Zimmer Recalls
550 recalls on record · September 5, 1978 to July 1, 2026 · Medical Devices, Vehicles
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
May 29, 2019Medical DevicesFDA
Zimmer GmbH recalls Drill, cannulated, 4x120mm, AO, Item Number ST502015402
Hazard: An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
May 29, 2019Medical DevicesFDA
Zimmer GmbH recalls Drill, 2.7x125mm, AO , Item Number ST502015217
Hazard: An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
May 29, 2019Medical DevicesFDA
Zimmer GmbH recalls Drill for 3.5mm screw, 2.5x120mm, AO, Item Number ST502015216
Hazard: An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
May 29, 2019Medical DevicesFDA
Zimmer GmbH recalls Drill for 2.7mm screw, 2x120mm, AO, Item Number ST502015212
Hazard: An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
May 29, 2019Medical DevicesFDA
Zimmer GmbH recalls Drill for 2.7mm screw, 2x100mm, AO, Item Number ST502015208
Hazard: An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
May 29, 2019Medical DevicesFDA
Zimmer GmbH recalls Drill for 2.7mm screw, 23mm stop, 2x103mm, AO, Item Number ST502015207
Hazard: An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
May 29, 2019Medical DevicesFDA
Zimmer GmbH recalls Drill for 2.7mm screw, 20mm stop, 2x105mm, Stryker, Item Number ST502015206
Hazard: An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
May 29, 2019Medical DevicesFDA
Zimmer GmbH recalls V-TEK", Micro-countersink, AO , Item Number ST28.66.113
Hazard: An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
May 29, 2019Medical DevicesFDA
Zimmer GmbH recalls V-TEK", standard-countersink, cannulated, AO, Item Number ST28.66.111
Hazard: An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
May 29, 2019Medical DevicesFDA
Zimmer GmbH recalls V-TEK", Micro-countersink, AO, Item Number 28.66.113
Hazard: An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
May 29, 2019Medical DevicesFDA
Zimmer GmbH recalls V-TEK", micro-countersink, round shaft, Item Number 28.66.112
Hazard: An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
May 29, 2019Medical DevicesFDA
Zimmer GmbH recalls V-TEK", standard-countersink, cannulated, AO, Item Number 28.66.111
Hazard: An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
May 29, 2019Medical DevicesFDA
Zimmer GmbH recalls V-TEK", standard-countersink, cannulated, round shaft, Item Number 28.66.110
Hazard: An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
May 29, 2019Medical DevicesFDA
Zimmer GmbH recalls CBS high, countersink, cannulated, AO, Item Number 503004542
Hazard: An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
May 29, 2019Medical DevicesFDA
Zimmer GmbH recalls CBS micro, countersink, cannulated, AO, Item Number 503004541
Hazard: An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
May 29, 2019Medical DevicesFDA
Zimmer GmbH recalls CBS 4.0 countersink, cannulated, 30mm stop, AO, Item Number 503004353
Hazard: An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
May 29, 2019Medical DevicesFDA
Zimmer GmbH recalls CBS 4.0 countersink, cannulated, 15mm stop, AO, Item Number 503004352
Hazard: An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
May 29, 2019Medical DevicesFDA
Zimmer GmbH recalls CBS 4.5 countersink, cannulated, 18mm stop, round-shaft, Item Number 503004351
Hazard: An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
May 29, 2019Medical DevicesFDA
Zimmer GmbH recalls CBS high, countersink, cannulated, round-shaft, Item Number 503004342
Hazard: An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
May 29, 2019Medical DevicesFDA
Zimmer GmbH recalls CBS micro, countersink, cannulated, round-shaft, Item Number 503004341
Hazard: An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
May 29, 2019Medical DevicesFDA
Zimmer GmbH recalls MaxiCan 4.5 countersink, cannulated, AO, Item Number 503004177
Hazard: An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
May 29, 2019Medical DevicesFDA
Zimmer GmbH recalls CBS 7.5 tap, cannulated, AO, Item Number 503002041
Hazard: An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
May 29, 2019Medical DevicesFDA
Zimmer GmbH recalls Drill, contra-angle, 1.5x85mm, Item Number 502015706
Hazard: An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
May 29, 2019Medical DevicesFDA
Zimmer GmbH recalls Drill, 3.2x145mm, AO, Item Number 502015650
Hazard: An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
May 29, 2019Medical DevicesFDA
Zimmer GmbH recalls Drill, cannulated, 4x90mm, round shaft, Item Number 502015640
Hazard: An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
May 29, 2019Medical DevicesFDA
Zimmer GmbH recalls V-TEK", IVP step drill 2.5-3.9x124mm, 16mm stop, AO, Item Number 502015638
Hazard: An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
May 29, 2019Medical DevicesFDA
Zimmer GmbH recalls V-TEK", IVP step drill 2.5-3.9x124mm, 16mm stop, contra-angle, Item Number 502015637
Hazard: An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
May 29, 2019Medical DevicesFDA
Zimmer GmbH recalls V-TEK", IVP step drill 2-3.4x124mm, 16mm stop, AO, Item Number 502015636
Hazard: An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
May 29, 2019Medical DevicesFDA
Zimmer GmbH recalls Drill, cannulated, 3.5x90mm, round shaft, Item Number 502015635
Hazard: An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
May 29, 2019Medical DevicesFDA
Zimmer GmbH recalls V-TEK", IVP step drill 2-3.4x124mm, 16mm stop, contra-angle, Item Number 502015634
Hazard: An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.