https://recallledger.net/Every U.S. food, drug, medical device and consumer product recall, in plain English, updated daily.https://recallledger.net/recalls/product-27088-boshengya-recalls-rugs-due-to-risk-of-serious-injury-or-death-from-fir/https://recallledger.net/recalls/product-27088-boshengya-recalls-rugs-due-to-risk-of-serious-injury-or-death-from-fir/Thu, 12 Nov 2026 12:00:00 +0000The recalled rugs violate the mandatory standard for the flammability of carpets and rugs, posing a risk of serious injury or death from fire hazard.https://recallledger.net/recalls/product-27087-cummins-recalls-portable-generators-due-to-risk-of-serious-injury-from/https://recallledger.net/recalls/product-27087-cummins-recalls-portable-generators-due-to-risk-of-serious-injury-from/Thu, 12 Nov 2026 12:00:00 +0000The valves in the recalled generators were installed incorrectly, preventing fuel vapors from venting properly from the gasoline tank, causing excessive pressure to build up. This pressure can cause fuel to discharge or the fuel cap to eject, posing a risk of serious injury from fire and burn hazards.https://recallledger.net/recalls/product-27086-huffy-recalls-buzz-bicycles-cerana-t2-e-trikes-due-to-risk-of-serious/https://recallledger.net/recalls/product-27086-huffy-recalls-buzz-bicycles-cerana-t2-e-trikes-due-to-risk-of-serious/Thu, 12 Nov 2026 12:00:00 +0000The recalled tricycles’ rear wheels can become loose or separate from the rear frame, posing a risk of serious injury from a fall hazard.https://recallledger.net/recalls/product-27085-kakgold-recalls-4wd-remote-controlled-car-toys-due-to-risk-of-serious/https://recallledger.net/recalls/product-27085-kakgold-recalls-4wd-remote-controlled-car-toys-due-to-risk-of-serious/Thu, 12 Nov 2026 12:00:00 +0000The recalled remote-controlled cars violate the mandatory standard for toys because they contain button cell and lithium-ion batteries in the remote control that can be easily accessed by children, posing a deadly ingestion hazard to children. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and deathhttps://recallledger.net/recalls/product-27084-qiomala-pressure-washers-recalled-due-to-serious-risk-of-injury-or-dea/https://recallledger.net/recalls/product-27084-qiomala-pressure-washers-recalled-due-to-serious-risk-of-injury-or-dea/Thu, 12 Nov 2026 12:00:00 +0000The recalled pressure washers lack an adequate-length power cord, which can encourage use of an extension cord, posing a serious risk of injury or death from shock and electrocution hazards.https://recallledger.net/recalls/product-27083-shein-distribution-corporation-recalls-baby-rattle-and-teether-toy-set/https://recallledger.net/recalls/product-27083-shein-distribution-corporation-recalls-baby-rattle-and-teether-toy-set/Thu, 12 Nov 2026 12:00:00 +0000The recalled toy sets violate the small parts ban because they are intended for children under three years old and the purple and orange knobs can detach from the product, posing a deadly choking hazard to young children.https://recallledger.net/recalls/product-27082-allstar-recalls-sharper-image-tabletop-and-infinity-fire-pits-due-to-r/https://recallledger.net/recalls/product-27082-allstar-recalls-sharper-image-tabletop-and-infinity-fire-pits-due-to-r/Thu, 12 Nov 2026 12:00:00 +0000Ignited flammable liquid can escape from the recalled fire pits or trigger flame jetting from the fuel containers, posing a risk of serious injury from burn and fire hazards.https://recallledger.net/recalls/product-27076-magnetopia-recalls-magnetic-building-cubes-and-blocks-due-to-risk-of-s/https://recallledger.net/recalls/product-27076-magnetopia-recalls-magnetic-building-cubes-and-blocks-due-to-risk-of-s/Thu, 05 Nov 2026 12:00:00 +0000The recalled magnetic building cubes contain magnets that can become loose if the cubes break or open, posing a magnet 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 https://recallledger.net/recalls/product-27074-u-s-titan-recalls-x-pro-youth-all-terrain-vehicles-atvs-due-to-risk/https://recallledger.net/recalls/product-27074-u-s-titan-recalls-x-pro-youth-all-terrain-vehicles-atvs-due-to-risk/Thu, 05 Nov 2026 12:00:00 +0000The recalled ATVs violate the mandatory ATV safety standard because the speed-adjusting module included with the vehicle allows for the ATV’s speed to be adjusted in excess of the maximum speed for vehicles intended for children 6 years old and older, posing a risk of serious injury or death from a crash.https://recallledger.net/recalls/product-27073-sanven-technology-recalls-vevor-bmx-bicycles-due-to-risk-of-serious-in/https://recallledger.net/recalls/product-27073-sanven-technology-recalls-vevor-bmx-bicycles-due-to-risk-of-serious-in/Thu, 05 Nov 2026 12:00:00 +0000The bicycles violate the mandatory safety regulation for bicycles, because they are not equipped with a chain guard. Loose clothing can get entrapped in the chain drive, posing a risk of serious injury or deadly crash hazard. In addition, the bicycles do not comply with the labeling requirements.https://recallledger.net/recalls/product-27072-baby-brezza-enterprises-recalls-superfast-sterilizer-dryers-due-to-ove/https://recallledger.net/recalls/product-27072-baby-brezza-enterprises-recalls-superfast-sterilizer-dryers-due-to-ove/Thu, 05 Nov 2026 12:00:00 +0000The recalled sterilizer dryers can overheat when plugged in and operating, posing a risk of injury from a burn hazard if the surface is handled.https://recallledger.net/recalls/product-27071-kikea-store-recalls-x-vesolje-nursing-pillows-due-to-risk-of-serious-i/https://recallledger.net/recalls/product-27071-kikea-store-recalls-x-vesolje-nursing-pillows-due-to-risk-of-serious-i/Thu, 05 Nov 2026 12:00:00 +0000The recalled nursing pillows violate the mandatory safety standards for nursing pillows because they can obstruct an infant’s breathing, posing a serious risk of injury or death from suffocation.https://recallledger.net/recalls/product-27070-c-a-m-p-recalls-mountain-ice-axes-due-to-risk-of-serious-injury-or-de/https://recallledger.net/recalls/product-27070-c-a-m-p-recalls-mountain-ice-axes-due-to-risk-of-serious-injury-or-de/Thu, 05 Nov 2026 12:00:00 +0000A screw on the recalled mountain ice axes can loosen during use, causing the handle or pick to detach, posing a risk of serious injury or death from fall hazard.https://recallledger.net/recalls/product-27069-gourmia-recalls-9-slice-digital-air-fryer-ovens-due-to-burn-hazard/https://recallledger.net/recalls/product-27069-gourmia-recalls-9-slice-digital-air-fryer-ovens-due-to-burn-hazard/Thu, 05 Nov 2026 12:00:00 +0000The oven’s doors can unexpectedly close when bumped, posing a burn hazard to consumers retrieving hot food.https://recallledger.net/recalls/product-27068-jiastfeng-recalls-hauoms-eight-drawer-dressers-due-to-risk-of-serious/https://recallledger.net/recalls/product-27068-jiastfeng-recalls-hauoms-eight-drawer-dressers-due-to-risk-of-serious/Thu, 05 Nov 2026 12:00:00 +0000The 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 standards as required by the STURDY Act.https://recallledger.net/recalls/product-27067-little-giant-recalls-ladders-with-rapid-locks-due-to-risk-of-serious-i/https://recallledger.net/recalls/product-27067-little-giant-recalls-ladders-with-rapid-locks-due-to-risk-of-serious-i/Thu, 05 Nov 2026 12:00:00 +0000The ladders can suddenly retract if the Rapid Locks are not fully engaged, posing a fall hazard to consumers.https://recallledger.net/recalls/product-27066-arlopu-recalls-slide-playsets-due-to-risk-of-serious-injury-and-death/https://recallledger.net/recalls/product-27066-arlopu-recalls-slide-playsets-due-to-risk-of-serious-injury-and-death/Thu, 05 Nov 2026 12:00:00 +0000The recalled products contain multiple openings where a child’s torso can fit through the opening, but a child’s head cannot, posing a risk of serious injury and death due to head and neck entrapment hazards. Additionally, the basketball nets on the recalled products with model number KT-CS17 can come unhooked from the rim, forming a loop large enough for a child’s head, posing entanglement and sthttps://recallledger.net/recalls/product-27065-bose-recalls-lithium-ion-battery-packs-for-s1-pro-and-s1-pro-bluetoot/https://recallledger.net/recalls/product-27065-bose-recalls-lithium-ion-battery-packs-for-s1-pro-and-s1-pro-bluetoot/Thu, 05 Nov 2026 12:00:00 +0000The recalled lithium-ion battery packs can overheat and ignite, posing a risk of injury from fire and overheating hazards.https://recallledger.net/recalls/product-27064-vanderhall-north-america-recalls-all-model-year-2024-2026-brawley-elec/https://recallledger.net/recalls/product-27064-vanderhall-north-america-recalls-all-model-year-2024-2026-brawley-elec/Thu, 05 Nov 2026 12:00:00 +0000The seat belts in Brawley ROVs can permanently lockup in the fully retracted position. If this occurs, consumers would be unable to reset the seat belt and put it on when the vehicle is operating, posing injury and crash hazards to consumers.https://recallledger.net/recalls/food-h-0186-2027-boner-bears-chocolate-3-doses-per-bar-net-wt-22g-male-enhancement/https://recallledger.net/recalls/food-h-0186-2027-boner-bears-chocolate-3-doses-per-bar-net-wt-22g-male-enhancement/Wed, 04 Nov 2026 12:00:00 +0000JXK Enterprises, Inc is voluntarily recalling Boner Bears Chocolate, Lot #BB21125, after being notified that FDA laboratory analysis confirmed the presence of sildenafil, an active ingredient in the FDA-approved prescription drug Viagra, which is not declared on the product label.https://recallledger.net/recalls/food-h-0185-2027-gluten-free-eat-g-a-n-g-s-t-e-r-pizza-crust-and-flat-bread-mix-5-8oz/https://recallledger.net/recalls/food-h-0185-2027-gluten-free-eat-g-a-n-g-s-t-e-r-pizza-crust-and-flat-bread-mix-5-8oz/Wed, 04 Nov 2026 12:00:00 +0000Products are recalled due to potential undeclared wheat glutenhttps://recallledger.net/recalls/food-h-0184-2027-gluten-free-truly-aip-rustic-bread-mix-14-oz/https://recallledger.net/recalls/food-h-0184-2027-gluten-free-truly-aip-rustic-bread-mix-14-oz/Wed, 04 Nov 2026 12:00:00 +0000Products are recalled due to potential