Intra-Aortic Balloon Catheter Kits and Percutaneous Insertion Kits 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Arrow International 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
    2016-02-26
  • 사례 출판 날짜
    2016-02-26
  • 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
    Medical device safety alert: arrow intra-aortic balloon catheter kits and percutaneous insertion kits the therapeutic goods administration (tga) of australia has posted a medical device safety alert concerning arrow intra-aortic balloon catheter kits and percutaneous insertion kits manufactured by arrow international, inc. the arrow intra-aortic balloon catheter kits and percutaneous insertion kits contain a percutaneous sheath introducer. the percutaneous sheath introducer is used by some clinicians in the intra-aortic balloon catheter insertion procedure. the issue pertains to the sheath introducer in the insertion kit only. the other components of the kits are unaffected. the manufacturer has advised there is the possibility that the percutaneous sheath introducer body may become separated from the sheath hub. if the separation occurs, there is a potential for bleeding from the device. if bleeding is not addressed with prompt intervention, it may result in loss of significant blood volume or exsanguination. in addition, delay of treatment, interruption of treatment, or loss of intra-aortic balloon therapy can occur. the manufacturer is advising customers to immediately quarantine all affected kits. the manufacturer will deliver replacement kits to the affected customers before the recovery of the affected kit. the manufacturer advises users that in the case of an emergency situation before the replacement kit can be delivered, the arrow intra-aortic balloon catheter can be inserted through the following alternative 8 fr. sheaths: -st jude medical diag maximum -terumo pinnacle -cordis avanti for details, please refer to the tga website:http://apps.Tga.Gov.Au/prod/sara/arn-detail.Aspx?k=rc-2016-rn-00204-1 if you are in possession of the affected products, please contact your supplier for necessary actions posted on 26 february 2016.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 의료기기 분류등급
  • 제품 설명
    Medical Device Safety Alert: ARROW Intra-Aortic Balloon Catheter Kits and Percutaneous Insertion Kits
  • Manufacturer

Manufacturer