Misago Peripheral Self-Expanding Stent System 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Terumo Corporation 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
    2016-08-12
  • 사례 출판 날짜
    2016-08-12
  • 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: terumo misago peripheral self-expanding stent system medical device manufacturer, terumo corporation, has issued a medical device safety alert concerning its misago peripheral self-expanding stent system. the affected devices are identified as follows:- product codes: all misago products starting with sf*f or sx-v lot number: all products on the market within the labeled expiration period (manufactured from september-2013 through august-2016) during the inspection process, the manufacturer identified a low occurrence rate of two types of non-conformances in comparison to the specifications as described in the regulatory applications: reduced diameter at one, or both ends of the stent due to incomplete self-expansion after release from the delivery catheter; and deformation of the stent strut shape due to the compression forces that are applied to compact, and mount the stent to the delivery catheter. according to the manufacturer, the body of clinical evidence as related to misago stents supports that clinical performance is not affected in that there are no new or additional complications, or adverse health consequences. the health hazard evaluation concluded that the nonconformity in the dimension (reduced diameter rat the ends of the stent), or in the stent shape (a bend or inconsistent alignment of the stent struts), will have no impact to safety, or effectiveness, of the product. therefore, there is no additional risk of serious health harm posed by these nonconforming products. the manufacturer has not received customer complaints, or adverse events, related to incomplete stent expansion, stent deployment failure, insufficient diameter, or stent deformation. product recall is ongoing. according to the local supplier, the affected products are distributed in hong kong. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 12 august 2016.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Terumo Misago Peripheral Self-Expanding Stent System
  • Manufacturer

Manufacturer