number": "26399", "title": "Shenzhen Baihang Recalls VEEKTOMX Mini Power Banks, Due to Fire and Burn Hazards; Sold on Amazon", "product": "VEEKTOMX Portable Charger Mini Power Banks", "reason": "The lithium-ion battery in the recalled power banks can overheat and ignite, posing fire and burn hazards to consumers.", "hazard_level": null, "company": "Shenzhen Baihang Technology Co., Ltd., of China", "company_location": "China", "date": "2026-04-09", "report_date": "2026-04-10", "status": "Announced", "distribution": "Sold in the United States at Amazon.com between January 2024 and September 2024, for between $24 and $30.", "states": [], "nationwide": true, "quantity": "About 8,000", "codes": "", "remedy": "Consumers should immediately stop using the recalled power banks and contact Shenzhen Baihang to verify power bank is part of the recall and receive a free replacement power bank. Replace", "retailers": ["Amazon.com between January 2024 and September 2024, for between $24 and $30."], "injuries": "Shenzhen Baihang has received three reports of fires resulting in minor property damage. No injuries have been reported.", "source_url": "https://www.cpsc.gov/Recalls/2026/Shenzhen-Baihang-Recalls-VEEKTOMX-Mini-Power-Banks-Due-to-Fire-and-Burn-Hazards-Sold-on-Amazon", "url": "https://recallledger.net/recalls/product-26399-shenzhen-baihang-recalls-veektomx-mini-power-banks-due-to-fire-and-bu/"}, {"id": "cpsc-26398", "source": "CPSC", "category": "consumer-product", "recall_number": "26398", "title": "ShymeryDirect LED Lights Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Coin Batteries", "product": "ShymeryDirect LED Lights", "reason": "The recalled LED lights violate the mandatory standard for consumer products containing button cell or coin batteries because they contain lithium coin batteries that can be accessed easily by children, posing an ingestion hazard. Additionally, the LED lights do not have the warnings required by Reese's Law. If coin batteries are swallowed, they can cause serious injuries, internal chemical burns and death.", "hazard_level": null, "company": "ShymeryDirect, of China", "company_location": "China", "date": "2026-04-09", "report_date": "2026-04-10", "status": "Announced", "distribution": "Sold in the United States at Online at Amazon.com from January 2026 through March 2026 for about $23.", "states": [], "nationwide": true, "quantity": "About 295", "codes": "", "remedy": "Consumers should immediately stop using the recalled LED lights and place them in an area where children cannot access them. Consumers will be asked to disassemble and submerge all components in water. To receive a full refund, email a photo showing the submerged product to Shymeryrecall0402@outlook.com. Note: Button cell and coin batteries are hazardous. Batteries should be disposed of or recycled by following local hazardous waste procedures. Refund", "retailers": ["Online at Amazon.com from January 2026 through March 2026 for about $23."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/ShymeryDirect-LED-Lights-Recalled-Due-to-Risk-of-Serious-Injury-or-Death-from-Battery-Ingestion-Violates-Mandatory-Standard-for-Consumer-Products-with-Coin-Batteries", "url": "https://recallledger.net/recalls/product-26398-shymerydirect-led-lights-recalled-due-to-risk-of-serious-injury-or-dea/"}, {"id": "cpsc-26397", "source": "CPSC", "category": "consumer-product", "recall_number": "26397", "title": "Yeeluzan Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violates Virginia Graeme Baker Pool & Spa Safety Act; Sold on Amazon by Yeeluzan", "product": "Yeeluzan Pool Drain Covers", "reason": "The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing entrapment and drowning hazards to swimmers and bathers.", "hazard_level": null, "company": "Weifang Luzhan Trade Co., Ltd., dba Yeeluzan, of China", "company_location": "China", "date": "2026-04-09", "report_date": "2026-04-10", "status": "Announced", "distribution": "Sold in the United States at Online at Amazon.com from May 2025 through March 2026 for about $32.", "states": [], "nationwide": true, "quantity": "About 640", "codes": "", "remedy": "Pool owners, pool operators and consumers should immediately stop using pools with the recalled pool drain covers. To receive a full refund to their original payment method, consumers should destroy the removed drain cover, take a clear photograph/video of the destroyed product as proof of destruction, and send the proof to the recalling firm by email at yeeluzanrecall@163.com. Ensure all pools and spas are fitted with VGBA-compliant drain covers and teach children to stay away from drains. Refund", "retailers": ["Online at Amazon.com from May 2025 through March 2026 for about $32."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/Yeeluzan-Pool-Drain-Covers-Recalled-Due-to-Risk-of-Serious-Injury-or-Death-from-Entrapment-and-Drowning-Hazards-Violates-Virginia-Graeme-Baker-Pool-Spa-Safety-Act-Sold-on-Amazon-by-Yeeluzan", "url": "https://recallledger.net/recalls/product-26397-yeeluzan-pool-drain-covers-recalled-due-to-risk-of-serious-injury-or-d/"}, {"id": "cpsc-26396", "source": "CPSC", "category": "consumer-product", "recall_number": "26396", "title": "Halloween Pumpkin Carving Kits Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Button Cell Batteries; Sold on Amazon by Besslly Store", "product": "Besslly Halloween Pumpkin Carving Kits", "reason": "The recalled carving kits violate the mandatory standard for consumer products with button cell and coin batteries because the button cell batteries in the tea lights can be accessed easily by children, posing an ingestion hazard. Additionally, the product and its packaging do not have the warnings required under Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns, and death.", "hazard_level": null, "company": "LinkInnow International Co., Ltd., dba Besslly Store, of China", "company_location": "China", "date": "2026-04-09", "report_date": "2026-04-10", "status": "Announced", "distribution": "Sold in the United States at Online at Amazon.com from March 2024 through December 2025 for between $9 and $20.", "states": [], "nationwide": true, "quantity": "About 650", "codes": "", "remedy": "Consumers should stop using the recalled carving kits immediately and contact Besslly Store for a full refund. Consumers will be asked to email a photograph of disposal to tingjmng@outlook.com to receive the refund. Note: Button cell batteries are hazardous. Batteries should be disposed of or recycled by following local hazardous waste procedures. Refund", "retailers": ["Online at Amazon.com from March 2024 through December 2025 for between $9 and $20."