Brand

Zimmer Biomet Spine Inc. Recalls

4 recalls on record. Search official CPSC, FDA, and USDA datasets for every recall issued for Zimmer Biomet Spine Inc..

4Total Recalls
0Critical
49,292Units Affected
Jul 30, 2018Most Recent
All Recalls

Every Zimmer Biomet Spine Inc. Recall

Sorted by most recent. Click any recall for full details.

4 recalls
High RiskFDA
Zimmer Biomet Spine Inc.
Vitality¿ Spinal Fixation System.Spinal Intervertebral Body, Appliance, Fixation (non-sterile). Pedicle screw fixation is indicated for ...
Medical Devices·16,429 affected·Jul 30, 2018
High RiskFDA
Zimmer Biomet Spine Inc.
Vitality¿ Spinal Fixation System. Thoracolumbosacral pedicle screw system (non-sterile). Pedicle screw fixation is indicated for skeletal...
Medical Devices·16,429 affected·Jul 30, 2018
High RiskFDA
Zimmer Biomet Spine Inc.
Vitality¿ Spinal Fixation System. Spinal Interlaminal, Appliance, Fixation, (non-sterile). Pedicle screw fixation is indicated for skelet...
Medical Devices·16,429 affected·Jul 30, 2018
High RiskFDA
Zimmer Biomet Spine, Inc
Zyston¿ Transform Instrument Case. Model Number PCR8200-2101. Device labeled sterile.
Medical Devices·5 affected·Jun 30, 2016