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
Zi Xiu Tang Success, LLC is recalling Ultimate Formula capsules because they contain undeclared sibutramine, an ingredient removed from the market for safety reasons.
Fabscout Entertainment is recalling 72HP Maximum Potency Male Sexual Enhancement because it contains undeclared sildenafil and was marketed without FDA approval.
Zi Xiu Tang Success, LLC is recalling Classic Zi Xiu Tang Bee Pollen Capsules because they contain undeclared sibutramine, an unapproved active ingredient.
Hospira Inc. is recalling 118,100 vials of 0.25% Bupivacaine Hydrochloride Injection due to the presence of visible particulate matter.
Fabscout Entertainment is recalling PRO POWER MAX Natural Energy Enhancer capsules because they contain undeclared sildenafil and tadalafil and were marketed without FDA approval.
Bethel Nutritional Consulting is recalling Quick Thin capsules because FDA analysis detected unapproved drugs sibutramine and phenolphthalein.
Fabscout Entertainment, Inc. is recalling Evil Root 1200 mg capsules because the product contains undeclared sildenafil and was marketed without FDA approval.
Altaire Pharmaceuticals is recalling specific lots of Carboxymethylcellulose Sodium 0.5% Ophthalmic Solution because the preservative may not be effective through expiry, posing a non-sterility risk.
Hospira Inc. is recalling 119,600 vials of Bupivacaine Hydrochloride Injection due to the presence of visible particulate matter.
Healthy Life Chemistry is recalling B-50 capsules because FDA analysis found undeclared steroids, making the product an unapproved new drug.
Myson Corporation is recalling Volcano Male Enhancement capsules because they contain undeclared active pharmaceutical ingredients, making them unapproved new drugs.
Main Street Family Pharmacy is recalling compounded methylprednisolone vials after seven reports of skin abscesses.
Main Street Compounding Pharmacy is recalling methylprednisolone vials after seven reports of skin abscesses potentially linked to the product.
Jack Rabbit, Inc. is recalling its J.R. Jack Rabbit All Natural Herbal Supplement because FDA testing found undeclared sildenafil and tadalafil.
Beamonstar Products is recalling Velextra All-Natural Herbal Supplement because it contains tadalafil, an unapproved drug ingredient.
Beamonstar Products is recalling SexVoltz All Natural Herbal Supplement because it contains tadalafil, an unapproved drug ingredient.
Fresenius Kabi is recalling 15,625 vials of Magnesium Sulfate Injection, USP, 50% due to the presence of glass particulate matter.
Hospira is recalling 264,432 bags of 0.9% Sodium Chloride Injection because the product may contain fibrous material.
Advance Pharmaceutical Inc. is recalling 16,440 bottles of Enteric Coated Aspirin 81 mg due to a label mix-up where one bottle contained Acetaminophen 500 mg.
Bethel Nutritional Consulting, Inc. is recalling Bethel 30 capsules because FDA analysis found undeclared sibutramine and phenolphthalein, making the product an unapproved new drug.
Chang Kwung Products is recalling Lightning ROD capsules because FDA analysis found an undeclared analogue of sildenafil, making the product an unapproved new drug.
Reumofan Plus tablets are being recalled because they were marketed without an approved NDA/ANDA and may contain undeclared active ingredients.
Chang Kwung Products is recalling Lightning ROD capsules because FDA analysis found an undeclared analogue of sildenafil, an unapproved new drug.
Green Planet Inc is recalling Night Bullet Capsules because they contain unapproved active ingredients for erectile dysfunction.
Med Prep Consulting is recalling 403,883 bags of Magnesium Sulfate 2 grams in Dextrose 5% for Injection due to non-sterility and mold contamination.