{
  "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": [
    {
      "country": "United States",
      "city": "Salt Lake City",
      "address_1": "384 N Wright Brothers Dr",
      "reason_for_recall": "GE Healthcare Surgery announces a voluntary field action for the OEC MiniView 6800, OEC 9900 Elite, and OEC 9800 because the workstation power cable assembly can result in intermittent power cord failures.",
      "address_2": "",
      "product_quantity": "",
      "code_info": "Manufactured between 1/1/16 to 11/1/16",
      "center_classification_date": "20170109",
      "distribution_pattern": "Worldwide Distribution - US including U.S. States: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS,  NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PUERTO RICO, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY and Internationally to Canada, Mexico, and Costa Rica",
      "state": "UT",
      "product_description": "The OEC 9900 Elite mobile fluoroscopy system is designed to provide fluoroscopic and spot-film images of the patient during diagnostic surgical and interventional procedure. Examples of clinical application may include cholangiography, endoscopy, urologic, orthopedic, neurologic, vascular, cardiac, critical care and emergency room procedure. The system may be used for other imaging applications at the physician's discretionOEC 9900 Elite. MDL Numbers: D148942, D155043",
      "report_date": "20170118",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "GE OEC Medical Systems, Inc",
      "recall_number": "Z-0975-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "76033",
      "termination_date": "20170822",
      "more_code_info": "",
      "recall_initiation_date": "20161219",
      "postal_code": "84116-2862",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}