Device recall
Z-1169-2025: Vios Monitoring System Bedside Monitor, Model BSM2050, Software Version Numbers…
FDA device recall · Class II · Murata Vios, Inc.
Key facts
| Recall number (Z-number) | Z-1169-2025 |
|---|---|
| Recall event | 96133 |
| Product | Vios Monitoring System Bedside Monitor, Model BSM2050, Software Version Numbers 1.54.20 and 1.56.00 |
| 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