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
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.
Teleflex Medical is recalling specific lots of Sheridan EZ-ENDO tracheal tubes because the 15 mm connector may disconnect, potentially causing insufficient oxygenation.
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.
Allergan is recalling 4 million textured breast implants and tissue expanders worldwide due to an increased risk of anaplastic large cell lymphoma.
Zimmer Biomet is recalling 45 units of XP-CR Tibial Trays because the locking bar may not fully engage.
Teleflex Medical is recalling specific lots of Sheridan/HVT Novaplus tracheal tubes because the 15 mm Sheridan connector may disconnect from the tube, potentially causing insufficient oxygenation.
Teleflex Medical is recalling specific lots of Hudson RCI Sheridan/HVT tracheal tubes because the 15 mm Sheridan connector may disconnect from the tube, potentially causing insufficient oxygenation.
Teleflex Medical is recalling Hudson RCI Sheridan/CF tracheal tubes because specific lots of the 15 mm Sheridan connector may disconnect from the endotracheal tube, potentially causing insufficient oxygenation.
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.
OMNIlife science Inc. is recalling six ApeX acetabular liners that failed oxidation testing. The defect may cause higher wear rates, potentially leading to revision surgery.
Stryker Communications is recalling 52 Berchtold Chromophare Dual Monitor Carrier Arms or Dual Flat Panels because the mounts may have insufficient welds.