{
  "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": "2026-08-27",
    "results": {
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      "product_res_number": "Z-0664-03",
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      "recall_status": "Terminated",
      "event_date_terminated": "2003-06-06",
      "res_event_number": "25714",
      "product_code": "DTR",
      "product_description": "Sarns MP4 Cardioplegia Sets; catalog number 15501.",
      "code_info": "Lot 322125",
      "firm_fei_number": "1828100",
      "recalling_firm": "Terumo Cardiovascular Systems Corp",
      "address_1": "6200 Jackson Rd.",
      "city": "Ann Arbor",
      "state": "MI",
      "postal_code": "48103",
      "additional_info_contact": "800-521-2818",
      "reason_for_recall": "There is a potential for delivery of a lower than intended amount of cardioplegia solution to the heart during surgery.",
      "root_cause_description": "Other",
      "action": "Initial customers were notified by telephone beginning on February 25, 2003.  A follow-up recall letter dated February 27, 2003 was sent to each customer.  Wholesalers were requested to either contact their customers or to provide their customer information to Terumo so that Terumo could notify the customers.",
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