{
  "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,
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  "results": [
    {
      "status": "Terminated",
      "city": "Oakville",
      "state": "Ontario",
      "country": "Canada",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "70157",
      "recalling_firm": "Natus Medical Incorporated",
      "address_1": "2568 Bristol Circle",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Nationwide Distribution",
      "recall_number": "Z-1068-2015",
      "product_description": "EPWorks software used in the Xltek Protektor Stimulator    Product Usage:  Intraoperative diagnosis of acute dysfunction in corticospinal axonal conduction brought about by mechanical trauma (traction, shearing, laceration, or compression) or vascular insufficiency.",
      "product_quantity": "928 units",
      "reason_for_recall": "Software error occurs when using remote monitoring; if the remote user tries to stop the free run waveform group, the system will display a message informing the user that they do not have sufficient privilege.",
      "recall_initiation_date": "20150102",
      "center_classification_date": "20150209",
      "termination_date": "20170322",
      "report_date": "20150218",
      "code_info": "EPWorks Software Versions prior to 6.0"
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}