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
HVL, LLC is recalling 278 bottles of Melatonin Control-Released Tablets that contained a vegetarian digestive enzyme instead of melatonin.
GM Manufacturing is recalling Ninja Mojo dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.
National Vitamin Co Inc is recalling Nature's Blend Ferrous Gluconate Tablets because the front panel incorrectly lists 65 mg of elemental iron instead of the correct 36 mg.
Nature's Way is voluntarily recalling Alive No Iron tablets because the raw material supplier reported that enzymes in the blend may contain the antibiotic chloramphenicol.
Pharmavite is voluntarily recalling all lots of Nature Made multivitamin softgels because quality tests show Vitamins B1 and B12 are losing potency faster than expected.
Pharmavite is voluntarily recalling Nature Made multivitamin softgels because quality tests show Vitamins B1 and B12 are losing potency faster than expected.
Pharmavite is voluntarily recalling Nature Made multivitamin softgels because quality tests show Vitamins B1 and B12 are losing potency faster than expected.
Pharmavite is recalling Nature Made Multi vitamins because quality tests show Vitamins B1 and B12 are losing potency faster than expected.
21st Century Healthcare is voluntarily recalling Digestive Enzymes capsules because raw materials may contain trace amounts of the antibiotic chloramphenicol.
Novartis Consumer Health is recalling specific lots of Benefibre Orange Creme Chewables because the lot number and expiration date may be illegible on the packaging.
Florida Nutri Labs is recalling 4HB Stack Bedtime caplets because they were not coated, making them difficult to swallow.
Brand New Energy, LLC is recalling EphBurn 25 supplements because they may contain ephedrine alkaloids, making them unapproved drugs.
Aptalis Pharma is recalling SourceCF Pediatric Drops because the formulation may not support the labeled shelf life. The recall covers 14,439 units distributed in the US, Italy, Canada, and Brazil.
Cardinal Health is recalling specific lots of Dairy Aid Lactase Enzyme Supplement caplets because the packaging incorrectly lists the strength as 9,000 FCC Units instead of 3,000 FCC Units.