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/Halloween-Pumpkin-Carving-Kits-Recalled-Due-to-Risk-of-Serious-Injury-or-Death-from-Battery-Ingestion-Violates-Mandatory-Standard-for-Consumer-Products-with-Button-Cell-Batteries-Sold-on-Amazon-by-Besslly-Store", "url": "https://recallledger.net/recalls/product-26396-halloween-pumpkin-carving-kits-recalled-due-to-risk-of-serious-injury/"}, {"id": "cpsc-26395", "source": "CPSC", "category": "consumer-product", "recall_number": "26395", "title": "Head USA Recalls Ski Boots Due to Risk of Serious Injury from Fall Hazard", "product": "Head Ski Boots", "reason": "The fluorescent yellow materials of the boot shell and sole inserts can deteriorate and break, posing a risk of serious injury from a fall.", "hazard_level": null, "company": "Head USA Inc., of Boulder, Colorado", "company_location": "Czech Republic", "date": "2026-04-09", "report_date": "2026-04-10", "status": "Announced", "distribution": "Sold in the United States at Various ski retailers nationwide and online from September 2015 through March 2026 for between $500 to $750.", "states": [], "nationwide": true, "quantity": "About 1,365 (In addition, about 525 were sold in Canada)", "codes": "", "remedy": "Consumers should stop using the recalled ski boots immediately and contact Head USA or a Head authorized retailer. For recalled boots with fluorescent boot shell materials, Head will provide free replacement boots in a newer equivalent model upon return of the recalled boots. For recalled boots with yellow sole inserts, Head will provide free replacement sole inserts, which can be installed by the consumer or by a ski shop. Replace Repair", "retailers": ["Various ski retailers nationwide and online from September 2015 through March 2026 for between $500 to $750."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/Head-USA-Recalls-Ski-Boots-Due-to-Risk-of-Serious-Injury-from-Fall-Hazard", "url": "https://recallledger.net/recalls/product-26395-head-usa-recalls-ski-boots-due-to-risk-of-serious-injury-from-fall-haz/"}, {"id": "cpsc-26394", "source": "CPSC", "category": "consumer-product", "recall_number": "26394", "title": "Seasonal Specialties Recalls Members Mark 7' Pre-Lit Twinkling Bucks Due to Burn Hazard", "product": "Members Mark 7' Pre-Lit Twinkling Buck", "reason": "If the wires are connected incorrectly, the current limiting resistor can overheat, posing a burn hazard.", "hazard_level": null, "company": "Seasonal Specialties, LLC, of Eden Prairie, Minnesota", "company_location": "China", "date": "2026-04-09", "report_date": "2026-04-10", "status": "Announced", "distribution": "Sold in the United States at Online at SamsClub.com from August 2025 through December 2025 for about $170.", "states": [], "nationwide": true, "quantity": "About 2,460", "codes": "", "remedy": "Consumers should stop using the Members Mark 7' Pre-Lit Twinkling Buck immediately and contact Seasonal Specialties to request either a full refund or a repair kit. The repair kit includes new instructions on how to connect the wires, color-coded wire labels and a cord tag warning sticker. Refund Repair", "retailers": ["Online at SamsClub.com from August 2025 through December 2025 for about $170."], "injuries": "The firm has received five reports of smoke and a burning smell. No injuries have been reported.", "source_url": "https://www.cpsc.gov/Recalls/2026/Seasonal-Specialties-Recalls-Members-Mark-7-Pre-Lit-Twinkling-Bucks-Due-to-Burn-Hazard", "url": "https://recallledger.net/recalls/product-26394-seasonal-specialties-recalls-members-mark-7-pre-lit-twinkling-bucks-d/"}, {"id": "cpsc-26393", "source": "CPSC", "category": "consumer-product", "recall_number": "26393", "title": "SCUBAPRO Recalls Monorail Weight Pockets for Buoyancy Compensator Devices (BCDs) Due to Risk of Serious Injury or Death from Drowning", "product": "SCUBAPRO Monorail Weight Pockets for BCDs", "reason": "The D-ring handle that is used to unlock the weight pocket from the Buoyancy Compensator Device (BCD) can detach during use. If this happens, the user will not be able to remove the weight pocket in an emergency, in order to rise to the surface, posing a risk of serious injury or death from a drowning hazard.", "hazard_level": null, "company": "Johnson Outdoors Diving LLC d/b/a SCUBAPRO, of Racine, Wisconsin", "company_location": "South Africa", "date": "2026-04-09", "report_date": "2026-04-10", "status": "Announced", "distribution": "Sold in the United States at Specialty dive shops nationwide and online at Scubapro.com and other authorized online retailers from November 2025 through February 2026 for about $200.", "states": [], "nationwide": true, "quantity": "About 2,800 (In addition, about 40 were sold in Canada)", "codes": "", "remedy": "Consumers should immediately stop using the recalled Monorail Weight Pocket and register online at https://scubapro.johnsonoutdoors.com/us/recalls for a free repair of the D-ring handle at a local authorized dealer or to obtain a prepaid shipping label to return the recalled weight pocket to SCUBAPRO for a free repair and free return shipping. Repair", "retailers": ["Specialty dive shops nationwide and online at Scubapro.com and other authorized online retailers from November 2025 through February 2026 for about $200."], "injuries": "The firm has received two reports of the D-ring handle detaching. No injuries have been