{
  "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": "Saint Paul",
      "address_1": "8200 Coral Sea St NE",
      "reason_for_recall": "Medtronic has identified an issue with a specific lot of the Archer 0.035 inch (0.89mm) Super Stiff Guidewire, model ARCSJ200W, where the PTFE (Teflon) coating has the potential to separate from the wire during in-vivo use.",
      "address_2": "",
      "product_quantity": "225 units",
      "code_info": "Lot number GFWA0387",
      "center_classification_date": "20130328",
      "distribution_pattern": "Worldwide Distribution-USA including the states of FL, OH, and MN and the countries of Belgium, France Germany, Netherlands, Turkey, and United Kingdom.",
      "state": "MN",
      "product_description": "Medtronic Archer Super Stiff Guidewire 0.035 inch (0.89mm), Model ARCSJ200W.    Intended to facilitate catheter placement and exchange during procedures in the aorta.",
      "report_date": "20130403",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Medtronic Inc. Cardiac Rhythm Disease Management",
      "recall_number": "Z-1017-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "64620",
      "termination_date": "20131121",
      "more_code_info": "",
      "recall_initiation_date": "20130313",
      "postal_code": "55112-4391",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}