undeclared wheat glutenhttps://recallledger.net/recalls/food-h-0183-2027-gluten-free-truly-aip-all-purpose-baking-mix-flour-15-3-oz/https://recallledger.net/recalls/food-h-0183-2027-gluten-free-truly-aip-all-purpose-baking-mix-flour-15-3-oz/Wed, 04 Nov 2026 12:00:00 +0000Products are recalled due to potential undeclared wheat glutenhttps://recallledger.net/recalls/food-h-0182-2027-sunny-sky-non-dairy-french-vanilla-creamer-96oz-bag-in-box-3-per-c/https://recallledger.net/recalls/food-h-0182-2027-sunny-sky-non-dairy-french-vanilla-creamer-96oz-bag-in-box-3-per-c/Wed, 04 Nov 2026 12:00:00 +0000Product sterility was potentially compromised.https://recallledger.net/recalls/food-h-0181-2027-riad-s-oliva-to-go-hummus/https://recallledger.net/recalls/food-h-0181-2027-riad-s-oliva-to-go-hummus/Wed, 04 Nov 2026 12:00:00 +0000contains undeclared sesamehttps://recallledger.net/recalls/food-h-0180-2027-riad-s-oliva-to-go-spicy-baba-ghanouj/https://recallledger.net/recalls/food-h-0180-2027-riad-s-oliva-to-go-spicy-baba-ghanouj/Wed, 04 Nov 2026 12:00:00 +0000contains undeclared sesamehttps://recallledger.net/recalls/food-h-0179-2027-riad-s-oliva-to-go-baba-ghanouj/https://recallledger.net/recalls/food-h-0179-2027-riad-s-oliva-to-go-baba-ghanouj/Wed, 04 Nov 2026 12:00:00 +0000contains undeclared sesamehttps://recallledger.net/recalls/food-h-0178-2027-miyoko-s-creamery-european-style-salted-plant-milk-butter-net-wt-8-o/https://recallledger.net/recalls/food-h-0178-2027-miyoko-s-creamery-european-style-salted-plant-milk-butter-net-wt-8-o/Wed, 04 Nov 2026 12:00:00 +0000Product recalled due to yeast, mold, and E. coli.https://recallledger.net/recalls/food-h-0177-2027-eden-brothers-broccoli-seeds-calabrese-sold-in-packets-net-wt-1oz/https://recallledger.net/recalls/food-h-0177-2027-eden-brothers-broccoli-seeds-calabrese-sold-in-packets-net-wt-1oz/Wed, 04 Nov 2026 12:00:00 +0000Salmonellahttps://recallledger.net/recalls/food-h-0176-2027-zestigreens-broccoli-seeds-for-sprouting-microgreens-8-oz-heirloom/https://recallledger.net/recalls/food-h-0176-2027-zestigreens-broccoli-seeds-for-sprouting-microgreens-8-oz-heirloom/Wed, 04 Nov 2026 12:00:00 +0000Broccoli seeds potentially contaminated with Salmonellahttps://recallledger.net/recalls/food-h-0175-2027-blue-bottle-coffee-4oz-sweet-blossom-simple-syrup-in-a-glass-boston-ro/https://recallledger.net/recalls/food-h-0175-2027-blue-bottle-coffee-4oz-sweet-blossom-simple-syrup-in-a-glass-boston-ro/Wed, 04 Nov 2026 12:00:00 +0000Potential contamination with mold (Aspergillus niger)https://recallledger.net/recalls/drug-d-0113-2027-atorvastatin-calcium-tablets-usp-40mg-1000-tablets-per-bottle-rx-o/https://recallledger.net/recalls/drug-d-0113-2027-atorvastatin-calcium-tablets-usp-40mg-1000-tablets-per-bottle-rx-o/Wed, 04 Nov 2026 12:00:00 +0000Presence of Foreign Tablets/Capsuleshttps://recallledger.net/recalls/drug-d-0111-2027-theophylline-extended-release-tablets-200-mg-rx-only-100-count-bott/https://recallledger.net/recalls/drug-d-0111-2027-theophylline-extended-release-tablets-200-mg-rx-only-100-count-bott/Wed, 04 Nov 2026 12:00:00 +0000CGMP Deviations: interruption in the ongoing stability testing program conducted at a third-party laboratoryhttps://recallledger.net/recalls/drug-d-0110-2027-theophylline-extended-release-tablets-100-mg-rx-only-100-count-bott/https://recallledger.net/recalls/drug-d-0110-2027-theophylline-extended-release-tablets-100-mg-rx-only-100-count-bott/Wed, 04 Nov 2026 12:00:00 +0000CGMP Deviations: interruption in the ongoing stability testing program conducted at a third-party laboratoryhttps://recallledger.net/recalls/drug-d-0109-2027-vecuronium-bromide-for-injection-20mg-10-single-dose-vials-per-carto/https://recallledger.net/recalls/drug-d-0109-2027-vecuronium-bromide-for-injection-20mg-10-single-dose-vials-per-carto/Wed, 04 Nov 2026 12:00:00 +0000Labeling: Label Lacks Warning or Rx Legendhttps://recallledger.net/recalls/drug-d-0108-2027-vecuronium-bromide-for-injection-10mg-10-single-dose-vials-per-carto/https://recallledger.net/recalls/drug-d-0108-2027-vecuronium-bromide-for-injection-10mg-10-single-dose-vials-per-carto/Wed, 04 Nov 2026 12:00:00 +0000Labeling: Label Lacks Warning or Rx Legendhttps://recallledger.net/recalls/drug-d-0107-2027-lidocaine-ointment-usp-5-0-50g-jar-rx-only-packaged-and-distribut/https://recallledger.net/recalls/drug-d-0107-2027-lidocaine-ointment-usp-5-0-50g-jar-rx-only-packaged-and-distribut/Wed, 04 Nov 2026 12:00:00 +0000Subpotent Drughttps://recallledger.net/recalls/drug-d-0106-2027-oxytocin-30-usp-units-added-to-0-9-sodium-chloride-500-ml-single/https://recallledger.net/recalls/drug-d-0106-2027-oxytocin-30-usp-units-added-to-0-9-sodium-chloride-500-ml-single/Wed, 04 Nov 2026 12:00:00 +0000Lack of Assurance of Sterilityhttps://recallledger.net/recalls/drug-d-0105-2027-phenylephrine-hcl-infusion-100-mg-per-250-ml-in-0-9-sodium-chloride/https://recallledger.net/recalls/drug-d-0105-2027-phenylephrine-hcl-infusion-100-mg-per-250-ml-in-0-9-sodium-chloride/Wed, 04 Nov 2026 12:00:00 +0000Lack of Assurance of