reported.", "source_url": "https://www.cpsc.gov/Recalls/2026/SCUBAPRO-Recalls-Monorail-Weight-Pockets-for-Buoyancy-Compensator-Devices-BCDs-Due-to-Risk-of-Serious-Injury-or-Death-from-Drowning", "url": "https://recallledger.net/recalls/product-26393-scubapro-recalls-monorail-weight-pockets-for-buoyancy-compensator-devi/"}, {"id": "cpsc-26392", "source": "CPSC", "category": "consumer-product", "recall_number": "26392", "title": "Magnetic Drinkware Charms Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Magnets; Sold on Amazon by Maitys", "product": "Maitys Drinkware Charms", "reason": "The recalled magnetic drinkware charms violate the mandatory standard for magnets because they contain loose magnets posing an ingestion hazard to children. When high-powered magnets are swallowed, the ingested magnets can attract each other, or other metal objects, and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning and death.", "hazard_level": null, "company": "Hefei Maitusilu Wangluokeji Youxiangongsi, dba Maitys, of China", "company_location": "China", "date": "2026-04-09", "report_date": "2026-04-10", "status": "Announced", "distribution": "Sold in the United States at Online at Amazon.com from October 2022 through January 2026 for about $8.", "states": [], "nationwide": true, "quantity": "About 16,400", "codes": "", "remedy": "Consumers should stop using the recalled drinkware charms immediately, take them away from children and contact Maitys for a full refund. Consumers will be asked to dispose of the charms and send a photo of the disposed product to maituus@outlook.com. Refund", "retailers": ["Online at Amazon.com from October 2022 through January 2026 for about $8."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/Magnetic-Drinkware-Charms-Recalled-Due-to-Risk-of-Serious-Injury-or-Death-from-Magnet-Ingestion-Violate-Mandatory-Standard-for-Magnets-Sold-on-Amazon-by-Maitys", "url": "https://recallledger.net/recalls/product-26392-magnetic-drinkware-charms-recalled-due-to-risk-of-serious-injury-or-de/"}, {"id": "cpsc-26389", "source": "CPSC", "category": "consumer-product", "recall_number": "26389", "title": "Silks Recall Children's Loungewear Sets Due to Risk of Serious Injury or Death from Burn Hazard; Violates Mandatory Flammability Standards for Children's Sleepwear", "product": "Children's Loungewear Sets", "reason": "The recalled children's loungewear violates mandatory flammability standards for children's sleepwear, posing a risk of serious injuries or deadly burn hazards to children.", "hazard_level": null, "company": "Silks, of Queen Creak, Arizona", "company_location": "China", "date": "2026-04-09", "report_date": "2026-04-10", "status": "Announced", "distribution": "Sold in the United States at Online at Silksdesign.com from January 2024 through September 2025 for between $40 and $50.", "states": [], "nationwide": true, "quantity": "About 7,900", "codes": "", "remedy": "Consumers should immediately stop using the recalled loungewear, take it away from children and contact Silks for a full refund or store credit. Consumers should destroy the garments by cutting the top and bottom in half and send a photo of the destroyed garments to silkssupport@silksdesign.com. Consumers should then dispose of the loungewear. Refund", "retailers": ["Online at Silksdesign.com from January 2024 through September 2025 for between $40 and $50."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/Silks-Recall-Childrens-Loungewear-Sets-Due-to-Risk-of-Serious-Injury-or-Death-from-Burn-Hazard-Violates-Mandatory-Flammability-Standards-for-Childrens-Sleepwear", "url": "https://recallledger.net/recalls/product-26389-silks-recall-children-s-loungewear-sets-due-to-risk-of-serious-injury/"}, {"id": "cpsc-26388", "source": "CPSC", "category": "consumer-product", "recall_number": "26388", "title": "SNOOZ Recalls Electrical Fans Due to Fire Hazard", "product": "Breez 2-in-1 Smart Bedroom Fan and White Noise Machine", "reason": "The power connector inside the fan can corrode and cause the fan to overheat, posing a risk of fire.", "hazard_level": null, "company": "Snooz, Inc., of Las Vegas, Nevada", "company_location": "China", "date": "2026-04-09", "report_date": "2026-04-10", "status": "Announced", "distribution": "Sold in the United States at Online at Amazon, Shopify, Kickstarter and other small retailers from June 2023 through December 2025 for about $200.", "states": [], "nationwide": true, "quantity": "About 11,900 (In addition, about 140 were sold in Canada)", "codes": "", "remedy": "Consumers should stop using the recalled fan immediately and go to the firm's website to register for a replacement fan. Breez 2nd Generation sound machines are not affected by this recall. To determine whether a product is affected, consumers should locate the serial number on the underside of the fan's wooden base. Serial numbers beginning with BZ10 or BZ02 are included in this recall. Consumers will be asked to cut the power cord and upload a photo of the cut power cord and a photo of the adapter showing the model number and all printed information. Replace", "retailers": ["Online at Amazon, Shopify, Kickstarter and other small retailers from June 2023 through December 2025 for about $200."], "injuries": "The firm reported six cases of the fans overheating and smoking with one report of fire. No injuries or property damage have been reported.", "source_url": "https://www.cpsc.gov/Recalls/2026/SNOOZ-Recalls-Electrical-Fans-Due-to-Fire-Hazard", "url": "https://recallledger.net/recalls/product-26388-snooz-recalls-electrical-fans-due-to-fire-hazard/"}, {"id": "cpsc-26387", "source": "CPSC", "category": "consumer-product", "recall_number": "26387", "title": "Easymake Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violates Mandatory Standard for Adult Portable Bed Rails; Imported by ZFZG-US", "product": "Easymake Adult Portable Bed Rails", "reason": "The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. In addition, the bed rails do not bear the required hazard warning labels.", "hazard_level": null, "company": "Zhongshan Yungu Daily Products, of China", "company_location": "China", "date": "2026-04-09", "report_date": "2026-04-10", "status": "Announced", "distribution": "Sold in the United States at Online at Amazon.com from August 2023 through February 2026 for about $55.", "states": [], "nationwide": true, "quantity": "About 19,000", "codes": "", "remedy": "Consumers should stop using the recalled bed rails immediately and contact ZFZG-US for a full refund. Consumers should destroy the bed rail by cutting the storage bag off the upper rail and the safety strap in half, write \"Recalled\" in permanent marker on the main frame and upload a photo of the marked bed rails to https://easymake-us.myshopify.com/recall. Consumers should then dispose of the recalled product in accordance with state and local waste disposal procedures. Refund", "retailers": ["Online at Amazon.com from August 2023 through February 2026 for about $55."