Device recall
Z-1485-04: The LTV Series ventilators provides continuous or intermittent ventilatory…
FDA device recall · Class I · Cardinal Health 203, Inc
Key facts
| Recall number (Z-number) | Z-1485-04 |
|---|---|
| Recall event | 29978 |
| Product | The LTV Series ventilators provides continuous or intermittent ventilatory support for the care of individuals who require mechanical ventilation. This is a prescription medical device intended for use by personnel under the direction of a physician. The ventilator is suitable for use in… |
| Product code | CBK |
| Recalling firm | Cardinal Health 203, Inc |
| Recall class | Class I |
| Status | Terminated |
| Termination date | May 28, 2008 |
| 510(k) numbers | K002881, K010608, K032226, K981371, K984056 |
| FEI number | 3002617992 |
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