Device recall
Z-0084-06: HoverMatt Patient Transfer Solution/Air Transfer Mattress
FDA device recall · Class III · D.T. Davis Enterprises Ltd.
Key facts
| Recall number (Z-number) | Z-0084-06 |
|---|---|
| Recall event | 33722 |
| Product | HoverMatt Patient Transfer Solution/Air Transfer Mattress |
| Product code | FRZ |
| Recalling firm | D.T. Davis Enterprises Ltd. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jun 7, 2006 |
| FEI number | 3001600982 |
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