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/Easymake-Adult-Portable-Bed-Rails-Recalled-Due-to-Risk-of-Serious-Injury-or-Death-from-Entrapment-and-Asphyxiation-Violates-Mandatory-Standard-for-Adult-Portable-Bed-Rails-Imported-by-ZFZG-US", "url": "https://recallledger.net/recalls/product-26387-easymake-adult-portable-bed-rails-recalled-due-to-risk-of-serious-inju/"}, {"id": "cpsc-26386", "source": "CPSC", "category": "consumer-product", "recall_number": "26386", "title": "Vitaquest International Recalls Multiple Iron Supplement Bottles and Packets Due to Risk of Serious Injury or Death from Poisoning to Young Children; Violates Mandatory Standard for Child-Resistant Packaging", "product": "Various Brands of Iron-Containing Dietary Supplements", "reason": "The dietary supplements contain iron, which must be in child-resistant packaging as required by the Poison Prevention Packaging Act. The packaging of the supplements is not child-resistant, posing a risk of serious injury or death from poisoning if the contents are swallowed by young children.", "hazard_level": null, "company": "Vitaquest International LLC of West Caldwell, New Jersey", "company_location": "United States", "date": "2026-04-09", "report_date": "2026-04-10", "status": "Announced", "distribution": "Sold in the United States at Credo Beauty, Erewhon, Healf, Nutrition World, The Vitamin Shoppe, Fullscript, Ulta Beauty stores nationwide, medical practitioners' offices, brands' websites and Amazon.com from April 2023 through February 2026 for between $13 and $130 depending on brand and size.", "states": [], "nationwide": true, "quantity": "About 356,140", "codes": "UPCs: 860007168901, 860007168994, 860012923930, 860010126417, 860010126479, 860010126493, 860013460136, 860013460174, 860013460143, 829584500061, 829584500153, 746888915028, 00709355144413, 0038407566232, 810067444910, 850067341338, 850067341314, 850067341321, 858151008334, 858151008341", "remedy": "Consumers should immediately store the supplements out of sight and reach of children and contact Vitaquest International for information on how to obtain a free child-resistant replacement cap or storage pouch. Brand / Product Name Remedy Arey Not Today, Grey (60ct and 180ct) Cap Bari Life Complete Bariatric Vitamin - Watermelon (60ct) Storage pouch Bird&Be The Prenatal Essentials for Females (30 pkts) Storage pouch Bird&Be The Power Prenatal for Females (30 pkts) Storage pouch Bird&Be The Power Prenatal for Females + CoQ10 Boost (30pkts) Storage pouch Bird&Be Female Fertility Power Prenatal Pack (30 pkts) Storage pouch Bird&Be Complete Prenatal Pack (30 pkts) Storage pouch Bird&Be Female Fertility Power Prenatal + CoQ10 Pack (30 pkts) Storage pouch Biote Nutraceutical Iron+ (30ct) Cap Dr. Fuhrman Gentle Prenatal Multivitamin + D3 (120ct) Cap Dr. Fuhrman Pixie Vites Children's Multivitamin (120ct) Cap NuLife Advanced Bariatrics Multivitamin Chewable Tablets (60ct) Cap HMR Multi Daily Vitamin and Mineral Supplement (60ct) Cap Bariatric Pal Ultra Multi Bariatric Multivitamin (90ct) Cap Noevir Inner Care Premium BioEssentials (120ct) Cap Zenbean Kids Café Instant Coffee + Nutrition Latte, Original, Caramel, Chocolate, and Vanilla (30srv) Storage pouch Sakara The Foundation (30pkts) Storage pouch Sakara The Foundation: Prenatal (30pkts) Storage pouch Replace", "retailers": ["Credo Beauty, Erewhon, Healf, Nutrition World, The Vitamin Shoppe, Fullscript, Ulta Beauty stores nationwide, medical practitioners' offices, brands' websites and Amazon.com from April 2023 through February 2026 for between $13 and $130 depending on brand and size."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/Vitaquest-International-Recalls-Multiple-Iron-Supplement-Bottles-and-Packets-Due-to-Risk-of-Serious-Injury-or-Death-from-Poisoning-to-Young-Children-Violates-Mandatory-Standard-for-Child-Resistant-Packaging", "url": "https://recallledger.net/recalls/product-26386-vitaquest-international-recalls-multiple-iron-supplement-bottles-and-p/"}, {"id": "cpsc-26385", "source": "CPSC", "category": "consumer-product", "recall_number": "26385", "title": "BISSELL Recalls Over One Million Steam Shot OmniReach Steam Cleaners Due to Risk of Serious Burn Hazard from Attachments", "product": "Steam Shot OmniReach and Steam Shot Omni Steam Cleaners with attachments", "reason": "The recalled steam cleaners' attachments can unexpectedly detach from the steam cleaners and expel hot water or steam onto users during use, posing a serious burn hazard.", "hazard_level": null, "company": "BISSELL Homecare Inc. of Grand Rapids, Michigan", "company_location": "China", "date": "2026-04-09", "report_date": "2026-04-10", "status": "Announced", "distribution": "Sold in the United States at Target, Walmart and other department and home goods stores nationwide and online at BISSELL.com, Amazon.com, HSN.com and other websites from October 2024 through March 2026 for between $9 and $55.", "states": [], "nationwide": true, "quantity": "About 1.7 million (In addition, about 96,000 were sold in Canada)", "codes": "", "remedy": "Consumers should stop using the recalled steam cleaner attachments immediately and contact BISSELL to receive free new attachments. Consumers should visit www.steamshot2026.com to register for the recall and for instructions on how to participate