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
Food Sensitivity Test Small kits are recalled for distribution without FDA premarket approval or clearance. Consumers should stop using and contact the manufacturer.
Siemens is recalling MAMMOMAT Revelation mammography systems where the operator table was sold together with a bus-installation kit, despite being designed for stationary operation only.
GET TESTED INTERNATIONAL AB is recalling its Fructose Intolerance Test because the product was distributed in the United States without FDA premarket approval or clearance.
GET TESTED INTERNATIONAL AB recalls its Vitamin D2 and D3 Test (EAN: 7340221709232) distributed nationwide without FDA premarket approval. All lots are affected.
GET TESTED INTERNATIONAL AB is recalling its Allergy & Food Intolerance Test (all lots) because it was distributed nationwide without FDA premarket approval or clearance.
GET TESTED INTERNATIONAL AB is recalling Ovulation Test (5 tests) nationwide due to distribution without FDA premarket approval or clearance.
Aizu Olympus is notifying customers of Olympus OER-Pro devices about important safety warnings and maintenance procedures. Only trained personnel should perform repairs and maintenance.
GET TESTED INTERNATIONAL AB recalled 27 units of the PSA Test distributed nationwide without FDA premarket approval or clearance.
A drug test device (4 substances) manufactured by GET TESTED INTERNATIONAL AB was distributed nationwide without FDA premarket clearance. Consumers should discontinue use and consult a healthcare provider.
GET TESTED INTERNATIONAL AB's Sperm Test (EAN 7340221710221, all lots) was distributed nationwide without required FDA premarket approval or clearance.
GET TESTED INTERNATIONAL AB is recalling the Sorbitol Intolerance Test distributed nationwide because it was sold without FDA premarket approval or clearance.
GET TESTED INTERNATIONAL AB is recalling 658 units of Parasite Test distributed nationwide without FDA premarket approval. The device lacks FDA validation for safety and effectiveness.
GET TESTED INTERNATIONAL AB is recalling Gut Microbiome Test Medium nationwide because the product was distributed without FDA premarket approval. Consumers should discontinue use.
GET TESTED INTERNATIONAL AB is recalling Peptic Ulcer Test (H. pylori) due to distribution without FDA premarket approval or clearance. Consumers should discontinue use and consult their healthcare provider.
GET TESTED INTERNATIONAL AB is recalling Gut Microbiome Test XL nationwide because the device was distributed without FDA premarket approval or clearance. Consumers should discontinue use and contact the manufacturer.
GET TESTED INTERNATIONAL AB is recalling the Food Intolerance Test Large (EAN: 616612785640) that was distributed nationwide without FDA premarket approval or clearance.
GET TESTED INTERNATIONAL AB is recalling its Serotonin Test distributed nationwide because the device was marketed without required FDA premarket approval or clearance. Stop using the product and contact the manufacturer for return instructions.
Food Sensitivity Test Medium manufactured by GET TESTED INTERNATIONAL AB has been recalled due to distribution without FDA premarket approval. Consumers should stop using and dispose of the product.
GET TESTED INTERNATIONAL AB is recalling the Female Fertility Test nationwide. The product was distributed without FDA premarket approval or clearance, which is required for medical devices.
GET TESTED INTERNATIONAL AB is recalling its Pet Allergy Test product (EAN: 616612785695) distributed in the U.S. without FDA premarket approval or clearance. Approximately 29 units distributed nationwide are subject to this Class II recall.
GET TESTED INTERNATIONAL AB is recalling its HPV Antigen Test (258 units, all lots) nationwide due to distribution without FDA premarket approval or clearance.
GET TESTED INTERNATIONAL AB is recalling Hair Mineral Analysis kits distributed nationwide without FDA premarket approval. Consumers should stop using this product.
GET TESTED INTERNATIONAL AB is recalling the NAD Profile Test (all lots) because it was distributed without FDA premarket approval or clearance.
GET TESTED INTERNATIONAL AB is recalling an Iron Deficiency Test (ferritin) that was distributed without FDA premarket approval. All lots should not be used.
GET TESTED INTERNATIONAL AB is recalling 754 units of its 2 in 1 Trichomonas / Gardnerella Test that was distributed nationwide without FDA premarket approval or clearance. The recall affects all lots.