FDA Device recall Z-1940-2025
Femoral Nail, RIGHT T2 GTN 8x300 mm
- FDA Device
- Class II
- ongoing
- Published 2025-06-18
On 2025-06-18 the FDA classified a Class II recall of Femoral Nail, RIGHT T2 GTN 8x300 mm by Stryker, citing 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 b….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1940-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-05-22 |
| Published | 2025-06-18 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Stryker |
| Distribution | US |
Product
Femoral Nail, RIGHT T2 GTN 8x300 mm. Catalog Number: 1851-0830S.
Reason
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.
Identifiers
| code_info | Catalog Number: 1851-0830S. GTIN: 04546540647184. Batch lot number: K09F17F |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1940-2025%22
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