{
  "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": "2026-04-22",
    "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": "72221",
      "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 Distribution -- US, including the states of CA, IN, MI, MO, TX and WI; and, the countries of Australia, Canada, Germany, Greece, India, Netherlands, New Zealand, Turkey, and the UK.",
      "recall_number": "Z-0112-2016",
      "product_description": "Monaco Radiation Treatment Planning System.    Used to make treatment plans for patients with prescriptions for external beam radiation therapy.",
      "product_quantity": "154 units",
      "reason_for_recall": "Dose and MU are incorrect when CT images are viewed from the head, and, when using multiple prescriptions with forced densities.",
      "recall_initiation_date": "20150915",
      "center_classification_date": "20151007",
      "termination_date": "20170404",
      "report_date": "20151014",
      "code_info": "Software Version 5.10.00"
    }
  ]
}