in the recall, including how to upload a photo showing the original attachment accessories have been disposed of in the trash. Repair", "retailers": ["Target, Walmart and other department and home goods stores nationwide and online at BISSELL.com, Amazon.com, HSN.com and other websites from October 2024 through March 2026 for between $9 and $55."], "injuries": "BISSELL has received 206 reports of hot water or steam unexpectedly escaping from the steam cleaners' attachments, including 161 reports of burn injuries with a report of one second degree burn.", "source_url": "https://www.cpsc.gov/Recalls/2026/BISSELL-Recalls-Over-One-Million-Steam-Shot-OmniReach-Steam-Cleaners-Due-to-Risk-of-Serious-Burn-Hazard-from-Attachments", "url": "https://recallledger.net/recalls/product-26385-bissell-recalls-over-one-million-steam-shot-omnireach-steam-cleaners-d/"}, {"id": "cpsc-26372", "source": "CPSC", "category": "consumer-product", "recall_number": "26372", "title": "Wybotics Recalls Robotic Pool Vacuums Due to Burn and Fire Hazards", "product": "Osprey 700 Max and S1 robotic pool vacuums", "reason": "The lithium-ion battery in the recalled pool vacuums can overheat, posing burn and fire hazards to consumers.", "hazard_level": null, "company": "Wybotics, Co. Ltd. of Tianjin, Chin", "company_location": "China", "date": "2026-04-09", "report_date": "2026-04-10", "status": "Announced", "distribution": "Sold in the United States at Online at Amazon.com, BestBuy.com and Wybotpool.com for between $500 and $700. The S1 was sold from April 2023 through September 2024 and the Osprey 700 Max was sold from April 2023 through November 2024.", "states": [], "nationwide": true, "quantity": "About 5,000", "codes": "", "remedy": "Consumers should stop using the recalled robotic pool vacuums immediately and contact Wybotics to receive a free replacement WYBOT C2 robotic pool vacuum. Wybotics will provide a free return label for consumers to send the recalled product back to Wybotics. Within 15 days of receiving the recalled pool vacuums, Wybotics will ship the replacement product. Wybotics is contacting all known purchasers directly. Replace", "retailers": ["Online at Amazon.com, BestBuy.com and Wybotpool.com for between $500 and $700. The S1 was sold from April 2023 through September 2024 and the Osprey 700 Max was sold from April 2023 through November 2024."], "injuries": "The firm has received ten reports of the pool vacuums overheating or catching fire while charging and not charging, resulting in nine incidents of property damage. No injuries have been reported.", "source_url": "https://www.cpsc.gov/Recalls/2026/Wybotics-Recalls-Robotic-Pool-Vacuums-Due-to-Burn-and-Fire-Hazards", "url": "https://recallledger.net/recalls/product-26372-wybotics-recalls-robotic-pool-vacuums-due-to-burn-and-fire-hazards/"}, {"id": "cpsc-26382", "source": "CPSC", "category": "consumer-product", "recall_number": "26382", "title": "Samson International Recalls Bellevue and Oaklynn Canopy Bed Frames Due to Impact and Injury Hazards", "product": "Universal Broadmoore brand Bellevue and Oaklynn model canopy bed frames", "reason": "The canopy beams of the bed frames can collapse primarily when the bed is moved, posing impact and injury hazards to consumers.", "hazard_level": null, "company": "Samson International, of High Point, North Carolina", "company_location": "Vietnam", "date": "2026-04-02", "report_date": "2026-04-03", "status": "Announced", "distribution": "Sold in the United States at Online at Costco.com from October 2024 through February 2026 for between $900 and $1,000.", "states": [], "nationwide": true, "quantity": "About 5,600 (In addition, about 516 units were sold in Canada)", "codes": "", "remedy": "Consumers should not move the recalled bed frames and contact Samson International immediately for a free repair and installation kit consisting of four metal brackets and mounting hardware. Repair", "retailers": ["Online at Costco.com from October 2024 through February 2026 for between $900 and $1,000."], "injuries": "The firm has received five reports of the bed canopy collapsing, including five reports of consumers being struck by the canopy beam and four resulting in shoulder and head contusion injuries.", "source_url": "https://www.cpsc.gov/Recalls/2026/Samson-International-Recalls-Bellevue-and-Oaklynn-Canopy-Bed-Frames-Due-to-Impact-and-Injury-Hazards", "url": "https://recallledger.net/recalls/product-26382-samson-international-recalls-bellevue-and-oaklynn-canopy-bed-frames-du/"}, {"id": "cpsc-26381", "source": "CPSC", "category": "consumer-product", "recall_number": "26381", "title": "Tuymec Minoxidil Hair Growth Spray Bottles Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging; Sold on Amazon by DrHealBeauty", "product": "Tuymec Minoxidil Hair Growth Kits, 5% Minoxidil with Biotin Spray", "reason": "The hair serum contains minoxidil, which must be in child-resistant packaging as required by the Poison Prevention Packaging Act. The hair serum's packaging is not child-resistant, posing a risk of serious injury or death from poisoning if the contents are swallowed by young children.", "hazard_level": null, "company": "DrHealBeauty, of Japan", "company_location": "China", "date": "2026-04-02", "report_date": "2026-04-03", "status": "Announced", "distribution": "Sold in the United States at Online at Amazon.com from June 2025 through August 2025 for about $24.", "states": [], "nationwide": true, "quantity": "About 6,200", "codes": "", "remedy": "Consumers should secure the recalled serum bottles out of sight and reach of children immediately and contact DrHealBeauty for a free empty replacement bottle with a child-resistant closure into which consumers should transfer the recalled bottle's contents. Replace", "retailers": ["Online at Amazon.com from June 2025 through August 2025 for about $24."