Device recall
Z-0603-2009: Pro 2000, Alternating Pressure Air Flotation Mattress, Model number 5613…
FDA device recall · Class II · Hill-Rom Manufacturing, Inc.
Key facts
| Recall number (Z-number) | Z-0603-2009 |
|---|---|
| Recall event | 50144 |
| Product | Pro 2000, Alternating Pressure Air Flotation Mattress, Model number 5613 Designed to provide enhanced static and pulsation pressure relieving therapies. |
| Product code | FNM |
| Recalling firm | Hill-Rom Manufacturing, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 10, 2009 |
| FEI number | 1045510 |
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