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FDAJanuary 10, 2017device

1.5mm System, Cranio-maxillofacial Bone Screws 1.5 x 4mm HT SD X-DR Screw, Bone Screw

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

The hazard

The identification of the devices was non-conforming with off-centered slots and the no-go gage starting in the pilot hole.

What to do

FDA enforcement status: Terminated

Brands named

zimmer biometzimmer

Recall history

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

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