Device recall
Z-2466-2015: Zippie IRIS Wheelchair. model EIZ5A in combination with option code 188M02…
FDA device recall · Class II · Sunrise Medical (US) LLC
Key facts
| Recall number (Z-number) | Z-2466-2015 |
|---|---|
| Recall event | 71829 |
| Product | Zippie IRIS Wheelchair. model EIZ5A in combination with option code 188M02 - MONO Backrest system with Dynamic Backrest option. 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 | Dec 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