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/Tuymec-Minoxidil-Hair-Growth-Spray-Bottles-Recalled-Due-to-Risk-of-Serious-Injury-or-Death-from-Child-Poisoning-Violates-Mandatory-Standard-for-Child-Resistant-Packaging-Sold-on-Amazon-by-DrHealBeauty", "url": "https://recallledger.net/recalls/product-26381-tuymec-minoxidil-hair-growth-spray-bottles-recalled-due-to-risk-of-ser/"}, {"id": "cpsc-26380", "source": "CPSC", "category": "consumer-product", "recall_number": "26380", "title": "Sam's Club Recalls Member's Mark Children's Pajama Sets Due to Burn Hazard; Violates Mandatory Flammability Standards for Children's Sleepwear", "product": "Member's Mark Children's Valentine SS Notch Collar Pajama Sets", "reason": "The recalled pajama sets violate the mandatory standards for flammability of children's sleepwear, posing a risk of burn injuries to children.", "hazard_level": null, "company": "Hansoll Textile Ltd., of South Korea", "company_location": "Indonesia", "date": "2026-04-02", "report_date": "2026-04-03", "status": "Announced", "distribution": "Sold in the United States at Online at Samsclub.com from December 2025 through January 2026 for about $14.", "states": [], "nationwide": true, "quantity": "About 18,000", "codes": "", "remedy": "Consumers should immediately stop using the recalled pajama sets, take them away from children and contact Sam's Club for information on how to receive a full refund. Consumers will be asked to return the product to their local store or to destroy the pajamas by cutting them in half and send a photo of the destroyed pajamas to Supersam@Samsclub.com then dispose of the product. Refund", "retailers": ["Online at Samsclub.com from December 2025 through January 2026 for about $14."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/Sams-Club-Recalls-Members-Mark-Childrens-Pajama-Sets-Due-to-Burn-Hazard-Violates-Mandatory-Flammability-Standards-for-Childrens-Sleepwear", "url": "https://recallledger.net/recalls/product-26380-sam-s-club-recalls-member-s-mark-children-s-pajama-sets-due-to-burn-ha/"}, {"id": "cpsc-26379", "source": "CPSC", "category": "consumer-product", "recall_number": "26379", "title": "HTRC and Haisito T400 Battery Chargers Recalled Due to Risk of Serious Injury and Death from Fire Hazard; Manufactured by Huizhou Haitan Technology", "product": "HTRC and Haisito battery chargers", "reason": "The chargers can ignite or cause a connected battery to ignite, posing a fire hazard and risk of serious injury and death.", "hazard_level": null, "company": "Huizhou Haitan Technology Co., Ltd., of China", "company_location": "China", "date": "2026-04-02", "report_date": "2026-04-03", "status": "Announced", "distribution": "Sold in the United States at AliExpress.us, Amazon.com, Banggood.com, eBay.com, and Pyrodrone.com from March 2019 through March 2026 for about $130.", "states": [], "nationwide": true, "quantity": "About 4,800", "codes": "", "remedy": "Consumers should immediately stop using the recalled chargers and contact Huizhou Haitan Technology for instructions on how to return the chargers for a full refund. Consumers will be instructed to contact the firm to request a prelabeled and prepaid return package to be sent to them so they can return the chargers to the firm for disposal. Refund", "retailers": ["AliExpress.us, Amazon.com, Banggood.com, eBay.com, and Pyrodrone.com from March 2019 through March 2026 for about $130."], "injuries": "Huizhou Haitan Technology has received 33 reports of fires and explosions, including three reports of burn and smoke inhalation injuries and 12 reports of property damage totaling $224,000.", "source_url": "https://www.cpsc.gov/Recalls/2026/HTRC-and-Haisito-T400-Battery-Chargers-Recalled-Due-to-Risk-of-Serious-Injury-and-Death-from-Fire-Hazard-Manufactured-by-Huizhou-Haitan-Technology", "url": "https://recallledger.net/recalls/product-26379-htrc-and-haisito-t400-battery-chargers-recalled-due-to-risk-of-serious/"}, {"id": "cpsc-26378", "source": "CPSC", "category": "consumer-product", "recall_number": "26378", "title": "Sangohe Reannounces and Expands Adult Portable Bed Rails Recall Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violates Mandatory Standard for Adult Portable Bed Rails", "product": "Sangohe Adult Portable Bed Rails", "reason": "The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. In addition, the bed rails do not bear the required warning labels.", "hazard_level": null, "company": "Zhongshan KDB Health Solutions Co., Ltd., of China", "company_location": "China", "date": "2026-04-02", "report_date": "2026-04-03", "status": "Announced", "distribution": "Sold in the United States at Online at Amazon.com from August 2023 through February 2026 for about $90 (model 504Q) and $110 (model 504E).", "states": [], "nationwide": true, "quantity": "About 36,500 (In January 2026, Sangohe previously recalled about 26,200 adult portable bed rails)", "codes": "", "remedy": "Consumers should immediately stop using the recalled adult portable bed rails and contact Sangohe for a full refund. Consumers should destroy the bed rails by cutting the handrails' foam padding and writing \"RECALLED\" on the upper and lower rails with permanent marker, take a photo of the destroyed rails and email the photo to SGHproductrecall@163.com. Refund", "retailers": ["Online at Amazon.com from August 2023 through February 2026 for about $90 (model 504Q) and $110 (model 504E)."