{
  "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": "Santa Rosa",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "78127",
      "recalling_firm": "Medtronic Vascular, Inc.",
      "address_1": "3576 Unocal Pl",
      "address_2": "N/A",
      "postal_code": "95403-1774",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to the states of : AZ, CA, FL, GA, MA, MI, MN and NH.",
      "recall_number": "Z-3227-2017",
      "product_description": "Medtronic Aptus Heli-FX Thoracic EndoAnchor System Heli-FX Guide 42 mm, REF HG-18-90-42, STERILE EO, Rx Only     The Heli-FX EndoAnchor System is intended to provide fixation and sealing between endovascular aortic grafts and the native artery. The Heli-FX System is indicated for use in patients who endovascular grafts have exhibited migration or endoleak, or are at risk for such complications, in whom augmented radial fixation and or sealing is required or regain or maintain adequate aneurysm exclusion.",
      "product_quantity": "20 units",
      "reason_for_recall": "It was determined that the deflection length indicated on the Guide catheter handle does not match the label on the box and sterile packaging for two lots.",
      "recall_initiation_date": "20170913",
      "center_classification_date": "20170927",
      "termination_date": "20200518",
      "report_date": "20171004",
      "code_info": "UDI 00763000006679, Lot Number 0008674156  UDI 00763000006655, Lot Number 0008674157"
    }
  ]
}