Device recall
Z-1825-2014: RUSH81 Prosthetic Foot Product Usage: Prosthetic foot for human use
FDA device recall · Class II · Ability Dynamics LLC
Key facts
| Recall number (Z-number) | Z-1825-2014 |
|---|---|
| Recall event | 68535 |
| Product | RUSH81 Prosthetic Foot Product Usage: Prosthetic foot for human use |
| Product code | ISW |
| Recalling firm | Ability Dynamics LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 22, 2014 |
| FEI number | 3008584163 |
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