{
  "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": "Pittsburgh",
      "address_1": "128 Gamma Dr",
      "reason_for_recall": "complaints of system malfunction and unintended, sudden movement at start up. No injuries reported.",
      "address_2": "",
      "product_quantity": "140",
      "code_info": "Model Numbers NOTC-S, NOTC-P, NOTC-C, NOTC-O, SVNG-1, SVNG-2, SVNG-3",
      "center_classification_date": "20150612",
      "distribution_pattern": "Worldwide distribution - US (nationwide) and Internationally to Canada and Mexico.",
      "state": "PA",
      "product_description": "I-Portal¿ NOTC and VNG; a device used to measure, record, or visually display the involuntary movements (nystagmus) of the eyeball, indicated for use as a diagnostic tool to assist trained clinicians in their analysis of vestibular disorders, which requires the separation of central vs. peripheral nervous system deficits.",
      "report_date": "20150624",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Neuro Kinetics, Inc.",
      "recall_number": "Z-1795-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "71264",
      "termination_date": "20170417",
      "more_code_info": "",
      "recall_initiation_date": "20150430",
      "postal_code": "15238-2920",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}