Device recall
Z-0600-2009: Synergy Pulse, Powered Flotation Therapy bed, Model number 5609. Designed to…
FDA device recall · Class II · Hill-Rom Manufacturing, Inc.
Key facts
| Recall number (Z-number) | Z-0600-2009 |
|---|---|
| Recall event | 50144 |
| Product | Synergy Pulse, Powered Flotation Therapy bed, Model number 5609. Designed to provide enhanced static and pulsation pressure relieving therapies. Provides sixteen pressure zones for customizing the support surface to each patient, and is capable of providing pulsation therapy. |
| 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