{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Woodbury",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "96133",
      "recalling_firm": "Murata Vios, Inc.",
      "address_1": "700 Commerce Dr Ste 190",
      "address_2": "",
      "postal_code": "55125-9239",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the state of NY.",
      "recall_number": "Z-1169-2025",
      "product_description": "Vios Monitoring System Bedside Monitor, Model BSM2050, Software Version Numbers 1.54.20 and 1.56.00",
      "product_quantity": "44 systems",
      "reason_for_recall": "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 \u001cPulse Ox Sensor Off\u001d warning condition will be incorrectly displayed by the system.",
      "recall_initiation_date": "20230606",
      "center_classification_date": "20250212",
      "report_date": "20250219",
      "code_info": "All systems with Software Version Numbers 1.54.20 and 1.56.00 affected; UDI-DI: B595BSM20500",
      "more_code_info": ""
    }
  ]
}