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
Cherry Hill Sales Co. is voluntarily recalling 7,200 cartons of MakeSense First Aid Cream due to Current Good Manufacturing Practice (CGMP) deviations.
MS Bionic is recalling MegaJex Herbal Supplement because it contains sildenafil and tadalafil, active ingredients in approved erectile dysfunction drugs, without FDA approval.
Jersey Shore Supplements, LLC is recalling SLIMFIT X capsules because they contain undeclared sibutramine and desmethylsibutramine and were marketed without an approved NDA/ANDA.
Aurobindo Pharma USA Inc is recalling 47,040 bottles of Venlafaxine Hydrochloride extended-release capsules because some contain punctured or clumped capsules.
Actavis Inc is recalling specific lots of Glipizide extended-release tablets because they failed to meet dissolution specifications at the 10-hour testing point.
Teva Pharmaceuticals USA is recalling specific lots of Mimvey Lo tablets because they failed impurity specifications for norethindrone.
Accord Healthcare is recalling 12,896 bottles of 5 mg Lisinopril tablets because the tablets are missing a break line. The recall covers the U.S. and Puerto Rico.
LEO Pharma Inc. is recalling Taclonex topical suspension because it was packaged with an out-of-date package insert.
VistaPharm is recalling 13,609 cases of Potassium Chloride Oral Solution because the unit dose cups may leak at the seal.
Aurobindo Pharma USA Inc is recalling 29,800 vials of Pantoprazole Sodium for Injection due to discoloration. The affected vials contain powder with a yellowish-brownish appearance.
Dr. Reddy's Laboratories is recalling Olanzapine tablets because an impurity exceeded specification limits during stability testing.
Apotex Inc. is recalling 67,946 bottles of 2 mg Aripiprazole tablets because the product may not meet specifications throughout its shelf life.
Fresenius Kabi is recalling specific lots of Midazolam Injection because they failed impurities and degradation specifications.
VistaPharm is recalling Hydrocodone Bitartrate and Acetaminophen Oral Solution because purified water used in manufacturing may have been contaminated with Burkholderia cepacia.
VistaPharm is recalling Oxycodone Hydrochloride Oral Solution because the purified water used in manufacturing may have been contaminated with Burkholderia cepacia.
Sun Pharmaceutical Industries is recalling 8,537 bottles of Carbidopa and Levodopa tablets because they failed dissolution specifications.
VistaPharm is recalling Lactulose Solution because the purified water used in manufacturing may have been contaminated with Burkholderia cepacia.
VistaPharm is recalling Lactulose Solution USP because purified water used in manufacturing may have been contaminated with Burkholderia cepacia.
VistaPharm is recalling Methadone Hydrochloride Oral Concentrate because purified water used in manufacturing may have been contaminated with Burkholderia cepacia.
VistaPharm is recalling Phenytoin Oral Suspension because the purified water used in manufacturing may have been contaminated with Burkholderia cepacia.
VistaPharm is recalling Nystatin Oral Suspension because the purified water used in manufacturing may have been contaminated with Burkholderia cepacia.
VistaPharm is recalling Nystatin Oral Suspension because the purified water used in manufacturing may have been contaminated with Burkholderia cepacia.
VistaPharm is recalling 3,354 bottles of Methadone Hydrochloride Oral Concentrate because the purified water used in manufacturing may have been contaminated with Burkholderia cepacia.
Dr. Reddy's Laboratories is recalling Flucanazole tablets because they failed dissolution and stability specifications.
VistaPharm is recalling specific lots of Metoclopramide Oral Solution because the purified water used in manufacturing may have been contaminated with Burkholderia cepacia.