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FDAJune 21, 2016device

MODIFIED LINEAR STANDARD/LATERAL NECK TRIALS WITH SPRING SIDES REF S-200635 and S-200636

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

The hazard

Reported failure of the instrument. The retaining ring component of a neck trial became disassembled from the body of the neck.

What to do

FDA enforcement status: Terminated

Brands named

encore medical lpencoreencore medical

Recall history

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

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MODIFIED LINEAR STANDARD/LATERAL NECK TRIALS WITH SPRING SIDES REF S-200635 and S-200636 — Recall Details · AllClear