{
  "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": "31777",
      "product_res_number": "Z-0593-04",
      "event_date_initiated": "2004-01-27",
      "event_date_posted": "2004-07-20",
      "recall_status": "Terminated",
      "event_date_terminated": "2005-10-31",
      "res_event_number": "28254",
      "product_code": "NFN",
      "k_numbers": [
        "K021363"
      ],
      "product_description": "Floppy Cronus Endovascular Guidewire, Length 180 cm (partial coat), Diameter 0.014 inch, Part Number 001-001232-3",
      "code_info": "Lots 0305-4024, 0305-4025, 0305-4026, 0306-4027,  0307-4028, 0307-4030, 0307-4031, and 0307-4050",
      "firm_fei_number": "3003084417",
      "recalling_firm": "Stereotaxis Inc",
      "address_1": "4041 Forest Park Ave",
      "city": "Saint Louis",
      "state": "MO",
      "postal_code": "63108-3213",
      "additional_info_contact": "Robert W. Calllahan\n314-615-6923",
      "reason_for_recall": "The magnet at the end of the guidewire could break off.",
      "root_cause_description": "Other",
      "action": "Consignees were sent a notice dated January 27, 2004.  The notice requested that consignees stop using the product and stated that a firm representative would contact the consignees.  The firm''s representatives have retrieved all of the product at the consignees.",
      "product_quantity": "72 guidewires",
      "distribution_pattern": "The product was shipped to consignees in Iowa, Massachusetts, Missouri, Oklahoma, and Texas in the United States and to consignees in Germany and The Netherlands.",
      "openfda": {}
    }
  ]
}