{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Oakville",
      "state": "N/A",
      "country": "Canada",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80239",
      "recalling_firm": "Natus Neurology DBA Excel Tech., Ltd. (XLTEK)",
      "address_1": "2568 Bristol Cir",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "USA Distribution:  AL, CA, CO, CT, FL, GA, IA, ID, IL, IN, KY, LA, MA, MD, ME, MI  MN, MO, NC, NE, NJ, NV, NY, OH, OR, PA, ,RI, SC, TN, TX, UT, VA, WA, WI.    World wide Distribution: Canada, China, Cyprus, Germany, Hong Kong, Italy,  Mexico, Saudi Arabia, Spain, United Kingdom",
      "recall_number": "Z-2570-2018",
      "product_description": "XLTEK EMU40EX EEG Headbox",
      "product_quantity": "462 Units Total",
      "reason_for_recall": "Possible degradation of an internal electronic component over time which may cause the XLTEK EMU 40EX Breakout box to fail.  It may feel hot and plastic case may start melting.",
      "recall_initiation_date": "20180515",
      "center_classification_date": "20180728",
      "termination_date": "20240506",
      "report_date": "20180808",
      "code_info": "Part Numbers: 10406, 002933"
    }
  ]
}