{
  "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.  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.  Medt",
      "address_2": "",
      "product_quantity": "",
      "code_info": "G13A00130  G13A01300  GT414  GU543  GV117  GV118  GV121  GV381  GV382  GV919  GW768  Additional Lots Identified:   GV143   GV926   GV927   G13A00133  G13A00134  G13A01167   G13A01912  G13A00136  G13A00137  G13A01938",
      "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": "ProVia¿ CROSSING GUIDEWIRE; Models:  15PROV300HS, 3PROV180HS, 3PROV180SS, 3PROV300HS, 3PROV300SS, 9PROV180HS, 9PROV180SS    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-0264-2014",
      "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"
    }
  ]
}