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 the agency’s own highest classification or reported deaths or serious injuries, 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
Biomet 3i is recalling specific Gingihue dental implants because pouches may not have been sealed during packing.
Biomet 3i, LLC is recalling Locator Abutment Impression Coping dental implants because pouches may not have been sealed during packing.
Biomet 3i is recalling 1,648,273 dental implant cover screws because pouches may not have been sealed during packing.
Biomet 3i, LLC is recalling specific Gingihue Post dental implants because pouches may not have been sealed during packing.
Biomet 3i is recalling specific dental implant copings because pouches may not have been sealed during packing, potentially compromising sterility.
Biomet 3i is recalling IOL Transfer Impression Coping dental implants because pouches may not have been sealed during packing.
Biomet 3i, LLC is recalling 1,648,273 Titanium Square Uniscrew Dental implants because pouches may not have been sealed during packing.
Biomet 3i is recalling IOL Pick-Up Impression Coping dental implant devices because pouches may not have been sealed during packing.
Biomet 3i, LLC is recalling Conical EP Pick-Up Coping dental implants because pouches may not have been sealed during packing.
Biomet 3i is recalling IOL Abutment and Screw dental implants because pouches may not have been sealed during packing.
Biomet 3i is recalling Micromini Flat Implant Cover Screws because pouches may not have been sealed during packing.
Biomet 3i, LLC is recalling 1,648,273 Healing Abutment Dental Implants because pouches may not have been sealed during packing.
Bard Peripheral Vascular Inc is recalling 1,250 TruGuide Disposable Coaxial Biopsy Needles because some units may contain two trocar or two blunt tip stylets instead of one of each.
Biomet 3i, LLC is recalling dental implant cover screws because pouches may not have been sealed during packing.
Biomet 3i, LLC is recalling Pick-up Coping Dental implants because pouches may not have been sealed during packing.
Biomet 3i is recalling headless dental implant cover screws because pouches may not have been sealed during packing.
Biomet 3i is recalling 1.6 million dental implant abutments because some pouches may not have been sealed during packing.
Ab Sciex is recalling MultiQuant MD software for 3200MD mass spectrometers because it may display incorrect quantitative results when using the Sum Multiple Ions feature.
Mindray is recalling Passport Series Patient Monitor CO2 Modules due to a potential leakage issue with the Dryline II Water Trap.
Biomet 3i, LLC is recalling IOL Healing Cap dental implants because pouches may not have been sealed during packing.
Biomet 3i, LLC is recalling Standard Abutment Temporary Screws because pouches may not have been sealed during packing.
Biomet 3i is recalling Gold-Tite Hexed Retaining Screws because pouches may not have been sealed during packing.
Biomet 3i is recalling specific dental implant abutments because pouches may not have been sealed during packing.
Biomet 3i, LLC is recalling 1,648,273 dental implant cover screws because pouches may not have been sealed during packing.
Biomet 3i is recalling Locator Extended Range Males dental implants because pouches may not have been sealed during packing.