{
  "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": [
    {
      "country": "United States",
      "city": "Ithaca",
      "address_1": "34 Dutch Mill Rd",
      "reason_for_recall": "Customer unable to obtain measurements due to the device seeing no flow or irrelevant flow condition during dialysis procedures.  The user saw a zero or a very low flow value displayed on HD03 and/or no measurements produced in other modes (recirculation; access flow; or cardiac output).",
      "address_2": "Warren Road Business Park",
      "product_quantity": "Domestic: 21 units, Foreign: 10 units",
      "code_info": "Serial Numbers HD03A60004; HD03A81167; HD03A81225; HD03A81237; HD03A91338; HD03A91394; HD03A91406; HD03B01461; HD03B21782; HD03B21803; HD03A60020; HD03A71082; HD03A81207; HD03A91255; HD03A91316; HD03Bl1679; HD03B11684; HD03B11705; HD03B21812; HD03B31971; HD03A81240; HD03A71086; HD03B01459; HD03B01594; HD03B11667; HD03B42175; HD03B42160; HD03B42161; HD03A91258; HD03A70046; HD03B31901",
      "center_classification_date": "20150318",
      "distribution_pattern": "Worldwide Distribution - USA Nationwide and the countries of: Australia, Canada, and South Korea",
      "state": "NY",
      "product_description": "Transonic Hemodialysis Monitor, Model HD03 --       Product Usage:  The Hemodialysis Monitor is intended for use by trained medical personnel to measure delivered blood flow, vascular access recirculation, vascular access blood flow and cardiac output on patients receiving hemodialysis treatment.",
      "report_date": "20150325",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Transonic Systems Inc",
      "recall_number": "Z-1295-2015",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "70647",
      "termination_date": "20160531",
      "more_code_info": "",
      "recall_initiation_date": "20150217",
      "postal_code": "14850-9785",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}