Device recall
Z-1083-04: VSP Shock Module (as part of a prosthetic foot).
FDA device recall · Class II · Ossur North America Inc
Key facts
| Recall number (Z-number) | Z-1083-04 |
|---|---|
| Recall event | 29386 |
| Product | VSP Shock Module (as part of a prosthetic foot). |
| Product code | ISH |
| Recalling firm | Ossur North America Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 17, 2005 |
| FEI number | 1000519909 |
At a glance
- None 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