FDA Device recall Z-3018-2017
Truliant Tibial Trial Handle
- FDA Device
- Class II
- terminated
- Published 2017-08-23
On 2017-08-23 the FDA classified a Class II recall of Truliant Tibial Trial Handle by Exactech, citing the Truliant Tibial Trial Handle's pin may disassociate from the main body.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-3018-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-06-23 |
| Published | 2017-08-23 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Exactech |
| Distribution | AZ, CA, CO, FL, IL, NV, NY, OH, OK, SC, TN |
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
Reason
The Truliant Tibial Trial Handle's pin may disassociate from the main body.
Identifiers
| code_info | Catalog Number 02-029-29-1000, Lot Number 83843-001. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3018-2017%22
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