Device recall
Z-1655-2008: Hill-Rom Procedural Stretcher with auto-contour option; Model P8000F. Wheeled…
FDA device recall · Class III · Hill-Rom, Inc.
Key facts
| Recall number (Z-number) | Z-1655-2008 |
|---|---|
| Recall event | 46858 |
| Product | Hill-Rom Procedural Stretcher with auto-contour option; Model P8000F. Wheeled hospital stretcher consisting of a platform mounted on a wheeled frame, designed to transport patients and to allow for patient care before, during and after transport. |
| Product code | FPO |
| Recalling firm | Hill-Rom, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Dec 29, 2009 |
| FEI number | 1824206 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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