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/Sangohe-Reannounces-and-Expands-Adult-Portable-Bed-Rails-Recall-Due-to-Risk-of-Serious-Injury-or-Death-from-Entrapment-and-Asphyxiation-Violates-Mandatory-Standard-for-Adult-Portable-Bed-Rails", "url": "https://recallledger.net/recalls/product-26378-sangohe-reannounces-and-expands-adult-portable-bed-rails-recall-due-to/"}, {"id": "cpsc-26377", "source": "CPSC", "category": "consumer-product", "recall_number": "26377", "title": "E Mishan Recalls Granitestone Diamond Pro Blue Stainless Sauté Pans Due to Impact and Burn Hazards", "product": "Granitestone Diamond Pro Blue Sauté Pans", "reason": "The metal cap on the screw that connects the sauté pan to the handle can become detached and forcefully eject when heated, posing impact and burn hazards to consumers.", "hazard_level": null, "company": "E Mishan & Sons, Inc., of New York, New York", "company_location": "China", "date": "2026-04-02", "report_date": "2026-04-03", "status": "Announced", "distribution": "Sold in the United States at The recalled sauté pans were sold in stores at Costco and online at Costco.com, Walmart.com, and Amazon.com from August 2021 through February 2026 for about $40.", "states": [], "nationwide": true, "quantity": "About 740,000", "codes": "UPCs: 080313081316", "remedy": "Consumers should stop using the recalled sauté pans immediately and contact E Mishan for a full refund. Consumers will be asked to return the recalled sauté pan. Refund", "retailers": ["The recalled sauté pans were sold in stores at Costco and online at Costco.com, Walmart.com, and Amazon.com from August 2021 through February 2026 for about $40."], "injuries": "E Mishan is aware of at least 98 incidents where the metal cap detached and ejected from the pan, including one report where a consumer received bruising and burn injuries.", "source_url": "https://www.cpsc.gov/Recalls/2026/E-Mishan-Recalls-Granitestone-Diamond-Pro-Blue-Stainless-Saute-Pans-Due-to-Impact-and-Burn-Hazards", "url": "https://recallledger.net/recalls/product-26377-e-mishan-recalls-granitestone-diamond-pro-blue-stainless-saute-pans-du/"}, {"id": "cpsc-26375", "source": "CPSC", "category": "consumer-product", "recall_number": "26375", "title": "TecFlox Hair and Beard Growth Serum Bottles Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging", "product": "TecFlox Hair and Beard Growth Serum Bottles", "reason": "The hair and beard growth serum contains minoxidil, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The bottles are not child-resistant, posing a risk of serious injury or death from poisoning if the contents are swallowed by young children.", "hazard_level": null, "company": "Jichehui Electronics Co. Ltd., dba TecFlox, of China", "company_location": "China", "date": "2026-04-02", "report_date": "2026-04-03", "status": "Announced", "distribution": "Sold in the United States at Amazon.com in October 2025 for about $30", "states": [], "nationwide": true, "quantity": "About 900", "codes": "", "remedy": "Consumers should immediately secure the recalled serum bottles out of sight and reach of children and contact TecFlox to receive free replacement serum bottles, including shipping. Only bottles with serum remaining will be replaced. Consumers will be asked to dispose of the bottles' contents and email a photo of the bottles in the trash, showing the manufacture date to TecFloxrecall@outlook.com Replace", "retailers": ["Amazon.com in October 2025 for about $30"], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/TecFlox-Hair-and-Beard-Growth-Serum-Bottles-Recalled-Due-to-Risk-of-Serious-Injury-or-Death-from-Child-Poisoning-Violates-Mandatory-Standard-for-Child-Resistant-Packaging", "url": "https://recallledger.net/recalls/product-26375-tecflox-hair-and-beard-growth-serum-bottles-recalled-due-to-risk-of-se/"}, {"id": "cpsc-26374", "source": "CPSC", "category": "consumer-product", "recall_number": "26374", "title": "ELENKER Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violates Mandatory Standard for Adult Portable Bed Rails; Sold on Amazon by Fuzhou Shiahaha Cultural Industry Development", "product": "ELENKER Bed Rails", "reason": "The recalled bed rails violate the mandatory standard for adult portable bed rails because when the bed rails are attached to a bed, users can become entrapped within the bed rail or between the bed rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. In addition, the bed rails do not bear the required hazard warning labels.", "hazard_level": null, "company": "Fuzhou Shiahaha Cultural Industry Development Co., Ltd., of China", "company_location": "China", "date": "2026-04-02", "report_date": "2026-04-03", "status": "Announced", "distribution": "Sold in the United States at Online at Amazon.com from August 2023 through February 2026 for about $80.", "states": [], "nationwide": true, "quantity": "About 30", "codes": "", "remedy": "Consumers should stop using the recalled bed rails immediately and contact Fuzhou Shiahaha Cultural Industry Development for a full refund. Consumers will be asked to write \"RECALL\" with permanent marker on the bed rails and then dispose of the recalled product in accordance with the state and local waste disposal procedure. Refund", "retailers": ["Online at Amazon.com from August 2023 through February 2026 for about $80."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/ELENKER-Portable-Bed-Rails-Recalled-Due-to-Risk-of-Serious-Injury-or-Death-from-Entrapment-and-Asphyxiation-Violates-Mandatory-Standard-for-Adult-Portable-Bed-Rails-Sold-on-Amazon-by-Fuzhou-Shiahaha-Cultural-Industry-Development", "url": "https://recallledger.net/recalls/product-26374-elenker-portable-bed-rails-recalled-due-to-risk-of-serious-injury-or-d/"}, {"id": "cpsc-26373", "source": "CPSC", "category": "consumer-product", "recall_number": "26373", "title": "OCUN NA Recalls Condor HMS Triple Carabiners Due to Risk of Serious Injury or Death from Fall Hazard", "product": "Ocun Condor HMS Triple Locking Carabiners", "reason": "The carabiner's gate can malfunction where the gate does not close automatically and has to be closed manually by hand, posing a risk of serious injury or death due to falling.", "hazard_level": null, "company": "OCUN NA LLC, of Park City, Utah", "company_location": "Taiwan", "date": "2026-04-02", "report_date": "2026-04-03", "status": "Announced", "distribution": "Sold in the United States at First Ascent Climbing and Fitness Arlington, and Vertical eXcape Climbing Center and online at Hownot2.com, backcountry.com, outdoorprolink.com, verticallstore.com from February 2025 through February 2026 for between $23 and $60.", "states": [], "nationwide": true, "quantity": "About 295 (in addition, about nine were sold in Canada)", "codes": "", "remedy": "Consumers should stop using the recalled carabiner immediately and contact OCUN NA for a free replacement. Consumers will be asked to fill out the recall form and email it to recall@ocun.com and follow the instructions to receive a prepaid return shipping label and return the recalled product. Replace", "retailers": ["First Ascent Climbing and Fitness Arlington, and Vertical eXcape Climbing Center and online at Hownot2.com, backcountry.com, outdoorprolink.com, verticallstore.com from February 2025 through February 2026 for between $23 and $60."