Murata Vios recalls Model 2050 bedside cardiac monitors where patient vital signs and ECG waveforms may flicker or flash during setup, affecting accuracy in monitoring.
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.
Murata Vios is recalling its Model 2050 bedside cardiac monitors because patient vital signs and ECG waveforms can become distorted and flicker during setup. This issue only affects the Central Station Monitor view and not other monitoring areas, so it may not cause immediate harm but could lead to inaccurate readings.
The monitor's Central Station Monitor (CSM) displays distorted patient vital signs and ECG waveforms that flicker or flash very quickly during setup. This issue only occurs in the patient tiles view and does not affect other monitoring areas or the bedside monitor.
Healthcare providers using the Model 2050 bedside cardiac monitor for patient monitoring are most at risk. Patients with cardiac conditions requiring close monitoring may be affected if the monitor provides inaccurate readings.
Check for the Model 2050 bedside cardiac monitor with software version 1.57.20. The product includes a cardiotachometer and alarm rate features. The recall applies to units sold with the UDI code +B595BSM20500/$$7V1.57.20/16D20231129Y.
Verify your monitor's software version is 1.57.20 by checking the device settings or label.
Reach out to Murata Vios directly for guidance on whether your unit is affected and next steps.
The recall states that vital signs and ECG waveforms may distort and flicker during setup, but it does not mention causing serious injury or death.
Check for the Model 2050 with software version 1.57.20 and UDI code +B595BSM20500/$$7V1.57.20/16D20231129Y.
The recall record does not specify a remedy or fix for the issue.
We’ve drafted a message you can send Murata Vios to request your refund or repair — edit it as you like.
Subject: Recall Z-1069-2025 — Murata Vios Murata Vios Hello, I own a Murata Vios that is covered by recall Z-1069-2025 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.
