FDAFDA · Food and drugs·Recall number Z-1292-2025
Vios Monitoring System Bedside Monitor Model BSM2050
Published March 12, 2025 · Recall initiated: August 9, 2024
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- Murata Vios, Inc.
- Distributor
- US Nationwide distribution in the states of Florida, Louisiana, Maryland, Montana, New York, Ohio, and Texas.
- Lot
- 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
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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