Sterilityhttps://recallledger.net/recalls/drug-d-0104-2027-ultra-strentgh-electric-midicated-balm-menthol-16-and-methyl-salicy/https://recallledger.net/recalls/drug-d-0104-2027-ultra-strentgh-electric-midicated-balm-menthol-16-and-methyl-salicy/Wed, 04 Nov 2026 12:00:00 +0000CGMP Deviationshttps://recallledger.net/recalls/drug-d-0103-2027-wechem-hand-guard8-1000ml-bag-manufactured-by-abc-compounding-co-i/https://recallledger.net/recalls/drug-d-0103-2027-wechem-hand-guard8-1000ml-bag-manufactured-by-abc-compounding-co-i/Wed, 04 Nov 2026 12:00:00 +0000CGMP Deviationshttps://recallledger.net/recalls/drug-d-0102-2027-suncoast-paper-inc-surgent-antiseptic-hand-soap-net-contents-1-gal/https://recallledger.net/recalls/drug-d-0102-2027-suncoast-paper-inc-surgent-antiseptic-hand-soap-net-contents-1-gal/Wed, 04 Nov 2026 12:00:00 +0000CGMP Deviationshttps://recallledger.net/recalls/drug-d-0101-2027-spurrier-antimicrobial-hand-soap-net-contents-1-gallon-3-8-l-man/https://recallledger.net/recalls/drug-d-0101-2027-spurrier-antimicrobial-hand-soap-net-contents-1-gallon-3-8-l-man/Wed, 04 Nov 2026 12:00:00 +0000CGMP Deviationshttps://recallledger.net/recalls/drug-d-0100-2027-chemseptic-net-contents-1-gallon-3-8-l-distributed-by-rmc-roches/https://recallledger.net/recalls/drug-d-0100-2027-chemseptic-net-contents-1-gallon-3-8-l-distributed-by-rmc-roches/Wed, 04 Nov 2026 12:00:00 +0000CGMP Deviationshttps://recallledger.net/recalls/drug-d-0099-2027-pro-chem-suds-hand-soap-net-contents-18-oz-532-ml-sold-by-pro-che/https://recallledger.net/recalls/drug-d-0099-2027-pro-chem-suds-hand-soap-net-contents-18-oz-532-ml-sold-by-pro-che/Wed, 04 Nov 2026 12:00:00 +0000CGMP Deviationshttps://recallledger.net/recalls/drug-d-0098-2027-pro-chem-ban-aid-antiseptic-hand-soap-net-contents-1-gallon-3-8-l/https://recallledger.net/recalls/drug-d-0098-2027-pro-chem-ban-aid-antiseptic-hand-soap-net-contents-1-gallon-3-8-l/Wed, 04 Nov 2026 12:00:00 +0000CGMP Deviationshttps://recallledger.net/recalls/drug-d-0097-2027-pro-chem-fresh-start-antibacterial-hand-soap-antiseptic-hand-soap-8/https://recallledger.net/recalls/drug-d-0097-2027-pro-chem-fresh-start-antibacterial-hand-soap-antiseptic-hand-soap-8/Wed, 04 Nov 2026 12:00:00 +0000CGMP Deviationshttps://recallledger.net/recalls/drug-d-0096-2027-people-s-fm-24-foaming-high-foaming-antiseptic-hand-and-body-wash-net/https://recallledger.net/recalls/drug-d-0096-2027-people-s-fm-24-foaming-high-foaming-antiseptic-hand-and-body-wash-net/Wed, 04 Nov 2026 12:00:00 +0000CGMP Deviationshttps://recallledger.net/recalls/drug-d-0095-2027-handtastic-foamy-mango-antiseptic-foam-soap-hand-body-wash-net-cont/https://recallledger.net/recalls/drug-d-0095-2027-handtastic-foamy-mango-antiseptic-foam-soap-hand-body-wash-net-cont/Wed, 04 Nov 2026 12:00:00 +0000CGMP Deviationshttps://recallledger.net/recalls/drug-d-0094-2027-lynx-antibacterial-hand-soap-refill-net-contents-1-gallon-3-8-l/https://recallledger.net/recalls/drug-d-0094-2027-lynx-antibacterial-hand-soap-refill-net-contents-1-gallon-3-8-l/Wed, 04 Nov 2026 12:00:00 +0000CGMP Deviationshttps://recallledger.net/recalls/drug-d-0093-2027-lynx-antibacterial-hand-soap-net-contents-1-gallon-3-8-l-manufac/https://recallledger.net/recalls/drug-d-0093-2027-lynx-antibacterial-hand-soap-net-contents-1-gallon-3-8-l-manufac/Wed, 04 Nov 2026 12:00:00 +0000CGMP Deviationshttps://recallledger.net/recalls/drug-d-0092-2027-lynx-lx0864-peachy-foam-antiseptic-handsoap-1000-ml-33-8-fl-oz-ma/https://recallledger.net/recalls/drug-d-0092-2027-lynx-lx0864-peachy-foam-antiseptic-handsoap-1000-ml-33-8-fl-oz-ma/Wed, 04 Nov 2026 12:00:00 +0000CGMP Deviationshttps://recallledger.net/recalls/drug-d-0091-2027-antiseptic-hand-soap-net-contents-1-gallon-3-8-l-distributed-by-i/https://recallledger.net/recalls/drug-d-0091-2027-antiseptic-hand-soap-net-contents-1-gallon-3-8-l-distributed-by-i/Wed, 04 Nov 2026 12:00:00 +0000CGMP Deviationshttps://recallledger.net/recalls/drug-d-0090-2027-delta-foremost-sani-foam-mango-net-contents-1000-ml-33-8-fl-oz-man/https://recallledger.net/recalls/drug-d-0090-2027-delta-foremost-sani-foam-mango-net-contents-1000-ml-33-8-fl-oz-man/Wed, 04 Nov 2026 12:00:00 +0000CGMP Deviationshttps://recallledger.net/recalls/drug-d-0089-2027-freshhands-premium-foamy-antibacterial-hand-soap-antiseptic-net-conte/https://recallledger.net/recalls/drug-d-0089-2027-freshhands-premium-foamy-antibacterial-hand-soap-antiseptic-net-conte/Wed, 04 Nov 2026 12:00:00 +0000CGMP Deviationshttps://recallledger.net/recalls/drug-d-0088-2027-certus-medical-satin-foam-750-ml-25-4-fl-oz-manufactured-for-ca/https://recallledger.net/recalls/drug-d-0088-2027-certus-medical-satin-foam-750-ml-25-4-fl-oz-manufactured-for-ca/Wed, 04 Nov 2026 12:00:00 +0000CGMP Deviationshttps://recallledger.net/recalls/drug-d-0087-2027-aero-foamy-mango-aloe-vera-antiseptic-hand-body-wash-net-contents/https://recallledger.net/recalls/drug-d-0087-2027-aero-foamy-mango-aloe-vera-antiseptic-hand-body-wash-net-contents/Wed, 04 Nov 2026 12:00:00 +0000CGMP