{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Ithaca",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79750",
      "recalling_firm": "Transonic Systems Inc",
      "address_1": "34 Dutch Mill Rd",
      "address_2": "N/A",
      "postal_code": "14850-9785",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) Distribution and to the states of :  NJ, NY, OH, PA, and TX., and to the countries of : Canada, South Korea, Thailand, Australia and Taiwan.",
      "recall_number": "Z-1776-2018",
      "product_description": "Transonic ADT1018 Flow QC Clear Advantage Tubing, Catalog No. ADT1018, ADT1018-40    The device is indicated for use as part of an extracorporeal blood circuit for hemodialysis when a monitor will be used to make access flow, recirculation, and/or cardiac output measurements during the patient s hemodialysis treatment.",
      "product_quantity": "6044",
      "reason_for_recall": "The sterility of the device cannot be assured. There is a potential for an increased risk of infection.",
      "recall_initiation_date": "20180215",
      "center_classification_date": "20180509",
      "termination_date": "20190430",
      "report_date": "20180516",
      "code_info": "Lots B151130E2 and B161115E0"
    }
  ]
}