{
  "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": "2026-08-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
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  },
  "results": [
    {
      "cfres_id": "141995",
      "product_res_number": "Z-0645-2016",
      "event_date_initiated": "2015-11-18",
      "event_date_posted": "2016-01-13",
      "recall_status": "Terminated",
      "event_date_terminated": "2017-09-06",
      "res_event_number": "72698",
      "product_code": "LYJ",
      "pma_numbers": [
        "P970003"
      ],
      "product_description": "Cyberonics Vagus Nerve Stimulator VNS Therapy AspireSR Generator,  Model 106",
      "code_info": "Serial numbers 36602, 37019, 39097, 40311, 40465",
      "firm_fei_number": "1000117004",
      "recalling_firm": "Cyberonics, Inc",
      "address_1": "100 Cyberonics Blvd",
      "city": "Houston",
      "state": "TX",
      "postal_code": "77058-2069",
      "additional_info_contact": "Clinical Technical Supprt\n866-882-8804",
      "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.",
      "root_cause_description": "Manufacturing material removal",
      "action": "Cyberonics sent out written recall notification beginning October 14, 2015, to all affected customers.  The letter identified the product, the problem, and the action to be taken by the customer.  For further questions, please call 866-882-8804",
      "product_quantity": "29 units",
      "distribution_pattern": "US Distributions to the states of : IL, NC, KS, and TX., and Internationally to the country of: United Kingdom.",
      "openfda": {
        "pma_number": [
          "P970003"
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        "device_name": "Stimulator, Autonomic Nerve, Implanted For Epilepsy",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "3",
        "registration_number": [
          "1644487"
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        "fei_number": [
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}