{
  "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": "Houston",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86776",
      "recalling_firm": "LivaNova USA 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": "International distribution in the countries of Austria and United Kingdom.",
      "recall_number": "Z-0535-2021",
      "product_description": "VNS Therapy SENTIVA DUO # 1000-D - Product Usage: indicated for the treatment of chronic or recurrent depression in patients who are experiencing a treatment-resistant or treatment- intolerant depressive episode.",
      "product_quantity": "8 generators",
      "reason_for_recall": "During internal testing, it was found that upon a device reset, the Generator exhibits the incorrect Model Number when interrogated.",
      "recall_initiation_date": "20201112",
      "center_classification_date": "20201204",
      "termination_date": "20230112",
      "report_date": "20201216",
      "code_info": "Model Number - Model 1000-D  Serial Numbers:  311298  310443  310068  310353  310531  310351  310380  310348"
    }
  ]
}