Dual Hemo MCable pod used with the Infinity Acute Care System (IACS) Monitoring Solution 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Dräger Medical Systems 에 의해 제조된 제품과 관련되어 있습니다.

이것은 무엇인가요?

안전성 경고는 의료기기 제품과 관련된 중요한 정보와 권고사항을 담고 있습니다. 물론 안전성 경고가 배포되었다고 해서 해당 제품이 무조건 안전하지 않은 제품이라는 것은 아닙니다. 보건의료업계 종사자와 의료기기 사용자들에게 배포되는 안전성 경고에는 회수(recall)도 포함될 수 있습니다. 제조사가 안전성 경고를 작성하기도 하지만, 보건당국에서 작성하는 경우도 있습니다.

데이터에 대해 더 자세히 알아보기 여기
  • 사례 유형
    Safety alert
  • 날짜
    2017-10-03
  • 사례 출판 날짜
    2017-10-03
  • 사례 국가
  • 사례 출처
    DH
  • 사례 출처 URL
  • 비고 / 경고
    Hong Kong data is current through September 2018. All of the data comes from the Department of Health (Hong Kong), 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 data from the U.S. and Hong Kong.
  • 데이터 추가 비고
    Medical Device Safety Alert
  • 원인
    Field safety notice: dräger dual hemo mcable pod used with the infinity acute care system (iacs) monitoring solution medical device manufacturer, dräger medical systems, inc., has issued a safety alert concerning its dual hemo mcable pod used with the infinity acute care system (iacs) monitoring solution. the manufacturer has determined through internal testing that dual hemo mcable pods with revision index (ri) 15 and 16, which are used with the dräger infinity acute care system, may permit liquid ingress inconsistent with their ipx4 rating, which could potentially result in an incorrect measured value of invasive blood pressure. the manufacturer has not received any complaints and is not aware of any negative patient consequences arising from this issue. revisions prior to ri 15, with proper orientation will still maintain its designated ipx1 rating and are not within the scope of this safety notice. in addition, revisions labelled ri 17 and greater are not affected by this notice because these revisions continue to meet the ipx4 standard. affected users are requested to take the following actions: contact the manufacturer to receive a sleeve that can be applied to protect against liquid ingress see the safety notice provided by the manufacturer for required upright orientation of the dual hemo mcable pod and installation instructions for the sleeve. according to the local supplier, the affected product is distributed in hong kong. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 3 october 2017.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Dräger Dual Hemo MCable pod used with the Infinity Acute Care System (IACS) Monitoring Solution
  • Manufacturer

Manufacturer