{
  "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": "Irvine",
      "state": "CA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "65248",
      "recalling_firm": "Endologix Inc",
      "address_1": "11 Studebaker",
      "address_2": "N/A",
      "postal_code": "92618-2013",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA Nationwide in the states of: NY, NH, IN, MI, FL and NJ and in the countries of: Europe and Latin America.",
      "recall_number": "Z-1436-2013",
      "product_description": "Brand Name: AFX\" Introducer System, Model Number S17-45.  Lot Numbers: 1079840, 1079843, 1079844, 1079845.    Product Usage:  The AFX Introducer System is intended for use to facilitate the introduction of catheters and other medical devices into the vasculature and to minimize blood loss associated with such introduction.",
      "product_quantity": "53",
      "reason_for_recall": "Endologix, Inc. initiated this voluntary recall of certain lots of Endologix, Inc. due to reports of dilator breakage during clinical procedures.",
      "recall_initiation_date": "20130513",
      "center_classification_date": "20130607",
      "termination_date": "20130819",
      "report_date": "20130619",
      "code_info": "Model Number S17-45.  Lot Numbers: 1079840, 1079843, 1079844, 1079845"
    }
  ]
}