Device recall
Z-1651-2008: Ambulift Classic, battery powered patient lift. The Ambulift is used to move and…
FDA device recall · Class II · Arjo, Inc.
Key facts
| Recall number (Z-number) | Z-1651-2008 |
|---|---|
| Recall event | 47885 |
| Product | Ambulift Classic, battery powered patient lift. The Ambulift is used to move and lift patients from their beds, transport them to the bathroom, and lift them in and out of the bath. Model KDB1890-04US - Ambulift Classic with chair and leg rest. Model KDB1895-04US - Ambulift Classic with chair, leg… |
| Product code | FSA |
| Recalling firm | Arjo, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 3, 2010 |
| FEI number | 1419652 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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