Device recall
Z-3178-2018: Permobil powered wheelchairs, Model Numbers: (a) M300 PS, (b) C300 PS, (c) C350…
FDA device recall · Class II · Permobil, Ab
Key facts
| Recall number (Z-number) | Z-3178-2018 |
|---|---|
| Recall event | 80686 |
| Product | Permobil powered wheelchairs, Model Numbers: (a) M300 PS, (b) C300 PS, (c) C350 PS, (d) C500 PS, (e) C400 PS Product Usage: The devices identified are intended to provide outdoor and indoor mobility to persons limited to a seated position that can operate a powered wheelchair. |
| Product code | ITI |
| Recalling firm | Permobil, Ab |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 3, 2021 |
| 510(k) numbers | K041219, K071650, K123290, 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