{
  "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
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  },
  "results": [
    {
      "cfres_id": "26525",
      "product_res_number": "Z-0743-03",
      "event_date_initiated": "2003-03-20",
      "event_date_posted": "2003-04-18",
      "recall_status": "Terminated",
      "event_date_terminated": "2021-05-12",
      "res_event_number": "25817",
      "k_numbers": [
        "K002902"
      ],
      "product_description": "Tandem-Cath Hemodialysis Cuffed Catheter with side holes\n10 Fr 23 cm Arterial Cuff/26cm Venous Cuff\nCode #: 8888-223266",
      "code_info": "All lots",
      "recalling_firm": "Tyco Healthcare/Kendall",
      "address_1": "15 Hampshire Street",
      "city": "Mansfield",
      "state": "MA",
      "postal_code": "02048",
      "additional_info_contact": "David  A. Olson\n508-261-8530",
      "reason_for_recall": "Tandem Hemodialysis Catheter may have splits in the catheter shaft  below the extension adapter",
      "root_cause_description": "Other",
      "action": "The firm notified accounts  by letter on 3/20/03 by overnight mail delivery. Users are requested to examine, remove and return product.",
      "product_quantity": "254",
      "distribution_pattern": "Nationwide\nInternational: Canada, Chile, Singapore. Belgium",
      "openfda": {}
    }
  ]
}