Deviationshttps://recallledger.net/recalls/drug-d-0086-2027-aerocare-sani-mango-antiseptic-hand-and-body-wash-net-contents-1-gal/https://recallledger.net/recalls/drug-d-0086-2027-aerocare-sani-mango-antiseptic-hand-and-body-wash-net-contents-1-gal/Wed, 04 Nov 2026 12:00:00 +0000CGMP Deviationshttps://recallledger.net/recalls/drug-d-0085-2027-palm-antiseptic-hand-soap-net-contents-1-gallon-3-8-l-manufactured/https://recallledger.net/recalls/drug-d-0085-2027-palm-antiseptic-hand-soap-net-contents-1-gallon-3-8-l-manufactured/Wed, 04 Nov 2026 12:00:00 +0000CGMP Deviationshttps://recallledger.net/recalls/drug-d-0081-2027-valuhealth-extra-strength-pain-relief-acetaminophen-500-mg-40-caplets/https://recallledger.net/recalls/drug-d-0081-2027-valuhealth-extra-strength-pain-relief-acetaminophen-500-mg-40-caplets/Wed, 04 Nov 2026 12:00:00 +0000Incorrect label placed on product: Outer carton label correctly identifies drug product in bottle as ValuHealth Extra Strength Pain Relief Acetaminophen 500 mg,but inner label on bottle says ValuHealth Extra Strength Pain Relief PMhttps://recallledger.net/recalls/drug-d-0080-2027-carboxymethylcellulose-sodium-0-5-lubricant-eye-drops-sterile-30-s/https://recallledger.net/recalls/drug-d-0080-2027-carboxymethylcellulose-sodium-0-5-lubricant-eye-drops-sterile-30-s/Wed, 04 Nov 2026 12:00:00 +0000Failed Impurities/Degradation Specification; detection of polyethylene (PE)-related oligomershttps://recallledger.net/recalls/drug-d-0077-2027-olmesartan-medoxomil-amlodipine-and-hydrochlorothiazide-tablets-40-m/https://recallledger.net/recalls/drug-d-0077-2027-olmesartan-medoxomil-amlodipine-and-hydrochlorothiazide-tablets-40-m/Wed, 04 Nov 2026 12:00:00 +0000Failed Dissolution Specifications.https://recallledger.net/recalls/drug-d-0075-2027-metoclopramide-tablets-usp-5-mg-100-tablets-per-bottle-rx-only-ma/https://recallledger.net/recalls/drug-d-0075-2027-metoclopramide-tablets-usp-5-mg-100-tablets-per-bottle-rx-only-ma/Wed, 04 Nov 2026 12:00:00 +0000Manufacturer is recalling batches due to co-mingled tablet.https://recallledger.net/recalls/drug-d-0074-2027-abiraterone-acetate-tablets-usp-500-mg-60-count-bottles-rx-only-dis/https://recallledger.net/recalls/drug-d-0074-2027-abiraterone-acetate-tablets-usp-500-mg-60-count-bottles-rx-only-dis/Wed, 04 Nov 2026 12:00:00 +0000Labeling: Not Elsewhere Classifiedhttps://recallledger.net/recalls/drug-d-0073-2027-formoterol-fumarate-inhalation-solution-20mcg-2ml-packaged-in-carton/https://recallledger.net/recalls/drug-d-0073-2027-formoterol-fumarate-inhalation-solution-20mcg-2ml-packaged-in-carton/Wed, 04 Nov 2026 12:00:00 +0000Failed Impurities/Degradation Specificationhttps://recallledger.net/recalls/device-z-0315-2027-carevo-height-adjustable-shower-trolley-model-number-bac1111-01/https://recallledger.net/recalls/device-z-0315-2027-carevo-height-adjustable-shower-trolley-model-number-bac1111-01/Wed, 04 Nov 2026 12:00:00 +0000The side support of the shower trolley may open unintentionally when the handles are not fully locked and additional force is applied during patient handling. If the side support is not fully locked and an additional force is applied by the caregiver on the handle (e.g., during turning or repositioning), the panel may open unintentionally, which can lead to a resident/patient fall and serious injuhttps://recallledger.net/recalls/device-z-0314-2027-precision-pointer-electromagnetic-8000-050-001/https://recallledger.net/recalls/device-z-0314-2027-precision-pointer-electromagnetic-8000-050-001/Wed, 04 Nov 2026 12:00:00 +0000Device may fracture during use at the laser welded joint on the pointer tube. If this happens, loose parts may fall out of the product while the device is inside the patient.https://recallledger.net/recalls/device-z-0311-2027-nalu-td2-therapy-disc-with-firmware-ref-34014-001-and-td2-patient-k/https://recallledger.net/recalls/device-z-0311-2027-nalu-td2-therapy-disc-with-firmware-ref-34014-001-and-td2-patient-k/Wed, 04 Nov 2026 12:00:00 +0000Therapy Disc (TD) that powers and sends stimulation signals to an Implantable Pulse Generator (IPG), part of a neurostimulation system, has a firmware issue that causes the TD to attempt to restart, then fail, leading it to become non-functional, and if a secondary TD is unavailable, this may lead IPG to become non-functional, thus unable to inhibit transmission of pain signals.https://recallledger.net/recalls/device-z-0310-2027-pentax-medical-water-bottle-assembly-model-number-os-h5/https://recallledger.net/recalls/device-z-0310-2027-pentax-medical-water-bottle-assembly-model-number-os-h5/Wed, 04 Nov 2026 12:00:00 +0000Warnings added to the IFU for ultrasound endoscopes and water bottle assembly to ensure there is deaerated sterile water in the assembly prior to and during the procedure.https://recallledger.net/recalls/device-z-0309-2027-pentax-medical-ultrasound-endoscope-model-number-eg-3270uk/https://recallledger.net/recalls/device-z-0309-2027-pentax-medical-ultrasound-endoscope-model-number-eg-3270uk/Wed, 04 Nov 2026 12:00:00 +0000Warnings added to the IFU for ultrasound endoscopes and water