Device recall
Z-0326-05: RemRest Non-Invasive Continuous Positive Airway Pressure System, Model 903. The…
FDA device recall · Class II · Medical Industries America Inc
Key facts
| Recall number (Z-number) | Z-0326-05 |
|---|---|
| Recall event | 30085 |
| Product | RemRest Non-Invasive Continuous Positive Airway Pressure System, Model 903. The firm name on the device is Medical Industries America Inc., Adel, IA. |
| Product code | BZD |
| Recalling firm | Medical Industries America Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 18, 2005 |
| 510(k) numbers | K002763 |
| FEI number | 1931654 |
At a glance
- 1–9 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