Device recall
Z-2767-2019: Aquilex Fluid Control System component: Bag deflector, REF AQL-100CBS Product…
FDA device recall · Class II · WOM World of Medicine AG
Key facts
| Recall number (Z-number) | Z-2767-2019 |
|---|---|
| Recall event | 83712 |
| Product | Aquilex Fluid Control System component: Bag deflector, REF AQL-100CBS Product Usage: Distends uterus with fluid during diagnostic and operative hysteroscopies. |
| Product code | HIG |
| Recalling firm | WOM World of Medicine AG |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 20, 2020 |
| 510(k) numbers | K172040 |
| FEI number | 3001556604 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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