bottle assembly to ensure there is deaerated sterile water in the assembly prior to and during the procedure.https://recallledger.net/recalls/device-z-0308-2027-pentax-medical-ultrasound-endoscope-model-numbers-eg-3870utk-eg-367/https://recallledger.net/recalls/device-z-0308-2027-pentax-medical-ultrasound-endoscope-model-numbers-eg-3870utk-eg-367/Wed, 04 Nov 2026 12:00:00 +0000Warnings added to the IFU for ultrasound endoscopes and water bottle assembly to ensure there is deaerated sterile water in the assembly prior to and during the procedure.https://recallledger.net/recalls/device-z-0307-2027-pentax-medical-ultrasound-endoscope-model-numbers-eg38-j10ut-eg34-j/https://recallledger.net/recalls/device-z-0307-2027-pentax-medical-ultrasound-endoscope-model-numbers-eg38-j10ut-eg34-j/Wed, 04 Nov 2026 12:00:00 +0000Warnings added to the IFU for ultrasound endoscopes and water bottle assembly to ensure there is deaerated sterile water in the assembly prior to and during the procedure.https://recallledger.net/recalls/device-z-0306-2027-pentax-medical-ultrasound-endoscope-model-number-eg36-j10ur/https://recallledger.net/recalls/device-z-0306-2027-pentax-medical-ultrasound-endoscope-model-number-eg36-j10ur/Wed, 04 Nov 2026 12:00:00 +0000Warnings added to the IFU for ultrasound endoscopes and water bottle assembly to ensure there is deaerated sterile water in the assembly prior to and during the procedure.https://recallledger.net/recalls/device-z-0304-2027-carelink-smartsync-device-manager-app-model-m01a02-pulse-generator/https://recallledger.net/recalls/device-z-0304-2027-carelink-smartsync-device-manager-app-model-m01a02-pulse-generator/Wed, 04 Nov 2026 12:00:00 +0000Software problem has the potential for an inaccurate displayed longevity estimate.https://recallledger.net/recalls/device-z-0303-2027-carelink-smartsync-rf-head-patient-connector-model-24967-pulse-gene/https://recallledger.net/recalls/device-z-0303-2027-carelink-smartsync-rf-head-patient-connector-model-24967-pulse-gene/Wed, 04 Nov 2026 12:00:00 +0000Software problem has the potential for an inaccurate displayed longevity estimate.https://recallledger.net/recalls/device-z-0302-2027-carelink-smartsync-programmer-model-24970a-pulse-generator-permanen/https://recallledger.net/recalls/device-z-0302-2027-carelink-smartsync-programmer-model-24970a-pulse-generator-permanen/Wed, 04 Nov 2026 12:00:00 +0000Software problem has the potential for an inaccurate displayed longevity estimate.https://recallledger.net/recalls/device-z-0301-2027-emag-system-model-catalog-number-418591-418591u-product-description/https://recallledger.net/recalls/device-z-0301-2027-emag-system-model-catalog-number-418591-418591u-product-description/Wed, 04 Nov 2026 12:00:00 +0000Delayed or no result when analyzing clinical samples with EMAG system (ref: 418591/418591U) due to a randomly occurring software error, Error 10003 Heater timeout after updating to recent firmware SP4 Patch 2https://recallledger.net/recalls/device-z-0300-2027-philips-azurion-s-model-number-722285/https://recallledger.net/recalls/device-z-0300-2027-philips-azurion-s-model-number-722285/Wed, 04 Nov 2026 12:00:00 +0000Solid-State Drives (SSDs) that are not specified in the Medical Device File may have been installed in various PCs. These SSDs may have different performance characteristics, which may include reduced reliability over time such as loss of imaging functionality or motorized movement, a blank or black display, and/or the inability to store newly acquired images or access previously acquired images.https://recallledger.net/recalls/device-z-0299-2027-philips-azurion-7-m20-model-numbers-722079-722224-722282/https://recallledger.net/recalls/device-z-0299-2027-philips-azurion-7-m20-model-numbers-722079-722224-722282/Wed, 04 Nov 2026 12:00:00 +0000Solid-State Drives (SSDs) that are not specified in the Medical Device File may have been installed in various PCs. These SSDs may have different performance characteristics, which may include reduced reliability over time such as loss of imaging functionality or motorized movement, a blank or black display, and/or the inability to store newly acquired images or access previously acquired images.https://recallledger.net/recalls/device-z-0298-2027-philips-azurion-7-m12-model-numbers-722078-722223/https://recallledger.net/recalls/device-z-0298-2027-philips-azurion-7-m12-model-numbers-722078-722223/Wed, 04 Nov 2026 12:00:00 +0000Solid-State Drives (SSDs) that are not specified in the Medical Device File may have been installed in various PCs. These SSDs may have different performance characteristics, which may include reduced reliability over time such as loss of imaging functionality or motorized movement, a blank or black display, and/or the inability to store newly acquired images or access previously acquired images.https://recallledger.net/recalls/device-z-0297-2027-philips-azurion-7-b20-model-numbers-722068-722226/https://recallledger.net/recalls/device-z-0297-2027-philips-azurion-7-b20-model-numbers-722068-722226/Wed, 04 Nov 2026 