Events

Device Recall Terumo Advanced Perfusion System 1 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Terumo Cardiovascular Systems Corporation 에 의해 제조된 제품과 관련되어 있습니다.

이것은 무엇인가요?

의료기기에 문제가 생겼을 경우 제조사가 이를 바로잡거나 시장에서 회수하는 조치를 말한다. 회수(Recall)는 의료기기에 결함이 있거나, 건강에 위협이 되거나, 또는 결함도 있고 건강에도 위협이 될 경우에 발생한다.

데이터에 대해 더 자세히 알아보기 여기
  • 사례 유형
    Recall
  • 사례 ID
    65381
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-1974-2013
  • 사례 시작날짜
    2013-07-26
  • 사례 출판 날짜
    2013-08-14
  • 사례 상황
    Terminated
  • 사례 국가
    United States
  • 사례 종료 날짜
    2017-02-08
  • 사례 출처
    USFDA
  • 사례 출처 URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=119861
  • 비고 / 경고
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • 데이터 추가 비고
    Console, heart-lung machine, cardiopulmonary bypass - Product Code DTQ
  • 원인
    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.
  • 조치
    Terumo Cardiovascular Systems (TCVS) notified their consignees of the Urgent Medical Device Recall letter dated 7/26/13 and was mailed 7/29/13. The notification provided reason for the device correction, affected product, how the device will be corrected, and the potential health hazard associated with a user's inaccurate interpretation of the service pump error message. Instructions for consignee responses to the recall notice communication may be faxed to 734-741-6149 or emailed to the address on the return form. If you have any questions or concerns, call Terumo Cardiovascular Systems (TCVS) Customer Service at 1-800-521-2818 M-F, 8am-6pm ET. Terumo Cardiovascular Systems (TCVS) will provide an addendum to the APS1 Manual to their consignees. The addendum will be placed at the beginning of Chapter 6, Centrifugal Control Unit.

Device

Device Recall Terumo Advanced Perfusion System 1
  • 모델명 / 제조번호(시리얼번호)
    Catalog Number or Part Number: 801764 Description: 220/240V AC, Advanced Perfusion System 1
  • 의료기기 분류등급
    Cardiovascular Devices
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    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
  • 제품 설명
    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.
  • Manufacturer
    Terumo Cardiovascular Systems Corporation

Manufacturer

Terumo Cardiovascular Systems Corporation
  • 제조사 주소
    Terumo Cardiovascular Systems Corporation, 6200 Jackson Rd, Ann Arbor MI 48103-9586
  • 제조사 모회사 (2017)
    Terumo Corp.
  • Source
    USFDA