FDAJune 9, 2014device

Total Toe Instrument Kit, Labeled in part: "Instrument Set, 15mm Toe, Dorsal Flange Combi" Part Number: 9000-3002 The component in question is the hex driver (part number 2009-4001).

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

The hazard

An oversight in the implementation of the design change record resulted in outdated components being shipped to customers. The component did not pass a half-cycle sterilization.

What to do

FDA enforcement status: Terminated

Brands named

arthrosurface

Recall history

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

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