Device recall
Z-0853-2022: EasyFuse Dynamic Compression System Instrument Pack
FDA device recall · Class II · Wright Medical Technology, Inc.
Key facts
| Recall number (Z-number) | Z-0853-2022 |
|---|---|
| Recall event | 89739 |
| Product | EasyFuse Dynamic Compression System Instrument Pack |
| Product code | JDR |
| Recalling firm | Wright Medical Technology, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 1, 2026 |
| 510(k) numbers | K203832 |
| 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