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.
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.
“Murata Vios BSM2050 Bedside Monitor Recall: Battery Depletion Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/54246-murata-vios-bsm2050-bedside-monitor-recall-battery-depletion-risk. Based on FDA recall #Z-1292-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1292-2025%22&limit=1).
The Food and Drug Administration announced on Aug. 9, 2024, that Murata Vios, Inc. is recalling the Vios Monitoring System Bedside Monitor Model BSM2050. The agency said batteries may deplete if devices are stored unplugged, potentially leading to tablet connectivity issues.
How to tell if you have it
Brand: Murata Vios
Product: Vios Monitoring System Bedside Monitor Model BSM2050
Distribution: US Nationwide, including Florida, Louisiana, Maryland, Montana, New York, Ohio, and Texas
The hazard
According to the FDA, batteries may deplete over time while not in use if devices are stored without being plugged into a wall outlet. This depletion may lead to tablet connectivity issues.
Context
GovInfoNow's records show Murata Vios, Inc. has had three other recalls since June 21, 2021. Other recent recalls of similar products include Philips Telemetry Monitor 5500 1.4 GHz Recall (June 5, 2026), Philips IntelliVue MP30 Monitor Recall (Oct. 31, 2025), and Philips IntelliVue MX70: Monitor May Not Alarm - Recall (Oct. 31, 2025).
How to tell if you have this one
Check for the model number BSM2050 on the device and software versions 1.56.01 or 1.57.20 on the label or packaging. The device was sold with specific UDI codes starting with +B595BSM20500.
Brand
Murata Vios
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Software Version
Look for software versions 1.56.01 or 1.57.20 on the device label or packaging.
Ensure Power Connection
If the device is stored without being plugged in, connect it to a wall outlet to prevent battery depletion.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 7 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “US Nationwide distribution in the states of Florida, Louisiana, Maryland, Montana, New York, Ohio, and Texas.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Florida, Louisiana, Maryland, Montana, New York, Ohio, Texas.
Recall timeline
FDA published this recall 7 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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.
Official source: FDA Recall #Z-1292-2025 (August 9, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1292-2025 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.