Z-1292-2025 Class II Ongoing
FDA device recall Z-1292-2025 was initiated by Murata Vios, Inc. on August 9, 2024 and is designated Class II. 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. The recall status is ongoing. Affected quantity: 50.
Recall Details
- Product Type
- Devices
- Report Date
- March 12, 2025
- Initiation Date
- August 9, 2024
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 50
Product Description
Vios Monitoring System Bedside Monitor Model BSM2050
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 Pattern
US Nationwide distribution in the states of Florida, Louisiana, Maryland, Montana, New York, Ohio, and Texas.
Code Information
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