{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Atlanta",
      "state": "GA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83604",
      "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": "Distribution within the US to Ohio and Indiana.      International distribution to Germany, Greece, Sweden.",
      "recall_number": "Z-2409-2019",
      "product_description": "Monaco Radiation Treatment Planning System (RTP) System",
      "product_quantity": "49 units",
      "reason_for_recall": "Monaco is displaying the Anatomy and Beam shift direction incorrectly on the Monaco Scan and Setup  Reference Report and is DICOM exporting incorrect (Anatomy/Beam) shift directions.",
      "recall_initiation_date": "20190823",
      "center_classification_date": "20190827",
      "termination_date": "20240628",
      "report_date": "20190904",
      "code_info": "Software Build: 5.50.00 & 5.51.00; UDI GTIN: (01)00858164002244(10) 5.50.00, (01)00858164002268(10) 5.51.00"
    }
  ]
}