{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Danvers",
      "address_1": "35-37A Cherry Hill Drive",
      "reason_for_recall": "Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach from Guidewire.",
      "address_2": "",
      "product_quantity": "58",
      "code_info": "G13A00117  G13A00735  G13A00792  G13A00794  G13A01324  GV259  GV261  GV276  GV287  GV847  GV848  GV849  GV851  GV852  GW690  GW758  GU141  GU959",
      "center_classification_date": "20131115",
      "distribution_pattern": "Worldwide distribution: US (Nationwide) including states of: AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, and WV; and countries of: Albania, Algeria, Argentina, Australia, Austria, Belgium, Brazil, Canada, Chile, China, Colombia, Croatia, Czech Republic, Denmark, Ecuador, Egypt, Finland, France, Georgia, Germany, Greece, Guyana, Honduras, Hong Kong,Hungary, Iceland, India, Ireland, Israel, Italy, Japan, Jordan, Kuwait, Lebanon, Libya, Luxembourg, Malaysia, Mexico, Montenegro, Nepal, Netherlands, New Zealand, Nepal, Nicaragua, Norway, Oman, Poland, Portugal Puerto Rico, Qatar, Russian Federation, Saudi Arabia, Serbia, Singapore, Slovakia, South Africa, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, United Kingdom, Uruguay, and Yemen.",
      "state": "MA",
      "product_description": "THUNDER¿  Extra Support Guidewire; Models: THNDR190J, THNDR190S, THNDR300J, THNDR300S    Medtronic guide wires are steerable guide wires that are used for the introduction and placement of diagnostics or interventional devices in the coronary and peripheral vasculature, and may be used to reach and cross a target lesion. Medtronic guide wires are not intended for cerebral vasculature. Medtronic steerable exchange guide wires are used to facilitate the substitution of one diagnostic or interventional device for another.",
      "report_date": "20131127",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "Medtronic Vascular",
      "recall_number": "Z-0263-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "66567",
      "termination_date": "20141215",
      "more_code_info": "",
      "recall_initiation_date": "20131021",
      "postal_code": "01923-2565",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}