{
  "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": "Pittsburgh",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "66995",
      "recalling_firm": "Neuro Kinetics, Inc.",
      "address_1": "128 Gamma Dr",
      "address_2": "N/A",
      "postal_code": "15238-2920",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Distributed USA (nationwide) and the country of Canada.",
      "recall_number": "Z-0966-2014",
      "product_description": "Normative Data Template CD for use with the I-Portal devices.    Used to measure, record, or visually display the involuntary movements (nystagmus) of the eyeball.",
      "product_quantity": "148",
      "reason_for_recall": "The data provided on the Normative Data Template CD for use with the I-Portal devices has not received clearance by FDA through the premarket 510(k) notification process.",
      "recall_initiation_date": "20131121",
      "center_classification_date": "20140210",
      "termination_date": "20150720",
      "report_date": "20140219",
      "code_info": "Software versions affected: 6.7.004, 6.8. 6.9, 6.10, 7.0, 7.0.1, and 7.1"
    }
  ]
}