Ultrafilter U9000 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Gambro 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
    2014-08-05
  • 사례 출판 날짜
    2014-08-05
  • 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: gambro ultrafilter u9000 medical device manufacturer, gambro, has issued a field safety notice (fsn) concerning its ultrafilter u9000. there is a possibility of external fluid leakage with ultrafilter u9000 as a result of multiple disinfections using a sodium carbonate-based solution. the housing of the ultrafilter u9000 is made of polycarbonate, a material that is known to undergo slow chemical degradation during long term exposure to alkaline substances. intensive use of sodium carbonate-based disinfection programs over several months may, therefore, cause degradation of the ultrafilter housing leading to an external fluid leakage at the position of the welding seal between the filter housing and the header cap. if a leakage is observed during treatment, the user should immediately stop the treatment and change the u9000 ultrafilter to avoid excessive fluid removal from the patient. furthermore, the use of sodium carbonate-based disinfection programmes has been broadly validated for the u9000 ultrafilter. however, to minimize the risk of an external fluid leak, the manufacturer strongly recommends adhering to the instructions mentioned in the fsn, when using sodium carbonate based disinfection programmes with u9000. according to the local supplier, the affected products were distributed in hong kong. if you are in possession of the products, please contact your supplier for necessary actions. posted on 5 aug 2014.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Gambro Ultrafilter U9000
  • Manufacturer

Manufacturer