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, LLC is recalling Locator Replacement Males dental implants because pouches may not have been sealed during packing.
Biomet 3i, LLC is recalling Preformance Post Dental implants because pouches may not have been sealed during packing.
Medtronic is recalling Valleylab Laparoscopic Flexible Argon Blade Electrodes because the packaging may be compromised, potentially breaching the sterile barrier.
MicroPort Orthopedics is recalling 14 units of Profemur Modular Necks due to a labeling error where item numbers were incorrectly assigned.
Biomet 3i, LLC is recalling specific Gingihue Post dental implants because pouches may not have been sealed during packing.
Medtronic is recalling 6,720 Valleylab Laparoscopic Straight Spatula Electrodes because the package may be compromised, potentially breaching the sterile barrier.
Biomet 3i is recalling Locator Light Retention Replacement Males because pouches may not have been sealed during packing.
Biomet 3i, LLC is recalling Prep-tite Cap Dental implants because pouches may not have been sealed during packing.
Biomet 3i is recalling Pick-Up Impression Coping dental implants because pouches may not have been sealed during packing.
Biomet 3i, LLC is recalling certain Pick-Up Coping dental implants because pouches may not have been sealed during packing.
Biomet 3i, LLC is recalling Preformance Temporary Cylinder Dental implants because pouches may not have been sealed during packing.
Biomet 3i, LLC is recalling Standard Abutment Transfer Coping Dental implants because pouches may not have been sealed during packing.
Biomet 3i is recalling 1,648,273 dental implant devices because pouches may not have been sealed during packing.
Biomet 3i is recalling Locator Abutment dental implants because pouches may not have been sealed during packing.
Teleflex Medical is recalling 45 units of the Weck EFx Classic Fascial Closure System because incorrect expiration dates were printed on the labels.
Biomet 3i is recalling Conical EP Pick-Up Coping dental implants because pouches may not have been sealed during packing.
Biomet 3i is recalling EP Twist Lock Coping Dental implants because pouches may not have been sealed during packing.
Biomet 3i, LLC is recalling certain Bellatek Encode Healing Abutment dental implants because pouches may not have been sealed during packing.
Ortho-Clinical Diagnostics is recalling VITROS TSH Reagent Packs because calibration curves frequently fall outside quality parameters, potentially delaying test results.
Biomet 3i is recalling certain Gingihue Post Dental implants because pouches may not have been sealed during packing.
Biomet 3i, LLC is recalling Locator Abutment dental implants because pouches may not have been sealed during packing.
Integra LifeSciences Corp. is recalling Universal Wire Fixation Bolts because the Slotted Post broke during use at the surgical site.
Invacare Corporation is recalling 1,011 Bariatric home care beds because the junction boxes may spark, posing a fire hazard in the presence of flammable materials.
BioMerieux is recalling NucliSENS easyMAG Magnetic Silica reagents due to customer complaints about amplification performance issues.
Richard-Allan Scientific Company is recalling 18 cases of 10% Neutral Buffered Formalin due to potential potassium hydroxide contamination that may affect immunohistochemistry test results.