Recalls in Illinois (page 16)
4177 recalls.
- Photera 600 3-D recall (Daavlin Distributing Company)
Medical deviceClass IIReported July 22, 2026 · Calibrated Output was not calculating correctly - UV Sensor GAIN being applied was incorrect - GAIN seemed to be "4/5" instead of "7" (counts were at ~1000... - Photera 600 recall (Daavlin Distributing Company)
Medical deviceClass IIReported July 22, 2026 · Calibrated Output was not calculating correctly - UV Sensor GAIN being applied was incorrect - GAIN seemed to be "4/5" instead of "7" (counts were at ~1000... - Photera 400 recall (Daavlin Distributing Company)
Medical deviceClass IIReported July 22, 2026 · Calibrated Output was not calculating correctly - UV Sensor GAIN being applied was incorrect - GAIN seemed to be "4/5" instead of "7" (counts were at ~1000... - The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System recall (Maquet Cardiovascular, LLC)
Medical deviceClass IIReported July 22, 2026 · Getinge identified that Vasoview Hemopro 2 devices from Lot 3000547797 were exposed to an out-of-specification sterilization dose during a gamma sterilization... - Medtronic Bio-Medicus Adult Cannula Kit recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported July 22, 2026 · Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood. - Medtronic DLP One-Piece Pediatric Arterial Cannula recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported July 22, 2026 · Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood. - Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK-LF ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 22, 2026 · Kits contain Zimmer Biomet mixing bowls and spatulas, which were recalled due to seal nonconformities which present risk of sterility breach. Health... - Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 22, 2026 · Kits contain Zimmer Biomet mixing bowls and spatulas, which were recalled due to seal nonconformities which present risk of sterility breach. Health... - Papablic Replacement Brush Heads. Model Number: PAPA317AA. recall (Papablic Inc)
Medical deviceClass IIReported July 22, 2026 · Potential for brush heads to break. - Papablic Replacement Brush Heads. Model Number: Papablic18B recall (Papablic Inc)
Medical deviceClass IIReported July 22, 2026 · Potential for brush heads to break. - Optima XR240amx recall (GE Medical Systems, LLC)
Medical deviceClass IIReported July 22, 2026 · GE HealthCare has become aware that in certain Optima XR200/220/240amx systems that have had a column replacement completed, functional testing of the safety... - Optima XR220amx recall (GE Medical Systems, LLC)
Medical deviceClass IIReported July 22, 2026 · GE HealthCare has become aware that in certain Optima XR200/220/240amx systems that have had a column replacement completed, functional testing of the safety... - Optima XR200amx recall (GE Medical Systems, LLC)
Medical deviceClass IIReported July 22, 2026 · GE HealthCare has become aware that in certain Optima XR200/220/240amx systems that have had a column replacement completed, functional testing of the safety... - Rapid Refill Continuous Injection System recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 22, 2026 · Devices contain recalled Medline Namic Angiographic Control Syringe with Rotating Adaptor. There is a risk of syringe loosening or disconnecting from the... - ICU Medical Plum Solo Precision IV Pump recall (ICU Medical, Inc.)
Medical deviceClass IIReported July 22, 2026 · In a specific scenario, the pump will not decrement the Volume to be Infused (VTBI) displayed on the Delivery screen and may deliver up to twice the VTBI at... - ICU Medical Plum Duo Infusion Pump recall (ICU Medical, Inc.)
