Device recall
Z-0834-03: Permobil Chairman 2K powered wheelchair
FDA device recall · Class II · Permobile Inc.
Key facts
| Recall number (Z-number) | Z-0834-03 |
|---|---|
| Recall event | 25733 |
| Product | Permobil Chairman 2K powered wheelchair |
| Product code | ITI |
| Recalling firm | Permobile Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 25, 2008 |
| 510(k) numbers | K991658 |
| FEI number | 1221084 |
At a glance
- 1–9 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