{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Rancho Cordova",
      "address_1": "2870 Kilgore Rd",
      "reason_for_recall": "The incorrect resistor has been used in affected CORE M2 Imaging Systems, which causes noise and results in an overly bright IVUS Image.",
      "address_2": "",
      "product_quantity": "8 devices",
      "code_info": "Serial #: 126620101597, 126620101599, 126620101600, 126620100718, 126620102313, 126620102315, 126620102307, and 126620093077.",
      "center_classification_date": "20180517",
      "distribution_pattern": "Worldwide Distribution -- U.S., to the states of California, Connecticut, Tennessee, North Carolina, Maryland, and Oregon; and, the country of Australia.",
      "state": "CA",
      "product_description": "Philips Volcano CORE M2 Vascular System, Part # 400-0100.17, Rx Only.    Used for the qualitative and quantitative evaluation of vascular morphology in the coronary arteries and vessels of the peripheral vasculature.",
      "report_date": "20180523",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Volcano Corporation",
      "recall_number": "Z-1891-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "79715",
      "termination_date": "20210428",
      "more_code_info": "",
      "recall_initiation_date": "20180322",
      "postal_code": "95670-6133",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}