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
Coastal Meds, LLC. is recalling 200 vials of ADENO-PLEX Injectable-30 mL MDV due to the presence of unknown particulate matter.
Premier Pharmacy Labs Inc is recalling 4,192 syringes of Morphine Sulfate 4 mg/mL PF Injection due to a lack of assurance of sterility.
Lyne Laboratories is recalling 23,453 units of Fluocinolone Acetonide Topical Oil because the product is subpotent. The recall is voluntary and classified as FDA Class II.
Coastal Meds, LLC. is recalling LIPO-B Injectable-30 mL vials due to the presence of unknown particulate matter.
Coastal Meds, LLC. is recalling 745 vials of Cyanocobalamin Injectable due to the presence of unknown particulate matter.
Coastal Meds, LLC. is recalling 1,309 vials of LIPO-DEN Injectable-30 mL because of the presence of unknown particulate matter.
Coastal Meds, LLC. is recalling 4,524 vials of Methylcobalamin Injectable due to the presence of unknown particulate matter.
Partell Specialty Pharmacy is recalling Testosterone 200 mg pellets in Nevada because they were sterilized using a non-approved method.
Partell Specialty Pharmacy is recalling Nandrolone decanoate 200mg/mL vials because they were sterilized using a non-approved method.
Partell Specialty Pharmacy is recalling Estradiol 20 mg pellets in Nevada because a non-approved sterilization method was used.
Partell Specialty Pharmacy is recalling specific testosterone and hormone pellet vials because they were sterilized using a non-approved method.
Partell Specialty Pharmacy is recalling specific lots of B-complex injectable vials because a non-approved sterilization method was used.
Partell Specialty Pharmacy is recalling Testosterone 37.5 mg pellets because they were sterilized using a non-approved method.
Partell Specialty Pharmacy is recalling Testosterone/Anastrozole pellets because a non-approved sterilization method was used, raising concerns about sterility assurance.
Partell Specialty Pharmacy is recalling Testosterone 40 mg pellets in Nevada due to a non-approved sterilization method.
Partell Specialty Pharmacy is recalling Estradiol 12.5 mg pellets in Nevada due to a non-approved sterilization method.
Partell Specialty Pharmacy is recalling HCG 1000 units/mL vials in Nevada because a non-approved sterilization method was used.
Partell Specialty Pharmacy is recalling Testosterone/Finasteride pellets because they were sterilized using a non-approved method.
Partell Specialty Pharmacy is recalling 7 vials of Testosterone Cypionate 200mg/mL in Nevada because the firm used a non-approved method of sterilization.
Partell Specialty Pharmacy is recalling Methionine 25mg/Inositol 50mg/Choline 50mg/B12 1mg injections because they were sterilized using a non-approved method.
Partell Specialty Pharmacy is recalling Pregnenolone 100 mg pellets because they were sterilized using a non-approved method.
Partell Specialty Pharmacy is recalling specific lots of Progesterone 50 mg pellets in Nevada because the products were sterilized using a non-approved method.
Partell Specialty Pharmacy is recalling Testosterone Propionate 100mg/mL vials because a non-approved method of sterilization was used.
Partell Specialty Pharmacy is recalling Vitamin D 50,000 unit/ml injectable liquid because it was sterilized using a non-approved method.
Partell Specialty Pharmacy is recalling Estradiol 15 mg pellets in Nevada due to a non-approved sterilization method.