{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Tustin",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "77880",
      "recalling_firm": "Microvention, Inc.",
      "address_1": "1311 Valencia Ave",
      "address_2": "N/A",
      "postal_code": "92780-6447",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution was made to medical facilities located in AZ, CA, CO, MA,  MI, MN, MO, NY, OH UT, VA, and WI.  There was no foreign/military/government distribution.",
      "recall_number": "Z-3103-2017",
      "product_description": "MicroVention Terumo Traxcess 7 Mini Guidewire with Hydrophilic Coating, Ref GW0721006M, 1 guidewire per package, sterile, RX.",
      "product_quantity": "34 units",
      "reason_for_recall": "There is a potential for the hydrophilic coating on the guidewire to delaminate from the guidewire.",
      "recall_initiation_date": "20170807",
      "center_classification_date": "20170901",
      "termination_date": "20181026",
      "report_date": "20170913",
      "code_info": "Lot numbers 17030521, 17032821, and 17041831"
    }
  ]
}