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
MyNicNaxs, Inc. is recalling Meizi Evolution Soft Gel Capsules because the product was marketed without an approved NDA/ANDA and contains undeclared active pharmaceutical ingredients.
Cubist Pharmaceuticals is recalling 51,500 vials of CUBICIN (daptomycin) because a customer reported a glass shard in one vial.
Hospira is recalling 85,680 vials of Marcaine (bupivacaine HCl) injection because a customer complaint confirmed the presence of visible metal particles and discolored solution.
Golden State Medical Supply Inc. is recalling Losartan Potassium 50 mg tablets because some bottles may contain debris swept up during cleaning.
Deseo Rebajar is recalling Burn 7 Capsules because they contain undeclared sibutramine and phenolphthalein, which were not approved for use in dietary supplements.
Herbal Give Care is recalling Esbelder Siloutte dietary supplements because they contain undeclared sibutramine, a drug removed from the U.S. market for safety reasons.
Herbal Give Care Llc is recalling Esbelder Man Herbal Blend because it contains undeclared sibutramine, a drug removed from the U.S. market for safety reasons.
Schindele Enterprises is recalling Sexy Monkey dietary supplements because they contain undeclared sildenafil, an analogue of sildenafil, and/or tadalafil.
Ben Venue Laboratories is recalling 5,131 vials of Acetylcysteine Solution, USP, 10% due to the presence of glass particulate matter.
Schindele Enterprises is recalling Boost Ultra sexual enhancement supplements because they contain undeclared sildenafil, an analogue of sildenafil, and/or tadalafil.
Schindele Enterprises is recalling XZONE GOLD dietary supplements because they contain undeclared sildenafil, an analogue of sildenafil, and/or tadalafil.
Pfizer is recalling specific lots of Effexor XR 150 mg capsules because a foreign Tikosyn capsule was found in a bottle.
Human Science Foundation is recalling PRO ArthMax tablets because FDA analysis found unapproved prescription drugs in the product.
Schindele Enterprises is recalling ExtenZe 600 mg tablets because they contain undeclared sildenafil or tadalafil, which were marketed without an approved NDA or ANDA.
Herbal Give Care Llc is recalling Esbelin Siloutte Mezcal Herbal because it contains undeclared sibutramine, a drug removed from the U.S. market for safety reasons.
Herbal Give Care Llc is recalling Esbelin Siloutte Te herbal tea because it contains undeclared sibutramine and related compounds, making it an unapproved new drug.
Herbal Give Care Llc is recalling Esbelder Fem Mezcla con L-Carnitina because it contains undeclared sibutramine, a drug removed from the U.S. market for safety reasons.
Schindele Enterprises is recalling Magic For Men dietary supplements because they contain undeclared sildenafil and tadalafil without FDA approval.
Schindele Enterprises is recalling XZEN Platinum dietary supplements because they contain undeclared sildenafil and tadalafil, which were marketed without FDA approval.
Tendex is recalling Naturect Capsules because FDA analysis found the product contains undeclared tadalafil, making it an unapproved drug.
Tendex is recalling P-Boost Capsules because FDA analysis found the product contains undeclared tadalafil, making it an unapproved drug.
Independent Nutrition Center is recalling Red Yeast Rice High Potency Dietary Supplement because it contains excessive levels of lovastatin, an FDA-approved drug.
Teva Pharmaceuticals is recalling 17,181 bottles of 2 mg Buprenorphine Hydrochloride Sublingual Tablets because stability testing revealed high out-of-specification impurity levels.
Fresenius Medical Care is recalling specific lots of phosLo (calcium acetate) GelCaps due to cross-contamination with a tricyclic antidepressant found on the packaging.
Teva Pharmaceuticals is recalling QVAR inhalation aerosol canisters because the delivery system and valve are defective.