{
  "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": "Miami Lakes",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "64273",
      "recalling_firm": "Cordis Corporation",
      "address_1": "14201 Nw 60th Ave",
      "address_2": "N/A",
      "postal_code": "33014-2802",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Worldwide distribution:  US states: AZ, FL, IL, LA, MA, NJ, OR, SC, and TX.  Armenia, Austria, Belgium, Colombia, Czech Republic, France, Hungary, Iran, Israel, India, Italy, Kuwait, Latvia, Lebanon, Luxembourg, Mexico, Morocco, Poland, Portugal, Russia, Saudi Arabia, South Africa, Spain, Switzerland, and United Arab Emirates.",
      "recall_number": "Z-1784-2014",
      "product_description": "Cordis EMPIRA RX PTCA Dilatation Catheter Catalog # 85R30300S  For cardiovascular use.",
      "product_quantity": "80 units",
      "reason_for_recall": "Dilatation catheters could exhibit radial versus axial tears should they burst during inflation.",
      "recall_initiation_date": "20130205",
      "center_classification_date": "20140611",
      "termination_date": "20140623",
      "report_date": "20140618",
      "code_info": "Catalog # 85R30300S LOT # CE0001447 exp date: 2014-08"
    }
  ]
}