{
  "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": "2026-05-06",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Salt Lake City",
      "address_1": "384 Wright Brothers Dr",
      "reason_for_recall": "Please be aware that this is not a new recall.  The firm has taken action; but, due to administrative issues this recall is now being classified by the Agency.  GE OEC recalled imaging devices OEC 9900, OEC 9800, and OEC 8800 as a result of an FDA inspection identifying that the vertical lift column power supply in the mainframe C-arm is defective and subject to early life failure.",
      "address_2": "",
      "product_quantity": "11,100 units",
      "code_info": "Part numbers: 00-884909-01, 00-884777-01, 00-884911-01, 00-885553-01, 00-884913-01, 00-885554-01, 00-885555-01, 00-886289-01.  All serial numbers.",
      "center_classification_date": "20120718",
      "distribution_pattern": "Worldwide Distribution.",
      "state": "UT",
      "product_description": "OEC 9800, OEC FluoroTrak 9800 Plus, OEC 9800 Plus, OEC 9800 MD Motorized C-arm System designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic, surgical and interventional procedures.    The OEC 9800 is designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic, surgical and interventional procedures. The system includes features specifically designed for use in diagnostic and interventional cardiac imaging procedures, and is also intended for cholangiography, endoscopic, urologic, orthopedic, neurologic, vascular, critical care and emergency room procedures. It may be used for other imaging applications at the physician's discretion.",
      "report_date": "20120725",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "GE OEC Medical Systems, Inc",
      "recall_number": "Z-2026-2012",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "62404",
      "termination_date": "20130128",
      "more_code_info": "",
      "recall_initiation_date": "20071119",
      "postal_code": "84116-2862",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}