Zilver PTX Drug-Eluting Peripheral Stent 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Cook Ireland Limited 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
    2013-04-19
  • 사례 출판 날짜
    2013-04-19
  • 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: cook ireland limited zilver ptx drug-eluting peripheral stent medical device manufacturer, cook ireland limited, has issued a field safety notice concerning zilver ptx drug-eluting peripheral stent [catalogue number: ziv6*****ptx] the manufacturer has received a number of complaint reports relating to the delivery system for the zilver ptx drug eluting stent (13 complaints with an occurrence rate of 0.043%; two occurrences were considered serious adverse events) involving fractures of the delivery system inner catheter after stent deployment, and separation of the inner catheter tip section. in december 2012, the manufacturer issued a field safety notice (fsca-identifier: 2012c0005) to customers advising of the potential risk of tip/inner catheter separation, but no root cause had been established at that time. since december 2012, the manufacturer has responded to complaint reports by carrying out an in-depth investigation to better understand the root cause and the risk to patients of these tip separations. as a result of their investigation, the manufacturer is initiating a voluntary withdrawal as they have determined that there is a higher than expected potential of inner delivery catheter breakage due to inconsistencies in the catheter manufacturing process. this withdrawal is intended to address the patient risks that may be associated with this potential occurrence. this is a potential failure mode of the delivery system and does not affect the safety or efficacy of the implantable stent. previously implanted stents are not affected by this withdrawal. this notice relates only to the zilver ptx drug eluting peripheral stent delivery system. any zilver flex and other bare metal stents from cook medical are not affected. according to the local supplier, the affected products were distributed in hong kong. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 19 april 2013.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 의료기기 분류등급
  • 제품 설명
    Medical Device Safety Alert: Cook Ireland Limited Zilver PTX Drug-Eluting Peripheral Stent
  • Manufacturer

Manufacturer