{
  "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": "Irvine",
      "address_1": "35 Hammond",
      "reason_for_recall": "Endologix initiated a correction by updating reports for the cumulative clinical data and information on the Powerlink System and the AFX Endovascular AAA System (AFX System).",
      "address_2": "",
      "product_quantity": "40,967",
      "code_info": "The correction is not lot specific. It applies to AFX procedures conducted after June 2013",
      "center_classification_date": "20170118",
      "distribution_pattern": "Worldwide Distribution - US Distribution and to the countries of :  Austria, Belgium, Czech Republic, France, Germany, Greece, Ireland, Israel, Italy, Latvia, Luxembourg, Monaco, Netherlands, Poland, Portugal, Spain, Sweden, Switzerland, Turkey and United Kingdom.",
      "state": "CA",
      "product_description": "AFX Endovascular AAA System, Endoleak Type IIIA",
      "report_date": "20170125",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Endologix",
      "recall_number": "Z-1035-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "76075",
      "termination_date": "20170428",
      "more_code_info": "",
      "recall_initiation_date": "20161227",
      "postal_code": "92618-1607",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}