Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Vios Monitoring System Bedside Monitor Recalled by Murata Vios, Inc. Due to A premature failure condition was identified with the...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Murata Vios, Inc. directly.
Affected Products
Vios Monitoring System Bedside Monitor, Model BSM2050, Software Version Numbers 1.54.20 and 1.56.00
Quantity: 44 systems
Why Was This Recalled?
A premature failure condition was identified with the L2050R pulse oximeter SpO2 sensor that connects to the L2050G Vios chest sensor device. When a failure occurs, a Pulse Ox Sensor Off warning condition will be incorrectly displayed by the system.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Murata Vios, Inc.
Murata Vios, Inc. has 4 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report