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/OCUN-NA-Recalls-Condor-HMS-Triple-Carabiners-Due-to-Risk-of-Serious-Injury-or-Death-from-Fall-Hazard", "url": "https://recallledger.net/recalls/product-26373-ocun-na-recalls-condor-hms-triple-carabiners-due-to-risk-of-serious-in/"}, {"id": "cpsc-26369", "source": "CPSC", "category": "consumer-product", "recall_number": "26369", "title": "Coluans Christmas Light-Up Rings Recalled Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violates Mandatory Standard for Toys; Sold on Amazon by BUDI Official", "product": "Coluans Christmas Light-Up Rings Party Favors", "reason": "The recalled light-up rings violate the mandatory safety standard for toys because the battery compartment within the LED light ring contains button cell batteries that can be easily accessed by children. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.", "hazard_level": null, "company": "Dongguan Oukatuo Electronic Technology Co., Ltd., dba BUDI Official, of China", "company_location": "China", "date": "2026-04-02", "report_date": "2026-04-03", "status": "Announced", "distribution": "Sold in the United States at Online at Amazon.com from August 2025 through December 2025 for between $15 to $20.", "states": [], "nationwide": true, "quantity": "About 3,540", "codes": "", "remedy": "Consumers should take the recalled light-up rings away from children, stop using them immediately and remove and properly dispose of the batteries. Consumers will be asked to throw away the light-up rings and send a photo of the disposed product to BUDIrecall@outlook.com for a full refund. Note: Button cell batteries are hazardous. Batteries should be disposed of or recycled by following local hazardous waste procedures. Refund", "retailers": ["Online at Amazon.com from August 2025 through December 2025 for between $15 to $20."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/Coluans-Christmas-Light-Up-Rings-Recalled-Due-to-Risk-of-Serious-Injury-or-Death-from-Battery-Ingestion-Hazard-Violates-Mandatory-Standard-for-Toys-Sold-on-Amazon-by-BUDI-Official", "url": "https://recallledger.net/recalls/product-26369-coluans-christmas-light-up-rings-recalled-due-to-risk-of-serious-injur/"}, {"id": "cpsc-26368", "source": "CPSC", "category": "consumer-product", "recall_number": "26368", "title": "Gavoyeat Halloween Light-Up Rings Recalled Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violates Mandatory Standard for Toys; Sold on Amazon by CSZWEICD", "product": "Gavoyeat Halloween Light-Up Rings Party Favors", "reason": "The recalled light-up rings violate the mandatory safety standard for toys because the battery compartment within the LED light ring contains button cell batteries that can be easily accessed by children. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.", "hazard_level": null, "company": "Shenzhen Weichaoda Technology Co., Ltd., dba CSZWEICD, of China", "company_location": "China", "date": "2026-04-02", "report_date": "2026-04-03", "status": "Announced", "distribution": "Sold in the United States at Online at Amazon.com from June 2025 through January 2026 for about $15.", "states": [], "nationwide": true, "quantity": "About 800 units", "codes": "", "remedy": "Consumers should take the recalled light-up rings from children, stop using the recalled toys immediately and remove and properly dispose of the batteries. Consumers will be asked to throw away the light-up rings and send a photo of the disposed product to recalledgavoyeat@yeah.net. Note: Button cell batteries are hazardous. Batteries should be disposed of or recycled by following local hazardous waste procedures. Refund", "retailers": ["Online at Amazon.com from June 2025 through January 2026 for about $15."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/Gavoyeat-Halloween-Light-Up-Rings-Recalled-Due-to-Risk-of-Serious-Injury-or-Death-from-Battery-Ingestion-Hazard-Violates-Mandatory-Standard-for-Toys-Sold-on-Amazon-by-CSZWEICD", "url": "https://recallledger.net/recalls/product-26368-gavoyeat-halloween-light-up-rings-recalled-due-to-risk-of-serious-inju/"}, {"id": "cpsc-26365", "source": "CPSC", "category": "consumer-product", "recall_number": "26365", "title": "Children's Toys Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Violates the Small Ball Ban; Sold on Amazon by Beestech", "product": "Beestech Children's Spiral Tower Toys", "reason": "The recalled spiral tower toy sets violate the mandatory standard for toys because they contain small balls and are intended for children under three years of age, posing a deadly choking hazard.", "hazard_level": null, "company": "Dongguan Qicaifeng Trading Co., Ltd., dba Beestech, of China", "company_location": "China", "date": "2026-04-02", "report_date": "2026-04-03", "status": "Announced", "distribution": "Sold in the United States at Online at Amazon.com from November 2025 through December 2025 for about $15.", "states": [], "nationwide": true, "quantity": "About 200", "codes": "", "remedy": "Consumers should take the toys away from children immediately and contact Beestech for a full refund. Consumers will be asked to write \"Recalled\" with permanent marker on the toy and send a photo of the marked toy to beestechballtowerrecall@hotmail.com. Consumers should then dispose of the recalled product. Refund", "retailers": ["Online at Amazon.com from November 2025 through December 2025 for about $15."], "injuries": "None reported", "source_url": "https://www.cpsc.gov/Recalls/2026/Childrens-Toys-Recalled-Due-to-Risk-of-Serious-Injury-or-Death-from-Choking-Hazard-Violates-the-Small-Ball-Ban-Sold-on-Amazon-by-Beestech", "url": "https://recallledger.net/recalls/product-26365-children-s-toys-recalled-due-to-risk-of-serious-injury-or-death-from-c/"}]}