Medical deviceClass IIReported July 22, 2026 · In a specific scenario, the pump will not decrement the Volume to be Infused (VTBI) displayed on the Delivery screen and may deliver up to twice the VTBI at... - Olympus Glass Body for 194 Ellik Evacuator. Model Number: 190A. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported July 22, 2026 · Some sterilization parameters included in the IFU may not consistently render the devices adequately sterile and therefore should no longer be used to... - Olympus Ellik Evacuator Includes Glass Body recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported July 22, 2026 · Some sterilization parameters included in the IFU may not consistently render the devices adequately sterile and therefore should no longer be used to... - Olympus Toomey Evacuator 50cc with Adaptor. Model Number: 188A. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported July 22, 2026 · Some sterilization parameters included in the IFU may not consistently render the devices adequately sterile and therefore should no longer be used to... - Olympus Toomey Evacuator 30cc with Adaptor. Model Number: 188. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported July 22, 2026 · Some sterilization parameters included in the IFU may not consistently render the devices adequately sterile and therefore should no longer be used to... - Bone Marrow Tray recall (Argon Medical Devices, Inc)
Medical deviceClass IReported July 22, 2026 · Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility. - Arterial Line Kit 20ga x 6 recall (Argon Medical Devices, Inc)
Medical deviceClass IReported July 22, 2026 · Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility. - T-Lok Bone Marrow Tray recall (Argon Medical Devices, Inc)
Medical deviceClass IReported July 22, 2026 · Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility. - General Biospy Tray recall (Argon Medical Devices, Inc)
Medical deviceClass IReported July 22, 2026 · Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility. - One-Piece Introducer Tray recall (Argon Medical Devices, Inc)
Medical deviceClass IReported July 22, 2026 · Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility. - Transvenous Pacing Electrode Tray w/ Bipolar Balloon Pacing Electrode 5F recall (Argon Medical Devices, Inc)
Medical deviceClass IReported July 22, 2026 · Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility. - MNIENT 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
Consumer productReported July 17, 2026 · 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... - Target Recalls Cat & Jack Children's Sandals Due to Risk of Serious Injury or Death from Choking Hazard
Consumer productReported July 17, 2026 · The sandals' decorative pearls can fall off, posing a risk of serious injury or death from a choking hazard. - SDADI Kitchen Step Stools Recalled Due to Risk of Serious Injury and Death from Entrapment and Fall Hazards; Imported by Yiwushi Bihe Trading
Consumer productReported July 17, 2026 · The recalled tower stools can collapse or tip over while in use, and a child's torso can fit through the openings on the front and back sides, posing a risk of... - Noerishia 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 Hurzein
Consumer productReported July 17, 2026 · 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... - Jobon Torch Lighters Recalled Due to Risk of Serious Injury or Death from Fire and Burn Hazards; Violate Mandatory Standard for Multipurpose Lighters
Consumer productReported July 17, 2026 · The lighters violate the mandatory safety standard for multipurpose lighters because they do not have the required child-resistant mechanisms posing a risk of... - Madewell Recalls Women's Sweaters Due to Due to Risk of Serious Injury or Death from Burn Hazard; Violate Mandatory Standard for Clothing Textiles
Consumer productReported July 17, 2026 · The recalled sweaters violate the mandatory standard for clothing textiles, posing a risk of serious burn injuries or death. - Huish Outdoors Recalls Hollis Diving Regulators Due to Risk of Serious Injury or Death from Drowning
Consumer productReported July 17, 2026 · The regulator inlet tube can crack and break, posing a risk of serious injury or death from drowning. - Warren James Recalls the Copper Cup Found in Flashgitz Relic Lunch Boxes Due to Risk of Serious Injury or Death from Lead Poisoning
Consumer productReported July 17, 2026 · The cup in the lunch boxes contains high lead concentration levels for drinking vessels, posing a lead poisoning hazard. Lead is toxic if ingested by adults or... - Wade Logan Annyka 9-Drawer Fabric Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units; Imported by Ningbo Jiangdong Peter International Trading
