AutoMate 2500 Family systems with Sorting-Drive software upgraded from version 4.1.2 to 4.2 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
    2016-05-31
  • 사례 출판 날짜
    2016-05-31
  • 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 automate 2500 family systems with sorting-drive software upgraded from version 4.1.2 to 4.2 medical device manufacturer, beckman coulter, has issued a medical device safety alert concerning its automate 2500 family systems with sorting-drive software upgraded from version 4.1.2 to 4.2. the manufacturer has identified a software error with sorting-drive version 4.2. this issue only impacts customers that have upgraded from sorting-drive software version 4.1.2 to version 4.2. the software error prevents the ability of the sorting-drive to process updates to original test orders received via the laboratory information system (lis). updates to original test orders consist of the following three (3) actions: an already completed test is rerun/repeated an additional test is added to an existing test order a test is removed or deleted from an existing test order any test updates to an original order will not be processed. the sorting-drive software provides no notification that the test updates were not processed. this may cause a delay in results for any tests which are requested after the original test order (i.E. reruns or added tests). any updates to original test orders (reruns or added tests) need to be processed manually, as described below: monitor the lis to identify test orders which have not been processed in the normal timeframe. identify which of these were requested after the original test order (i.E., reruns or added tests). locate the associated samples and load these directly onto the analyzer for processing, bypassing the automate system. 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 31 may 2016.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Beckman Coulter AutoMate 2500 Family systems with Sorting-Drive software upgraded from version 4.1.2 to 4.2
  • Manufacturer

Manufacturer