{
  "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": "2026-04-01",
    "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": "88028",
      "recalling_firm": "Medtronic Vascular, Inc.",
      "address_1": "3850 Brickway Blvd",
      "address_2": "N/A",
      "postal_code": "95403-8223",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S. Nationwide distribution in the state of GA.    O.U.S.: None",
      "recall_number": "Z-1976-2021",
      "product_description": "Endurant II/IIs Stent Graft System: STENT GRAFT ETBF3216C145E ENDUR II BIF.  For treatment of vascular aneurysms.",
      "product_quantity": "3 devices",
      "reason_for_recall": "Incorrect stentstop assembly (18fr) was used to build the delivery system component of the device.  Correct stentstop assembly is 20fr.",
      "recall_initiation_date": "20210428",
      "center_classification_date": "20210628",
      "termination_date": "20240405",
      "report_date": "20210707",
      "code_info": "Model Number: ETBF3216C145E  GTIN: 00613994990983  Serial Numbers:  V30064787;  V30064789;  V30064790;"
    }
  ]
}