Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Virage OCT Spinal Fixation System. Intended to promote fusion of Recalled by Zimmer Spine, Inc. Due to Zimmer Biomet Spine is initiating a Medical Device...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Zimmer Spine, Inc. directly.
Affected Products
Virage OCT Spinal Fixation System. Intended to promote fusion of the Occipital-Cervical-Thoracic spine (Occiput-T3).
Quantity: 15,753
Why Was This Recalled?
Zimmer Biomet Spine is initiating a Medical Device Correction regarding the Virage OCT Spinal Fixation System by providing additional guidance in the Virage OCT Surgical Technique Manual.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Zimmer Spine, Inc.
Zimmer Spine, Inc. has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report