Device recall
Z-1720-2015: Roscoe Mini Neb Compressor User Manual for the NEB-ROS Product Usage: Inhaler…
FDA device recall · Class II · Compass Health Brands
Key facts
| Recall number (Z-number) | Z-1720-2015 |
|---|---|
| Recall event | 71112 |
| Product | Roscoe Mini Neb Compressor User Manual for the NEB-ROS Product Usage: Inhaler therapy that converts liquid medicine into a fine mist that is easily inhaled. |
| Product code | CAF |
| Recalling firm | Compass Health Brands |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 25, 2016 |
| 510(k) numbers | K031413 |
| FEI number | 3005182235 |
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