FDA Device recall Z-2338-2018
Cannulated Driver Handle, Catalog #: 210-00-003, Rx Only, Non Sterile
- FDA Device
- Class II
- terminated
- Published 2018-07-11
On 2018-07-11 the FDA classified a Class II recall of Cannulated Driver Handle, Catalog #: 210-00-003, Rx Only, Non Sterile by Trilliant Surgical, citing 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 ret….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2338-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-03-27 |
| Published | 2018-07-11 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Trilliant Surgical |
| Distribution | AZ, CA, DE, FL, GA, IA, KS, MA, MN, MO, MT, NE, NJ, OH, OK, OR, PA, TX, UT, VA, WA, WI |
Product
Cannulated Driver Handle, Catalog #: 210-00-003, Rx Only, Non Sterile
Reason
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.
Identifiers
| code_info | Lot: 603599 |
|---|
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-2338-2018%22
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