Device recall
Z-1650-2008: Ambulift, standard basic model manually powered patient lift. The Ambulift is…
FDA device recall · Class II · Arjo, Inc.
Key facts
| Recall number (Z-number) | Z-1650-2008 |
|---|---|
| Recall event | 47885 |
| Product | Ambulift, standard basic model manually 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 AB1102 - Standard basic model Ambulift with chair and leg rest. Model AB1552 - Standard basic… |
| 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