Device recall
Z-2781-2015: NebuTech Nebulizer, Model number: Series 8660, 8960, 8961, 8966, 8984. Nebulizer…
FDA device recall · Class II · Salter Labs
Key facts
| Recall number (Z-number) | Z-2781-2015 |
|---|---|
| Recall event | 71909 |
| Product | NebuTech Nebulizer, Model number: Series 8660, 8960, 8961, 8966, 8984. Nebulizer used to generate aerosols delivered directly to the patient for breathing. Designed to be used in either a hospital or homecare environment. |
| Product code | CAF |
| Recalling firm | Salter Labs |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 6, 2016 |
| 510(k) numbers | K961476, K962879 |
| FEI number | 1314417 |
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