K-Wire — Class II medical device recall Z-1035-2022
Terminated recall by Arthrex, Inc., reported 2022-05-11, distributed nationwide. Products do not meet length and diameter specifications.
| Recall number | Z-1035-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Arthrex, Inc., Naples, FL, United States |
| Recall initiated | 2022-03-25 |
| Classified | 2022-05-05 |
| Reported by FDA | 2022-05-11 |
| Terminated | 2026-05-15 |
| Distributed | Nationwide (US) |
| Countries outside the US | BE, DE, EG, ES, FI, FR, IT, NL, NO, PL, PT |
| Quantity | 300 units |
| UPC / GTIN / UDI-DI | 00888867197084 |
| Lot numbers | 1298116640 |
| Model numbers | AR-8610K-43 |
Product
K-Wire, 1.35 mm x 170 mm
Reason for recall
Products do not meet length and diameter specifications.
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-1035-2022. 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.