{
  "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": "Houston",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72698",
      "recalling_firm": "Cyberonics, Inc",
      "address_1": "100 Cyberonics Blvd",
      "address_2": "N/A",
      "postal_code": "77058-2069",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distributions to the states of : IL, NC, KS, and TX., and Internationally to the country of: United Kingdom.",
      "recall_number": "Z-0645-2016",
      "product_description": "Cyberonics Vagus Nerve Stimulator VNS Therapy AspireSR Generator,  Model 106",
      "product_quantity": "29 units",
      "reason_for_recall": "Certain Model 106 Pulse Generators demonstrate delays in sensing during use of the 'Verify Heartbeat Detection' feature and exhibit the potential for decreased battery longevity.",
      "recall_initiation_date": "20151118",
      "center_classification_date": "20160119",
      "termination_date": "20170906",
      "report_date": "20160127",
      "code_info": "Serial numbers 36602, 37019, 39097, 40311, 40465",
      "more_code_info": ""
    }
  ]
}