FDA Device recall Z-2324-2016
V-TEK TWIST D 40X90MM 30MM Cann 12MM Rnd
- FDA Device
- Class II
- terminated
- Published 2016-08-10
On 2016-08-10 the FDA classified a Class II recall of V-TEK TWIST D 40X90MM 30MM Cann 12MM Rnd by Zimmer, citing zimmer Biomet initiated a voluntary recall of the Twist Drill & V-Tek Twist Drill due to to a potential tolerance stack up identified between the twist drill and the mating Kirsch….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2324-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-06-27 |
| Published | 2016-08-10 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Zimmer |
| Distribution | CO, IL |
Product
V-TEK TWIST D 40X90MM 30MM Cann 12MM Rnd; The twist drill is used to drill holes into bones/tissues for foot, ankle and hand implant systems.
Reason
Zimmer Biomet initiated a voluntary recall of the Twist Drill & V-Tek Twist Drill due to to a potential tolerance stack up identified between the twist drill and the mating Kirschner Wire (K-Wire) component.
Identifiers
| code_info | Part No.: 502015640; Lot Numbers:27374, 104547/188A9 |
|---|
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-2324-2016%22
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