{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "35720",
      "product_res_number": "Z-0209-05",
      "event_date_initiated": "2003-08-12",
      "event_date_posted": "2004-11-18",
      "recall_status": "Terminated",
      "event_date_terminated": "2005-09-22",
      "res_event_number": "30352",
      "product_code": "DTQ",
      "k_numbers": [
        "K022947"
      ],
      "product_description": "Terumo Advanced Perfusion System 1; 220V -240V, 7A (circuit breaker), 50/60 Hz (10A power source required); Model 801764.",
      "code_info": "All units bearing serial numbers 20 through 109.",
      "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 central control monitor screen may go blank during use because of a bad wiring connection in the wiring harness or a low voltage setting on the potentiometer.",
      "root_cause_description": "Other",
      "action": "Service representatives were sent a service bulletin dated 8/12/03 instructing them to correct units in the field bearing serial numbers between 20 and 109.",
      "distribution_pattern": "United States, Belgium, Canada, Dubai, Egypt, Germany, Hong Kong, India, Japan, Korea, Singapore and United Kingdom.",
      "openfda": {
        "k_number": [
          "K870976",
          "K022947",
          "K221373",
          "K172220",
          "K942582",
          "K091007",
          "K133598",
          "K002116",
          "K915183",
          "K232291",
          "K801097",
          "K842138",
          "K093882",
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          "K982014",
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          "K851615",
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          "K163531",
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          "K770002",
          "K813034",
          "K210130",
          "K950990",
          "K871131",
          "K090006",
          "K103762",
          "K173834",
          "K002118",
          "K202125",
          "K070213",
          "K060053",
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          "K861388",
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          "K052555",
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          "K151349",
          "K190282"
        ],
        "registration_number": [
          "9611109",
          "3019807891",
          "3002807090",
          "1828100",
          "3011554160",
          "3007427881",
          "8010762",
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          "3010703925",
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          "3005941719",
          "2916596",
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        "fei_number": [
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          "3006073153",
          "3001589655",
          "3006003617",
          "1218444",
          "2916596",
          "3002808267"
        ],
        "device_name": "Console, Heart-Lung Machine, Cardiopulmonary Bypass",
        "medical_specialty_description": "Cardiovascular",
        "regulation_number": "870.4220",
        "device_class": "2"
      }
    }
  ]
}