CARDIOHELP-I 의 리콜

Health Canada (via FOI)에 따르면, 해당 리콜 는 Canada 에서 MAQUET-DYNAMED INC. 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
    82612
  • 사례 위험등급
    III
  • 사례 시작날짜
    2013-09-04
  • 사례 국가
  • 사례 출처
    HC
  • 비고 / 경고
    Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
  • 데이터 추가 비고
  • 원인
    In certain rare instances the cardiohelp-i device may display an error message with audible alarm indicating "battery defective". the alarm will occur while booting or when the main power supply is unplugged from the main power source. this is due to a defective capacitor within the battery manager board. further when alarming the hmi (human machine interface) will gradually become black due to the hmi back light shutting down. the defective capacitor behavior leads to the shutdown of the battery booster that boosts the voltage of the batteries from 12v to 24v. this in turn leads to the state that the voltage is insufficient to ignite the backlight of the display. blood flow is not affected during the shutdown time of the hmi therefore there is no risk of circulatory impairment.

Device

  • 모델명 / 제조번호(시리얼번호)
    Model Catalog: 70104.8012 (Lot serial: 90410704); Model Catalog: 70104.8012 (Lot serial: 90410486); Model Catalog: 70104.8012 (Lot serial: 90410493)
  • 제품 설명
    CARDIOHELP-i
  • Manufacturer

Manufacturer

  • 제조사 주소
    MISSISSAUGA
  • 제조사 모회사 (2017)
  • Source
    HC