FDAMarch 20, 2018device

Epic Extremity Plate System, Midfoot/Flatfoot Insert, Part 2111-0005 with Extended Butterfly Plate (2000-5002)

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

The hazard

There is an error in the caddy artwork that misidentifies a specific plate and screw.

What to do

FDA enforcement status: Terminated

Brands named

epic extremityepic

Recall history

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

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