Remel Streptex Group D Latex Reagent 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Thermo Fisher Scientific 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
    2013-04-09
  • 사례 출판 날짜
    2013-04-09
  • 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: thermo fisher remelstreptex group d latex reagent medical device manufacturer, thermo fisher scientific issued a medical device safety alert concerning remelstreptex group d latex reagent with model number r30950901 and lot number 1215767. according to the manufacturer,an internal technical investigation has confirmed that streptex group d latex lot: 1215767 sold separately as r30950901 lot: 1215642 and contained within the kits detailed below, may give weak or false negative test results: streptex latex agglutination test (200 tests) r30164701 lot: 1215568 streptex latex agglutination test (50 tests) r30950501 lot: 1215567 streptex latex agglutination test (50 tests) r30950901 lot: 1215642 the positive control reagent continues to react satisfactorily with the latex and will not indicate that the reagent is weak. continued use of these kits may result in false negative test results with some cultures. the manufacturer advises the affected customers to: destroy any remaining stock; contact customer services or local oxoid supplier who will issue a replacement; review results reported using this lot; and consider retesting and/or seek appropriate expert advice. if you are in possession of the affected product, please contact your supplier for necessary actions. posted on 9 april 2013.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Thermo Fisher RemelStreptex Group D Latex Reagent
  • Manufacturer

Manufacturer