Recall Z-1292-2025— Murata Vios, Inc.

Name: FDA recall Z-1292-2025
Creator: U.S. Food and Drug Administration
Published: 2024-08-09

Class II · Ongoing

Class II FDA medical device recall by Murata Vios, Inc., initiated 2024-08-09. It names one FDA 510(k) clearance: K172586. Product: Vios Monitoring System Bedside Monitor Model BSM2050. Reason: Batteries may deplete over time while not in use if devices are stored without being plugged in to wall outlet. Depleted batteries may lead to tablet connectivity issues..

Recalling firm: Murata Vios, Inc.
Classification: Class II
Status: Ongoing
Initiated: 2024-08-09
Firm location: Woodbury, MN, United States

510(k) clearances named in this recall

1 on FDA's record

K172586 — Vios Monitoring System Model 2050Vios Medical, Inc.·cleared 2018-06-22

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

Vios Monitoring System Bedside Monitor Model BSM2050

Reason for recall

Batteries may deplete over time while not in use if devices are stored without being plugged in to wall outlet. Depleted batteries may lead to tablet connectivity issues.

Data sourced from openFDA. This site is unofficial and independent of the FDA.