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FDAFebruary 3, 2016device

Virage OCT Spinal Fixation System. Intended to promote fusion of the Occipital-Cervical-Thoracic spine (Occiput-T3).

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Terminated

Brands named

zimmer spinezimmer

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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