FDAMarch 16, 2017device

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 origi...

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

The hazard

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.

What to do

FDA enforcement status: Terminated

Brands named

zimmer biomet spinezimmerzimmer biomet

Recall history

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

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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 origi... — Recall Details · AllClear