Zimmer Biomet Spine recalls

Zimmer Biomet Spine appears in 8 official U.S. recall notices indexed by RecallRadar, most recently on 2024-01-10.

Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.

• Vitality Polyaxial Screw, 7.5mmx 50mm, REF: 07.02000.118, used with Vitality and Vital Spinal Fixation System
  FDA Device · Class II · 2024-01-10 · Zimmer Biomet Spine
• Vitality¿ Spinal Fixation System.Spinal Intervertebral Body, Appliance, Fixation (non-sterile)
  FDA Device · Class II · 2019-03-06 · Zimmer Biomet Spine
• Vitality¿ Spinal Fixation System
  FDA Device · Class II · 2019-03-06 · Zimmer Biomet Spine
• Vitality¿ Spinal Fixation System
  FDA Device · Class II · 2019-03-06 · Zimmer Biomet Spine
• Vitality Spinal Fixation System, Vitality T27 Final Drivers and Vitality Torque Limiting Handle  90 in-lbs Model Number(s): 07.02066.001,…
  FDA Device · Class II · 2017-06-14 · Zimmer Biomet Spine
• Altius M-INI OCT Posterior Spinal Fixation System, Model Number 1200-9216 The AltiusTM OCT and AltiusTM M-INITM OCT Systems when intended t…
  FDA Device · Class II · 2017-04-05 · Zimmer Biomet Spine
• Zyston¿ Transform Instrument Case
  FDA Device · Class II · 2016-08-17 · Zimmer Biomet Spine
• Zyston¿ Transform Implant Kit
  FDA Device · Class II · 2016-08-17 · Zimmer Biomet Spine