vitros 3600 immunodiagnostics system and vitros 5600 integrated system, software version 3.2.2 and below 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Ortho-clinical Diagnostics Inc 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
    2016-04-14
  • 사례 출판 날짜
    2016-04-14
  • 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: ortho-clinical vitros 3600 immunodiagnostics system and vitros 5600 integrated system, software version 3.2.2 and below the therapeutic goods administration (tga) of australia has posted a medical device safety alert concerning vitros 3600 immunodiagnostics system and vitros 5600 integrated system, software version 3.2.2 and below, manufactured by ortho-clinical diagnostics inc. product code: 6802783 and 6802413 unique device id: 10758750002979 and10758750002740 according to the manufacturer, a vitros system software timing anomaly has been identified that could cause two different sample metering scenarios that may lead to erroneous results: scenario 1: the vitros system could aspirate sample from an unintended sample container causing assay result(s) obtained from that sample to be incorrectly associated with the intended sample. scenario 2: a sample could be aspirated from a sample container (sample a) and be dispensed into an unintended container (sample b) to be contaminated and diluted by sample a. there is the potential for false negative and false positive results which may lead to an inappropriate diagnosis and patient management leading to serious patient injury. the manufacturer is providing users with interim instructions to follow to decrease the probability of the issues occurring, and can review the affected systems to determine if the errors have occurred. besides, the manufacturer is providing users with a software update (and associated modification modules) as a permanent correction. for details, please refer to the tga website: http://apps.Tga.Gov.Au/prod/sara/arn-detail.Aspx?k=rc-2016-rn-00420-1 if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 14 april 2016.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Ortho-clinical VITROS 3600 Immunodiagnostics System and VITROS 5600 Integrated System, software version 3.2.2 and below
  • Manufacturer

Manufacturer