{
  "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": "Saint Paul",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "78323",
      "recalling_firm": "Boston Scientific Corporation",
      "address_1": "4100 Hamline Ave N",
      "address_2": "N/A",
      "postal_code": "55112-5700",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Visit",
      "distribution_pattern": "The devices were distributed to medical facilities located in MN and OH.  There was no foreign/government/military distribution.",
      "recall_number": "Z-0078-2018",
      "product_description": "RESONATE EL ICD DR, Model D433, Sterile.",
      "product_quantity": "12 devices",
      "reason_for_recall": "The devices have an incorrect firmware configuration.",
      "recall_initiation_date": "20171004",
      "center_classification_date": "20171108",
      "termination_date": "20191015",
      "report_date": "20171115",
      "code_info": "Serial numbers 530802, 531123, 531237, 531292, 531301, 531446, 531492, 531520, 531536, 531539, 531545, and 531767."
    }
  ]
}