{
  "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": [
    {
      "country": "United States",
      "city": "Atlanta",
      "address_1": "400 Perimeter Center Ter Ne",
      "reason_for_recall": "The beam is displayed at the \"gantry\" angle, but the dose is calculated at the \"rotation_start\" angle.",
      "address_2": "Ste 50",
      "product_quantity": "13",
      "code_info": "Versions 3.20.00 and 3.20.01",
      "center_classification_date": "20130220",
      "distribution_pattern": "Nationwide Distribution-including the states of AK, CA, FL, NJ, NC, OH, OR, TN, TX, WA, and WI.",
      "state": "GA",
      "product_description": "Monaco RTP System.    Radiation treatment planning.",
      "report_date": "20130227",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Elekta, Inc.",
      "recall_number": "Z-0841-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "64328",
      "termination_date": "20140121",
      "recall_initiation_date": "20130211",
      "postal_code": "30346-1227",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}