Consumer productReported July 17, 2026 · 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... - Currey & Company Recalls Nottaway Chandeliers Due to Risk of Serious Injury or Death from Electrocution Hazard
Consumer productReported July 17, 2026 · The recalled chandeliers lack proper electrical grounding, posing a risk of serious injury or death from electrocution hazard. - TOMY Recalls Boon PIVOT Collapsible Toddler Tower Kitchen Step Stools Due to Risk of Serious Injury and Death from Tip-Over and Fall Hazards
Consumer productReported July 17, 2026 · The recalled toddler towers can tip over while in use, posing a risk of serious injury and death, due to tip over and fall hazards. - Liizousuda Paint Thinner Bottles Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violate Mandatory Standard for Child-Resistant Packaging; Sold on Amazon.com by Shenzhen Gudebo Technology
Consumer productReported July 17, 2026 · The paint thinner contains low-viscosity petroleum distillates, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act.... - Panasonic Recalls Electric Toaster Ovens Due to Shock and Fire Hazards
Consumer productReported July 17, 2026 · The power cord insulation can be insufficient due to a protective fiberglass sleeve not covering it adequately, posing a risk of shock and/or fire hazard. - Oitnlaughter Projecting Finger Light Toys Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Toys; Sold on Amazon by Delightmi
Consumer productReported July 17, 2026 · The recalled finger lights violate the mandatory safety standard for toys because they contain button cell batteries that can be easily accessed by children.... - GSP Neonatal GALT Kit. Product Codes: 3303-001U recall (WALLAC OY)
Medical deviceClass IIReported July 15, 2026 · Reduction in the on-board stability of the GSP GALT assay. This may increase the likelihood of run-QC failures and consequently delay the reporting of patient... - Brand Name: Geneva Product Name: Brachytherapy Applicator Product Description: The... recall (Elekta, Inc.)
Medical deviceClass IIReported July 15, 2026 · Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient. - Brand Name: Brachytherapy Applicator Product Name: Advanced Gynecological Applicator ... recall (Elekta, Inc.)
Medical deviceClass IIReported July 15, 2026 · Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient. - Brand Name: Fletcher CT/MR Shielded Applicator Set Product Name: Intracavitary Remote... recall (Elekta, Inc.)
Medical deviceClass IIReported July 15, 2026 · Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient. - 5008X Blood Tubing Set recall (Fresenius Medical Care Holdings, Inc.)
Medical deviceClass IIReported July 15, 2026 · Potential for Online Port Errors due to connection issues when connecting the SafeLine of the 5008X CAREset to the substitution fluid port of the 5008X... - Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS recall (Encore Medical, LP)
Medical deviceClass IIReported July 15, 2026 · Due to packaging discrepancy with incorrect product size mixed up. - Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS recall (Encore Medical, LP)
Medical deviceClass IIReported July 15, 2026 · Due to packaging discrepancy with incorrect product size mixed up. - Intracept Access Instruments recall (Boston Scientific Neuromodulation Corporation)
Medical deviceClass IIReported July 15, 2026 · 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... - Aquacel Ag Surgical SP REF: 413556 9cm x 15cm/3.5 in. x 6 in. recall (ConvaTec, Inc)
Medical deviceClass IIReported July 15, 2026 · Surgical dressing manufactured out of specification (greater thickness). - High Valley Orchard Chocolate Covered Raisins recall (Lehi Valley Trading Company, Inc)
FoodClass IReported July 15, 2026 · Undeclared Peanut. High Valley Orchard Chocolate Covered Raisins contains unintended undeclared peanut due to mis-packaging. - Azacitidine for Injection 100mg/Vial recall (Reliance Life Sciences Private Limited)
DrugClass IIReported July 15, 2026 · Lack of Sterility Assurance - Bortezomib for Injection 3.5mg/Vial recall (Reliance Life Sciences Private Limited)
DrugClass IIReported July 15, 2026 · Lack of Sterility Assurance - Pemetrexed for Injection 500mg/Vial recall (Reliance Life Sciences Private Limited)
DrugClass IIReported July 15, 2026 · Lack of Sterility Assurance - Pemetrexed for Injection 100mg/Vial recall (Reliance Life Sciences Private Limited)
DrugClass IIReported July 15, 2026 · Lack of Sterility Assurance - Drogueria San Juan Puerto Rico Isopropyl Alcohol 70% recall (Gasco Industrial Corp.)
DrugClass IIReported July 15, 2026 · Subpotent drug - Drogueria San Juan Puerto Rico Isopropyl Alcohol 70% recall (Gasco Industrial Corp.)
