{
  "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": "Ann Arbor",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "65381",
      "recalling_firm": "Terumo Cardiovascular Systems Corporation",
      "address_1": "6200 Jackson Rd",
      "address_2": "",
      "postal_code": "48103-9586",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worlwide Distribution - US Nationwide: AL,AR,AZ, CA, CO, CT, DC, DE, FL,GA, HI, IA, ID, IL, IN, KY, LA, MA , MD, MI, MN, MO, MS, MT, NC, ND, NE, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN,  TX, UT,  VA, VT, WA, WI, WV  and the countries of: AUSTRALIA,UNITED ARAB EMIRATES (UAE),Hong Kong,  onesia,Singapore,Taiwan,Thailand, Philippines,CHILE,    Malaysia,USA,South Korea,BELGIUM,Japan,Mexico,CANADA",
      "recall_number": "Z-1974-2013",
      "product_description": "Terumo¿ Advanced Perfusion System 1 (APS1, System 1)  Description: 220/240V AC    Product Usage:  The Terumo¿ Advanced Perfusion System 1 is indicated for use in extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures only when used by a qualified perfusionist who is experienced in the operation of Sarns TM or similar equipment.",
      "product_quantity": "1657",
      "reason_for_recall": "Terumo Cardiovascular Systems (TCVS) has become aware that an Advanced Perfusion  System 1 (APS1) Centrifugal Pump 'Service Pump' message may occur due to user induced  motor movement.  In this instance, the APS1 will identify the movement (as it is  designed) and display a Service Pump message error. The user might interpret this as a  pump which requires service rather than a message displayed due to pump movement while  not activated.",
      "recall_initiation_date": "20130726",
      "center_classification_date": "20130814",
      "termination_date": "20170208",
      "report_date": "20130821",
      "code_info": "Catalog Number or Part Number: 801764  Description: 220/240V AC, Advanced Perfusion System 1",
      "more_code_info": ""
    }
  ]
}