pedal of footswitch for philips multidiagnost eleva fd systems and allura xper systems 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Philips Healthcare 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
    2014-07-11
  • 사례 출판 날짜
    2014-07-11
  • 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: pedal of footswitch for philips multidiagnost eleva fd systems and allura xper systems medical device manufacturer, philips healthcare, has issued a field safety notice concerning its footswitches for multidiagnost eleva fd systems and allura xper systems. according to the manufacturer, if a footswitch is frequently used on an anti-fatigue mat, on a not flat surface or in the pedestal, the footswitch pedals may get bent. this might cause an intermittent or continuous inability of making live fluoro images or exposures. in case the fluoro pedal is bent and live fluoro is not available, the exposure pedal of the footswitch or the handswitch may be used to generate a live image in order to finish a procedure. this will lead to a higher dose but it outweighs a possible safety risk. the manufacturer advises users that before the start of a procedure, the footswitch should be inspected for possible bent pedals. if bent pedals are found, the procedure should not continue. furthermore, the manufacturer would arrange a mechanical hardware update of the footswitch in order to prevent bent pedals. 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 11 july 2014.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Pedal of footswitch for Philips MultiDiagnost Eleva FD Systems and Allura Xper Systems
  • Manufacturer

Manufacturer

  • 제조사 모회사 (2017)
  • Source
    DH