Recalls
Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.
Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.
The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.
Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.
Minimum severity
Medline is recalling CURAD Germ-Shield Touch-Free Fabric Bandages because packaging seals may be open, potentially compromising product sterility. Consumers should stop using affected units.
The Safe-T-Centesis 6 Fr Catheter Drainage Tray has a faulty safety indicator that may show the catheter is in the wrong position, potentially causing treatment delays or internal organ injury.
Stryker is voluntarily recalling 297 Arise 1000EX mattresses sold near MV3 beds because these products were not tested for compatibility and are not designed to be used together.
Medline is recalling Curad Quick Strip Fabric Bandages (18,000 units) due to open seals that may compromise sterility. Distribution affected: US, Guam, Canada, and United Arab Emirates.
Stryker has issued a voluntary recall of 294 MV3 bariatric beds because these units were sold in proximity to Arise 1000EX mattresses that have not been tested for compatibility and are not designed to be used together.
Medline's DEXLOCK Achilles Repair Implant Kits may experience drill bit fusion to the drill guide bushing during surgery, potentially prolonging procedures. 163 units were distributed nationwide.
Medline Industries recalled Perfusion Syringes containing BD Luer Tip Caps that failed biocompatibility testing. The caps may cause sensitization, irritation, pyrogenicity, or acute systemic toxicity, though no patient injuries have been reported.
Medline is recalling all lots of Quick Strip Plastic Sterile Adhesive Bandages (1" x 3") due to open seals in packaging that may compromise sterility. No injuries have been reported.
BD InLay Optima Ureteral Stent Kit (Lot# NGJU4328) recalled due to labeling discrepancy where actual stent size may not match product label. Approximately 116 units distributed worldwide.
C.R. Bard is recalling BD InLay Optima Ureteral Stent Kits (4.7 Fr x 26 cm) due to a labeling discrepancy where actual stent size may not match the product label. Lot NGJU4181 with approximately 4,350 units affected worldwide.
Nipro Medical Corporation is recalling Hemodialysis System Surdial DX units due to a screw that may loosen or fall out. Affected systems were distributed nationwide. Patients should contact their healthcare provider immediately.
A knee fusion nail component was distributed with a locking screw incorrectly inserted from the wrong side into the taper. This manufacturing defect could compromise proper implant fixation and stability.
Medline is recalling approximately 1.7 million Quick Strip Plastic Sterile Adhesive Bandages due to open packaging seals that may compromise product sterility. Affected products were distributed in the US, Guam, Canada, and UAE.
Medline Industries is recalling Curad Touch-Free and Quick-Strip Sterile Adhesive Bandages due to potential open package seals that could compromise product sterility. Approximately 1.57 million units were distributed in the US, Guam, Canada, and UAE.
Philips recalled 110 Azurion 7 M20 fluoroscopic X-ray systems in the U.S. shipped without a required Source-to-Skin Distance Spacer. The missing component may prevent systems from meeting FDA radiation safety distance requirements.
Datascope Corp. is updating the preventative maintenance schedule for the Cardiosave Rescue Intra-Aortic Balloon Pump system in an FDA Class II recall. The Instructions for Use addendum aligns maintenance procedures with updates to the Service Manual from June 2023.
Orthofix U.S. LLC is recalling 61,977 CONSTRUX Mini PTC Spacer System units due to labeling that contains claims not consistently present. No injuries or illnesses have been reported.
Orthofix U.S. LLC is recalling the Pillar SA PTC Spacer System due to product labeling containing claims that are not consistently present. Approximately 13,317 units were distributed worldwide.
Steris Corporation recalls AMSCO 7052HP Washer/Disinfectors because a wire in the electrical box may shift and cause internal electrical arcing. No shock risk is posed to users.
The Cardiosave Hybrid intra-aortic balloon pump maintenance schedule is being updated. Datascope Corp. revised preventative maintenance procedures to align with June 2023 service manual updates.
Orthofix U.S. LLC is recalling CONSTRUX Mini Ti Spacer System due to labeling inconsistencies where claims are not consistently present on affected devices.
Beckman Coulter is recalling 38,225 Access 2 Reaction Vessels that may have manufacturing deformities causing instrument errors and delays in patient test results.
GE Medical Systems is recalling certain Senographe mammography systems due to missing or incorrect X-Ray warning labels. The recall affects approximately 1,818 units globally.
Orthofix U.S. LLC recalls FIREBIRD SI Fusion System surgical screws due to labeling claims that are not consistently present. All 19,431 units distributed worldwide are affected.
Cardinal Health is recalling ChemoPlus protective gowns (251,165 units) distributed nationwide and in Canada due to incorrect expiration dating on packaging. The gowns have a three-year shelf-life but are mislabeled as five years.