DrugClass IIReported July 15, 2026 · Subpotent drug - Drogueria San Juan Puerto Rico Isopropyl Alcohol 70% recall (Gasco Industrial Corp.)
DrugClass IIReported July 15, 2026 · Subpotent drug - Gasco Isopropyl Alcohol 70% recall (Gasco Industrial Corp.)
DrugClass IIReported July 15, 2026 · Subpotent drug - Gasco Isopropyl Alcohol 70% recall (Gasco Industrial Corp.)
DrugClass IIReported July 15, 2026 · Subpotent drug - Gasco Isopropyl Alcohol 70% recall (Gasco Industrial Corp.)
DrugClass IIReported July 15, 2026 · Subpotent drug - Methohexital Sodium recall (QuVa Pharma, Inc.)
DrugClass IIReported July 15, 2026 · Failed Impurities/Degradation Specifications - Medline Remedy Specialized Silicone Cream recall (BioMed Laboratories, LLC.)
DrugClass IIReported July 15, 2026 · Failed Impurities/Degradation Specifications; Formaldehyde levels exceeded specification. - Methohexital Sodium for Injection recall (ONESOURCE SPECIALTY PHARMA LIMITED)
DrugClass IIReported July 15, 2026 · Failed Impurities/Degradation Specifications - Brand Name: Versius Surgical System US Product Name: Vesius Surgeon Console US ... recall (CMR SURGICAL LIMITED)
Medical deviceClass IIReported July 15, 2026 · Secure Boot was mistakenly not enabled at manufacturing time, which presents a potential cybersecurity risk. - TMINI Femur Tracking Array REF 109003 UDI-DI code: M9461090030 TMINI Tibia... recall (Think Surgical, Inc.)
Medical deviceClass IIReported July 15, 2026 · Due to manufacturing/design issue where the knob on the tracking array may loosen causing potential misalignment of the array. - OmniTract Surgical Retractor System recall (Integra LifeSciences Corp. (NeuroSciences))
Medical deviceClass IIReported July 15, 2026 · The current Omni-Tract Surgical Retractor System IFU states a dry time of 30 minutes. Integra LifeSciences has identified that the dry time needs to be... - Atellica CH Enzymatic Hemoglobin A1c recall (Siemens Healthcare Diagnostics, Inc.)
Medical deviceClass IIReported July 15, 2026 · The potential for intermittent well-to-well bias on the A1c_E assay on the Atellica CH and Atellica CI analyzer which could cause falsely depressed or falsely... - KL Owen Custom Orthodontic Solution recall (Klowen Braces)
Medical deviceClass IIReported July 15, 2026 · A product error defect may cause incorrect bracket placement. - Medline Convenience Kits: 1) OPEN HEART PEDS PACK recall (Medline Industries, LP)
Medical deviceClass IIReported July 15, 2026 · Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the... - Medline Convenience Kits: 1) OPEN HEART PEDS PACK recall (Medline Industries, LP)
Medical deviceClass IIReported July 15, 2026 · Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the... - Medline Convenience Kits: 1) ANESTHESIA KIT PEDS 90-LF recall (Medline Industries, LP)
Medical deviceClass IIReported July 15, 2026 · Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the... - Olympus Single Use Distal Cover recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported July 15, 2026 · Olympus has developed and released newly designed version of the Distal Cover (MAJ-2315) to replace previous design of the Single Use Distal Covers. - Greenworks Tools Recalls 24V and 48V Kobalt Yard Power Tools with USB-C Batteries Due to Risk of Serious Injury from Fire Hazard
Consumer productReported July 10, 2026 · Charging the lithium-ion batteries through the USB-C port, while the batteries are inserted in the yard power tools can cause the batteries to short-circuit... - Flaunt Recalls Magsafe Battery Chargers Due to Risk of Serious Injury or Death from Fire and Burn Hazards
Consumer productReported July 10, 2026 · The lithium-ion battery in the recalled power banks (chargers) can overheat and ignite, posing a risk of serious injury or death from fire and burn hazards. - WonderStone Infant Walkers Recalled Due to Risk of Serious Injury or Death from Fall Hazard; Violate Mandatory Standard for Infant Walkers; Sold on Walmart.com by Wonder Stone Toys
Consumer productReported July 10, 2026 · The recalled infant walkers violate the mandatory standard for infant walkers because they can fit through a standard doorway and fail to stop at the edge of a... - Moodooy Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails; Sold on Amazon by Yuezhang
