{
  "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": "2026-06-24",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Atlanta",
      "state": "GA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98980",
      "recalling_firm": "Elekta, Inc.",
      "address_1": "400 Perimeter Center Ter NE Ste 50",
      "address_2": "N/A",
      "postal_code": "30346-1227",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide - US Nationwide distribution in the states of WI, FL, LA, NY, NY, NJ, KS, FL, IA, NM, TX and the countries of Bahrain, Belgium, Canada, China, Denmark, France, Germany, \tHong Kong, India, Israel, Italy, Japan, Lithuania, Malta, Mexico, Netherlands, Pakistan, \tPanama, Poland, Spain, Sweden, Switzerland, Taiwan, Thailand, Turkey, United Kingdom.",
      "recall_number": "Z-2406-2026",
      "product_description": "MOSAIQ Oncology Information System",
      "product_quantity": "12 programs",
      "reason_for_recall": "Software may fail to load adapted baseline shift plan during treatment delivery when a communication error occurs.",
      "recall_initiation_date": "20260521",
      "center_classification_date": "20260611",
      "report_date": "20260617",
      "code_info": "Software Version: MOSAIQ 3.2/UDI: 07340201500071"
    }
  ]
}