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
SCA Pharmaceuticals is recalling 3,932 bags of Heparin Sodium 5,000 units due to out-of-specification potency results at the 30-day stability timepoint.
Eosera, Inc. is voluntarily recalling specific lots of Ear Itch MD sprays nationwide due to cGMP deviations.
Eosera, Inc. is voluntarily recalling 43,424 bottles of Ear Itch MD Anti-Itch Spray due to cGMP deviations. The product was distributed nationwide in the United States.
Eosera, Inc. is voluntarily recalling 125,874 bottles of Ear Pain MD Pain Relief Drops with 4% Lidocaine due to current Good Manufacturing Practice (cGMP) deviations.
Taro Pharmaceuticals is recalling specific lots of Clobetasol Propionate Cream 0.05% because the bulk material failed content uniformity testing.
Lupin Pharmaceuticals is recalling Mibelas 24 Fe chewable tablets because they failed impurity specifications. The recall covers 560,922 pouches distributed nationwide.
Eosera, Inc. is voluntarily recalling 45,673 bottles of Ear Pain MD Pain Relief Drops For Kids due to cGMP deviations.
Teva Pharmaceuticals is recalling Lidocaine 5% Patches because individual pouches are missing lot and expiration dates. The recall covers 28,596 cartons distributed nationwide.
Pharmaceutical Associates, Inc. is recalling Nystatin Oral Suspension because it failed potency testing. Patients should consult their healthcare provider.
Golden State Medical Supply Inc. is recalling specific lots of Clobetasol Propionate Cream, USP, 0.05% because the bulk material failed content uniformity testing.
West-Ward Columbus Inc. is recalling 2,300 bottles of Leucovorin Calcium 10 mg tablets because they are imprinted with the incorrect identification code.
Michigan Herbal Remedies is recalling 100 bottles of Pathway To Wellness CBD Oil due to elevated levels of undeclared lead. The product was sold nationwide via internet and retail channels.
Michigan Herbal Remedies is recalling Tasty Drops CBD oil bottles due to elevated levels of undeclared lead. The product was sold nationwide via internet and retail channels.
Michigan Herbal Remedies is recalling Tasty Drops CBD oil due to elevated levels of undeclared lead. Consumers should stop using the product.
Michigan Herbal Remedies is recalling 496 bottles of Made by Hemp 1000MG Hemp Extract due to elevated levels of undeclared lead.
Michigan Herbal Remedies is recalling A Clean Choice CBD tinctures due to elevated levels of undeclared lead. Consumers should stop using the product.
Michigan Herbal Remedies is recalling Tasty Drops Hemp Oil Extract due to elevated levels of undeclared lead. Consumers should stop using the product.
Michigan Herbal Remedies is recalling Tasty Drops Hemp Oil Extract because it contains elevated levels of undeclared lead.
Michigan Herbal Remedies is recalling Tasty Drops CBD oil bottles due to elevated levels of undeclared lead.
Michigan Herbal Remedies is recalling 25 bottles of BC Hemp Co. CBD Oil due to elevated levels of undeclared lead.
Michigan Herbal Remedies is recalling 25 bottles of SP Berry CBD hemp oil because the product contains elevated levels of undeclared lead.
Michigan Herbal Remedies is recalling 486 bottles of Made by Hemp 1000MG Hemp Extract due to elevated levels of undeclared lead.
Michigan Herbal Remedies is recalling 50 bottles of BC Hemp Co. CBD Oil due to elevated levels of undeclared lead.
Mylan Institutional LLC is recalling 18,480 vials of Daptomycin for Injection due to the presence of particulate matter. The product is distributed nationwide.
Michigan Herbal Remedies is recalling 33 bottles of Herbzeedy Hemp Oil due to elevated levels of undeclared lead. The product was sold nationwide via internet and retail channels.