Reported Aug 23, 2017 · Terminated
Truliant Tibial Trial Handle. To assist the surgeon in the implantation of Truliant Knee system components according to…
Exactech, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Exactech, Inc. · 2320 NW 66th Ct · Gainesville, FL · 32653-1630
Is this the product you have?
- 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
- Lot codes and dates
Catalog Number 02-029-29-1000Lot Number 83843-001
- Amount recalled
- 68 devices
Where it was sold
Why it was recalled
The Truliant Tibial Trial Handle's pin may disassociate from the main body.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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