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 the agency’s own highest classification or reported deaths or serious injuries, 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
Greenstone LLC is recalling 4,848 bottles of Spironolactone 50 mg tablets because the manufacturing site change resulted in an unapproved dissolution profile.
Affirm XL is recalling its nutritional supplement because FDA analysis found it contains sulfoaildenafil, an unapproved analogue of sildenafil.
Hospira Inc. is recalling 251,400 vials of Metoclopramide Injection because glass spicules were found during a site inspection.
Hospira Inc. is recalling 681,400 vials of Ondansetron Injection because glass spicules were found during a site inspection.
Boehringer Ingelheim is recalling 10,267 bottles of Oxcarbazepine Oral Suspension because the product failed to meet resuspendability requirements.
L. Perrigo is recalling 108,828 bottles of infants' acetaminophen because some cartons may contain dosing syringes without dose markings.
Kremers Urban Pharmaceuticals is recalling 3,867 bottles of Omeprazole 20 mg capsules because some may not meet acid resistance specifications.
Pfizer is recalling Aldactone (spironolactone) 100 mg tablets because the manufacturing site change resulted in an unapproved dissolution profile.
L. Perrigo Co. is recalling 143,892 bottles of infants' acetaminophen suspension because some may be packaged with dosing syringes lacking dose markings.
Greenstone LLC is recalling 2,796 bottles of Spironolactone 25 mg tablets because they were manufactured at an unapproved site, altering the dissolution profile.
Pharmavite is voluntarily recalling Nature Made multivitamin softgels because quality tests show Vitamins B1 and B12 are losing potency faster than expected.
L. Perrigo is recalling 35,136 bottles of Infants' Pain and Fever acetaminophen because the included oral dosing syringes may lack dose markings.
Pharmavite is recalling Nature Made Multi vitamins because quality tests show Vitamins B1 and B12 are losing potency faster than expected.
L. Perrigo Co. is recalling 27,504 bottles of TopCare Infants' Pain and Fever because some cartons may contain dosing syringes without dose markings.
Pharmavite is voluntarily recalling Nature Made multivitamin softgels because quality tests show Vitamins B1 and B12 are losing potency faster than expected.
Pharmavite is voluntarily recalling all lots of Nature Made multivitamin softgels because quality tests show Vitamins B1 and B12 are losing potency faster than expected.
Hill Dermaceuticals is recalling specific lots of Derma-Smoothe/FS topical oil because routine testing found the active ingredient to be subpotent.
Hill Dermaceuticals is recalling Derma-Smoothe/FS topical oil because routine testing found the active ingredient to be subpotent.
21st Century Healthcare is voluntarily recalling Digestive Enzymes capsules because raw materials may contain trace amounts of the antibiotic chloramphenicol.
Hospira Inc. is recalling 70,450 vials of Propofol Injectable Emulsion because visible particles were found in the glass during inspection.
Mylan Pharmaceuticals is recalling specific lots of Amlodipine Besylate and Benazepril HCl capsules because they were not manufactured according to Good Manufacturing Practices.
Mylan Pharmaceuticals is recalling 521 bottles of Ciprofloxacin 250 mg tablets because they were not manufactured according to Good Manufacturing Practices.
Mylan Pharmaceuticals is recalling specific lots of Amlodipine Besylate and Benazepril HCl capsules because they were not manufactured according to Good Manufacturing Practices.
Mylan Pharmaceuticals is recalling Amlodipine Besylate Tablets 10 mg because they were produced with active ingredients not manufactured according to Good Manufacturing Practices.
Mylan Pharmaceuticals is recalling Amlodipine Besylate Tablets, 5 mg, because they were produced with active ingredients not manufactured according to Good Manufacturing Practices.