DePuy ADEPT 12/14 Modular Head 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 DePuyOrthopaedics 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
    2013-01-22
  • 사례 출판 날짜
    2013-01-22
  • 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 adept 12/14 modular head the medicines and healthcare products regulatory agency (mhra), united kingdom posted a medical device safety alert concerning adept 12/14 modular head, manufactured bydepuyorthopaedics(a johnson & johnson company). review of post‐market surveillance data suggests a higher than expected revision rate for the adept 12/14 modular head when used in conventional total hip arthroplasty. analysis of uk national joint registry supplier feedback data indicates a cumulative revision rate of 12.1% (95% ci 9.5% to 15.4%) at 7 years for the affected product when used in conventional total hip arthroplasty. in september 2012, the australian orthopaedic association national joint replacement registry reported a cumulative revision rate of 7.1% (95% ci 3.6% to 13.6%) at 3 years with 8 revisions in a cohort of 121 adept 12/14 modular head cases used in conventional total hip arthroplasty. the manufacturer advises that patients who have received the affected products should be followed according to local guidance/standard of care for patients receiving metal on metal (mom) articulations. also, refer to the local orthopaedic association for detailed information related to the treatment of patients with mom articulations. for details, please refer to mhra website: http://www.Mhra.Gov.Uk/safetyinformation/safetywarningsalertsandrecalls/ fieldsafetynotices/con224428 if you are in possession of the affected product, please contact your supplier for necessary actions. posted on 22 january 2013.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: DePuy ADEPT 12/14 Modular Head
  • Manufacturer

Manufacturer