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Exactech, Inc. recalls Truliant Tibial Trial Handle. To assist the surgeon in the implantation of Truliant Knee system components according
Recalled August 23, 2017 · FDA recall Z-3018-2017 · Exactech
Hazard
The Truliant Tibial Trial Handle's pin may disassociate from the main body. · FDA Class II
Units
68 devices
Sold at
US Distribution to the states of : AZ, CA, CO, FL, IL, OH, OK, NV, NY, SC and TN.
Description
The Truliant Tibial Trial Handle's pin may disassociate from the main body.
Product
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
Manufacturer(s)
Exactech, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →