PK7300 Automated Microplate 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
    2017-06-27
  • 사례 출판 날짜
    2017-06-27
  • 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 pk7300 automated microplate system medical device manufacturer, beckman coulter, has issued a medical device safety alert concerning its pk7300 automated microplate system. the manufacturer has confirmed that, during sample processing under certain conditions, the pk7300 does not always generate a reagent dispensing pressure error when the reagent vial becomes empty and no reagent is dispensed. sample processing will continue after a vial is empty only when the reagent alarm volume, limit volume and associated mode shift alarm have not been set. the above issue may lead to false negative test results with blood grouping reagents. results will not be generated for tests using cellular or particle reagents. wells without cellular or particle reagents will be flagged as empty (.E flags). the manufacturer advises users to take the following actions:- verify that the following are all set on all pk7300 analyzers in the laboratory: alarm volume and limit volume in the common test parameter -name (reagent tab) menu. either “to pause” or “to measure 2” is selected for “at short reagent volume alarm” on the mode shift tab in the system- system menu. if the parameters described above have not been set on all pk7300s in the laboratory, affected users should follow the instructions in the pk7300 user’s guide and the information provided by the manufacturer to set them. when users place the reagent vials in the reagent tray, they should make sure that each vial is fully seated to the bottom of the tray. the manufacturer will update the pk7300 user’s guide to include the information described in the actions above to indicate that the settings for the alarm volume, limit volume and associated mode shift are required. additionally, a statement will be added to insure that the reagent vials are fully seated to the bottom of the reagent tray. 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 27 june 2017.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Beckman Coulter PK7300 Automated Microplate System
  • Manufacturer

Manufacturer