Sterility problems recalls (page 5)
732 recalls.
- Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PULL ... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PULL ... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PULL ... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PUSH OTW ... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PUSH OTW ... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PUSH OTW ... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: CORFLO Safety PEG Kit with ENFit Connector Model/Catalog Number:... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-6312 recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-5320 recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-4320 recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6316 recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6312 recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Brand Name: CORFLO Product Name: CORFLO Safety PEG Kit Model/Catalog Number: 30-5320 recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Brand Name: CORFLO Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-4320 recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Brand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE recall (HF Acquisition Co LLC)
Medical deviceClass IIReported June 17, 2026 · Due to incorrect incubation process being performed on product. - Brand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE recall (HF Acquisition Co LLC)
Medical deviceClass IIReported June 17, 2026 · Due to incorrect incubation process being performed on product. - Lidocaine HCl Injection USP recall (Spectra Medical Devices, Llc)
DrugClass IIReported June 10, 2026 · Lack of Assurance of Sterility - DeRoyal Industries Inc. Ref 46-406 recall (DeRoyal Industries Inc)
Medical deviceClass IIReported June 10, 2026 · Sterile wound dressing, lacks sterility assurance - Covidien EndoStitch" Polysorb Single Use Loading Unit recall (Covidien, LP)
Medical deviceClass IIReported June 10, 2026 · 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. - PRED MILD recall (AbbVie Inc.)
DrugClass IIIReported June 3, 2026 · Failed Stability Specifications - Medline medical convenience kit labeled as EYE TRAY-LF recall (Medline Industries, LP)
Medical deviceClass IIReported June 3, 2026 · Specific Medline Kits contain Cardinal Health Monoject 1mL Luer Lock Syringes, Tuberculin Print, Sterile. Cardinal Health has recalled these syringes because... - MG217 Multi-Symptom Treatment Cream & Skin Protectant recall (Wisconsin Pharmacal Company)
DrugClass IReported May 27, 2026 · Microbial Contamination of Non-Sterile Products: confirmed presence of Staphylococcus Aureus. - fentaNYL Citrate recall (IntegraDose Compounding Services LLC)
DrugClass IIReported May 27, 2026 · Subpotent Drug - cimzia recall (UCB Biosciences Inc.)
DrugClass IIReported May 27, 2026 · Lack of Assurance of Sterility - Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach. - Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach. - Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach. - Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach. - Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach. - Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach. - Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach. - Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 15FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach. - Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 13FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach. - Oasis Tears PF recall (Oasis Medical, Inc.)
DrugClass IIReported May 20, 2026 · 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... - Medtronic Marinr Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - Daig Livewire Steerable BDB recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - Daig Livewire Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - Daig Livewire Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - Daig Livewire Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - Daig Livewire Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - Daig Livewire Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - Daig Livewire Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - Daig Livewire Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - Daig Livewire Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - Daig Livewire Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - Daig Livewire Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - Daig Livewire Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - Daig Livewire Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - CS Uni-Directional w Auto ID recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - CS Uni-Directional w Auto ID recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - BW Webster Duo-Decapolar recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - BARD EP XT Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - BARD EP XT Decapolar Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - BARD Dynamic XT Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - BARD Dynamic XT Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - BARD Dynamic XT Deca Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - BARD Dynamic Tip Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - BARD Dynamic Tip Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - BARD Dynamic Tip Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - BARD Dynamic Deca Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - Edwards EVOQUE tricuspid delivery system REF:9850TDS Sterile EO recall (Edwards Lifesciences, LLC)
Medical deviceClass IIReported May 20, 2026 · Labeling update to provide warning if functionality of the valve replacement delivery system is compromised. - Rolls of label stock used with the Omnicell i.v.Station. 1. Part Number 258920028 recall (Omnicell, Inc.)
Medical deviceClass IReported May 20, 2026 · Potential for mislabeled syringe produced by the i.v.STATION device. - Octreotide Acetate for Injectable Suspension recall (Teva Pharmaceuticals USA, Inc)
DrugClass IIReported May 13, 2026 · Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract... - BD PurPrep recall (CareFusion 213, LLC)
DrugClass IIReported May 13, 2026 · Lack of assurance of Sterility: potential product contamination - BD PurPrep recall (CareFusion 213, LLC)
DrugClass IIReported May 13, 2026 · Lack of assurance of Sterility: potential product contamination - DELFLEX recall (Fresenius Medical Care Holdings, Inc.)
DrugClass IIReported May 13, 2026 · Lack of Assurance of Sterility: Potential leaks from perforations in bags. - DELFLEX recall (Fresenius Medical Care Holdings, Inc.)
DrugClass IIReported May 13, 2026 · Lack of Assurance of Sterility: Potential leaks from perforations in bags. - Medline Surgical Packs: 1) PACK recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - See complete list in RES recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Surgical Drapes: 1) SHEET recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) ARTHROSCOPY CDS recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) KIT UROLOGY SLING recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) LVAD DRIVELINE TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) DRAPE PACK recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) KIT TRIPLE LUMEN INSERTION recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) DRAPE PACK-CHOICE recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) KIT GENERAL CLOSURE recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) BURN PACK recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) WMC I D PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) PICC CATHETER INSERTION TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) BAPTIST FLOYD ENDO GI KIT recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) BASIC NERVE BLOCK TRAY W/LINEN recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) KIT STC TRACHEOSTOMY recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - See RES for complete list. Medline Convenience Kits: 1) SPINAL CDS recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) KIT OPHTHALMIC RUPTURE GLOBE recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) BAP NORTH ROBOTIC SURGERY CDS recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) HYSTEROSCOPY recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) C-SECTION PACK recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - See full list in RES recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) OB KIT recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) NEURO SHUNT- CODMAN recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) CHEST TUBE INSERTION TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) ADMIT KIT recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) PPE KIT recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) CENTRAL LINE UNIVERSAL INSERTI recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) CVC PACK recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - See RES for complete list. Medline Convenience Kits: 1) DRAWER 6-IV FLUIDS GLOVES recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) LITHOTOMY PACK recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - See RES for complete list. Medline Convenience Kits: 1) PLASTIC BIN W/MISC KITS recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated...