Device recall
Z-2290-2016: Quickie Q7 wheelchair. Model EIR4 Physical Medicine. The Quickie Q7 series of…
FDA device recall · Class II · Sunrise Medical (US) LLC
Key facts
| Recall number (Z-number) | Z-2290-2016 |
|---|---|
| Recall event | 74596 |
| Product | Quickie Q7 wheelchair. Model EIR4 Physical Medicine. The Quickie Q7 series of wheelchair's intended use is to provide mobility to persons limited to a sitting position. |
| Product code | IOR |
| Recalling firm | Sunrise Medical (US) LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 11, 2017 |
| 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