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 the agency’s own highest classification or reported deaths or serious injuries, 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
Wright Medical Technology is recalling 34 Charlotte Claw Screws because missing threads on the screwheads may prevent secure engagement with the plate, potentially prolonging surgery.
American Nitrile Operations LLC is recalling 36.8 million Opportunity Flex blue nitrile gloves due to defects like tears and debris that may expose users to pathogens or chemicals.
TOJI CO. is recalling Cloud Cafe Collagen Milk due to an undeclared fish allergen. The product was sold to a single distributor in Los Angeles.
SV Labs Toronto Corporation is recalling specific lots of Benzoyl Peroxide Wash, USP, 5% due to microbial contamination. The product was distributed in Illinois.
Cardinal Health 200, LLC is recalling 2,957 gynecological laparoscopy kits because the handpieces may leak fluid, creating a slip and fall hazard.
Cardinal Health 200, LLC is recalling 22 Presource Packs containing Stryker StrykeFlow PS and AHTO tube sets because the handpieces may leak fluid, creating a slip and fall hazard.
American Contract Systems Inc. is recalling medical convenience kits containing BD CliniClean Pericare Wipes due to potential lubricant contamination.
Shanghai United Imaging Healthcare is recalling 11 uCT ATLAS CT systems due to a software issue that may hide patient images, potentially requiring rescans.
ASP Global is recalling sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life, while the correct validated shelf life is 5 years.
TerSera Therapeutics is recalling 296 cartons of Zoladex (goserelin) implants because the product sat in a non-temperature-controlled trailer for 25.5 hours.
ASP Global is recalling 6,100 units of Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global is recalling MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global, LLC. is recalling 240 units of Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global, LLC. is recalling MPR Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life, but the validated shelf life is only 5 years.
ASP Global, LLC. is recalling 1,899 units of Expressaire Disposable Tourniquet Cuffs because the products are labeled with a 10-year shelf life, but the validated shelf life is 5 years.
SLT Foods Inc. is recalling Khazana Fennel Candy due to undeclared food dyes Yellow 5, Yellow 6, Red 3, and Blue 1.
ASP Global, LLC. is recalling 70 units of Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global is recalling sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life, but the validated shelf life is only 5 years.
Shanghai United Imaging Healthcare is recalling six uMI Panvivo S PET/CT systems due to a software defect that may hide patient images, potentially requiring rescans.
ASP Global, LLC. is recalling Expressaire disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global, LLC. is recalling 850 sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global is recalling sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global, LLC. is recalling MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global, LLC. is recalling 1,692 units of Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global, LLC. is recalling 396 units of Expressaire Disposable Tourniquet Cuffs because the products are labeled with a 10-year shelf life, but the correct validated shelf life is 5 years.