{
  "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": "Ann Arbor",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "66344",
      "recalling_firm": "Xoran Technologies, Inc.",
      "address_1": "5210 S State Rd",
      "address_2": "N/A",
      "postal_code": "48108-7936",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US nationwide",
      "recall_number": "Z-0041-2014",
      "product_description": "Xoran MiniCAT CT Scanner ID ENT00001",
      "product_quantity": "320",
      "reason_for_recall": "Failure of the gantry to rotate. The complaint alleged that the scanner would emit radiation but would not rotate.",
      "recall_initiation_date": "20091214",
      "center_classification_date": "20131025",
      "termination_date": "20140911",
      "report_date": "20131106",
      "code_info": "minicat"
    }
  ]
}