Bone fixation nail — Class II medical device recall Z-0772-2021
Terminated recall by Smith & Nephew, Inc., reported 2021-01-13, distributed nationwide. Manufacturing packaging error.
| Recall number | Z-0772-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Smith & Nephew, Inc., Memphis, TN, United States |
| Recall initiated | 2020-11-02 |
| Classified | 2021-01-06 |
| Reported by FDA | 2021-01-13 |
| Terminated | 2023-01-06 |
| Distributed | Nationwide (US) |
| Quantity | 41 units |
| Lot numbers | 20CM25278, 20DM01466 |
| Model numbers | 71675532, 71675535 |
Product
Bone fixation nail. TRIGEN INTERTAN - Product Usage: indicated for fractures of the femur including simple shaft fractures, comminuted shaft fractures, spiral shaft fractures, long oblique shaft fractures and segmental shaft fracture;
Reason for recall
Manufacturing packaging error.
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-0772-2021. 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.