{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "50426",
      "product_res_number": "Z-0658-2007",
      "event_date_initiated": "2007-01-12",
      "event_date_posted": "2007-03-27",
      "recall_status": "Terminated",
      "event_date_terminated": "2008-06-19",
      "res_event_number": "37366",
      "product_code": "DTW",
      "k_numbers": [
        "K900815"
      ],
      "product_description": "Terumo Perfusion System 8000 Base, 5 pump, 220/240v; Model 8000; Catalog No. 16406.",
      "code_info": "Hand crank serial numbers 1197 through 1214.",
      "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 hand crank may crack in the bearing/shaft area due to a manufacturing defect.  (Note:  Some of the hand cranks subject to this recall were shipped as replacements for hand cranks recalled in the Summer of 2006.)",
      "root_cause_description": "Other",
      "action": "Consignees were notified by phone between 1/12/07 and 2/23/07 and informed replacement hand cranks would be shipped.",
      "product_quantity": "18",
      "distribution_pattern": "Worldwide, including USA, Belgium, Hong Kong, Japan, Taiwan and United Arab Emirates.",
      "openfda": {
        "k_number": [
          "K781145",
          "K915337",
          "K860076",
          "K924354",
          "K041558",
          "K823712",
          "K900815",
          "K873206",
          "K910599",
          "K831879",
          "K955152",
          "K992857",
          "K822821",
          "K900910",
          "K150530",
          "K852407",
          "K843802"
        ],
        "registration_number": [
          "2032112",
          "3015431638",
          "1828100",
          "2184009",
          "9617604",
          "2025816"
        ],
        "fei_number": [
          "3015431638",
          "1000116158",
          "1828100",
          "3003076831",
          "3002558692",
          "2025816"
        ],
        "device_name": "Monitor And/Or Control, Level Sensing, Cardiopulmonary Bypass",
        "medical_specialty_description": "Cardiovascular",
        "regulation_number": "870.4340",
        "device_class": "2"
      }
    }
  ]
}