{
  "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": "77590",
      "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 in the states of AK, CT, GA, KY, LA, MA, MD, MN, NC, NM, OH, OK, OR, PA, SC, SD, TN, TX, VA, WA and countries of Hawaii  Australia, Austria, Belgium, Denmark, France, Germany, Hong Kong, India, Indonesia, Ireland, Italy, Japan, Netherlands, New Zealand, Poland, Slovenia, Spain, Sweden, Switzerland, United Kingdom, & Vietnam.",
      "recall_number": "Z-3017-2017",
      "product_description": "iGUIDE Software 2.2     Product Usage:  Control of accurate patient positioning with assistance of a 30 Tracking System in a radiotherapy environment.",
      "product_quantity": "110 units",
      "reason_for_recall": "Incorrect PEC values.",
      "recall_initiation_date": "20170619",
      "center_classification_date": "20170810",
      "termination_date": "20191105",
      "report_date": "20170816",
      "code_info": "Scope; iGUIDE 2.2.0, iGUIDE 2.2.1"
    }
  ]
}