Murata Vios, Inc. recalls Vios Monitoring System Bedside Monitor Model BSM2050
- Recall date
- August 9, 2024
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1292-2025
- FDA classification
- Class II
- Brand / firm
- Murata Vios, Inc.
- Sold / distributed
- US Nationwide distribution in the states of Florida, Louisiana, Maryland, Montana, New York, Ohio, and Texas.
Why it was recalled
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.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Vios Monitoring System Bedside Monitor Model BSM2050
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