{
  "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": "2026-04-29",
    "results": {
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  "results": [
    {
      "country": "United States",
      "city": "Salt Lake City",
      "address_1": "384 Wright Brothers Dr",
      "reason_for_recall": "GE Healthcare initiated a field correction because prior revision of components were potentially installed on certain OEC 9800, FlexiView 8800, OEC MiniView 6800 and OEC UroView 2800 systems.",
      "address_2": "",
      "product_quantity": "5",
      "code_info": "Serial No: 3120PU3, 4851PU2, 5640PU8, 6052PU5, FIB0064",
      "center_classification_date": "20141107",
      "distribution_pattern": "Worldwide Distribution.",
      "state": "UT",
      "product_description": "FlexiView 8800 Digital Mobile Imaging System.    The FlexiView 8800 Digital Mobile Imaging System is designed to provide fluoroscopic and spot film, imaging of the patient during diagnostic, surgical and interventional procedures.",
      "report_date": "20141119",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "GE OEC Medical Systems, Inc",
      "recall_number": "Z-0194-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "69474",
      "termination_date": "20150323",
      "more_code_info": "",
      "recall_initiation_date": "20141003",
      "postal_code": "84116-2862",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}