Device recall
Z-1464-2008: Viasys healthcare, Pulmonetic Systems LTV 950 Ventilator The ventilator is…
FDA device recall · Class II · Cardinal Health 203, Inc
Key facts
| Recall number (Z-number) | Z-1464-2008 |
|---|---|
| Recall event | 46850 |
| Product | Viasys healthcare, Pulmonetic Systems LTV 950 Ventilator The ventilator is suitable for use in institutional, home or transport settings. Fully self-contained ventilator in a compact and lightweight design. It can operate from an internal battery, external battery or AC power. Applications include… |
| Product code | CBK |
| Recalling firm | Cardinal Health 203, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 16, 2012 |
| 510(k) numbers | K002881, K040540, K981371, K984056 |
| FEI number | 3002617992 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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