{
  "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 I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87014",
      "recalling_firm": "Boston Scientific Corporation",
      "address_1": "4100 Hamline Ave N Bldg 3",
      "address_2": "N/A",
      "postal_code": "55112-5700",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution including US and US territories, Canada, Latin America, Europe, Middle East, Africa, and Asia-Pacific region",
      "recall_number": "Z-0879-2021",
      "product_description": "EMBLEM S-ICD Subcutaneous Electrode Model 3501.  Component of implantable cardioverter defibrillator (ICD)",
      "product_quantity": "47000 units",
      "reason_for_recall": "There is potential for fractures which results in the inability to delivery therapy.",
      "recall_initiation_date": "20201113",
      "center_classification_date": "20210119",
      "termination_date": "20240723",
      "report_date": "20210127",
      "code_info": "All serialized EMBLEM Subcutaneous Electrodes Model 3501 manufactured and distributed are subject to this worldwide advisory communication.",
      "more_code_info": ""
    }
  ]
}