{
  "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": "2026-08-27",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "25805",
      "product_res_number": "Z-0593-03",
      "event_date_initiated": "2002-11-21",
      "event_date_posted": "2003-02-28",
      "recall_status": "Terminated",
      "event_date_terminated": "2003-02-28",
      "res_event_number": "25424",
      "k_numbers": [
        "K000825"
      ],
      "product_description": "JOGRAPHY Cardiovascular Angiographic Catheter, 5F *** pigtail  *** tapered with perfusion ports *** MEDI-DYNE, INC., 604 Queensbury Ave., Queensbury, New York 12804 *** Single use, sterile, disposable intravascular catheters with an atraumatic tip.",
      "code_info": "Lot Number 41340",
      "firm_fei_number": "1000120334",
      "recalling_firm": "Jomed Catheters, Inc.",
      "address_1": "604 Queensbury Avenue",
      "city": "Queensbury",
      "state": "NY",
      "postal_code": "12804",
      "reason_for_recall": "6 Fr. catheters packaged and labeled as 5 Fr.",
      "root_cause_description": "Other",
      "action": "Consignees  notified via e-mail on 11/21/2002.  The consignees were instructed to contact their customers and return product to Jomed''sdistribution center in the Netherlands.",
      "product_quantity": "50 catheters",
      "distribution_pattern": "There was no U.S. distribution.  The product was distributed to three consignees in Germany, Hungary and Italy.",
      "openfda": {}
    }
  ]
}