Device recall
Z-3016-2011: AirLife Nebulizer Heater, Catalog Code 2M8021 The AirLife Nebulizer Heater is…
FDA device recall · Class II · Carefusion 211 Inc
Key facts
| Recall number (Z-number) | Z-3016-2011 |
|---|---|
| Recall event | 59376 |
| Product | AirLife Nebulizer Heater, Catalog Code 2M8021 The AirLife Nebulizer Heater is part of the heated nebulizer system intended to provide warm bland aerosol therapy to respiratory patients. The system is used in conjunction with a standard oxygen flowmeter, which by providing pressurized oxygen powers… |
| Product code | CAF |
| Recalling firm | Carefusion 211 Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 30, 2012 |
| 510(k) numbers | K780456 |
| FEI number | 3013421741 |
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