FDAOctober 2, 2019device

Medicrea TLIF-B Holder, short intended for Intervertebral body fusion device Catalog: Number A24200010

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

The hazard

Inner draw rod, which threads into the cage may potentially be separated from the proximal knob of the inserter

What to do

FDA enforcement status: Terminated

Brands named

medicrea

Recall history

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

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