{
  "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": "Ann Arbor",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79624",
      "recalling_firm": "Terumo Cardiovascular Systems Corporation",
      "address_1": "6200 Jackson Rd",
      "address_2": "N/A",
      "postal_code": "48103-9586",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Worldwide Distribution -- USA, including the states of IL, KY, and MI; and, the country of Singapore.",
      "recall_number": "Z-1478-2018",
      "product_description": "Flowmeter Module (accessory to Terumo Advanced  Perfusion System 1).    Provides the interface between the flow sensor and the system.",
      "product_quantity": "7",
      "reason_for_recall": "Inaccurrate flow readings.  Depending on the degree of inaccuracy, this issue may not be easy for the user to detect during setup or use (for example, following a Flow Probe relocation or manipulation).",
      "recall_initiation_date": "20180119",
      "center_classification_date": "20180420",
      "termination_date": "20180718",
      "report_date": "20180502",
      "code_info": "Catalog # - 802018  Serial #: 01662, 01672, 01680, 01681,01682, 01683 , and 01687.  UDI: 00886799000687."
    }
  ]
}