Class II — Stryker GmbH
| Recalling firm | STRYKER CORP. |
|---|---|
| Registered facility | View this company's 61 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Ongoing |
| 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. |
| Product | Femoral Nail, RIGHT T2 GTN 8x300 mm. Catalog Number: 1851-0830S. |
| Quantity | 2 |
| Distribution | Worldwide - US Nationwide distribution in the states of California and Missouri. The countries of Belgium, Japan, Netherlands. |
| Initiated | 2025-05-22 |
| Classified | 2025-06-10 |
| Recall number | Z-1940-2025 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Stryker GmbH (Z-1940-2025).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/96924/
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