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
MyNicKnaxs is recalling weight reduction pills marketed without FDA approval because they contain undeclared phenolphthalein.
MyNicNaxs, Inc. is recalling Slim Xtreme Weight loss capsules because they contain undeclared active pharmaceutical ingredients, including sibutramine, and were marketed without FDA approval.
MyNicNaxs, Inc. is recalling Magic Slim capsules because they contain undeclared active pharmaceutical ingredients and were marketed without an approved NDA or ANDA.
Pure Edge Nutrition is recalling Bella Vi BTrim MAX dietary supplements because they contain undeclared sibutramine and phenolphthalein and were marketed without FDA approval.
MyNicNaxs, Inc. is recalling REDUCE WEIGHT FRUTA PLANTA Capsules because they contain undeclared phenolphthalein and were marketed without FDA approval.
MyNicNaxs, Inc. is recalling Fruta BIO 400 mg capsules because they contain undeclared sibutramine and phenolphthalein.
Cubist Pharmaceuticals is recalling 51,500 vials of CUBICIN (daptomycin) because a customer reported a glass shard in one vial.
Legacy Pharmaceutical Packaging is recalling Pantoprazole Sodium tablets because some cartons may contain Lorazepam tablets instead.
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.
Sandoz, Inc. is recalling Cefpodoxime Proxetil tablets because they contain stainless steel particles. The recall covers 22,818 bottles distributed nationwide.
Ben Venue Laboratories is recalling 5,131 vials of Acetylcysteine Solution, USP, 10% due to the presence of glass particulate matter.
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 Magic For Men dietary supplements because they contain undeclared sildenafil and tadalafil without FDA approval.
Schindele Enterprises is recalling Sexy Monkey dietary supplements because they contain undeclared sildenafil, an analogue of sildenafil, and/or tadalafil.
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 XZEN Platinum dietary supplements because they contain undeclared sildenafil and tadalafil, which were marketed without FDA approval.
Pfizer is recalling specific lots of Effexor XR 150 mg capsules because a foreign Tikosyn capsule was found in a bottle.
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.
Schindele Enterprises is recalling XZONE GOLD dietary supplements because they contain undeclared sildenafil, an analogue of sildenafil, and/or tadalafil.
Schindele Enterprises is recalling Boost Ultra sexual enhancement supplements because they contain undeclared sildenafil, an analogue of sildenafil, and/or tadalafil.
Human Science Foundation is recalling PRO ArthMax tablets because FDA analysis found unapproved prescription drugs in the product.
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.
Schindele Enterprises is recalling ExtenZe 600 mg tablets because they contain undeclared sildenafil or tadalafil, which were marketed without an approved NDA or ANDA.