Murata Vios, Inc. recalls Vios Monitoring System Bedside Monitor, Model BSM2050, Software Version Numbers 1.54.20 and 1.56.00
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…
Read the official notice →- Date
- 2025-02-19
- Country
- United States
- Brand
- Murata Vios
- Product
- Vios Monitoring System Bedside Monitor, Model BSM2050, Software Version Numbers 1.54.20 and 1.56.00
- Classification
- Class II
- Units
- US Nationwide distribution in the state of NY.
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
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- Check the product name, strength and lot number against the official notice.
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General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
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Murata Vios, Inc. recalls Vios Monitoring System Bedside Monitor Model BSM2050
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Murata Vios, Inc. recalls muRata Vios Monitoring System Model 2050; bedside cardiac monitor, including cardiotachometer and alarm rate
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FDA · DeviceMurata Vios, Inc.Worldwide - US Nationwide distribution in the states of NY, TX, OH, MD and the…Official notice →- 2025-01-22
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During the set-up and workflow to begin Vios monitoring, it has been noticed that patient vital signs and ECG waveforms can become distorted and will flicker or flash very fast. This issue only occurs on the Central…
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