UniCel DxH 800 Coulter Cellular Analysis System and UniCel DxH 600 Coulter Cellular Analysis System 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
    2018-08-10
  • 사례 출판 날짜
    2018-08-10
  • 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 unicel dxh 800 coulter cellular analysis system and unicel dxh 600 coulter cellular analysis system medical device manufacturer, beckman coulter, has issued a medical device safety alert concerning its following devices: unicel dxh 800 coulter cellular analysis system [reference: 629029, b24465, b24802, b68304, b66445, b63322; software version: 3.2.0 and below]; unicel dxh 600 coulter cellular analysis system [reference: b23858; software version: 1.3.0 and below]. the manufacturer has confirmed complaints of sporadic erroneously elevated platelet results without flags or system messages. other parameters are not affected by the issue. patient results may be affected. no injury has been reported in association with the issue. during patient’s follow-up, the affected users are advised to consider unexpected elevated platelet levels as possible erroneous results due to the failure and ensure implementation of the following actions: use all available features to assess patient results, including reference ranges, action and critical limits, instrument system flags, codes, messages, delta checks, xm, and decision rules; follow their laboratory’s standard operating procedure for confirming unexpected results; communicate to their medical director the need to avoid patient treatment based solely on any single test result, and to interpret all results in the context of other clinical and laboratory features; consult with the medical director to determine if a retrospective review of results is warranted. according to the manufacturer, dxh 800 version 3.2.1 and dxh 600 version 1.3.1 are not affected by the issue. the manufacturer will be prioritizing the upgrades for the systems. alternatively, the manufacturer is working on the development of a self-installable software patch option, in lieu of the software upgrade, to expedite resolution and minimize impact on laboratory workflow. 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 10 august 2018.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Beckman Coulter UniCel DxH 800 Coulter Cellular Analysis System and UniCel DxH 600 Coulter Cellular Analysis System
  • Manufacturer

Manufacturer