Device recall
Z-2744-2018: AbViser AutoValve IAP (intra- abdominal pressure) Monitoring Device, Patient…
FDA device recall · Class II · ConvaTec, Inc
Key facts
| Recall number (Z-number) | Z-2744-2018 |
|---|---|
| Recall event | 80539 |
| Product | AbViser AutoValve IAP (intra- abdominal pressure) Monitoring Device, Patient mount: a) REF ABV300, b) REF ABV301 AbViser is a sterile non-invasive disposable intra- abdominal pressure monitoring device containing aspiration tubing, infusion tubing, valves and optional pressure transducers for the… |
| Product code | FEN |
| Recalling firm | ConvaTec, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 24, 2023 |
| FEI number | 3011987967 |
At a glance
- None 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