{
  "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": "Rancho Cordova",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71881",
      "recalling_firm": "Volcano Corporation",
      "address_1": "2870 Kilgore Rd",
      "address_2": "N/A",
      "postal_code": "95670-6133",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US (nationwide) Canada, Europe, Saudi Arabia, Iran, Egypt, and Qatar.",
      "recall_number": "Z-2718-2015",
      "product_description": "Volcano Pioneer Plus Re-Entry Catheter;  Product Code PPLUS20, Catheter for Crossing Total Occlusions.    Cardiovascular: The Volcano Pioneer Plus Intravascular Ultrasound Re-Entry Catheter (Pioneer Plus) is intended to facilitate the placement and positioning of catheters within the peripheral vasculature.",
      "product_quantity": "5042 devices",
      "reason_for_recall": "Due to a manufacturing defect, there is the possibility that a small wire could extend through the catheter shaft of the Pioneer Plus intravascular Ultrasound Guided Re-Entry Catheters.",
      "recall_initiation_date": "20150722",
      "center_classification_date": "20150902",
      "termination_date": "20160428",
      "report_date": "20150909",
      "code_info": "Product Code PPLUS20; All lots"
    }
  ]
}