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.
September 18, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls XP-XP Tibial Tray - Interlok 69 mm Item # 195754
Hazard: The locking bar not fully engaging
September 18, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls XP-XP Tibial Tray - Interlok 71 mm Item # 195755
Hazard: The locking bar not fully engaging
September 18, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls XP-XP Tibial Tray - Interlok 73 mm Item # 195756
Hazard: The locking bar not fully engaging
September 18, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls XP-XP Tibial Tray - Interlok 75 mm Item # 195757
Hazard: The locking bar not fully engaging
September 18, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls XP-XP Tibial Tray - Interlok 79 mm Item # 195758
Hazard: The locking bar not fully engaging
September 18, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls XP-XP Tibial Tray - Interlok 83 mm Item # 195759
Hazard: The locking bar not fully engaging
September 18, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls XP-XP Tibial Tray - Interlok 87 mm Item # 195760
Hazard: The locking bar not fully engaging
September 18, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls XP-XP Tibial Tray - Interlok 91mm Item # 195761
Hazard: The locking bar not fully engaging
September 18, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls XP-CR Tibial Tray - Porous Plasma 91 mm Item # 195291
Hazard: The locking bar not fully engaging
September 18, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls XP-CR Tibial Tray - Interlok 91 mm Item # 195279
Hazard: The locking bar not fully engaging
September 18, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls XP-CR Tibial Tray - Interlok 87 mm Item # 195278
Hazard: The locking bar not fully engaging
September 18, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls XP-CR Tibial Tray - Interlok 83 mm Item # 195277
Hazard: The locking bar not fully engaging
September 18, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls XP-CR Tibial Tray - Interlok 79 mm Item # 195276
Hazard: The locking bar not fully engaging
September 18, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls XP-CR Tibial Tray - Interlok 75mm Item # 195275
Hazard: The locking bar not fully engaging
September 18, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls XP-CR Tibial Tray - Interlok 73mm Item # 195274
Hazard: The locking bar not fully engaging
September 18, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls XP-CR Tibial Tray - Interlok 71mm Item # 195273
Hazard: The locking bar not fully engaging
September 18, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls XP-CR Tibial Tray - Interlok 69mm Item # 195272
Hazard: The locking bar not fully engaging
September 18, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls XP-CR Tibial Tray - Interlok 67mm Item # 195271
Hazard: The locking bar not fully engaging
September 18, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls XP-CR Tibial Tray - Interlok 65mm Item # 195270
Hazard: The locking bar not fully engaging
September 18, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls XP-CR Tibial Tray - Interlok 63mm Item # 195269
Hazard: The locking bar not fully engaging
September 18, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls XP- CR Tibial Tray- Interlok 59mm Item # 195268
Hazard: The locking bar not fully engaging
August 21, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151815
Hazard: Cleaning processes potentially being ineffective
August 21, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151814
Hazard: Cleaning processes potentially being ineffective
August 21, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151813
Hazard: Cleaning processes potentially being ineffective
August 21, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151812
Hazard: Cleaning processes potentially being ineffective
August 21, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151811
Hazard: Cleaning processes potentially being ineffective
August 21, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151810
Hazard: Cleaning processes potentially being ineffective
July 24, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Ultra-Drive Irrigation Tubing Assembly, Reference Number 423834 - Product Usage: Item used with the UltraDrive System to
Hazard: The products do not have sufficient data to support the labeled shelf life of 10 years.
July 24, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Ultra-Drive Hose/Drape Assembly, Reference Number 423833 - Product Usage: Item used with the UltraDrive System to provid
Hazard: The products do not have sufficient data to support the labeled shelf life of 10 years.
July 24, 2019Medical DevicesFDA
Zimmer Biomet, Inc. recalls Comprehensive Reverse Shoulder Instrument Case Total (Outer Case Vault Only), Item Number 595510
Hazard: Lack of an adequate sterilization validation.