{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "27526",
      "product_res_number": "Z-0018-04",
      "event_date_initiated": "2001-10-19",
      "event_date_posted": "2003-10-15",
      "recall_status": "Terminated",
      "event_date_terminated": "2004-05-11",
      "res_event_number": "26334",
      "k_numbers": [
        "K003925"
      ],
      "product_description": "Product is  labeled as Cordis Pre-shaped Prowler Plus MP Infusion Catheter (3 F proximal OD, 2.3 F Distal OD, 45 cm distal length, total length 155 cm) with an MP (45 degree) dual marker band tip. Also the package states that it is distributed by Cordis Endovascular systems, Inc, Miami, FL 33102 a Johnson & Johnson Company.",
      "code_info": "Catalog No. 606-2511 FX UPN H7396062511FX3 Lot T0601010, expiration date 2004-05",
      "firm_fei_number": "1000222137",
      "recalling_firm": "Cordis Neurovascular, Inc.",
      "address_1": "14000 NW 57th Ct.",
      "city": "Miami Lakes",
      "state": "FL",
      "postal_code": "33014",
      "additional_info_contact": "Jacqueline Maestri\n800-898-9481",
      "reason_for_recall": "These catheters have  J-shape tips instead of the labeled MP (multipurpose) tips and also are packed into the incorrect tip tray.",
      "root_cause_description": "Other",
      "action": "The firm initiated a recall of the product shipped to Japan via an  e-mail notification on 8/20/2001 requesting return of the devices.  The firm mailed recall notification letters to accounts in the United States on 10/19/2001.  The firm considers the recall complete and effective and has accounted for all devices involved.",
      "product_quantity": "54",
      "distribution_pattern": "Product was distributed to 4 US hospital accounts and to one Distirbutor in Japan.",
      "openfda": {}
    }
  ]
}