Device recall
Z-2246-2016: DeVilbiss Model 7305P-D Powered Suction Unit
FDA device recall · Class II · DeVilbiss Healthcare LLC
Key facts
| Recall number (Z-number) | Z-2246-2016 |
|---|---|
| Recall event | 74308 |
| Product | DeVilbiss Model 7305P-D Powered Suction Unit |
| Product code | JCX |
| Recalling firm | DeVilbiss Healthcare LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 30, 2017 |
| 510(k) numbers | K982304 |
| FEI number | 2515872 |
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