Device recall
Z-0177-05: Aeroneb Go Micropump Nebulizer Featuring OnQ electronic micropump, RX…
FDA device recall · Class II · Medical Industries America Inc
Key facts
| Recall number (Z-number) | Z-0177-05 |
|---|---|
| Recall event | 30068 |
| Product | Aeroneb Go Micropump Nebulizer Featuring OnQ electronic micropump, RX, Manufactured by Medical Industries America Inc., Adel, IA. The product is sold individually or in master packs of 8 under the following model numbers (all using the same box label): Model 7000 - Consisting of the Aeroneb Go… |
| Product code | CAF |
| Recalling firm | Medical Industries America Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 24, 2005 |
| 510(k) numbers | K032849 |
| FEI number | 1931654 |
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