Device recall
Z-3192-2018: Xper Flex Cardio Physiomonitoring System Model # 453564669081 Software Version…
FDA device recall · Class II · Invivo Corporation
Key facts
| Recall number (Z-number) | Z-3192-2018 |
|---|---|
| Recall event | 80761 |
| Product | Xper Flex Cardio Physiomonitoring System Model # 453564669081 Software Version 1.6.0.0388 |
| Product code | MWI |
| Recalling firm | Invivo Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 15, 2021 |
| 510(k) numbers | K101571 |
| FEI number | 1051786 |
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