Device recall
Z-0948-03: StayFuse PROX 03.3 MM sterile intramedullary bone screw distributed by Zimmer
FDA device recall · Class II · Pioneer Surgical Technology
Key facts
| Recall number (Z-number) | Z-0948-03 |
|---|---|
| Recall event | 26405 |
| Product | StayFuse PROX 03.3 MM sterile intramedullary bone screw distributed by Zimmer |
| Product code | HWC |
| Recalling firm | Pioneer Surgical Technology |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 12, 2003 |
| 510(k) numbers | K990804 |
| FEI number | 1000115331 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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