{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Saint Paul",
      "state": "MN",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "63855",
      "recalling_firm": "St Jude Medical Inc",
      "address_1": "177 E County Road B",
      "address_2": "N/A",
      "postal_code": "55117-1951",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution only including the states of FL, KY and OK.",
      "recall_number": "Z-0617-2013",
      "product_description": "Fast-Cath Transseptal Guiding Introducer, 90, 8F, REF 406586, Length 60 cm, Sterile EO, Rx only, St. Jude Medical, 14901 DeVeau Place, Minnetonka, MN 55343    Indicated for introducing various cardiovascular catheters into the left side of the heart through the interatrial septum.",
      "product_quantity": "26",
      "reason_for_recall": "St. Jude Medical is recalling a single batch of Fast Cath Transseptal Guiding Introducers which was packaged as a 180 degree curve style introducer instead of a 90 degree curve style introducer as indicated on the labeling.",
      "recall_initiation_date": "20120328",
      "center_classification_date": "20121228",
      "termination_date": "20130712",
      "report_date": "20130109",
      "code_info": "Model no. 406586  Batch no. 3619533"
    }
  ]
}