{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Plymouth",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "69965",
      "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": "International Only Distribution -- RUSSIA, ROMANIA, UNITED KINGDOM, GERMANY, ITALY, SPAIN, FRANCE, TURKEY, POLAND, and JAPAN.",
      "recall_number": "Z-0878-2015",
      "product_description": "ev3 Protege Rx Tapered Carotid Stent System, SECX-10-7-40-135, Sterile EO,  Rx only.    Indicated for the treatment of patients at high risk for adverse events from carotid endarterectomy who require percutaneous carotid revascularization and meet outlined criteria.",
      "product_quantity": "14",
      "reason_for_recall": "Two production lots of the Protege Rx Tapered Carotid Stent Systems (SECX-10-7-40-135, Lot # 9922452 & SEPX-8-6-40-135, Lot # 9922795) because of a product labeling error.",
      "recall_initiation_date": "20141204",
      "center_classification_date": "20141229",
      "termination_date": "20150717",
      "report_date": "20150107",
      "code_info": "Lot # 9922452"
    }
  ]
}