Ratcheting Cannulated Driver Handle — Class II medical device recall Z-2339-2018
Terminated recall by Trilliant Surgical Ltd., reported 2018-07-11, distributed in AZ, CA, DE, FL, GA, IA, KS, MA…. Firm is voluntarily recalling cannulated driver handles (210-00-003 and 210-00-004) that may demonstrate a deg
| Recall number | Z-2339-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Trilliant Surgical Ltd., Houston, TX, United States |
| Recall initiated | 2018-03-27 |
| Classified | 2018-07-02 |
| Reported by FDA | 2018-07-11 |
| Terminated | 2020-06-04 |
| Distributed | AZ, CA, DE, FL, GA, IA, KS, MA, MN, MO, MT, NE, NJ, OH, OK, OR, PA, TX, UT, VA, WA, WI |
| Quantity | 90 |
| Reason classes | specification failure |
| Lot numbers | 603600 |
| Model numbers | 210-00-004 |
Product
Ratcheting Cannulated Driver Handle, Catalog #: 210-00-004, Rx Only, Non Sterile
Reason for recall
Firm is voluntarily recalling cannulated driver handles (210-00-003 and 210-00-004) that may demonstrate a degradation of function with the adapter collar sticking, and/or not retaining the mating adapter male shaft.
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-2339-2018. 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.