Every recall we track for Murata Vios, Inc. — 4 in all — plus the complaints and injury reports the public filed about them.
Murata Vios recalls bedside monitors with software versions 1.56.01 and 1.57.20 due to potential battery depletion when stored unplugged, causing tablet connectivity issues.
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.
Murata Vios recalls bedside monitors with specific software versions due to potential incorrect pulse oximeter warnings. Affected units may display false 'Pulse Ox Sensor Off' alerts.
Murata Vios recalls Model 2050 bedside cardiac monitors with software versions 1.49.02 and 1.52.00. Distorted ECG waveforms and flickering vital signs may occur during setup, potentially causing inaccurate readings.
