FDAMay 25, 2017device

Logic Fit Tibial Tamp Head

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

The hazard

The firm determined that the labeling (surgical technique) should be updated to clarify the proper technique and instrumentation to remove the tamp assembly from the bone, i.e., to include a caution statement about the potential for instrument breakage if the tamp handle/guide is misused by impacting in retro-grade.

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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