{
  "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": [
    {
      "country": "United States",
      "city": "Atlanta",
      "address_1": "400 Perimeter Center Ter NE Ste 50",
      "reason_for_recall": "Incorrect Enhanced Dynamic Wedge (EDW) or Virtual Wedge (VW) Calculations.",
      "address_2": "",
      "product_quantity": "279",
      "code_info": "Software Versions 5.00 and higher",
      "center_classification_date": "20170111",
      "distribution_pattern": "Worldwide Distribution - US Nationwide in the state of CA, IN, KY, MA, NJ, NY, NC, PA, TX, WI, and the countries of Brazil, Canada, China, Croatia, Estonia, Germany, India, Japan, Netherlands, New Zealand, Norway, Poland, Serbia, South Africa, Spain, Russia, Turkey",
      "state": "GA",
      "product_description": "Monaco RTP System    Product Usage:  Used to make treatment plans for patients with prescriptions for external beam radiation therapy.",
      "report_date": "20170118",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Elekta, Inc.",
      "recall_number": "Z-1009-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "76028",
      "termination_date": "20210716",
      "more_code_info": "",
      "recall_initiation_date": "20161221",
      "postal_code": "30346-1227",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}