Device recall
Z-2605-2016: Panacea Air Pro Mattress Control Unit, Model: Platinum 5000, US Model Number…
FDA device recall · Class II · American National Mfg Inc
Key facts
| Recall number (Z-number) | Z-2605-2016 |
|---|---|
| Recall event | 74737 |
| Product | Panacea Air Pro Mattress Control Unit, Model: Platinum 5000, US Model Number 5000. Use with alternating pressure air flotation mattress. |
| Product code | FNM |
| Recalling firm | American National Mfg Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 17, 2017 |
| FEI number | 3000204953 |
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