Device recall
Z-1102-2020: WRIGHT EVOLVE Proline Head, Size: +2, OD: 22mm, REF 496H222
FDA device recall · Class II · Wright Medical Technology, Inc.
Key facts
| Recall number (Z-number) | Z-1102-2020 |
|---|---|
| Recall event | 84673 |
| Product | WRIGHT EVOLVE Proline Head, Size: +2, OD: 22mm, REF 496H222 |
| Product code | KWI |
| Recalling firm | Wright Medical Technology, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 23, 2021 |
| 510(k) numbers | K060731 |
| 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