Device recall
Z-1020-2015: Quickie Q7 Adult Rigid Wheelchair Model EIR4.
FDA device recall · Class II · Sunrise Medical (US) LLC
Key facts
| Recall number (Z-number) | Z-1020-2015 |
|---|---|
| Recall event | 70141 |
| Product | Quickie Q7 Adult Rigid Wheelchair Model EIR4. |
| Product code | IOR |
| Recalling firm | Sunrise Medical (US) LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 10, 2015 |
| 510(k) numbers | K123975 |
| 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