Axxess Drug Eluting Coronary Bifurcation Stent System 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Biosensors 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
    2013-12-13
  • 사례 출판 날짜
    2013-12-13
  • 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: biosensors international axxess drug eluting coronary bifurcation stent system medical device manufacturer, biosensors international, has issued a field safety notice concerning 4.0 x 9mm model of axxess drug eluting coronary bifurcation stent system (axbf-4009) (lot numbers: w13090159 and w13080132). several cases with deployment difficulty have been reported to biosensors international group to date, concerning the affected device. physicians in these cases found it either difficult or impossible to pull back the deployment actuator. this could potentially lead to a sub-optimal deployment. in most cases, the stent was successfully deployed, resulting in a positive clinical patient outcome. in the remaining cases, deployment was aborted and patients were administered alternative treatment, with positive patient outcomes. there have been no reports of adverse patient events. the manufacturer has the following recommendations: for all successfully implanted devices, no action is necessary and patients should continue to be managed in accordance with standard patient management protocol. quarantine and return any remaining stocks of affected product. according to the local supplier, the affected products were not distributed in hong kong. if you are in possession of the affected product, please contact your supplier for necessary actions. posted on 13 december 2013.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Biosensors International Axxess Drug Eluting Coronary Bifurcation Stent System
  • Manufacturer

Manufacturer