FDAApril 27, 2018device

Femoral Nail, LEFT T2 GTN ¿12x360 mm, Product Number 18501236S

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

The hazard

The manufacturer has discovered that potentially out-of-specification products may have left the factory. Non-conforming cannulation of the nails may result in reduced component strength and potentially premature nail breakage.

What to do

FDA enforcement status: Terminated

Brands named

stryker

UPCs

04546540646842

Recall history

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

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