FDANovember 22, 2016device

Ceres-C Standalone Cervical Interbody The product is a stand-alone anterior cervical interbody fusion device indicated for use in skeletally mature patients with degenerative disc disease (DDD) with accompanying radicular symptoms at the one level from C2-T1.

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

The hazard

Absent tantalum market pin.

What to do

FDA enforcement status: Terminated

Brands named

amendia

Recall history

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

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