Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
muRata Vios Monitoring System Model 2050 Recalled by Murata Vios, Inc. Due to During the set-up and workflow to begin Vios...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Murata Vios, Inc. directly.
Affected Products
muRata Vios Monitoring System Model 2050; bedside cardiac monitor, including cardiotachometer and alarm rate
Quantity: 62 units
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Murata Vios, Inc.
Murata Vios, Inc. has 4 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report