Device recall
Z-0863-2012: Gas cylinders used in Gunnell manual wheelchairs with dynamic recline feature…
FDA device recall · Class II · Gunnell, Inc.
Key facts
| Recall number (Z-number) | Z-0863-2012 |
|---|---|
| Recall event | 60180 |
| Product | Gas cylinders used in Gunnell manual wheelchairs with dynamic recline feature, including: Rehab Kidster( Kidster). Product Usage: The purpose of these wheelchairs is to provide mobility to individuals limited to a seating position. They may also be used as attendant propelled transport devices in a… |
| Product code | IOR |
| Recalling firm | Gunnell, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 29, 2013 |
| FEI number | 3009255757 |
At a glance
- None 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