Murata Vios recalls bedside monitors with specific software versions due to potential incorrect pulse oximeter warnings. Affected units may display false 'Pulse Ox Sensor Off' alerts.
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.
Murata Vios is recalling bedside monitors with software versions 1.54.20 and 1.56.00 because a faulty sensor can cause false warnings about low oxygen levels. This could lead to unnecessary alarm or delayed medical response.
The L2050R pulse oximeter sensor can malfunction and incorrectly show a 'Pulse Ox Sensor Off' warning. This might cause healthcare workers to think oxygen levels are low when they're actually normal, potentially delaying critical care.
Patients using bedside monitors with specific software versions are affected. Healthcare providers using these monitors may be at risk if they rely on the device for oxygen monitoring.
Check for the model BSM2050 with software versions 1.54.20 or 1.56.00. The unique identifier (UDI-DI) is B595BSM20500.
Look for the software version number on the device label or in the device settings.
A premature failure condition was identified with the L2050R pulse oximeter sensor that can cause incorrect warnings about low oxygen levels.
The recall record does not specify a remedy, so contact Murata Vios directly for guidance.
The recall record states the hazard is a false warning, which is unlikely to cause serious injury but could delay medical care.
We’ve drafted a message you can send Murata Vios to request your refund or repair — edit it as you like.
Subject: Recall Z-1169-2025 — Murata Vios Murata Vios Hello, I own a Murata Vios that is covered by recall Z-1169-2025 from Murata Vios. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
