{
  "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": "26599",
      "product_res_number": "Z-0800-03",
      "event_date_initiated": "2003-03-17",
      "event_date_posted": "2003-05-09",
      "recall_status": "Terminated",
      "event_date_terminated": "2008-02-19",
      "res_event_number": "25847",
      "k_numbers": [
        "K981198"
      ],
      "product_description": "Z2 Guiding Catheter 6 F JR3.5 SH\nItem No. : Z26JR35SH",
      "code_info": "Lot Number: 122596",
      "firm_fei_number": "1220452",
      "recalling_firm": "Medtronic, Inc.",
      "address_1": "35-37A Cherry Hill Drive",
      "city": "Danvers",
      "state": "MA",
      "postal_code": "01923-2565",
      "additional_info_contact": "Fred L. Boucher, R.A.C.\n978-739-3116",
      "reason_for_recall": "The PTCA catheter is mislabeled:  the curve style (Judkin Left vs. Judkin Right ) of the catheter may not correctly match the box label.",
      "root_cause_description": "Other",
      "action": "Medtronic AVE notified the firm''s sales representatives on 3/17/03 by e-mail to retrieve affected product from the hospital and return it Danvers, MA.  Each sales rep. is required to document the notification and accounting for the devices returned from the field.",
      "distribution_pattern": "AL, AR, KY, LA, MT, NH, NY, PA, WI\nForeign: Japan, Hungary",
      "openfda": {}
    }
  ]
}