{
  "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": "Flagstaff",
      "state": "AZ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85434",
      "recalling_firm": "W L Gore & Associates, Inc.",
      "address_1": "1500 N 4th St",
      "address_2": "N/A",
      "postal_code": "86004-5866",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Visit",
      "distribution_pattern": "International the country of Japan.",
      "recall_number": "Z-2052-2020",
      "product_description": "Conformable Thoracic Stent Graft, Rx only, Sterile EO - Product Usage: This device is intended for endovascular repair of lesions of the descending thoracic aorta.",
      "product_quantity": "15 stents",
      "reason_for_recall": "The incorrect label was placed on both the primary and secondary package.",
      "recall_initiation_date": "20191217",
      "center_classification_date": "20200520",
      "termination_date": "20210428",
      "report_date": "20200527",
      "code_info": "Part number of the device is TGM343420J  Serial numbers:  21225065  21225066  21225067  21225068  21225069  21225070  21225071  21225072  21225073  21225074  21225075  21225076  21225077  21225078  21225079  21225080  21225081  21225082  21225083  21225084"
    }
  ]
}