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
Invisiblu International LLC is recalling LGD-Xtreme capsules containing unapproved ligandrol because the product was marketed without an approved NDA or ANDA.
Baptist Health Medical Towers Pharmacy is recalling seven bags of TPN 1 (amino acid 20%) in Arkansas due to a lack of sterility assurance.
Baptist Health Medical Towers Pharmacy is recalling two bags of Vancomycin IV solution in Arkansas due to a lack of sterility assurance.
Baptist Health Medical Towers Pharmacy is recalling 11 bags of Nafcillin 12 grams in 322 mL 0.9% NS due to a lack of sterility assurance.
Baptist Health Medical Towers Pharmacy recalled Deferoxamine syringes in Arkansas due to lack of sterility assurance.
Baptist Health Medical Towers Pharmacy is recalling three bags of Hydromorphone 2 mg/mL IV solution in Arkansas due to a lack of sterility assurance.
Baptist Health Medical Towers Pharmacy is recalling 24 bags of Invanz 1 gram in 100 mL 0.45% NS due to lack of sterility assurance.
Baptist Health Medical Towers Pharmacy is recalling 84 bags of Vancomycin 1250 mg in 250 mL 0.9% NS due to lack of sterility assurance.
Baptist Health Medical Towers Pharmacy is recalling 11 bags of Cefazolin 6 grams in 292 mL 0.9% NS due to a lack of sterility assurance.
Baptist Health Medical Towers Pharmacy is recalling 14 bags of Daptomycin 650 mg in 50 mL 0.9% NS due to a lack of sterility assurance.
Baptist Health Medical Towers Pharmacy is recalling 7 bags of 1/2 Normal Saline due to lack of sterility assurance. The product was distributed in Arkansas.
Baptist Health Medical Towers Pharmacy is recalling Ceftriaxone IV bags in Arkansas due to a lack of sterility assurance.
Baptist Health Medical Towers Pharmacy is recalling 7 bags of Water for Injection in Arkansas due to a lack of sterility assurance.
Baptist Health Medical Towers Pharmacy is recalling 59 bags of Vancomycin 1000 mg in 250 mL 0.9% NS due to a lack of sterility assurance.
Baptist Health Medical Towers Pharmacy is recalling 11 bags of Vancomycin IV solution in Arkansas due to a lack of sterility assurance.
Baptist Health Medical Towers Pharmacy is recalling 18 syringes of 70% Ethanol-lock Solution in Arkansas due to a lack of sterility assurance.
R Thomas Marketing, LLC is recalling Weekend Prince capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
R Thomas Marketing, LLC is recalling Samurai-X capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Pharmakon Pharmaceuticals is recalling 75 syringes of Morphine Sulfate 0.5 mg/mL due to out-of-specification potency results indicating high levels.
The FDA is recalling 'Bigger Longer More Time More Sperms' because it was marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
R Thomas Marketing, LLC is recalling Stree Overlord capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Lucy's Weight Loss System is recalling Pink Bikini capsules because they contain undeclared Sibutramine, Phenolphthalein, and/or Diclofenac.
Master Herbs is recalling Licorice Coughing Liquid because it contains undeclared morphine and was marketed without an approved NDA or ANDA.
Lucy's Weight Loss System is recalling Shorts on the Beach capsules because they contain undeclared Sibutramine, Phenolphthalein, and/or Diclofenac.
Centro Naturista is recalling Smart Lipo Dietary Supplement capsules because they contain undeclared sibutramine, desmethylsibutramine, and phenolphthalein.