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
The Medicine Shoppe Pharmacy is recalling Hydromorphone Oral 1 mg/mL Solution due to lack of processing control. The product was distributed in Florida.
The Medicine Shoppe Pharmacy in Port Charlotte, Florida, is recalling Tretinoin 0.1% in Versabase Cream due to a lack of processing control.
The Medicine Shoppe Pharmacy is recalling Bi-Est (8:2)/Progesterone capsules in Florida due to a lack of processing control.
Filltech USA is recalling Dermatone Sunscreen Lotion due to positive tests for yeast and bacteria.
The Medicine Shoppe Pharmacy is recalling Testosterone Cream due to a lack of processing control. The product was distributed in Florida.
The Medicine Shoppe Pharmacy is recalling Bi-Est cream due to lack of processing control. The product was distributed in Florida.
The Medicine Shoppe Pharmacy is recalling specific lots of Progesterone 200 mg Capsules due to a lack of processing control.
H J Harkins Company is recalling 9,000 tablets of Acetaminophen and Codeine Phosphate 300/30 mg due to cGMP deviations. The product was distributed in California and Arizona.
PharMEDium Services, LLC is recalling 46 lots of fentanyl citrate injection products because of a lack of sterility assurance.
Innovative Compounding Pharmacy is recalling Testosterone Cypionate In Sesame Oil 200mg/ml injectable vials because the firm cannot assure the sterility of the product.
Innovative Compounding Pharmacy is recalling Hydroxyprogesterone Caproate injections because the FDA cannot ensure the product is sterile. Patients in California, Maine, and Texas should stop using the medication.
Avet Pharmaceuticals is recalling Losartan Potassium Tablets 50 mg because FDA testing found an impurity above acceptable levels.
Herbal Doctor Remedies is recalling Hernia Off because the product is misbranded as an unapproved new drug.
Innovative Compounding Pharmacy is recalling specific lots of Methylcobalamin Injectable due to a lack of assurance of sterility. Patients in California, Maine, and Texas should stop using the product.
Herbal Doctor Remedies is recalling Bleeding Stop because the product is misbranded as an unapproved new drug. The product was sold online in the US and internationally.
Innovative Compounding Pharmacy is recalling MIC-8 injectable vials because the firm cannot assure the product's sterility. Patients in California, Maine, and Texas should stop using the product.
Herbal Doctor Remedies is recalling Lipidtrol 500mg capsules because the products were found to be misbranded as unapproved new drugs due to CGMP deviations.
Herbal Doctor Remedies is recalling Herpes Off because the product is misbranded as an unapproved new drug. The product was sold online in the U.S. and internationally.
Teva Pharmaceuticals USA is recalling bulk Losartan Potassium Tablets 100 mg because an impurity called NMBA was detected in the active ingredient.
Herbal Doctor Remedies is recalling Thyro-H 500mg capsules because the products were found to be misbranded as unapproved new drugs.
PharMEDium Services, LLC is recalling 46 lots of fentanyl citrate infusions because of a lack of sterility assurance. The products were distributed nationwide in the US.
Teva Pharmaceuticals USA is recalling bulk Losartan Potassium Tablets because an impurity was detected in the active pharmaceutical ingredient.
Teva Pharmaceuticals USA is recalling bulk Losartan Potassium Tablets 50 mg because an impurity, NMBA, was detected in the active pharmaceutical ingredient.
PharMEDium Services, LLC is recalling 46 lots of fentanyl citrate injection products because of a lack of sterility assurance.
PharMEDium Services LLC is recalling 46 lots of nICARdipine HCl injection products because of a lack of sterility assurance.