Device recall
Z-2376-2016: Volker 2080, 2082, S 280 and S 282 series beds with lateral release button. A/C…
FDA device recall · Class II · Hill-Rom, Inc.
Key facts
| Recall number (Z-number) | Z-2376-2016 |
|---|---|
| Recall event | 74615 |
| Product | Volker 2080, 2082, S 280 and S 282 series beds with lateral release button. A/C Powered Adjustable Hospital Bed Product Usage: Volker model 2080/3010/3080 nursing beds are intended for the care of residents in rooms in nursing homes, in residential homes for the elderly and in suitable rooms in… |
| Product code | FNL |
| Recalling firm | Hill-Rom, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 15, 2017 |
| 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