{
  "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": "2026-08-13",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "cfres_id": "30166",
      "product_res_number": "Z-0102-04",
      "event_date_initiated": "2003-10-16",
      "event_date_posted": "2003-11-07",
      "recall_status": "Terminated",
      "event_date_terminated": "2005-07-07",
      "res_event_number": "27604",
      "product_code": "DTQ",
      "k_numbers": [
        "K022947"
      ],
      "product_description": "Terumo Advanced Perfusion System 1 Roller Pump; 4 inch diameter; Catalog number 801040.",
      "code_info": "Serial numbers 0001 through 0599.",
      "firm_fei_number": "1828100",
      "recalling_firm": "Terumo Cardiovascular Systems Corp",
      "address_1": "6200 Jackson Rd",
      "city": "Ann Arbor",
      "state": "MI",
      "postal_code": "48103-9586",
      "additional_info_contact": "800-521-2818",
      "reason_for_recall": "The roller pump tube clamp mechanism may fail to release , making it difficult to remove or insert the tubing, and thereby delaying perfusion.",
      "root_cause_description": "Other",
      "action": "Letters entitled Urgent Safety Alerts were sent to each customer on 10/16/03.  Customers were made away of the problem and advised to develop a protocol for action, in case the problem occurred in their facility.",
      "product_quantity": "285",
      "distribution_pattern": "United States, Belgium, Canada, Dubai, Egypt, Germany, Hong Kong, India, Indonesia, Japan, Malaysia, Singapore, South Korea.",
      "openfda": {
        "k_number": [
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          "K813034",
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          "K090006",
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          "K173834",
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        "registration_number": [
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          "3019807891",
          "3002807090",
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          "3010703925",
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        "fei_number": [
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          "3001589655",
          "3006003617",
          "1218444",
          "2916596",
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        "device_name": "Console, Heart-Lung Machine, Cardiopulmonary Bypass",
        "medical_specialty_description": "Cardiovascular",
        "regulation_number": "870.4220",
        "device_class": "2"
      }
    }
  ]
}