{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Plymouth",
      "state": "MN",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89470",
      "recalling_firm": "ev3 Inc.",
      "address_1": "4600 Nathan Ln N",
      "address_2": "N/A",
      "postal_code": "55442-2890",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of AZ, CA, FL, IA, IL, KS, LA, MI, MS, NC, NJ, NY, OR, SC, SD, TN, TX, and VA.",
      "recall_number": "Z-0694-2022",
      "product_description": "Medtronic TurboHawk Plus Directional Atherectomy System 6F, Multi-vessel, Catalog number THP-M. For use in peripheral vasculature.",
      "product_quantity": "441 devices",
      "reason_for_recall": "The device has similarities in design to another device that the firm recently issued a field correction on due to instances of tip detachment and embolization.",
      "recall_initiation_date": "20220204",
      "center_classification_date": "20220307",
      "termination_date": "20241002",
      "report_date": "20220316",
      "code_info": "GTIN 00763000402396"
    }
  ]
}