Device recall
Z-0382-05: Medication Bottle (U22-3), a component of the MicroAir Vibrating Mesh Nebulizer…
FDA device recall · Class II · Omron Healthcare, Inc.
Key facts
| Recall number (Z-number) | Z-0382-05 |
|---|---|
| Recall event | 30363 |
| Product | Medication Bottle (U22-3), a component of the MicroAir Vibrating Mesh Nebulizer, Model NE-U22V/NE-22VAC; Distributed by: Omron Healthcare, Inc., 300 Lakeview Parkway, Vernon Hills, IL 60061 |
| Product code | CAF |
| Recalling firm | Omron Healthcare, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 26, 2007 |
| 510(k) numbers | K923024 |
| FEI number | 1450057 |
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