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 | Terminated |
| Reason | The manufacturer has discovered that potentially out-of-specification products may have left the factory. Non-conforming cannulation of the nails may result in reduced component strength and potentially premature nail breakage. |
| Product | Femoral Nail, LEFT T2 GTN 12x360 mm, Product Number 18501236S |
| Distribution | The products were distributed to the following US states: AL, Co, FL, KY, NC, TN, UT, and WA. |
| Initiated | 2018-04-27 |
| Classified | 2018-07-10 |
| Terminated | 2020-05-21 |
| Recall number | Z-2403-2018 |
| 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-2403-2018).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/80131/
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