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 faceplates may incorrectly identify the T2 Basic Long Instrument Set as T2 Basic Short Instrument Set. |
| Product | Instrument Tray, Basic T2 Femur Long Catalog #: 1806-9900 Product Usage: Knee Arthroplasty |
| Quantity | 17 units |
| Distribution | In the countries of Canada and Korea |
| Initiated | 2019-01-21 |
| Classified | 2019-03-06 |
| Terminated | 2020-04-02 |
| Recall number | Z-0980-2019 |
| 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-0980-2019).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/82140/
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