Device recall
Z-2741-2011: JASMINE Full Body (Patient) Lift, electrically-powered device with a 500 lb…
FDA device recall · Class II · Invacare Corporation
Key facts
| Recall number (Z-number) | Z-2741-2011 |
|---|---|
| Recall event | 58655 |
| Product | JASMINE Full Body (Patient) Lift, electrically-powered device with a 500 lb. weight capacity. The recalled product is an electrically-powered device either fixed or mobile, used to lift and transport patients in the horizontal or other required position from one place to another. |
| Product code | FNG |
| Recalling firm | Invacare Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 28, 2013 |
| FEI number | 1525712 |
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