Device recall
Z-1075-2007: AirLife nCPAP System Driver; a nasal continuous positive airway pressure device…
FDA device recall · Class II · Cardinal Health
Key facts
| Recall number (Z-number) | Z-1075-2007 |
|---|---|
| Recall event | 38062 |
| Product | AirLife nCPAP System Driver; a nasal continuous positive airway pressure device, which is part of a larger system that includes an nCPAP generator, fixation device and patient interface (prongs and.or mask); Cardinal Health, McGaw Park, IL 60085; cat. 006900 |
| Product code | BZD |
| Recalling firm | Cardinal Health |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 12, 2007 |
| 510(k) numbers | K051226 |
| FEI number | 3001236905 |
At a glance
- 1–9 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