FDA Device recall Z-0139-2023
Stryker INBONE Tibial Tray, Left Plasma Spray Ti6Al4V, CPti, Use w/ 16mm Stem Base, REF 200252903, Size 3
- FDA Device
- Class II
- terminated
- Published 2022-11-02
On 2022-11-02 the FDA classified a Class II recall of Stryker INBONE Tibial Tray, Left Plasma Spray Ti6Al4V, CPti, Use w/ 16mm Stem Base, REF 200252903, Size 3 by Wright Medical Technology, citing the tibial tray lock detail is oversized (larger than specification).
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0139-2023 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2022-09-30 |
| Published | 2022-11-02 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Wright Medical Technology |
| Distribution | US |
Product
Stryker INBONE Tibial Tray, Left Plasma Spray Ti6Al4V, CPti, Use w/ 16mm Stem Base, REF 200252903, Size 3
Reason
The tibial tray lock detail is oversized (larger than specification).
Identifiers
| code_info | GTIN 00840420124142, Lot Code: 1726308 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0139-2023%22
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