Nextra CH Cannulated Hammertoe Mini Instrument Kit-indicated for… — Class II medical device recall Z-0739-2022
Terminated recall by Nextremity Solutions, reported 2022-03-16, distributed nationwide. During insertion of the middle phalanx implant into bone, the driver may deform the implant locking mechanism
| Recall number | Z-0739-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Nextremity Solutions, Warsaw, IN, United States |
| Recall initiated | 2022-01-13 |
| Classified | 2022-03-09 |
| Reported by FDA | 2022-03-16 |
| Terminated | 2024-05-24 |
| Distributed | Nationwide (US) |
| Quantity | 23 units |
| UPC / GTIN / UDI-DI | 00817701026389 |
| Lot numbers | 1578401 |
Product
Nextra CH Cannulated Hammertoe Mini Instrument Kit-indicated for small bone reconstruction limited to inter-digital repair and fusion of the lesser toes SKU: CH-MINI-KT
Reason for recall
During insertion of the middle phalanx implant into bone, the driver may deform the implant locking mechanism and result in inadequate mating force between the middle and proximal phalanx implants, resulting in surgical delay, in-situ removal of the implant, use of alternative surgical approach, disassembly of the implants post-operatively, and revision
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-0739-2022. 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.