{
  "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": "Ashland",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80283",
      "recalling_firm": "Terumo Cardiovascular Systems Corp",
      "address_1": "28 Howe St",
      "address_2": "N/A",
      "postal_code": "01721-1305",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "US state of FL",
      "recall_number": "Z-2550-2018",
      "product_description": "Tubing Pack Convenience Kit, Product Code 65217    Product Usage:  Intended for use only in the extracorporeal circuit of the cardiopulmonary bypass procedures for which the user designed it.",
      "product_quantity": "30 cases/2 units (Total 60 units)",
      "reason_for_recall": "Kit was labeled with the incorrect Expiration Date of April 30, 2019.",
      "recall_initiation_date": "20170512",
      "center_classification_date": "20180726",
      "termination_date": "20181026",
      "report_date": "20180801",
      "code_info": "Lot Number: VE17"
    }
  ]
}