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
Bokser Home is recalling about 2,300 units of 100% cotton mattress pads because they violate federal flammability regulations and pose a fire hazard. No injuries have been reported.
Eban's Bakehouse Sweet Indulgences cookies are recalled due to undeclared milk and soy allergens not listed on the label. Consumers with allergies to milk or soy should not consume this product.
Valley View Candies recalled Chocolate Fudge due to undeclared egg allergen. The recall affects 348 containers distributed to retail stores in Iowa.
All lots of Peanut Butter Fudge sold in Iowa are recalled due to undeclared egg allergen. The manufacturer initiated the voluntary recall.
Eban's Bakehouse LLC is recalling Sweet Indulgences cookies for containing undeclared milk and soy allergens, which pose serious health risks to allergic consumers.
InvaGen Pharmaceuticals recalls Vigabatrin for Oral Solution nationwide due to defective containers that may leak. Consumers with affected lot should contact their pharmacy or healthcare provider.
Eban's Bakehouse Sweet Indulgences lemon cookies are being recalled due to undeclared milk and soy allergens. Consumers with allergies to these ingredients should not consume the product.
Eban's Bakehouse Sweet Indulgences Brown Butter Snickerdoodles are recalled due to undeclared milk and soy allergens. The FDA Class I recall affects 876 units distributed to 33 states.
Valley View Candies is recalling Maple Nut Fudge 8oz containers due to undeclared egg allergen. The product was distributed to retail stores in Iowa.
Eban's Bakehouse has recalled Sweet Indulgences Chocolate Chili Coconut cookies due to undeclared milk and soy allergens. The product was distributed nationwide and poses a risk to allergic consumers.
Eban's Bakehouse Sweet Indulgences cookies are being recalled due to undeclared milk and soy allergens. Consumers with allergies should not consume these products and should discard or return them.
Eban's Bakehouse LLC is recalling Turtle Brownie cookies that contain undeclared milk and soy allergens. Consumers with allergies should not consume the product.
Abiomed is recalling its Oscor Introducer Kit due to holes in the outer pouch that may compromise the sterile barrier. Non-sterile introducers could expose patients to infection, bacteremia, or sepsis.
The Scoot Control R-net wheelchair attendant controller's throttle lever may stick and fail to return to neutral, potentially causing unwanted chair movement. A total of 129 units were distributed in Tennessee and Texas.
Dr. Reddy's Laboratories is recalling Tizanidine 4mg tablets due to the presence of 2mg tablets in bottles. About 38,952 bottles were distributed nationwide.
Abbott Laboratories is recalling 1,325 Alinity i Processing Module systems due to unlabeled dry natural rubber (latex) subcomponents. Users with latex allergies may be at risk of exposure.
BioFire Diagnostics recalls 57 kits of the BIOFIRE Respiratory Panel 2.1 due to a manufacturing defect that may produce false negative results, potentially causing treatment delays or missing infections.
Abiomed is recalling 84 introducer kits that may have holes in the outer pouch, compromising the sterile barrier. This exposes patients to microbial contamination and risk of serious infections including bacteremia and sepsis.
Icotec Ag is recalling VADER pedicle system torque wrenches (Catalog Number 42-702) because the torque limiting function may malfunction, potentially leaving nut screws insufficiently tightened during implant surgery. No injuries have been reported.
Ingomar Packing Co is recalling 3/4" diced tomatoes in juice sold in 55-gallon drums due to potential plastic contamination. Affected products were distributed to California, Washington, and Japan.
Rising Pharma Holdings is recalling 47,976 bottles of Bupropion Hydrochloride 150mg tablets nationwide due to foreign tablets or capsules found in some bottles. Consumers should stop use and contact their pharmacist immediately.
Olympus has updated cleaning instructions for the Model CYF-VH Cysto-Nephro Videoscope. Reusable cleaning brushes are no longer recommended for manual cleaning; single-use brushes remain compatible.
Philips BrightView X gamma cameras may create a gap between patient support and detector during quality assurance scans, potentially trapping a patient's extremity.
Immunostics is recalling H. Pylori diagnostic test kits due to mislabeled expiration dates. Using the product after expiration may produce false positive, false negative, or invalid results.
Abiomed Introducer Kits may have holes in outer pouches that compromise sterility, exposing patients to bacterial contamination and risk of infection, bacteremia, or sepsis.