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Murata Vios, Inc. recalls muRata Vios Monitoring System Model 2050; bedside cardiac monitor, including cardiotachometer and alarm rate
Recalled February 5, 2025 · FDA recall Z-1069-2025 · Murata Vios
Hazard
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 Station Monitor (CSM) in the patient tiles view and is not seen at any other point during patient monitoring & not on the Bedside Monitor. · FDA Class II
Units
62 units
Sold at
Worldwide - US Nationwide distribution in the states of NY, TX, OH, MD and the country of India.
Description
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 Station Monitor (CSM) in the patient tiles view and is not seen at any other point during patient monitoring & not on the Bedside Monitor.
Product
muRata Vios Monitoring System Model 2050; bedside cardiac monitor, including cardiotachometer and alarm rate
Manufacturer(s)
Murata Vios, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →