Events

CARESCAPE R860 의 리콜

Health Canada (via FOI)에 따르면, 해당 리콜 는 Canada 에서 GENERAL ELECTRIC CANADA (OPERATING AS GE HEALTHCARE) 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
    78518
  • 사례 위험등급
    II
  • 사례 시작날짜
    2015-07-28
  • 사례 국가
    Canada
  • 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
    The following issue is being addressed by ge healthcare file no. fmi 34066: the evair component manufacturer imtmedical ag is conducting a field corrective action. imtmedical has identified that potential friction of cables and tubing internal to the evair compressor may result in an inability for the compressor to output compressed air. there is a potential for temporary oversupply of oxygen to the patient as a result of this failure because the ge healthcare ventilators are designed to ventilate with 100% oxygen in the case of loss of input air supply pressure.

Device

CARESCAPE R860

Manufacturer

GENERAL ELECTRIC CANADA (OPERATING AS GE HEALTHCARE)