Device recall
Z-1966-2023: bellavista 1000 Ventilator, Catalogue Number 301.100.030; Continuous Use…
FDA device recall · Class II · Vyaire Medical
Key facts
| Recall number (Z-number) | Z-1966-2023 |
|---|---|
| Recall event | 92243 |
| Product | bellavista 1000 Ventilator, Catalogue Number 301.100.030; Continuous Use Ventilator |
| Product code | CBK |
| Recalling firm | Vyaire Medical |
| Recall class | Class II |
| Status | Completed |
| 510(k) numbers | K183364 |
| FEI number | 3013421741 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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