Murata Vios BSM2050 Bedside Monitor Recall: Battery Depletion Risk

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Recalling firmMurata Vios, Inc.700 Commerce Dr Ste 190 · Woodbury, MN 55125-9239

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Murata Vios is recalling bedside monitors model BSM2050 with specific software versions because batteries can deplete over time when not plugged in, leading to tablet connectivity problems. This affects users who store the device without a power source.

Why it’s dangerous

Batteries in these monitors can deplete over time when not connected to a power source. This depletion may cause tablet connectivity issues, but it does not pose a risk of injury or damage to the user.

Who’s affected

Users of the Vios Monitoring System Bedside Monitor Model BSM2050 with software versions 1.56.01 or 1.57.20 are most at risk if they store the device without being plugged in to a wall outlet.

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.

✎ GovInfoNow

Questions people ask

Why is this monitor being recalled?

Batteries may deplete over time when the device is stored without being plugged in, leading to tablet connectivity issues.

What software versions are affected?

Software versions 1.56.01 and 1.57.20.

How can I tell if my monitor is affected?

Check for the model number BSM2050 and software versions 1.56.01 or 1.57.20 on the device label or packaging.

Take action

Contact Murata Vios

We’ve drafted a message you can send Murata Vios to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-1292-2025 — Murata Vios Murata Vios

Hello,

I own a Murata Vios that is covered by recall Z-1292-2025 from Murata Vios.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

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.

Murata Vios, Inc. recalls Vios Monitoring System Bedside Monitor Model BSM2050

Lower-risk recall