{
  "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": "74087",
      "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": "IL, LA, Austria, Australia, Botswana, Germany, Denmark, France, India, Japan",
      "recall_number": "Z-1705-2016",
      "product_description": "iGUIDE System, for patient positioning, with assistance of a 30 Tracking System in a radiotherapy environment.",
      "product_quantity": "20",
      "reason_for_recall": "If by mistake the initial pre-treatment imaging was performed BEFORE the HexaPOD was moved to the DRIVE (*START) position, iGUIDE offers the possibility to branch into a specific catch-up workflow, which was implemented to use the initial scan data.",
      "recall_initiation_date": "20160512",
      "center_classification_date": "20160523",
      "termination_date": "20210716",
      "report_date": "20160601",
      "code_info": "Software iGUIDE 2.1 and 2.2"
    }
  ]
}