Stryker INBONE Tibial Tray — Class II medical device recall Z-0139-2023
Terminated recall by Wright Medical Technology, Inc., reported 2022-11-02, distributed nationwide. The tibial tray lock detail is oversized (larger than specification).
| Recall number | Z-0139-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Wright Medical Technology, Inc., Memphis, TN, United States |
| Recall initiated | 2022-09-30 |
| Classified | 2022-10-27 |
| Reported by FDA | 2022-11-02 |
| Terminated | 2026-08-21 |
| Distributed | Nationwide (US) |
| Quantity | 1 units |
| UPC / GTIN / UDI-DI | 00840420124142 |
| Lot numbers | 1726308 |
| Model numbers | 200252903 |
Product
Stryker INBONE Tibial Tray, Left Plasma Spray Ti6Al4V, CPti, Use w/ 16mm Stem Base, REF 200252903, Size 3
Reason for recall
The tibial tray lock detail is oversized (larger than specification).
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-0139-2023. 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.