Device recall
Z-1069-2025: muRata Vios Monitoring System Model 2050; bedside cardiac monitor, including…
FDA device recall · Class II · Murata Vios, Inc.
Key facts
| Recall number (Z-number) | Z-1069-2025 |
|---|---|
| Recall event | 96169 |
| Product | muRata Vios Monitoring System Model 2050; bedside cardiac monitor, including cardiotachometer and alarm rate |
| Product code | DRT |
| Recalling firm | Murata Vios, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K172586 |
| FEI number | 3015328411 |
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