{
  "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": [
    {
      "country": "United States",
      "city": "Miami Lakes",
      "address_1": "14201 Nw 60th Ave",
      "reason_for_recall": "Due to a labeling error related to the conversion of the inner diameter of the catheter from inches to millimeters.  The English dimension is correct and is the primary dimension.",
      "address_2": "",
      "product_quantity": "1238 units",
      "code_info": "Catalog           Lots   ----------------------------------  67200000       15918614  67200200       15892736  67200400       15892737, 15897416  67200500       15901314  67203400       15922021  67203600       15897418  67204000       15925687  67205200       15892738, 15892739  67205400       15885645, 15887472, 15897420  67205600       15901319  67206000       15897422  67207200       15892740  67208000       15892741  67208200       15887473, 15887474, 15897424  67208300       15901321  67212600       15916942  67213000       15916943  67227000       15901323",
      "center_classification_date": "20131001",
      "distribution_pattern": "Worldwide Distribution - USA Nationwide in the states of AZ, CA, FL, ID, LA, MA, MD, MI, MN, MO, NC, NH, NY, OH, OK, PA, SC, TX, VA, WI, and WV and the countries of: Austria, Belgium, Czech Republic, France, Germany, Greece,Hungary, Israel, Italy, Latvia, Netherlands, Poland, Portugal, Russian Federation, Slovenia, Spain, Sweden, Switzerland, United Arab, and United Kingdom",
      "state": "FL",
      "product_description": "Cordis ADROIT 6F Guiding Catheter    Product Usage:  For intravascular introduction of interventional and/or diagnostic devices into the coronary or peripheral vascular system.",
      "report_date": "20131009",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Cordis Corporation",
      "recall_number": "Z-0003-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "66026",
      "termination_date": "20140930",
      "more_code_info": "",
      "recall_initiation_date": "20130812",
      "postal_code": "33014-2802",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}