Device recall
Z-2319-2013: DeVilbiss Vacu-Aide QSU Suction Unit (Disposable Suction Container/Filter), 800…
FDA device recall · Class II · DeVilbiss Healthcare LLC
Key facts
| Recall number (Z-number) | Z-2319-2013 |
|---|---|
| Recall event | 66347 |
| Product | DeVilbiss Vacu-Aide QSU Suction Unit (Disposable Suction Container/Filter), 800 ML DISP Container, Unassembled, 800 ML DISP Container w/6' patient tubing, and 800 ML DISP Container w/6' patient tubing, assembled. DeVilbiss Vacu-Aide QSU Suction Unit (Disposable Suction Container/Filter) is used to… |
| Product code | JCX |
| Recalling firm | DeVilbiss Healthcare LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 6, 2014 |
| 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