{
  "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": "Salt Lake City",
      "state": "UT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76074",
      "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": "Worldwide including govt/VA/military and foreign consignees.",
      "recall_number": "Z-1060-2017",
      "product_description": "OEC 9900 Elite. MDL Numbers: D148942, D155043",
      "product_quantity": "26,256 total",
      "reason_for_recall": "GE Healthcare Surgery announces a voluntary field action for the OEC 9800 and OEC 9900 Elite due to additional supplementation to the user documentation to include areas for enhanced planned maintenance and component replacement frequencies.",
      "recall_initiation_date": "20161227",
      "center_classification_date": "20170120",
      "termination_date": "20180712",
      "report_date": "20170201",
      "code_info": "Manufactured from Oct 2005 to present"
    }
  ]
}