Device recall
Z-0831-2011: Manual Wheelchairs with Transit System Option, Model: Quickie LXI (EILXI)…
FDA device recall · Class II · Sunrise Medical Inc
Key facts
| Recall number (Z-number) | Z-0831-2011 |
|---|---|
| Recall event | 51260 |
| Product | Manual Wheelchairs with Transit System Option, Model: Quickie LXI (EILXI), Product is manufactured and distributed by Sunrise Medical, Inc. Fresno, CA Intended to provide mobility to persons restricted to a sitting position and are unable to transfer from their wheelchairs when traveling in motor… |
| Product code | IOR |
| Recalling firm | Sunrise Medical Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 3, 2011 |
| 510(k) numbers | K973673 |
| 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