Reported Feb 19, 2025 · Ongoing
Vios Monitoring System Bedside Monitor, Model BSM2050, Software Version Numbers 1.54.20 and 1.56.00
Murata Vios, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Murata Vios, Inc. · 700 Commerce Dr Ste 190 · Woodbury, MN · 55125-9239
Is this the product you have?
Vios Monitoring System Bedside MonitorModel BSM2050Software Version Numbers 1.54.20 and 1.56.00
- Lot codes and dates
- All systems with Software Version Numbers 1.54.20 and 1.56.00 affected
- UDI-DIB595BSM20500
- Amount recalled
- 44 systems
Where it was sold
- Nationwide
- NY
Why it was 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.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
Free recall alerts
Get alerted about new Murata Vios, Inc. recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.