Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Altius M-INI OCT Posterior Spinal Fixation System Recalled by Zimmer Biomet Spine, Inc Due to Zimmer Biomet is recalling the Altius M-INI OCT...
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 Biomet Spine, Inc directly.
Affected Products
Altius M-INI OCT Posterior Spinal Fixation System, Model Number 1200-9216 The AltiusTM OCT and AltiusTM M-INITM OCT Systems when intended to promote fusion of the cervical spine and occipitocervico-thoracic junction (Occiput-T3), these systems are indicated for: DDD (neck pain of discogenic origin with degeneration of the disc as confirmed by patient history and radiographic studies); spondylolisthesis; spinal stenosis; fracture/dislocation; atlantoaxial fracture with instability; occipitocervical dislocation; revision of previous cervical spine surgery; and tumors. The occipital bone screws are limited to occipital fixation only
Quantity: 141
Why Was This Recalled?
Zimmer Biomet is recalling the Altius M-INI OCT Posterior Spinal Fixation System because the driver is unable to mate with the screw head tulip.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Zimmer Biomet Spine, Inc
Zimmer Biomet 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