12:00:00 +0000Solid-State Drives (SSDs) that are not specified in the Medical Device File may have been installed in various PCs. These SSDs may have different performance characteristics, which may include reduced reliability over time such as loss of imaging functionality or motorized movement, a blank or black display, and/or the inability to store newly acquired images or access previously acquired images.https://recallledger.net/recalls/device-z-0296-2027-philips-azurion-7-b12-model-numbers-722067-722225/https://recallledger.net/recalls/device-z-0296-2027-philips-azurion-7-b12-model-numbers-722067-722225/Wed, 04 Nov 2026 12:00:00 +0000Solid-State Drives (SSDs) that are not specified in the Medical Device File may have been installed in various PCs. These SSDs may have different performance characteristics, which may include reduced reliability over time such as loss of imaging functionality or motorized movement, a blank or black display, and/or the inability to store newly acquired images or access previously acquired images.https://recallledger.net/recalls/device-z-0295-2027-philips-azurion-5-m20-model-numbers-722228-722281/https://recallledger.net/recalls/device-z-0295-2027-philips-azurion-5-m20-model-numbers-722228-722281/Wed, 04 Nov 2026 12:00:00 +0000Solid-State Drives (SSDs) that are not specified in the Medical Device File may have been installed in various PCs. These SSDs may have different performance characteristics, which may include reduced reliability over time such as loss of imaging functionality or motorized movement, a blank or black display, and/or the inability to store newly acquired images or access previously acquired images.https://recallledger.net/recalls/device-z-0294-2027-philips-azurion-5-m12-model-number-722227/https://recallledger.net/recalls/device-z-0294-2027-philips-azurion-5-m12-model-number-722227/Wed, 04 Nov 2026 12:00:00 +0000Solid-State Drives (SSDs) that are not specified in the Medical Device File may have been installed in various PCs. These SSDs may have different performance characteristics, which may include reduced reliability over time such as loss of imaging functionality or motorized movement, a blank or black display, and/or the inability to store newly acquired images or access previously acquired images.https://recallledger.net/recalls/device-z-0293-2027-philips-azurion-3-m15-model-number-722064-722222-722280/https://recallledger.net/recalls/device-z-0293-2027-philips-azurion-3-m15-model-number-722064-722222-722280/Wed, 04 Nov 2026 12:00:00 +0000Solid-State Drives (SSDs) that are not specified in the Medical Device File may have been installed in various PCs. These SSDs may have different performance characteristics, which may include reduced reliability over time such as loss of imaging functionality or motorized movement, a blank or black display, and/or the inability to store newly acquired images or access previously acquired images.https://recallledger.net/recalls/device-z-0292-2027-philips-azurion-3-m12-model-numbers-722063-722221/https://recallledger.net/recalls/device-z-0292-2027-philips-azurion-3-m12-model-numbers-722063-722221/Wed, 04 Nov 2026 12:00:00 +0000Solid-State Drives (SSDs) that are not specified in the Medical Device File may have been installed in various PCs. These SSDs may have different performance characteristics, which may include reduced reliability over time such as loss of imaging functionality or motorized movement, a blank or black display, and/or the inability to store newly acquired images or access previously acquired images.https://recallledger.net/recalls/device-z-0291-2027-alphenix-interventional-angiography-system-ref-infx-8000v/https://recallledger.net/recalls/device-z-0291-2027-alphenix-interventional-angiography-system-ref-infx-8000v/Wed, 04 Nov 2026 12:00:00 +0000Due to software issue, X-ray interventional system may experience internal error if F-Store or imagine acquisition is performed while clinical analysis function is use.https://recallledger.net/recalls/device-z-0290-2027-alphenix-interventional-angiography-system-ref-infx-8000f/https://recallledger.net/recalls/device-z-0290-2027-alphenix-interventional-angiography-system-ref-infx-8000f/Wed, 04 Nov 2026 12:00:00 +0000Due to software issue, X-ray interventional system may experience internal error if F-Store or imagine acquisition is performed while clinical analysis function is use.https://recallledger.net/recalls/device-z-0289-2027-alphenix-interventional-angiography-system-ref-infx-8000c/https://recallledger.net/recalls/device-z-0289-2027-alphenix-interventional-angiography-system-ref-infx-8000c/Wed, 04 Nov 2026 12:00:00 +0000Due to software issue, X-ray interventional system may experience internal error if F-Store or imagine acquisition is performed while clinical analysis function is use.https://recallledger.net/recalls/device-z-0288-2027-model-number-712010/https://recallledger.net/recalls/device-z-0288-2027-model-number-712010/Wed, 04 Nov 2026 12:00:00 +0000Potential for the device to fail immediately after an