Medicine, medical device and cosmetics recalls in United States
Recalls of medicines, medical devices, supplements, cosmetics and personal care products published in United States, newest first.
1,518 recalls, newest first · Checked 14 minutes ago
United StatesArrowhead DE LLC recalls Arrow-LOK Implant
Implant did not undergo required gamma radiation dose audit.Fort Defiance Industries, LLC recalls Fort Defiance Industries
The Automated Field Steam Sterilizer's water recovery system 120V Amphenol connector may experience an intermittent loss of ground continuity, which could result in an…Beckman Coulter Inc. recalls Beckman Coulter DxC 500i Clinical Analyzer Modules using software version 1.5 or lower… and 1 more products
a software defect in which the Parameter Package (PP) import logic overwrites all predefined calculated test rules, including those previously modified by the user…Bard Access Systems, Inc. recalls BD Needle Kit for Powered Driver 15mm x 15Ga
After placement of intraosseous (IO) needle sets, used when intravenous access is difficult or impossible to obtain in emergent, urgent, or medically necessary cases…Spectral Instruments Inc recalls Lago X and 1 more products
Momentary absence of On-Screen "X-Ray On" banner during run readiness check.Boston Scientific Corporation recalls Boston Scientific ENROUTE Transcarotid Neuroprotection System and 1 more products
Potential for arterial sheath tip separation or partial tip separation during use.ConvaTec, Inc recalls Esteem Body Soft Convex Urostomy Pouch Model/Catalog Numbers: 423703
Urostomy Pouches may leak from cap during use.BMC Medical Co., Ltd. recalls BMC/REACTHEALTH Luna G3 APAP REF LG 3600
Retroactive reporting for 2024 rework conducted at the 3B/React Health warehouseCovidien, LLC recalls EndoFLIP System that includes: ENDOFLIP 1 SYSTEM EF-100 05391530810050 10884521809307…
The system's 24-hour usage limit results in catheters incorrectly flagged as expired, making them unavailable for clinical procedures.Paragon 28, Inc. recalls Custom Made Device Implant 6123 Navicular Cage Small Right Rev A and 1 more products
Device was recalled due to an elevated oxygen level in excess of the allowable limit.Siemens Healthcare Diagnostics Products Ltd. recalls Siemens Healthineers Immulite 2000 Systems SYP Syphilis Screen REF:L2KSY2 and 1 more products
Syphilis Screen assay may contain a negative patient bias resulting in low reactive patient results being reported as nonreactive.Philips North America Llc recalls Cardiac Workstation 5000. Product Number: 860439. and 1 more products
Device will intermittently provide inaccurate data related to native heart rate.Medtronic MiniMed, Inc. recalls MiniMed 640G Insulin Pump and 2 more products
Loaner insulin pumps may have been cleaned with chemically incompatible products that could damage the pump case or keypad, allow moisture ingress, and result in…Foundation Medicine, Inc. recalls Hamilton Microlab STAR Liquid Handler
Software issue that can cause an increase in spontaneous software closures.Kico Knee Innovation Company recalls Brand Name: Kico Knee Innovation Product Name: ARVIS SURGICAL NAVIGATION SYSTEM GEN 2…
Due to an internal sensor issue, image displayed with eyepiece may appear tilted relative to the eyepiece housingTobii Dynavox Llc recalls TD Navio Midi Speech Generating Device Model/Catalog Number: 1000798 and 1 more products
Under certain conditions, the battery mounting tabs may become damaged, allowing the battery to move within the device enclosure, potentially leading to an internal…Paragonix Technologies Inc. recalls Paragonix Technologies Inc. KidneyVault Portable Renal Perfusion System REF#…
Due to a firmware defect, the portable organ transfer device datalogger may lose its configuration, resulting in a blank screen and loss of displayed preservation…restor3d Inc. recalls Brand Name: Veritas Standard Reverse Total Shoulder Product Name: Veritas Standard…
Due to incorrect machining of peripheral screw hole resulting in potential for improper engagement of the peripheral screws.Gentherm Medical, LLC recalls Blanketrol II Model 222S and 2 more products
Overheating of the 115V CPU board may cause the device to shut down.Siemens Healthcare Diagnostics, Inc. recalls Syva EMIT 2000 Quinidine Assay REF: 4Q019UL Contents: 1x28 mL and 1 more products
Due to unacceptable precision performance exhibited in certain lots of the Emit 2000 Quinidine Assay, which may lead to erroneously elevated quinidine measurements…American Contract Systems Inc recalls American Contract Systems medical procedure kits and trays labeled as: 1) CRANI PACK and 1 more products
The recall notice was initiated due to a Medicom Urgent Medical Device Recall.AVID Medical, Inc. recalls Halyard LAVH PACK
The kit component was subjected to EO sterilization, contrary to the manufacturer recommendation, which may have led to the component leaking in a kit.Boston Scientific Corporation recalls OverStitch Suture Cinch and 1 more products
Device may fail to deploy the cinch implant and/or fail to cut the suture as intended.A little guidance
Get more from your tools
Practical guide 3 min read
Recall classes explained: Class I, II and III
What the FDA's recall classes, Canada's classes and types, and UK and EU alert levels mean, with how often each one comes up.
Practical guide 3 min read
How to check if your car has a recall
Find the recalls for your make and model, confirm with your VIN whether your car is affected, and know what do-not-drive and park-outside warnings mean.
Practical guide 3 min read
What to do if something you own is recalled
Refunds, repairs, replacements and proof of destruction: what to expect, and how to handle recalled food, medicines, batteries and children's products safely.