{
  "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": [
    {
      "status": "Terminated",
      "city": "Lindon",
      "state": "UT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "74273",
      "recalling_firm": "ZYTO Technologies, Inc.",
      "address_1": "387 S 520 W Ste 200",
      "address_2": "N/A",
      "postal_code": "84042-1961",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Nationwide. Canadian and other foreign consignees. No VA/govt/military.",
      "recall_number": "Z-2121-2016",
      "product_description": "The ZYTO Select and ZYTO Elite software programs are used to rank pairs of galvanic skin response measurements from most coherent (the second scan is closest in time measurement to the baseline original scan) to least coherent (further away from the baseline).",
      "product_quantity": "1252 total",
      "reason_for_recall": "ZYTO Technologies Inc. Announces a Voluntary Recall of the ZYTO Tower and ZYTO Select and Elite Software Due to Claims Exceeding the 510(k) Clearance.",
      "recall_initiation_date": "20151123",
      "center_classification_date": "20160701",
      "termination_date": "20171221",
      "report_date": "20160713",
      "code_info": "Not Applicable."
    }
  ]
}