Device recall
Z-0468-2007: Re-Flex VSP and Low Profile Re-Flex VSP external prosthetic foot modules with…
FDA device recall · Class II · Ossur
Key facts
| Recall number (Z-number) | Z-0468-2007 |
|---|---|
| Recall event | 36883 |
| Product | Re-Flex VSP and Low Profile Re-Flex VSP external prosthetic foot modules with integrated shock absorber, Model numbers RFXS0002, RFXS0003, RFLS0006 and RFL50007 |
| Product code | ISH |
| Recalling firm | Ossur |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 28, 2008 |
| FEI number | 3003764610 |
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