FDAJune 23, 2017device

Truliant Tibial Trial Handle. To assist the surgeon in the implantation of Truliant Knee system components according to a conventional technique for total knee replacement. Specifically, these instruments are reusable, surgically invasive, and intended for transient use.t Tibial Trial Handle

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

The hazard

The Truliant Tibial Trial Handle's pin may disassociate from the main body.

What to do

FDA enforcement status: Terminated

Brands named

exactech

UPCs

02029291000

Recall history

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

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