{
  "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": [
    {
      "country": "United States",
      "city": "Houston",
      "address_1": "100 Cyberonics Blvd",
      "reason_for_recall": "The recalled product was distributed with an incorrect serial number printed on the device's label.",
      "address_2": "",
      "product_quantity": "1 unit",
      "code_info": "Serial Number: 31309; UDI: (01)05425025750054(11)140917(17)160808(21)31309(99)10-0009-5705.",
      "center_classification_date": "20141223",
      "distribution_pattern": "Distributed to PA.",
      "state": "TX",
      "product_description": "Cyberonics VNS Therapy AspireHC, Model 105 Generator. The Cyberonics VNS Therapy System consists of the implantable VNS Therapy Generator, the VNS Therapy Lead, and the external programming system used to change the stimulation settings.    Indicated for use as an adjunctive therapy in reducing the frequency of seizures.",
      "report_date": "20141231",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Cyberonics, Inc",
      "recall_number": "Z-0858-2015",
      "initial_firm_notification": "Visit",
      "product_type": "Devices",
      "event_id": "69844",
      "termination_date": "20160208",
      "more_code_info": "",
      "recall_initiation_date": "20141120",
      "postal_code": "77058-2069",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}