--- title: "Murata Vios, Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Murata Vios, Inc. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/murata-vios-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Murata Vios, Inc. recall records **3** reported ongoing 3 records in this archive. Latest source date Aug 9, 2024. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Aug 9, 2024 FDA device enforcement ### [Vios Monitoring System Bedside Monitor Model BSM2050](https://isitonrecall.com/recall/fda-device-z-1292-2025-vios-monitoring-system-bedside-monitor-model-bsm2050/) 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. Class II Reported ongoing Distribution: US Nationwide distribution in the states of Florida, Louisiana, Maryland, Montana, New York, Ohio, and Texas. [Official source for Vios Monitoring System Bedside Monitor Model BSM2050](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1292-2025%22) Apr 22, 2024 FDA device enforcement ### [muRata Vios Monitoring System Model 2050; bedside cardiac monitor, including cardiotachometer and alarm rate](https://isitonrecall.com/recall/fda-device-z-1069-2025-murata-vios-monitoring-system-model-2050-bedside-cardiac-monitor-including-cardiotachometer-and-alar/) During the set-up and workflow to begin Vios monitoring, it has been noticed that patient vital signs and ECG waveforms can become distorted and will flicker or flash very fast. This issue only occurs on the Central Station Monitor (CSM) in the patient tile... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of NY, TX, OH, MD and the country of India. [Official source for muRata Vios Monitoring System Model 2050; bedside cardiac monitor, including cardiotachometer and...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1069-2025%22) Jun 6, 2023 FDA device enforcement ### [Vios Monitoring System Bedside Monitor, Model BSM2050, Software Version Numbers 1.54.20 and 1.56.00](https://isitonrecall.com/recall/fda-device-z-1169-2025-vios-monitoring-system-bedside-monitor-model-bsm2050-software-version-numbers-1-54-20-and-1-56-00/) A premature failure condition was identified with the L2050R pulse oximeter SpO2 sensor that connects to the L2050G Vios chest sensor device. When a failure occurs, a Pulse Ox Sensor Off warning condition will be incorrectly displayed by the system. Class II Reported ongoing Distribution: US Nationwide distribution in the state of NY. [Official source for Vios Monitoring System Bedside Monitor, Model BSM2050, Software Version Numbers 1.54.20 and 1.56.00](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1169-2025%22) ## Reasons in these listed records - 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. - During the set-up and workflow to begin Vios monitoring, it has been noticed that patient vital signs and ECG waveforms can become distorted and will flicker or flash very fast. This issue only occurs on the Central Station Monitor (CSM) in the patient tiles view and is not se... - A premature failure condition was identified with the L2050R pulse oximeter SpO2 sensor that connects to the L2050G Vios chest sensor device. When a failure occurs, a Pulse Ox Sensor Off warning condition will be incorrectly displayed by the system. These examples come from this result page and are not a ranking of every recall reason. ## Checking Murata Vios, Inc. ### Is there a recall on murata vios, inc. right now? This archive contains 3 records, including 3 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search Murata Vios, Inc.](https://isitonrecall.com/check/?q=Murata%20Vios%2C%20Inc.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)