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
Gadget Island, Inc. is recalling FIFTY SHADES 6000 capsules because they contain undeclared active pharmaceutical ingredients sildenafil, desmethyl carbodenafil, and tadalafil.
Gadget Island, Inc. is recalling Rhino 7 Platinum 5000 capsules because they contain undeclared active pharmaceutical ingredients and were marketed without FDA approval.
Gadget Island, Inc. is recalling PapaZen 3300 capsules because they contain undeclared prescription drugs sildenafil, desmethyl carbodenafil, and tadalafil.
Lucky Mart Inc. is recalling Piyamping Anti-Itch Lotion because it contains dexamethasone instead of the labeled hydrocortisone.
Vitility is recalling MAN OF STEEL capsules because FDA analysis found they contain undeclared sildenafil, an unapproved drug with unestablished safety and efficacy.
Chiavna Saffron LLC is recalling Super Panther 7K Capsules because FDA analysis found the product was tainted with sildendafil and tadalafil and marketed without an approved NDA/ANDA.
The FDA is recalling CaverFlo Natural Herbal Coffee because it contains undeclared sildenafil, tadalafil, and milk. The product was marketed without an approved NDA or ANDA.
C. O. Truxton is recalling Phenobarbital 15 mg tablets that were actually 30 mg due to a labeling error.
Dynamic Technical Formulations is recalling Biotech Underground Tri-Ton Hardcore Formula capsules because FDA testing found unapproved drug ingredients.
Genetic Edge Compounds LLC is recalling GEC LX Laxoplex dietary supplements because FDA analysis found the product tainted with undeclared anabolic steroids and steroid-like substances.
Organic Herbal Supply is recalling ZRECT for Women herbal capsules because FDA testing found undeclared prescription drugs, including tadalafil and sildenafil.
Organic Herbal Supply is recalling Enhancerol Herbal Dietary Supplement Capsules because FDA analysis found undeclared tadalafil, sildenafil, and Flibanserin.
Organic Herbal Supply is recalling Xrect Male Enhancement capsules because FDA analysis found undeclared prescription drugs tadalafil, sildenafil, and Flibanserin.
Organic Herbal Supply is recalling Rectalis Male Enhancement Capsules because FDA analysis found undeclared prescription drugs, including tadalafil and sildenafil.
Organic Herbal Supply is recalling BIGnHARD Male Enhancement Capsules because FDA testing found undeclared prescription drugs, including tadalafil and sildenafil.
Organic Herbal Supply is recalling Cummor Natural Male Enhancement capsules because FDA analysis found undeclared prescription drugs, including tadalafil and sildenafil.
Organic Herbal Supply is recalling Tornado Male Enhancement capsules because FDA analysis found undeclared prescription drugs, including tadalafil and sildenafil.
Organic Herbal Supply is recalling UPROAR male enhancement capsules because FDA testing found undeclared prescription drugs, including tadalafil and sildenafil.
Organic Herbal Supply is recalling ZRECT Male Enhancement capsules because FDA analysis found undeclared prescription drugs, including tadalafil and sildenafil.
Organic Herbal Supply is recalling LabidaMAX Herbal Dietary Supplement Capsules because FDA analysis found undeclared prescription drugs.
Organic Herbal Supply is recalling ZDaily Testosterone and Libido Booster capsules because FDA analysis found undeclared prescription drugs, including tadalafil, sildenafil, and flibanserin.
Complete Pharmacy and Medical Solutions LLC is recalling 1,890 syringes of Human Chorionic Gonadotropin (HCG) due to confirmed mold contamination.
Complete Pharmacy and Medical Solutions LLC is recalling 49 vials of Human Chorionic Gonadotropin due to confirmed bacterial contamination.
Standard Homeopathic Company is recalling Hyland's Baby Nighttime Teething Tablets because FDA analysis found inconsistent amounts of belladonna alkaloids.
Hospira is recalling 71,550 syringes of Infant 25% Dextrose Injection because human hair was found in an internal sample. The product was distributed nationwide and in Puerto Rico.