Device recall
Z-0638-2007: VIASYS VELA Ventilator, Catalog Number-16186; Viasys Respiratory Care, Inc.
FDA device recall · Class II · Viasys Respiratory Care, Inc.dba Bird Products
Key facts
| Recall number (Z-number) | Z-0638-2007 |
|---|---|
| Recall event | 37318 |
| Product | VIASYS VELA Ventilator, Catalog Number-16186; Viasys Respiratory Care, Inc. |
| Product code | CBK |
| Recalling firm | Viasys Respiratory Care, Inc.dba Bird Products |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 18, 2008 |
| 510(k) numbers | K032451 |
| FEI number | 2021710 |
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