FDA Device recall Z-1292-2025
Vios Monitoring System Bedside Monitor Model BSM2050
- FDA Device
- Class II
- ongoing
- Published 2025-03-12
On 2025-03-12 the FDA classified a Class II recall of Vios Monitoring System Bedside Monitor Model BSM2050 by Murata Vios, citing batteries may deplete over time while not in use if devices are stored without being plugged in to wall outlet. Depleted batteries may lead to tablet connectivity issues.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1292-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-08-09 |
| Published | 2025-03-12 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Murata Vios |
| Distribution | US |
Product
Vios Monitoring System Bedside Monitor Model BSM2050
Reason
Batteries may deplete over time while not in use if devices are stored without being plugged in to wall outlet. Depleted batteries may lead to tablet connectivity issues.
Identifiers
| code_info | 1.56.01 UDI: +B595BSM20500/$$7V1.56.01/16D20230630S 1.57.20 UDI: +B595BSM20500/$$7V1.57.20/16D20231129Y Software Versions 1.56.01 and 1.57.20 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1292-2025%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.