Vios Monitoring System Bedside Monitor Model BSM2050
This recall is currently active, issued March 6, 2025. It was issued by Murata Vios, Inc..
- Company
- Murata Vios, Inc.
- Recall Initiated
- August 9, 2024
- Posted
- March 6, 2025
- Recall Number
- Z-1292-2025
- Quantity
- 50
- Firm Location
- Woodbury, MN
- Official Source
- View on FDA website ↗
Reason for Recall
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.
Distribution
US Nationwide distribution in the states of Florida, Louisiana, Maryland, Montana, New York, Ohio, and Texas.
Lot / 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
Root Cause
Labeling design
Action Taken
The firm sent a single page of instructions to customers on August 9, 2024 via email. Customers were informed that tablets should remain plugged into a wall outlet when the tablet is not in use. The tablet battery should not be allowed to fully deplete at any time during patient monitoring or when not in use.