Device recall
Z-1697-2011: Liko Capella 201 Lift, Liko, Sweeden. The Sabina and Capella sit-to-stand lifts…
FDA device recall · Class II · Hill-Rom, Inc.
Key facts
| Recall number (Z-number) | Z-1697-2011 |
|---|---|
| Recall event | 57734 |
| Product | Liko Capella 201 Lift, Liko, Sweeden. The Sabina and Capella sit-to-stand lifts are especially designed for people who have difficulty in standing on their own. The lifts are intended to be used with patients who are able to bear weight on their legs and actively participate in the standing… |
| Product code | FSA |
| Recalling firm | Hill-Rom, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 19, 2014 |
| FEI number | 1824206 |
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