Synchron Enzyme Validator 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
    2018-01-03
  • 사례 출판 날짜
    2017-01-03
  • 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, synchron enzyme validator medical device manufacturer, beckman coulter, has issued a medical device safety alert concerning its synchron enzyme validator [product code: 441350; lot number (expiration date): m612600 (31 march 2018)]. the manufacturer has identified that a supplemental product information notification is missing from the affected lot. according to the manufacturer, customers switching from enzyme validator lots m510750 or older to lot m612600 may observe differences in ifcc enzyme methods for ggt (ref 442650 and 476846) and ast- (ref 467845 and 467849). a positive bias up to 13 u/l for ggt was observed with synchron control level 1. a negative bias up to 9% for ast- was observed with synchron control level 3. shifts in ggt and ast- were observed with other levels; however the recoveries were within the control insert ranges. customers switching from enzyme validator lot m605630 to lot m612600 are not impacted. the affected users are advised to read the supplemental product information and determine if control ranges need to be reassessed. retrospective review of patient results is at the discretion of the laboratory director. 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 03 january 2017.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Beckman Coulter, Synchron Enzyme Validator
  • Manufacturer

Manufacturer