FDA Device recall Z-1035-2022
K-Wire, 1.35 mm x 170 mm
- FDA Device
- Class II
- terminated
- Published 2022-05-11
On 2022-05-11 the FDA classified a Class II recall of K-Wire, 1.35 mm x 170 mm by Arthrex, citing products do not meet length and diameter specifications.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1035-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2022-03-25 |
| Published | 2022-05-11 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Arthrex |
| Distribution | US |
Product
K-Wire, 1.35 mm x 170 mm
Reason
Products do not meet length and diameter specifications.
Identifiers
| code_info | Part Number: AR-8610K-43, Batch 1298116640 UDI: 00888867197084 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1035-2022%22
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