Fully Automated Blood Coagulation Analyzer 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Sysmex Corporation 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
    2013-11-20
  • 사례 출판 날짜
    2013-11-20
  • 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: sysmex fully automated blood coagulation analyzer the medicines and healthcare products regulatory agency (mhra), united kingdom (uk) has posted a medical device safety alert concerning fully automated blood coagulation analyzer [model no.: cs-2000i & cs-2100i; software versions: 01-57, 01-60, 01-63], manufactured by sysmex corporation. the manufacturer is informing users about a software bug which has occurred recently concerning fully automated blood coagulation analyzer cs-2000i/cs-2100i. under certain circumstances, measurement results could be assigned to a wrong sample. when the operator registers an order for micro mode and tries to modify the order by pushing the button in the order screen or the job list screen, there is a risk of a mismatch between results and sample id numbers. the problem concerns qc as well as sample measurements which are measured in normal-mode. this problem occurs even if no modification of the sample order has been done. pushing the button already triggers the error which is caused by a possible wrong feed forward of the sample rack. the affected users should take a precaution by carry out the following instructions until the software update is available:- once an order is set for micro mode measurement, do not press the button neither in the order screen nor in the job list screen. if user would like to change the order, he/she should delete the original micro mode order first on the job list screen and then register a new order. the software bug will be fixed with a software update that is expected to be released in the first quarter of 2014. the manufacturer does not recommend a look back of previously generated results since the coagulation status changes over the time, and does recommend that this communication is reviewed with the laboratory medical director. for details, please visit the following mhra website: http://www.Mhra.Gov.Uk/safetyinformation/safetywarningsalertsandrecalls/fieldsafetynotices/con334789 if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 20 november 2013.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Sysmex Fully Automated Blood Coagulation Analyzer
  • Manufacturer

Manufacturer