Zimmer Biomet Recalls
875 recalls on record · January 20, 2016 to December 30, 2020 · Medical Devices
Recalls by year
16
17
18
19
20
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
February 7, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail, RH 130 DEG 13MM X 460MM
Hazard: During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.
February 7, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail, RH 130 DEG 13MM X 440MM
Hazard: During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.
February 7, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail, RH 130 DEG 13MM X 300MM
Hazard: During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.
February 7, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail, RH 130 DEG 13MM X 280MM
Hazard: During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.
February 7, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail, RH 130 DEG 11MM X 440MM
Hazard: During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.
February 7, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail, RH 130 DEG 11MM X 420MM
Hazard: During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.
February 7, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail, RH 130 DEG 11MM X 400MM
Hazard: During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.
February 7, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail, RH 130 DEG 11MM X 380MM
Hazard: During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.
February 7, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail, RH 130 DEG 11MM X 360MM
Hazard: During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.
February 7, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail, RH 130 DEG 11MM X 340MM
Hazard: During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.
February 7, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail, RH 130 DEG 11MM X 320MM
Hazard: During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.
February 7, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail, RH 130 DEG 11MM X 300MM
Hazard: During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.
February 7, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail, RH 130 DEG 11MM X 280MM
Hazard: During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.
February 7, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail, RH 130 DEG 11MM X 260MM
Hazard: During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.
February 7, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail, RH 125 DEG 9MM X 460MM
Hazard: During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.
February 7, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail, RH 125 DEG 9MM X 440MM
Hazard: During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.
February 7, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail, RH 125 DEG 9MM X 420MM
Hazard: During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.
February 7, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail, RH 125 DEG 9MM X 400MM
Hazard: During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.
February 7, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail, RH 125 DEG 9MM X 360MM
Hazard: During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.
February 7, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail, RH 125 DEG 9MM X 340MM
Hazard: During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.
February 7, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail, RH 125 DEG 9MM X 320MM
Hazard: During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.
February 7, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail, RH 125 DEG 9MM X 260MM
Hazard: During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.
February 7, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail, RH 125 DEG 13MM X 320MM
Hazard: During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.
February 7, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail, RH 125 DEG 13MM X 260MM
Hazard: During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.
February 7, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail, RH 125 DEG 11MM X 460MM
Hazard: During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.
February 7, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail, RH 125 DEG 11MM X 440MM
Hazard: During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.
February 7, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail, RH 125 DEG 11MM X 380MM
Hazard: During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.
February 7, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail, RH 125 DEG 11MM X 300MM
Hazard: During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.
February 7, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail, LH 130 DEG 9MM X 440MM
Hazard: During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.
February 7, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail, LH 130 DEG 9MM X 420MM
Hazard: During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.