Device recall
Z-0005-2018: Electric Wheelchairs: a) C300 CORPUS II b) C350 CORPUS II c) C400 CORPUS II d)…
FDA device recall · Class II · Permobil, Ab
Key facts
| Recall number (Z-number) | Z-0005-2018 |
|---|---|
| Recall event | 78079 |
| Product | Electric Wheelchairs: a) C300 CORPUS II b) C350 CORPUS II c) C400 CORPUS II d) C400 CORPUS II LR e) C500 CORPUS II f) C500 CORPUS II LR |
| Product code | ITI |
| Recalling firm | Permobil, Ab |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 4, 2021 |
| 510(k) numbers | K041219, K071650, K991658 |
| FEI number | 3002807844 |
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