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, LH 130 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, LH 130 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, LH 130 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, LH 130 DEG 9MM 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 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, LH 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, LH 130 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, LH 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, LH 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, LH 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, LH 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, LH 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, LH 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, LH 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, LH 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, LH 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, LH 125 DEG 9MM 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, LH 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, LH 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, LH 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, LH 125 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, LH 125 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, 130 DEG 9MM X 180MM
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, 130 DEG 11MM X 180MM
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, 125 DEG 9MM X 180MM
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, 125 DEG 11MM X 180MM
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.
January 24, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Persona Partial Knee System, Size 8, Finishing Guide
Hazard: Finishing guide does not adequately account for shape differences present in Size 8 of Persona Partial Knee System, potentially resulting in additional surgery time or sensation of tightness during knee flexion.
January 10, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls PPS RingLoc+ Acetabular Shell, RNGLC+ LTD HOLE SHELL SZ62 The Porous Plasma Spray (PPS) Ringloc¿+ Acetabular System
Hazard: Device was distributed with the etching missing from the product.
January 10, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls RED SEXP DSTL FEM 19CM LT ASSY, model # CP111828
Hazard: Possibility that the patient label inside the product box was incorrectly labeled. The outer box label and actual product are correctly identified but the internal patient label could be incorrect.
January 10, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls RED SEXP DSTL FEM 19CM RT ASSY, model # CP111817
Hazard: Possibility that the patient label inside the product box was incorrectly labeled. The outer box label and actual product are correctly identified but the internal patient label could be incorrect.