{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Irvine",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72165",
      "recalling_firm": "Micro Therapeutics Inc, Dba Ev3 Neurovascular",
      "address_1": "9775 Toledo Way",
      "address_2": "N/A",
      "postal_code": "92618-1811",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distributions to states of: TN, KY, VA, WI, MO, IL, UT, OR, and MD.     No foreign consignees.",
      "recall_number": "Z-0120-2016",
      "product_description": "-Pipeline Embolization Device  -Pipeline Flex Embolization Device    The Pipeline and Pipeline Flex Embolization Devices consist of a permanent implant combined with a guidewire based delivery system.  The Pipeline and Pipeline Flex embolization device implant is a braided, multi-alloy, mesh cylinder woven from platinum/tungsten and cobalt-chromium-nickel alloy wires.    The Pipeline and Pipeline Flex Embolization Devices are indicated for the endovascular treatment of adults (22 years of age or older) with large or giant wide-necked intracranial aneurysms (IAs) in the internal carotid artery from the petrous to the superior hypophyseal segments.",
      "product_quantity": "23 devices",
      "reason_for_recall": "The firm is recalling Pipeline and Pipeline Flex Embolization Devices from U.S. since the devices were shipped with an EU version of the Instructions for Use.",
      "recall_initiation_date": "20150904",
      "center_classification_date": "20151014",
      "termination_date": "20170518",
      "report_date": "20151021",
      "code_info": "Pipeline  Model Number Lot Number  FA-77250-16V06 9724629  FA-77350-16V10 A024276  FA-77350-16V12 A012865  FA-77350-18Vl0 A013596  FA-77350-20V12 A012039  FA-77375-14V12 A013029  FA-77375-16Vl2 A011629  FA-77375-16Vl2 A029223  FA-77375-16Vl2 A031361  FA-77375-18V10 A024213  FA-77375-20Vl2 A029315  FA-77400-14V12 A012885  FA-77425-18V12 A026942  FA-77450-14V12 A013028  FA-77475-20Vl2 A012383  FA-77500-16Vl2 A029316      Pipeline Flex  Model Number Lot Number  PED-400-20VO1 9977371  PED-475-20V01 A047151  PED-375-18V01 9971250"
    }
  ]
}