Device recall
Z-0240-2008: Hill-Rom VersaCare Hospital Bed System; Models P3200 and P3201, Hill-Rom…
FDA device recall · Class II · Hill-Rom, Inc.
Key facts
| Recall number (Z-number) | Z-0240-2008 |
|---|---|
| Recall event | 38256 |
| Product | Hill-Rom VersaCare Hospital Bed System; Models P3200 and P3201, Hill-Rom, Batesville, IN 47006 |
| Product code | FIN |
| Recalling firm | Hill-Rom, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 22, 2010 |
| FEI number | 1824206 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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