Murata Vios, Inc.: Medical Device Recall in 2025 - (Recall #: Z-0956-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

muRata Vios Monitoring System Model 2050; bedside cardiac monitor, including cardiotachometer and alarm rate

Product Classification:

Class II

Date Initiated: June 21, 2021

Date Posted: January 22, 2025

Recall Number: Z-0956-2025

Event ID: 96078

Reason for Recall:

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.

Status: Completed

Product Quantity: 275 units

Code Information:

Soft ware version 1.49.02 UDI: +B595BSM20500/\$\$7V1.49.02/16D20200504S and Software version 1.52.00 UDI: +B595BSM20500/\$\$7V1.52.00/16D20210305K

Distribution Pattern:

Worldwide - US Nationwide distribution in the states of NY, LA and the country of India.

Voluntary or Mandated:

Voluntary: Firm initiated