{
  "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": "2026-04-22",
    "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": "58185",
      "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": "Letter",
      "distribution_pattern": "Worldwide Distribution: US (nationwide) and the countries of  Canada, Brazil, Hong Kong, Korea, and Thailand.",
      "recall_number": "Z-0158-2015",
      "product_description": "Terumo  Cardioplegia Delivery Set-               Item Number: 16130    Product Usage:  The Cardioplegia Delivery Sets are indicated for delivery of cardioplegic solutions to the heart during cardiopulmonary bypass surgery.",
      "product_quantity": "777 units",
      "reason_for_recall": "Defect in the luer connector can compromise the seal on the female side of the connector. and the compromised seal can introduce air in the table line",
      "recall_initiation_date": "20110301",
      "center_classification_date": "20141031",
      "termination_date": "20141106",
      "report_date": "20141112",
      "code_info": "Lot Numbers:  MN08,  MNI5,  MM11,  MM18,  MM25.    Manufacturing dates October 1I, 2010 through Novemberl5, 20 I 0."
    }
  ]
}