{
  "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,
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  "results": [
    {
      "country": "United States",
      "city": "Rancho Cordova",
      "address_1": "2870 Kilgore Rd",
      "reason_for_recall": "Visions PV .035 Intravascular Ultrasound (IVUS) Catheters (catalog number 88901 adnd81234) due to the potential inability to pass the guidewire through the y-port of the catheter.",
      "address_2": "",
      "product_quantity": "6870 units",
      "code_info": "Batch Numbers:  0301438588  0301450806  0301457390  0301457394  0301461995  0301487960  0301457393  0301450808  0301435421  0301442654  0301446201  0301469590  0301469593  0301442649  0301446202  0301476726  0301480937  0301485800  0301465886  0301498206  0301420742  0301485801  0301441407  0301469591  0301465885  0301476727  0301450809  0301480927  0301453527  0301440822  0301450812  0301453524  0301461996  0301476725  0301480928  0301492147  0301422648  0301450811  0301461999  0301450810  0301430794  0301430795  0301446203  0301472637  0301430796  0301465887",
      "center_classification_date": "20190111",
      "distribution_pattern": "Worldwide Distribution",
      "state": "CA",
      "product_description": "Visions PV .035 Digital IVUS Catheter, Catalog Number/Part Number 88901/400-0200.173    Product Usage:  The Volcano PV .035 Digital IVUS Catheter is an over the wire imaging catheter with a digital ultrasound transducer on the distal tip. The transducer utilizes a 64-element cylindrical array that radiates acoustic energy into the surrounding tissue and detects the subsequent echoes. The information from the echoes is used to generate real-time images of the peripheral vessels. The devices are provided sterile and are single use disposable devices.",
      "report_date": "20190123",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Volcano Corporation",
      "recall_number": "Z-0726-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "81882",
      "termination_date": "20210430",
      "more_code_info": "",
      "recall_initiation_date": "20181017",
      "postal_code": "95670-6133",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}