ARGENE reagents 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Biomérieux 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
    2016-05-13
  • 사례 출판 날짜
    2016-05-13
  • 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: biomérieux argene reagents medical device manufacturer, biomérieux, has issued a medical device safety alert concerning its argene reagents. the following products with the reference numbers are affected by this issue described below:- product name (reference number): adenovirus r-gene kit (69-010b); ebv r-gene (69-002b; bk virus r-gene kit (69-013b); cmv r-gene (69-003b); hsv1 hsv2 vzv r-gene kit (69-004b); cmv hhv6,7,8 r-gene (69-100b); quanti fiua qs r-gene (68-006); parvovirus b19 r-gene (69-019b); quanti hhv8 qs r-gene (68-008); enterovirus r-gene (69-005b); hhv6 premix r-gene (69-100r6); bordetella parapertussis r-gene (71-012); hhv7 premix r-gene (69-100r7); influenza a/b r-gene (71-040); hhv8 premix r-gene (69-100r8) ; rsv/hmpv r-gene (71-041) ; cell control r-gene (71-106) ; rhino&ev/cc r-gene (71-042) ; parechovirus r-gene (71-020) ; adv/hbov r-gene (71-043) ; hcov/piv r-gene (71-045) ; chla/myco pneumo r-gene (71-044) ; hsv1 r-gene (71-015); legio pneumo/cc r-gene (71-046) ; hsv2 r-gene (71-016) ; flu a(m) & h1ni 2009 r-gene (71-300) ; vzv r-gene (71-017); bordetella r-gene ( 69-011b) the use of the argene reagents on rotorgene system was validated during reagent development using the rotorgene consumable “strips 4 tubes”. this specification on rotor-gene consumable associated with argene reagent performance has not been specified in argene reagents’ instruction for use. following a customer complaint and an internal investigation, the manufacturer has been confirmed that an interaction between the other rotorgene disposables could cause validation issues. for the tests including hsv2 parameter, the test’s sensibility is reduced due to the interaction with the consumable causing low positive results to shift to (false) negative. according to the manufacturer, there is a potential risk to cause delayed results considering the incompatibility between the reagents and the consumable appears immediately and could lead to invalid results. the ability to obtain a false result associated to a valid run has been estimated as remote. the manufacturer requests the user to validate the use of the other consumables than strips 4 tubes in their applications, in case they would like to continue using them on the rotor-gene system in conjunction with argener reagents. 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 13 may 2016.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Biomérieux ARGENE products
  • Manufacturer

Manufacturer