Device recall
Z-1532-2008: Quickie Groove Power Wheelchair with QC (non-expandable) electronics, Model…
FDA device recall · Class II · Sunrise Medical Inc
Key facts
| Recall number (Z-number) | Z-1532-2008 |
|---|---|
| Recall event | 46908 |
| Product | Quickie Groove Power Wheelchair with QC (non-expandable) electronics, Model number EIPW13. |
| Product code | ITI |
| Recalling firm | Sunrise Medical Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 16, 2009 |
| 510(k) numbers | K060531 |
| FEI number | 2937137 |
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