Device recall
Z-1149-2007: VS-1000 Senator Prosthetic Foot, (Categories 5 and 6, sizes 22-30 cm, both Left…
FDA device recall · Class II · Applied Composite Technology
Key facts
| Recall number (Z-number) | Z-1149-2007 |
|---|---|
| Recall event | 38289 |
| Product | VS-1000 Senator Prosthetic Foot, (Categories 5 and 6, sizes 22-30 cm, both Left and Right) Applied Composite Technology, Gunnison, UT. |
| Product code | ISH |
| Recalling firm | Applied Composite Technology |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 5, 2008 |
| FEI number | 3004737223 |
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