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
The One Minute Miracle Inc. is recalling Miracle Rock 48 capsules because they contain undeclared thiosildenafil, an unapproved drug analogue.
The One Minute Miracle Inc. is recalling Miracle Diet 30 capsules because they contain undeclared phenolphthalein, an unapproved drug ingredient.
Hartley Medical Center Pharmacy is recalling 10 vials of Prolotherapy with Phenol due to non-sterility concerns. The product was distributed in California and Nevada.
PharMEDium Services is recalling 20 bags of Bupivacaine HCl 0.0625% for epidural use because they contain human hair particulate matter.
PharMEDium Services, LLC is recalling 48 bags of Epinephrine HCl injection due to the presence of particulate matter in the solution.
Teva Pharmaceuticals USA is recalling ADRUCIL (fluorouracil injection) vials due to the presence of silicone rubber and fluorouracil crystals in the solution.
PharMEDium Services, LLC is recalling 240 bags of Heparin Sodium Injection USP 25,000 Units in 250 mL bags due to the presence of particulate matter.
PharMEDium Services, LLC is recalling 264 bags of Epinephrine HCl injection due to the presence of particulate matter in the saline solution.
PharMEDium Services is recalling 36 bags of Epinephrine HCl injection due to the presence of particulate matter in the solution.
Baxter Healthcare is recalling 189,120 bags of 0.9% Sodium Chloride Injection USP due to a customer complaint of an insect found inside a bag.
Mylan Institutional LLC is recalling 2,455 vials of Gemcitabine for Injection due to the presence of particulate matter.
Mylan Institutional LLC is recalling Methotrexate Injection vials due to the presence of particulate matter.
Baxter Healthcare is recalling specific lots of Lactated Ringers Injection due to the presence of metal particulate matter.
Bethel Nutritional Consulting is recalling SLIM-K capsules because FDA testing found unapproved ingredients including sibutramine and phenolphthalein.
Baxter Healthcare is recalling 18,324 bags of 10% Dextrose Injection due to the presence of metal particulate matter. The affected products were distributed in the US, Puerto Rico, and Bermuda.
Baxter Healthcare is recalling 202,824 bags of 0.9% Sodium Chloride Injection due to the presence of metal particulate matter.
Baxter Healthcare is recalling 402,284 bags of 5% Dextrose Injection due to the presence of metal particulate matter.
Strohecker's Pharmacy is recalling 365 vials of Testosterone Cypionate 200 mg/mL because they contain Estradiol Valerate 20 mg/mL instead.
Physician Preferred Medical, LLC is recalling Epel 18 mg Estradiol Pellets because the specific lot failed sterility testing. The product was distributed in Arizona and Kansas.
Ultra ZX Labs is recalling Ultra ZX dietary supplements because FDA testing found undeclared sibutramine and phenolphthalein. The product was marketed without an approved NDA or ANDA.
Anabolic Science Labs LLC is recalling Estrastain Pro-Anabolic Mass and Hardening Complex capsules because they contain unapproved synthetic hormone ingredients.
Detox Transforms is recalling iNDiGO capsules because they contain undeclared phenolphthalein, making the product an unapproved drug.
REFA Enterprises is recalling Forever Beautiful INFINITY capsules because FDA analysis found the product contains sibutramine and phenolphthalein without an approved NDA/ANDA.
The FDA is recalling iNSANE Bee Pollen capsules because they contain undeclared phenolphthalein and fluoxetine, making them unapproved drugs.
Detox Transforms is recalling EDGE Amplified Weight Release capsules because the product contains undeclared phenolphthalein and fluoxetine, making it an unapproved drug.