{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Saint Paul",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90985",
      "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": "Worldwide distribution - US Nationwide distribution in the countries of AL, AR, CA, CO, DE, GA, IL, IA, MA, MI, MN, NV, NJ, NY, OH, PA, TN, TX, and VA.  The countries of Canada, France, Germany, Latvia, Netherlands, Poland, Sweden, Switzerland, and United Kingdom.",
      "recall_number": "Z-0151-2023",
      "product_description": "EMBLEM S-ICD, Subcutaneous Implantable Defibrillators, Model A209, sterile.",
      "product_quantity": "7 devices",
      "reason_for_recall": "There is an incorrect manufacturing date/timestamp within the software which causes an inaccurate display of battery capacity.",
      "recall_initiation_date": "20220930",
      "center_classification_date": "20221031",
      "report_date": "20221109",
      "code_info": "UPN:  00802526548406; Serial numbers 169276, 169509, 169645, 169774, 169876, 169671, 169297."
    }
  ]
}