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
Instrumentation Laboratory is recalling 364 ROTEM ex-tem kits because they may produce prolonged clotting times. The recall affects specific lots distributed in the US and internationally.
Zimmer Biomet is recalling 454 units of XP-CR Tibial Trays because the locking bar may not fully engage.
Zimmer Biomet is recalling 50 units of the XP-XP Tibial Tray - Interlok 59 mm because the locking bar may not fully engage.
Zimmer Biomet is recalling Vanguard XP Tibial Trays because the locking bar may not fully engage. The recall covers units distributed in the US and internationally.
Zimmer Biomet is recalling 973 units of the XP-XP Tibial Tray because the locking bar may not fully engage.
Zimmer Biomet is recalling 1,282 units of the XP-XP Tibial Tray because the locking bar may not fully engage.
Zimmer Biomet is recalling 369 units of the XP-CR Tibial Tray - Interlok 75mm because the locking bar may not fully engage.
Zimmer Biomet is recalling 84 units of Vanguard XP Tibial Tray 73 mm because the locking bar may not fully engage.
Zimmer Biomet is recalling 45 units of XP-CR Tibial Trays because the locking bar may not fully engage.
Zimmer Biomet is recalling 1,221 units of the XP-XP Tibial Tray because the locking bar may not fully engage.
Zimmer Biomet is recalling 180 units of XP-CR Tibial Trays because the locking bar may not fully engage.
Zimmer Biomet is recalling 857 units of XP-XP Tibial Trays because the locking bar may not fully engage.
Zimmer Biomet is recalling 327 units of XP-CR Tibial Trays because the locking bar may not fully engage.
Zimmer Biomet is recalling 43 units of Vanguard XP Tibial Tray 65 mm because the locking bar may not fully engage.
Instrumentation Laboratory Co. is recalling 44 ROTEM ex-tem kits (Lot 42255801) because they may produce prolonged clotting times.
Zimmer Biomet is recalling 123 units of Vanguard XP Tibial Trays because the locking bar may not fully engage.
Zimmer Biomet is recalling 375 units of the XP-CR Tibial Tray - Interlok 65mm because the locking bar may not fully engage.
Zimmer Biomet is recalling 1,210 units of the XP-XP Tibial Tray because the locking bar may not fully engage.
Zimmer Biomet is recalling 319 units of XP-CR Tibial Trays because the locking bar may not fully engage.
Exactech, Inc. is recalling 22 Threaded Offset Cup Impactors because the threaded mechanism may be gritty and difficult to turn, potentially due to entrapped blast media.
Philips is recalling 5-Lead ECG sets because the connector thickness may prevent or impede I 2-Lead ECG measurements.
Smith & Nephew is recalling 12 units of Legion Hemi Step Tibial Wedges because they were inadvertently packaged with an incorrect screw component.
Philips North America, LLC is recalling two HeartStart MRx Monitor/Defibrillators because they may not have received applicable corrections from prior field actions.
Randox Laboratories is recalling calibration sera due to realigned targets for AST and ALT. The recall affects 307 kits distributed nationwide and in several foreign locations.
Medtronic is updating the Micra Pacemaker Instructions for Use and Implant Procedure Tip Card to include specific information on tether removal during implant.