{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Danvers",
      "address_1": "35-37A Cherry Hill Drive",
      "reason_for_recall": "Medtronic has determined that the French size indicator on the inner pouch may incorrectly reflect a 6 French size, rather than the correct 5 French size. The catheters inside the pouch are the correct U5TRAN35 item, the outer carton has all the correct labeling, and all the other information and configuration details on both the carton and the pouch are correct.",
      "address_2": "",
      "product_quantity": "250 units",
      "code_info": "UDI/GTIN:  20643169738717  Lot Number 60068186",
      "center_classification_date": "20180926",
      "distribution_pattern": "CA, IA, NE, TN, TX, VA, WA, Jamaica, New Zealand, Thailand",
      "state": "MA",
      "product_description": "Medtronic DxTerity(TM) TRA 5F, Diagnostic Catheter, REF U5TRAN35",
      "report_date": "20181003",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Medtronic Vascular",
      "recall_number": "Z-3253-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "80919",
      "termination_date": "20210507",
      "more_code_info": "",
      "recall_initiation_date": "20180816",
      "postal_code": "01923-2565",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}