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Search every CPSC, FDA, USDA and NHTSA recall on record, or scan a barcode. The last 90 days are below.
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Page 28 of 28Moderate
Medline Curad bandages recalled for compromised sterility riskMedline is recalling seven Curad bandage products, including Germ-Shield Touch-Free, Quick Strip, and Fur Friends fabric and plastic bandages. Some packages may have open seals, which could compromise the sterility of the bandages. No injuries have been reported.
ModerateFDADec 17, 20257 products
- Check expiration dates on ChemoPlus gowns
Cardinal Health ChemoPlus protective gowns and sleeves have been mislabeled with a five-year shelf life when the actual shelf life is three years. The affected gowns may be used past their true expiration date if the incorrect label is relied upon. No injuries have been reported.
ModerateFDADec 17, 2025
- Check Waldemar Link knee fusion nail implant
Waldemar Link knee fusion nails in certain lots were shipped with a locking screw installed incorrectly—inserted from the wrong side into the femoral component. This misalignment could affect how the device functions after implantation. Eighteen units were distributed to Alabama, Georgia, and Texas.
ModerateFDADec 17, 2025
- Stop using affected Beckman Coulter reaction vessels
Certain lots of Beckman Coulter Access 2 Reaction Vessels contain small defects on the bottom that may cause errors in laboratory immunoassay instruments. These defects could delay patient test results. The recall affects specific lot numbers distributed nationwide and globally.
ModerateFDADec 17, 2025
- Stop using Bard Safe-T-Centesis drainage trays
Bard Peripheral Vascular Inc. is recalling Safe-T-Centesis 6 Fr Catheter Drainage Trays because the safety indicator on the catheter may show the wrong position—displaying "sharp" when the catheter is actually "blunt." This could lead medical staff to believe the catheter hasn't entered the body cavity when it actually has, potentially causing discomfort, treatment delays, or injury to organs or blood vessels.
ModerateFDADec 17, 2025
- Check Medline Perfusion Syringe lot 25FMJ081
Medline is recalling specific batches of Medline Perfusion Syringes (model DYNJ39223C) that contain BD Luer Tip Caps. BD's testing found that certain tip cap trays failed biocompatibility tests, meaning the plastic may cause skin irritation, allergic reactions, or other adverse effects if it contacts patients during use. No injuries have been reported so far.
ModerateFDADec 17, 2025
- Check your GE Senographe Pristina mammography system
Some GE Senographe Pristina, Pristina Serena, and Pristina Serena 3D mammography systems were distributed with a missing or incorrect X-ray warning label. This label is required by federal regulation to inform users of radiation hazards. No injuries have been reported.
ModerateFDADec 17, 2025
- Check your Philips Azurion 7 M20 X-ray system
Between July 2024 and June 2025, some Philips Azurion R3.0 fluoroscopic X-ray systems (model 722234) were shipped without a required safety spacer. This spacer ensures the X-ray tube maintains a safe distance from patients during standard fluoroscopy procedures, as required by FDA regulations.
ModerateFDADec 17, 2025