FACET WEDGE System 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Depuy Synthes 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
    2016-10-25
  • 사례 출판 날짜
    2016-10-25
  • 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: depuy synthes facet wedge system medical device manufacturer, depuy synthes, has issued a field safety notice (fsn) concerning its instruction for use (ifu) and surgical technique guide for the facet wedge system. the affected ifu number is se_463713 and surgical technique guide number is 036.001.121. the manufacturer issued this fsn in order to communicate changes being made to the ifu and surgical technique guide in order to clarify the intended use of the facet wedge device. the intended use section is being updated to remove stand-alone use of the facet wedge device and clarify multi-level use. in addition, further clarification is being added to the indications section in regards to pseudarthrosis. according to the manufacturer, there has been no change to the design or manufacture of the facet wedge implants or instruments. the fsn impacts information in the ifu and technique guide only. a post market clinical study conducted for the facet wedge system determined that patients implanted with stand-alone facet wedge devices may potentially display signs of radiological non-fusion. however, there have been no confirmed complaints of patient harm associated with stand-alone use of facet wedge devices to date. the customers are advised to review the revisions being made to the ifu and surgical technique guide. the updated ifu document will be included with facet wedge implants and the technique guide will become available at the manufacture’s website. for patients with stand-alone facet wedge devices implanted, there is no recommendation for prophylactic removal. patients should be monitored in accordance with standard practice for the facet wedge treatment process. 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 25 october 2016.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Depuy Synthes FACET WEDGE System
  • Manufacturer

Manufacturer