Consumer productReported July 10, 2026 · 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... - Biometric Gun Safes Recalled Due to Serious Injury Hazard and Risk of Death; Sold Exclusively on Amazon.com by BBRKIN
Consumer productReported July 10, 2026 · The biometric lock on the gun safes can be opened by unauthorized users, posing a serious injury hazard and risk of death. - Best Buy Recalls Insignia® Gas Ranges Due to Risk of Serious Injury from a Fire Hazard
Consumer productReported July 10, 2026 · The recalled ranges' front-mounted knobs can be activated accidentally by humans or pets, posing a risk of serious injury from a fire hazard. - Conair Recalls Cuisinart Propel+ Four Burner 3-In-1 Gas Grills Due to Risk of Serious Injury from Laceration Hazard
Consumer productReported July 10, 2026 · The tempered glass window in the pizza oven can shatter during use, posing a risk of serious injury from laceration hazard. - MorningStar Farms Hot & Spicy Sausage Patties recall (MARS SNACKING)
FoodClass IIReported July 8, 2026 · Potential contamination with plastic material - MorningStar Farms Buffalo Chik'n Nuggets recall (MARS SNACKING)
FoodClass IIReported July 8, 2026 · Potential contamination with plastic material - GORE¿ TAG¿ Thoracic Branch Endoprosthesis Side Branch Component Catalog Numbers recall (W L Gore & Associates, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to catheter separation - 4380 ECONOMY SOFT TISSUE BIOPSY TRAY UDI-DI Code: 0110885403108563 4382A SOFT... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - CK000880 Provena Midline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741188770 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - 1174108 PowerPICC Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741154935 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - 7617408 Groshong NXT ClearVue Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741035258 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - CK000525B PowerPICC Provena SOLO Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741236129... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - CK000980A PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741236150 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - CK000727 PowerMidline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741138478 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - 5855240 Power-Trialysis Slim-Cath Straight Short-Term Dialysis Catheter 12 Fr... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - 5605150 Power-Trialysis Short-Term Straight Dialysis Catheter 13 Fr Triple-Lumen ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - 1274108D PowerPICC SV Catheter 4 Fr Dual-Lumen REKW2449 00801741087110 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - CK000662 PowerPICC SOLO HF Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741129674 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - 5625240 DuoGlide Short-Term Straight Dialysis Catheter 13 Fr Dual-Lumen UDI-DI Code:... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - CK000495A Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741121609 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - OTP5000 THORA/PARA TRAY recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - MEDLINE 111 GRAVITY SET W/3 Needle Free Y-Sites REF DYNDTN0555 Catalog Number:... recall (BD SWITZERLAND SARL)
Medical deviceClass IIReported July 8, 2026 · Due to engineering sample labeled "Not for Human Use" being inadvertently shipped it the U.S. market. - Covidien Shiley Disposable Decannulation Plug REF DDCP UDI-DI code: 10884522004060 ... recall (Covidien LLC)
Medical deviceClass IIReported July 8, 2026 · Due to product labeling incorrectly including the symbol indicating non-DEHP (Bis(2-ethylhexyl) phthalate as the product includes 30 to 35% DEHP. - Brand Name: Medela Product Name: ENFit ExSet Strl 60 2.0ml PV 1ct EN Model/Catalog... recall (Medela Inc)
Medical deviceClass IIReported July 8, 2026 · May contain incorrect connectors and will not attach or misconnect to ENFit connections and is thus incompatible. Issue could lead to slight delay in delivery... - Brand Name: Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges recall (TELEFLEX LLC)
Medical deviceClass IIReported July 8, 2026 · Due to out-of-specification, or potential out-of-specification, levels of endotoxins