Murata Vios, Inc. recalls
Every recall we track for Murata Vios, Inc. — 4 in all, from 2021–2024 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
4 recalls since 2017.
All FDA recall records for Murata Vios, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 1 | 0 | 1 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 1 | 0 | 1 |
| 2024 | 0 | 0 | 2 | 0 | 2 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Murata Vios, Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Murata Vios, Inc. recalls
4 shown- Lower riskMedical device
Murata Vios, Inc. recalls Vios Monitoring System Bedside Monitor Model BSM2050
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.
Murata ViosAug 9, 2024 - Lower riskMedical device
Murata Vios, Inc. recalls muRata Vios Monitoring System Model 2050; bedside cardiac monitor, including cardiotachometer and alarm rate
Murata Vios recalls Model 2050 bedside cardiac monitors where patient vital signs and ECG waveforms may flicker or flash during setup, affecting accuracy in monitoring.
Murata ViosApr 22, 2024 - Lower riskMedical device
Murata Vios, Inc. recalls Vios Monitoring System Bedside Monitor, Model BSM2050, Software Version Numbers 1.54.20 and 1.56.00
Murata Vios recalls bedside monitors with specific software versions due to potential incorrect pulse oximeter warnings. Affected units may display false 'Pulse Ox Sensor Off' alerts.
Murata ViosJun 6, 2023 - Lower riskMedical device
Murata Vios, Inc. recalls muRata Vios Monitoring System Model 2050; bedside cardiac monitor, including cardiotachometer and alarm rate
Murata Vios recalls Model 2050 bedside cardiac monitors with software versions 1.49.02 and 1.52.00. Distorted ECG waveforms and flickering vital signs may occur during setup, potentially causing inaccurate readings.
Murata ViosJun 21, 2021
Murata Vios, Inc. recall questions
How many recalls has Murata Vios, Inc. had?
4 recalls from Murata Vios, Inc. are on record with U.S. safety agencies, from 2021–2024.
What is the most recent Murata Vios, Inc. recall?
Murata Vios, Inc. recalls Vios Monitoring System Bedside Monitor Model BSM2050, dated Aug 9, 2024. Every Murata Vios, Inc. recall is listed on this page, newest first.
What should I do if I have a recalled Murata Vios, Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Murata Vios, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.