Device recall
Z-0809-2013: Chenica Gunnell Rehab Series of Wheelchairs (GRSW); Mechanical Wheelchair, Sold…
FDA device recall · Class II · CHENICA INC.
Key facts
| Recall number (Z-number) | Z-0809-2013 |
|---|---|
| Recall event | 64110 |
| Product | Chenica Gunnell Rehab Series of Wheelchairs (GRSW); Mechanical Wheelchair, Sold as Rehab Tough and Tilt (TNT), Rehab Recline and Mobility (RAM), Rehab Kidster (Kidster). Provide mobility to individuals limited to a seating position. |
| Product code | IOR |
| Recalling firm | CHENICA INC. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 15, 2014 |
| 510(k) numbers | K111636 |
| FEI number | 3009255757 |
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