Truliant Tibial Trial Handle — Class II medical device recall Z-3018-2017
Terminated recall by Exactech, Inc., reported 2017-08-23, distributed in AZ, CA, CO, FL, IL, NV, NY, OH…. The Truliant Tibial Trial Handle's pin may disassociate from the main body.
| Recall number | Z-3018-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Exactech, Inc., Gainesville, FL, United States |
| Recall initiated | 2017-06-23 |
| Classified | 2017-08-11 |
| Reported by FDA | 2017-08-23 |
| Terminated | 2020-11-30 |
| Distributed | AZ, CA, CO, FL, IL, NV, NY, OH, OK, SC, TN |
| Quantity | 68 devices |
| Lot numbers | 83843-001 |
| Model numbers | 02-029-29-1000 |
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 for recall
The Truliant Tibial Trial Handle's pin may disassociate from the main body.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-3018-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.