VITEK 2 AST-P586 Test Kit 20 Cards 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 BioMérieux 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
    2017-02-15
  • 사례 출판 날짜
    2017-02-15
  • 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: biomérieux vitek 2 ast-p586 test kit 20 cards medical device manufacturer, biomérieux, has issued a field safety notice concerning its vitek 2 ast-p586 test kit 20 cards (lot number: 366386410; expiration: 13 jul 2017). the manufacturer received customer reports regarding an issue related to out-of-range-low (oorl) ampicillin/sulbactam qc results for escherichia coli atcc 35218, a package insert qc strain, in association with vitek 2 ast-p586 test kit, lot 366386410. internal investigation at the manufacturing site has confirmed the oorl ampicillin/sulbactam qc results. in addition, the investigation determined the ampicillin/sulbactam mic results for the gram-positive organisms claimed by the vitek 2 ast-p586 test kit are not affected (i.E. staphylococcus spp., enterococcus spp. and streptococcus agalactiae). according to the manufacturer, the issue is limited to the affected lot. there are no reports or evidence to suggest the issue exists for any other test kit lot. evaluation of the identified issue indicates no potential for erroneous patient mic results due to the oorl ampicillin/sulbactam qc result. however, escherichia coli atcc 35218 must be repeated to success, or an alternate method must be used to obtain ampicillin/sulbactam mic results the manufacturer advises users to dispose of the remaining affected lot in their stock. product replacement is on-going according to the local supplier, the affected products are distributed in hong kong. if you are in possession of the products, please contact your supplier for necessary actions. posted on 15 february 2017.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: BioMérieux VITEK 2 AST-P586 Test Kit 20 Cards
  • Manufacturer

Manufacturer