{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Danvers",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79591",
      "recalling_firm": "Medtronic Vascular",
      "address_1": "35-37A Cherry Hill Drive",
      "address_2": "N/A",
      "postal_code": "01923-2565",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US and AUSTRIA, Canada, Germany, ROMANIA, SLOVENIA,",
      "recall_number": "Z-1479-2018",
      "product_description": "Medtronic DxTerity Diagnostic Catheter, JL 4.0, REF DXT5JL40, marked with 6F color code on box.",
      "product_quantity": "855 units",
      "reason_for_recall": "The color coded French size indicator on the outer box may incorrectly reflect a 6 French size, rather than the correct 5 French size. The catheters inside the carton are the correct DXT5JL40 item, the inner pouch has correct 5F labeling, information and configuration details.",
      "recall_initiation_date": "20180313",
      "center_classification_date": "20180420",
      "termination_date": "20210507",
      "report_date": "20180502",
      "code_info": "UDI 20643169689309, Lot Number 60074805"
    }
  ]
}