{
  "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": "Salt Lake City",
      "state": "UT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76568",
      "recalling_firm": "GE OEC Medical Systems, Inc",
      "address_1": "384 N Wright Brothers Dr",
      "address_2": "N/A",
      "postal_code": "84116-2862",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "One consignee in CA.",
      "recall_number": "Z-1469-2017",
      "product_description": "OEC FlexiView 8800, Digital Mobile Imaging System, GE Medical Systems",
      "product_quantity": "1",
      "reason_for_recall": "OEC FlexiView 8800 workstation power cable assembly issue which can result in a loss of imaging functionality due to intermittent power cord failures.",
      "recall_initiation_date": "20170221",
      "center_classification_date": "20170314",
      "termination_date": "20170424",
      "report_date": "20170322",
      "code_info": "OEC FlexiView 8800 systems that had NEMA 5-15 15 Amp power cords replaced between January 28, 2016 and November 23, 2016."
    }
  ]
}