Device recall
Z-0300-04: MVP-10 Pediatric/ Neonatal Volume Ventilator
FDA device recall · Class II · Bio-Med Devices, Inc.
Key facts
| Recall number (Z-number) | Z-0300-04 |
|---|---|
| Recall event | 27937 |
| Product | MVP-10 Pediatric/ Neonatal Volume Ventilator |
| Product code | MNT |
| Recalling firm | Bio-Med Devices, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 1, 2016 |
| FEI number | 3003952420 |
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