Class II — Murata Vios, Inc.
| Recalling firm | Murata Vios, Inc. |
|---|---|
| Registered facility | View this company's 2 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Ongoing |
| 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. |
| Product | Vios Monitoring System Bedside Monitor Model BSM2050 |
| Quantity | 50 |
| Distribution | US Nationwide distribution in the states of Florida, Louisiana, Maryland, Montana, New York, Ohio, and Texas. |
| Initiated | 2024-08-09 |
| Classified | 2025-03-06 |
| Recall number | Z-1292-2025 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Murata Vios, Inc. (Z-1292-2025).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/96252/
Alerts for Murata Vios, Inc.
Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.
Want a one-page facility brief?
A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.