exposure, causing the system to remain stationary.https://recallledger.net/recalls/device-z-0286-2027-orthoscan-versa-accessory-cart-ref-1000-0021-and-versa-mini-c-arm-sy/https://recallledger.net/recalls/device-z-0286-2027-orthoscan-versa-accessory-cart-ref-1000-0021-and-versa-mini-c-arm-sy/Wed, 04 Nov 2026 12:00:00 +0000The accessory cart weldment does not conform to weld dimensional specifications which may result in separation of the monitor arm mounting structure from the cart.https://recallledger.net/recalls/device-z-0285-2027-omniasecure-model-3930m-lead-3930m74-74-cm-df4-mr-3930m74-lead/https://recallledger.net/recalls/device-z-0285-2027-omniasecure-model-3930m-lead-3930m74-74-cm-df4-mr-3930m74-lead/Wed, 04 Nov 2026 12:00:00 +0000Affected leads require additional engineering evaluation due to complaints regarding difficulty in achieving fixation during implantation. Potential harm of tissue trauma due to implant difficulty.https://recallledger.net/recalls/device-z-0284-2027-ethilon-nylon-suture-product-code-697g/https://recallledger.net/recalls/device-z-0284-2027-ethilon-nylon-suture-product-code-697g/Wed, 04 Nov 2026 12:00:00 +0000Nylon suture indicated for use in general soft tissue approximation and/or ligation may have needles with distorted curvature, that may break during use, or could cause additional soft tissue or vessel injury, including tearing or bleeding intraoperatively.https://recallledger.net/recalls/device-z-0210-2027-impella-connect-optical-aic-packaged-primary-user-control-interface/https://recallledger.net/recalls/device-z-0210-2027-impella-connect-optical-aic-packaged-primary-user-control-interface/Wed, 04 Nov 2026 12:00:00 +0000Retrospective review of servicing records identified AIC units requiring various hardware, firmware, and/or software update(s): 1. RFID firmware issue that may result in failure of the AIC to recognize the purge cassette during case setup or cassette change. This issue may result in delay in procedure or therapy. 2. Potential for the rotary push button (RPB) sticking and unreliable actuation imhttps://recallledger.net/recalls/device-z-0209-2027-impella-optical-controller-packaged-primary-user-control-interface-f/https://recallledger.net/recalls/device-z-0209-2027-impella-optical-controller-packaged-primary-user-control-interface-f/Wed, 04 Nov 2026 12:00:00 +0000Retrospective review of servicing records identified AIC units requiring various hardware, firmware, and/or software update(s): 1. RFID firmware issue that may result in failure of the AIC to recognize the purge cassette during case setup or cassette change. This issue may result in delay in procedure or therapy. 2. Potential for the rotary push button (RPB) sticking and unreliable actuation imhttps://recallledger.net/recalls/device-z-0208-2027-automated-impella-controller-packaged-primary-user-control-interface/https://recallledger.net/recalls/device-z-0208-2027-automated-impella-controller-packaged-primary-user-control-interface/Wed, 04 Nov 2026 12:00:00 +0000Retrospective review of servicing records identified AIC units requiring various hardware, firmware, and/or software update(s): 1. RFID firmware issue that may result in failure of the AIC to recognize the purge cassette during case setup or cassette change. This issue may result in delay in procedure or therapy. 2. Potential for the rotary push button (RPB) sticking and unreliable actuation imhttps://recallledger.net/recalls/product-27061-longjili-trading-recalls-pamag-pieeoo-mattresses-due-to-risk-of-seriou/https://recallledger.net/recalls/product-27061-longjili-trading-recalls-pamag-pieeoo-mattresses-due-to-risk-of-seriou/Thu, 29 Oct 2026 12:00:00 +0000The recalled mattresses violate the mandatory flammability standard for mattresses, posing a risk of serious injury or death from fire.https://recallledger.net/recalls/product-27060-harkla-recalls-childrens-sensory-swings-due-to-risk-of-serious-injury/https://recallledger.net/recalls/product-27060-harkla-recalls-childrens-sensory-swings-due-to-risk-of-serious-injury/Thu, 29 Oct 2026 12:00:00 +0000The recalled swings’ ceiling hook can separate from its plate, posing a risk of serious injury from a fall hazard.https://recallledger.net/recalls/product-27059-yinklev-recalls-jocoevol-6-drawer-dressers-due-to-risk-of-serious-inju/https://recallledger.net/recalls/product-27059-yinklev-recalls-jocoevol-6-drawer-dressers-due-to-risk-of-serious-inju/Thu, 29 Oct 2026 12:00:00 +0000The 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 standards as required by the STURDY Act.https://recallledger.net/recalls/product-27058-rootstim-recalls-minoxidil-hair-regrowth-treatment-bottles-due-to-risk/https://recallledger.net/recalls/product-27058-rootstim-recalls-minoxidil-hair-regrowth-treatment-bottles-due-to-risk/Thu, 29 Oct 2026 12:00:00 +0000The recalled hair regrowth products contain minoxidil, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The bottle is not child-resistant, posing a risk of serious injury or death from poisoning if the contents are ingested by young children.