{
  "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": "Wilmington",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "73410",
      "recalling_firm": "Neurotherm, Inc.",
      "address_1": "600 Research Dr Ste 1",
      "address_2": "N/A",
      "postal_code": "01887-4438",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "CA, CO, IA, ME, NJ,  NY,  SC, TX, WI",
      "recall_number": "Z-1361-2016",
      "product_description": "Neurotherm  NT2000iX RF Generator  Model Number: RFG-NT -2000iX",
      "product_quantity": "25",
      "reason_for_recall": "NT2000iX software shipped with the international setting turned on. The international settings include access to Corodotomy, Bi-Polar, and No Temperature modes were not cleared in the United States for use.",
      "recall_initiation_date": "20131009",
      "center_classification_date": "20160409",
      "termination_date": "20160414",
      "report_date": "20160420",
      "code_info": "Serial Numbers:  2593-13, 2717-13,  2616-13, 2704-13, 2735-13, 2360-12, 2732-13, 2727-13,   2284-11, 2726-13,  2728-13, 2426-12, 2700-13, 2508-12, 2643-13, 2733-13,   2730-13,  2724-13, 2453-12,  2631-13, 2171-11, 2059-10, 2729-13 ,2294-12,  2725-13",
      "more_code_info": ""
    }
  ]
}