DxH 500 Hematology Analyser 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
    2017-05-29
  • 사례 출판 날짜
    2017-05-29
  • 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 hematology analyser medical device manufacturer, beckman coulter, has issued a medical device safety alert concerning its dxh 500 hematology analyser [reference: b40601; software versions 1.0.2]. as a result of internal investigations, the manufacturer has become aware that when the instrument temperature (<18°c to >36.5°c) is exceeded, the dxh 500 allows sample processing and result reporting despite the instructions for use stating that “the run sample is inaccessible”. results generated in this scenario may be erroneous. additionally: the message on the results screen/printout reads “instrument temperature” instead of “instrument temperature out of range”. the results are transmitted to the laboratory information system (lis) without the accompanying “instrument temperature out of range” message. using the auto-transmit option could lead to the release of erroneous results to the lis. if the instrument is operating out of the temperature range and the warnings on the screen are ignored and the results are used, then: these cbc, wbc-diff or cbc/wbc-diff results may be erroneous. if these erroneous results are released to the physician, this could result in inappropriate patient management. the manufacturer advises affected users to take the following actions:- when the message “instrument temperature out of range” or “instrument temperature” is displayed on the system or printouts, do not report the patient results. ensure the laboratory ambient temperature is within specifications (18°c -32°c) when processing samples. disable the auto-transmit option if there is a potential for the operational temperature to be exceeded. consult with the medical director to determine if a retrospective review of results is warranted. 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 29 may 2017.

Device

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

Manufacturer