{
  "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": "Irvine",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80831",
      "recalling_firm": "Micro Therapeutics Inc, Dba Ev3 Neurovascular",
      "address_1": "9775 Toledo Way",
      "address_2": "N/A",
      "postal_code": "92618-1811",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution to US states of KS, CA, FL, GA, AZ, MI, LA, TX, NE, KY, and China",
      "recall_number": "Z-3022-2018",
      "product_description": "ev3 TurboHawk PERPHERAL PLAQUE EXCISION SYSTEM FOR SURGICAL USE, LARGE VESSEL XTENDED TIP FOR CALCIUM, Model THS-LX-C  for peripheral vascular use.",
      "product_quantity": "67 units",
      "reason_for_recall": "The Distal Flush Tool (DFT) accessories that were packaged in this lot number are not compatible with the TurboHawk LX-C catheter. This may result in the inability to remove excised material from the tip of the catheter.",
      "recall_initiation_date": "20180810",
      "center_classification_date": "20180911",
      "termination_date": "20200804",
      "report_date": "20180919",
      "code_info": "Lot Number A495368"
    }
  ]
}