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 GmbH is recalling V-TEK micro-countersinks because an investigation found they may be made from a different material than specified.
Zimmer GmbH is recalling V-TEK standard-countersink screws because they may have been manufactured from a different material than specified.
Zimmer GmbH is recalling CBS micro countersink cannulated round-shaft screws because they may be made from the wrong material.
Zimmer GmbH is recalling 2.7x125mm AO Drills because they may be made from a different material than specified.
Zimmer GmbH is recalling 15mm surgical drills that may have been manufactured from incorrect materials. The products were distributed to 41 US states.
Elekta Instrument AB is recalling Leksell GammaPlan 11.1 software because the margin tool overestimates treatment margins in certain areas.
Boston Scientific is recalling eight Auriga 30 laser systems worldwide because a mechanical cooling issue may cause faster-than-normal power degradation and low power errors.
Zimmer GmbH is recalling specific cannulated drills because they may have been manufactured from a material different from the defined specifications.
Zimmer GmbH is recalling specific cannulated drills because they may have been manufactured from a material different from the specifications.
Stryker is recalling 3,176 EDS Light Suspension components for the Visum LED Surgical Lighting System due to a potential assembly defect in the joint.
Zimmer GmbH is recalling 26mm orthopedic drills that may have been manufactured from a different material than specified.
Zimmer GmbH is recalling MaxiCan 4.5 countersinks because they may be made from a different material than specified. The products were distributed to 40 US states.
Zimmer GmbH is recalling CBS 4.0 countersinks because they may have been manufactured from a material different from the defined specifications.
Zimmer GmbH is recalling V-TEK IVP step drills because an investigation found they may be made from a different material than specified.
Zimmer GmbH is recalling contra-angle drills that may have been manufactured from a different material than specified.
Zimmer GmbH is recalling 2.7mm orthopedic drills because they may be made from a different material than specified. The products were distributed to 40 US states.
Zimmer GmbH is recalling V-TEK standard-countersink, cannulated, AO screws because they may have been manufactured from a material different from the defined specifications.
Boston Scientific is recalling 27 Auriga XL 4007 laser systems worldwide due to a mechanical cooling issue that may cause the device to stop emitting laser pulses during surgery.
Zimmer GmbH is recalling Stryker orthopedic drills because they may have been manufactured from a different material than specified.
Zimmer GmbH is recalling specific cannulated drills because they may have been manufactured from a material different from the defined specifications.
Boston Scientific is recalling 18 Auriga 30 laser systems worldwide because a mechanical cooling issue may cause faster-than-normal power degradation and low power errors.
Zimmer GmbH is recalling specific cannulated drills because they may have been manufactured from a material different from the defined specifications.
Zimmer GmbH is recalling Stryker 15mm drills because an investigation found they may have been manufactured from a different material than specified.
Zimmer GmbH is recalling specific 3.5mm orthopedic drills because they may have been manufactured from a different material than specified.
Zimmer GmbH is recalling specific cannulated drills because they may have been manufactured from a different material than specified.