{
  "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": "Fremont",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "68373",
      "recalling_firm": "Boston Scientific Corporation",
      "address_1": "47215 Lakeview Blvd",
      "address_2": "N/A",
      "postal_code": "94538-6530",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution.",
      "recall_number": "Z-1798-2014",
      "product_description": "IntellaTip MiFi XP Temperature Ablation Catheter; 10m x 8F (2.67mm) Large Curve.    The BSC Controller and Accessories are indicated for use in conjunction with standard and high power catheters for cardiac ablation procedures.",
      "product_quantity": "968 units total all models",
      "reason_for_recall": "Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not manufactured according to specification.",
      "recall_initiation_date": "20140515",
      "center_classification_date": "20140616",
      "termination_date": "20150625",
      "report_date": "20140625",
      "code_info": "Catalog Number: PM4790K2;  Material Number: M004PM47900K2;  Serial numbers: 16739673, 16739674, 16739675, 16739676, 16739677, 16739678, 16739679, 16739860, 16872121, 16872935  Expiry Dates:  May 11, 2014 to January 13, 2017",
      "more_code_info": ""
    }
  ]
}