Device recall
Z-0796-2016: T-piece Nebulizer with in-line connectors, Part number 8915-7-50. Single patient…
FDA device recall · Class II · Salter Labs
Key facts
| Recall number (Z-number) | Z-0796-2016 |
|---|---|
| Recall event | 73130 |
| Product | T-piece Nebulizer with in-line connectors, Part number 8915-7-50. Single patient use, non-sterile prescription device designed for use in a hospital or home care environment. |
| Product code | CAF |
| Recalling firm | Salter Labs |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 21, 2016 |
| 510(k) numbers | K884947 |
| 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