FDAJuly 13, 2018device

Tibial Alignment Guide, REF 351-10-00 Vantage Fixed Ankle system components for ankle replacements.

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

The hazard

Exactech is recalling the Tibial Alignment Guide because the Global Trade Item Number (GTIN) on the device is incorrect. The GTIN on the device reads 10885862525629, when it should read 10885862525628.

What to do

FDA enforcement status: Terminated

Brands named

exactech

Recall history

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

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