{
  "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": [
    {
      "status": "Terminated",
      "city": "Marlborough",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "65317",
      "recalling_firm": "Boston Scientific Corporation",
      "address_1": "100 Boston Scientific Way",
      "address_2": "N/A",
      "postal_code": "01752-1234",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution: USA (nationwide) including states of:  NJ, NY, OH, IL, MI, MD, MA and countries of: Denmark, Great Britain, and Spain.",
      "recall_number": "Z-1672-2013",
      "product_description": "NephroMax high Pressure Nephrostomy Balloon Catheter. Material Number/Catalog Number: M0062101400/210-140, M062101440/210144    Dilation of the nephrostomy tract.",
      "product_quantity": "27",
      "reason_for_recall": "Incorrect sized renal sheath was packaged with the NephroMax high pressure nephrostomy Balloon Catheter.",
      "recall_initiation_date": "20130528",
      "center_classification_date": "20130709",
      "termination_date": "20140123",
      "report_date": "20130717",
      "code_info": "Lot Number: 15875861, 15875860, 15875299, 15872797, 15872799, 15872798"
    }
  ]
}