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
AuroMedics Pharma LLC is recalling 308,112 bags of Levofloxacin in 5% Dextrose Injection due to a lack of assurance of sterility and a confirmed report of mold.
AuroMedics Pharma LLC is recalling Linezolid Injection bags due to a lack of assurance of sterility and a confirmed report of leaking bags with mold.
AuroMedics Pharma LLC is recalling 67,300 bags of Levetiracetam Injection due to a confirmed report of leaking bags and mold found between the outer bag and overwrap.
AuroMedics Pharma LLC is recalling 261,250 bags of Levetiracetam Injection due to a confirmed report of leaking bags and mold found between the outer bag and overwrap.
AuroMedics Pharma LLC is recalling specific lots of Levofloxacin in 5% Dextrose Injection due to a lack of assurance of sterility and reports of leaking bags with mold.
Coastal Meds, LLC. is recalling 200 vials of ADENO-PLEX Injectable-30 mL MDV due to the presence of unknown particulate matter.
Coastal Meds, LLC. is recalling LIPO-PLEX Injectable-30 mL vials nationwide due to the presence of unknown particulate matter.
Premier Pharmacy Labs is recalling specific lots of Morphine Sulfate Injection because routine testing of other lots detected microbial contamination risks.
Premier Pharmacy Labs is recalling NeoStigmine Methylsulfate syringes because routine testing of other lots detected microbial contamination risks.
Coastal Meds, LLC. is recalling 635 vials of Pyridoxine Injectable due to the presence of unknown particulate matter.
Premier Pharmacy Labs is recalling 3,570 hydromorphone syringes because routine testing of other lots found microbial contamination risks.
Coastal Meds, LLC. is recalling 3,733 vials of LIPO-DEN EXTREME Injectable-30 mL 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.
Coastal Meds, LLC. is recalling 1,457 vials of LIPO-DEN PLUS Injectable because of the presence of unknown particulate matter. The product was distributed nationwide in the USA.
Coastal Meds, LLC. is recalling 1,506 vials of Hydroxocobalamin Injectable due to the presence of unknown particulate matter. The product was distributed nationwide.
Bayer is recalling specific Alka-Seltzer Plus packages because the ingredients listed on the front sticker may not match the actual product inside the carton.
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/Anastrozole pellets in Nevada 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 CoEnzymeQ10 25mg/mL vials because they were sterilized using a non-approved method.
Partell Specialty Pharmacy is recalling Ascorbic Acid (Tapioca) 500 mg/mL vials because they were sterilized using a non-approved method.
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 Estradiol 35 mg pellets in Nevada due to the use of a non-approved sterilization 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 four vials of Glutathione 200mg/mL in Nevada because the products were sterilized using a non-approved method.