Food, drugs, devices › Murata Vios, Inc.
Device recall: Vios Monitoring System Bedside Monitor Model BSM2050
FDA enforcement event 96252 is a device recall by Murata Vios, Inc. of Woodbury, MN, initiated 9 Aug 2024 and classified Class II, with 1 product record.
FDA defines Class II as a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote. 87% of the 970 device enforcement events initiated in 2024 carry the same class.
Status: Ongoing. Initiation: voluntary: firm initiated. Murata Vios, Inc. has 4 enforcement events on this register, with a median of 1 product record per event.
Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.
Recalling firm
Murata Vios, Inc., Woodbury, MN.
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."
Distribution
"US Nationwide distribution in the states of Florida, Louisiana, Maryland, Montana, New York, Ohio, and Texas."
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| Z-1292-2025 | Vios Monitoring System Bedside Monitor Model BSM2050 | 50 | Class II | Ongoing | 12 Mar 2025 |
Context
Other enforcement events for Murata Vios, Inc.
| Initiated | Product (first record) | Type | Class | Records |
|---|---|---|---|---|
| 22 Apr 2024 | muRata Vios Monitoring System Model 2050; bedside cardiac monitor, including cardiotachometer and alarm rate | Device | Class II | 1 |
| 6 Jun 2023 | Vios Monitoring System Bedside Monitor, Model BSM2050, Software Version Numbers 1.54.20 and 1.56.00 | Device | Class II | 1 |
| 21 Jun 2021 | muRata Vios Monitoring System Model 2050; bedside cardiac monitor, including cardiotachometer and alarm rate | Device | Class II | 1 |
All 4 events for Murata Vios, Inc.
Questions and answers
Why was this device recalled?
FDA's record gives the reason for recall as: "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."
What does Class II mean?
FDA classifies recalls by relative degree of health hazard. Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.
Where was the product distributed?
FDA's distribution pattern field reads: "US Nationwide distribution in the states of Florida, Louisiana, Maryland, Montana, New York, Ohio, and Texas."
Is the recall still ongoing?
FDA lists the status as Ongoing. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.
Where does this data come from?
openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.
Provenance
Source: openFDA device enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.