{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "32321",
      "product_res_number": "Z-0794-04",
      "event_date_initiated": "2004-03-11",
      "event_date_posted": "2004-07-20",
      "recall_status": "Terminated",
      "event_date_terminated": "2005-10-31",
      "res_event_number": "28498",
      "product_code": "DQR",
      "k_numbers": [
        "K021284",
        "K021455"
      ],
      "product_description": "Guidant EasyTrak 8 French Guiding Catheter, Inner Diameter .087'', 2.21 mm, Overall Length 49 cm, Coronary Sinus - Hook Tip Shape, CS-H, REF 6754",
      "code_info": "Lots 4012051, 4020551, 4020551, 4021151, 4022151, 4022151, and 4022551",
      "firm_fei_number": "2124215",
      "recalling_firm": "Guidant Corp-Cpi Division",
      "address_1": "4100 Hamline Ave N",
      "city": "Saint Paul",
      "state": "MN",
      "postal_code": "55112-5700",
      "additional_info_contact": "Steven C. Roth\n651-582-4260",
      "reason_for_recall": "The terminal hub component in a some of the catheters has an unintended abrupt transition  between the entry port and the catheter lumen which  can result in difficulty introducing or removing delivery system components during lead placement.",
      "root_cause_description": "Other",
      "action": "Starting on March 11, 2003, the firm''s representatives visited consignees, to whom the recalled catheters  had been consigned, and retrieved the catheters.",
      "product_quantity": "150 catheters",
      "distribution_pattern": "Nationwide in the United States.",
      "openfda": {
        "k_number": [
          "K960098",
          "K882977",
          "K902674",
          "K894784",
          "K780079",
          "K884628",
          "K073559",
          "K880776",
          "K873012",
          "K872983",
          "K870825",
          "K881884",
          "K884478",
          "K870826",
          "K803002",
          "K880771",
          "K874618",
          "K894243",
          "K884375",
          "K770512",
          "K030398",
          "K813144",
          "K131446",
          "K820102",
          "K051655"
        ],
        "registration_number": [
          "9680841",
          "8020785",
          "1000523114",
          "3018940143",
          "3003418325",
          "9710524",
          "3005334138",
          "1417485",
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          "3011237770",
          "3003944071",
          "3005809810",
          "3002807264",
          "1319211",
          "3009291251",
          "3031571797"
        ],
        "device_name": "Cannula, Catheter",
        "medical_specialty_description": "Cardiovascular",
        "regulation_number": "870.1300",
        "device_class": "2"
      }
    }
  ]
}