{
  "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": "66340",
      "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 - Nationwide",
      "recall_number": "Z-0040-2014",
      "product_description": "Xoran MiniCAT00202",
      "product_quantity": "320",
      "reason_for_recall": "The MiniCAT CT Scanners subject to this notification failed to meet Xoran's specifications for dose rate of 125 ¿ 3 kVp. These 18 complaints received include dose rates both on the high and low end of Xorans specifications.",
      "recall_initiation_date": "20100727",
      "center_classification_date": "20131025",
      "termination_date": "20140911",
      "report_date": "20131106",
      "code_info": "minicat"
    }
  ]
}