{
  "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": "Knoxville",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "69897",
      "recalling_firm": "Siemens Medical Solutions USA Inc.",
      "address_1": "810 Innovation Dr",
      "address_2": "N/A",
      "postal_code": "37932-2562",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed in the states of NC and MA and the countries of  Australia, Canada, Switzerland, and Germany.",
      "recall_number": "Z-0810-2015",
      "product_description": "Biograph mCT S(64)-4R, System Material Number 10248672.    The Siemens Biograph mCT systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic information.",
      "product_quantity": "8 units total",
      "reason_for_recall": "Possibility for system display freeze during CT interventional procedures.",
      "recall_initiation_date": "20141113",
      "center_classification_date": "20141216",
      "termination_date": "20150709",
      "report_date": "20141224",
      "code_info": "Serial Number:  11021"
    }
  ]
}