DxH 500 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Beckman Coulter 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
    2016-03-09
  • 사례 출판 날짜
    2016-03-09
  • 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: beckman coulter dxh 500 medical device manufacturer, beckman coulter, has issued a medical device safety alert concerning its dxh 500 (part number: b40601, software versions 1.0.0 and 1.0.1). the manufacturer is notifying users regarding an error in the result abnormal flags field transmitted from the dxh 500 to the laboratory information system (lis). test values are not affected. according to the manufacturer, the logic for the “a” code used in the result abnormal flags field is reversed for all test parameters. this letter does not apply if the user’s laboratory is not transmitting results to an lis or if the lis driver does not use the result abnormal flags field. the test results and flags generated by the instrument are correct and are not affected by this issue. the definitive messages, system messages, parameter flags and codes, reference intervals and action limit flags are displayed, printed and transmitted to the lis correctly. however, there is an additional flag, result abnormal flag, which is only transmitted to the lis that is incorrect. if the lis is using the result abnormal flags field, the lis may incorrectly interpret results. specifically, correct normal values may be erroneously flagged as abnormal and correct yet abnormal results may be missing the abnormal flag. this issue will be corrected in a future software release. 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 9 march 2016.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Beckman Coulter DxH 500
  • Manufacturer

Manufacturer