Device recall
Z-0139-2023: Stryker INBONE Tibial Tray, Left Plasma Spray Ti6Al4V, CPti, Use w/ 16mm Stem…
FDA device recall · Class II · Wright Medical Technology, Inc.
Key facts
| Recall number (Z-number) | Z-0139-2023 |
|---|---|
| Recall event | 90965 |
| Product | Stryker INBONE Tibial Tray, Left Plasma Spray Ti6Al4V, CPti, Use w/ 16mm Stem Base, REF 200252903, Size 3 |
| Product code | HSN |
| Recalling firm | Wright Medical Technology, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 21, 2026 |
| 510(k) numbers | K051023 |
| FEI number | 3010667733 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database