Femoral Nail — Class II medical device recall Z-1939-2025
Ongoing recall by Stryker GmbH, reported 2025-06-18, distributed nationwide. Investigation determined that one lot of the T2 Greater Trochanter Nail (GTN) was labeled as left version but
| Recall number | Z-1939-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker GmbH, Selzach, Switzerland |
| Recall initiated | 2025-05-22 |
| Classified | 2025-06-10 |
| Reported by FDA | 2025-06-18 |
| Distributed | Nationwide (US) |
| Countries outside the US | BE, JP, NL |
| Quantity | 1 |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 04546540646293 |
| Lot numbers | K09F126 |
| Model numbers | 1850-0830S |
Product
Femoral Nail, LEFT T2 GTN 8x300 mm. Catalog Number: 1850-0830S.
Reason for recall
Investigation determined that one lot of the T2 Greater Trochanter Nail (GTN) was labeled as left version but contained a right nail and another lot was labeled as right version but contained a left nail.
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-1939-2025. 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.