{
  "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": "Saint Paul",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "69512",
      "recalling_firm": "St Jude Medical",
      "address_1": "1 Saint Jude Medical Dr",
      "address_2": "N/A",
      "postal_code": "55117-1789",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution including the states of CA, GA, NJ, NY, OR and PA.",
      "recall_number": "Z-0177-2015",
      "product_description": "St. Jude Medical, Fixed Curve Response 6F Electrophysiology Catheter, CSL, Model 401353",
      "product_quantity": "26",
      "reason_for_recall": "St. Jude Medical is performing a voluntary recall of batch 4671318, model number 401353 of the Response Fixed Curve DECA 6F 65cm CSL 2/8 Catheter. Specifically, the firm has identified that every device packaged within batch 4671318 contains the incorrect catheter (Supreme FC QUAD 5F catheter) within the packaging.  To date, no serious injuries have occurred as a result of this issue",
      "recall_initiation_date": "20141014",
      "center_classification_date": "20141106",
      "termination_date": "20141210",
      "report_date": "20141112",
      "code_info": "Batch # 4671318"
    }
  ]
}