FDAJuly 18, 2018device

P.F.C. SIGMA Revision Knee System Distal Augment, Model Number 960830

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

The hazard

This unit may be missing the screw/collet Assembly

What to do

FDA enforcement status: Terminated

Brands named

depuy orthopaedicsdepuy

UPCs

10603295234135

Recall history

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

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