CARTOSOUND Module of the CARTO 3 EP Navigation System 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Biosense Webster 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
    2015-10-02
  • 사례 출판 날짜
    2015-10-02
  • 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: biosense webster cartosound module of the carto 3 ep navigation system medical device manufacturer, biosense webster, has issued a medical device safety alert concerning its cartosound module of the carto 3 ep navigation system, [catalogue number: c3sound] when used with the soundstar eco 8f and eco 10f diagnostic ultrasound catheter, [catalogue number: 10439236, 10439072, 10439011 & 10438577]. the manufacturer has received one complaint of image disappearance from the cardiac ultrasound system when the carto 3 ep navigation system needed restarting. this occurred while the patient was experiencing pericardial effusion. based on medical evaluation of the health risk profile, the manufacturer believes that the likelihood of harm to the patient is generally low if the ultrasound imaging is not available. however, if the intra-cardiac ultrasound is used to actively monitor an ongoing effusion, the lack of imaging may present a safety issue due to the delay in procuring the resources/equipment to use another imaging modality. the manufacturer will be updating the product labeling to include and further reinforce the above-mentioned precautionary safety information. according to the local supplier, the affected product [cartosound module for the cartro 3 ep navigation system] is distributed to hospitals in hong kong for demonstration purposes. however, soundstar eco 8f and eco 10f catheter are not distributed in hong kong. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 2 october 2015.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Biosense Webster CARTOSOUND Module of the CARTO 3 EP Navigation System
  • Manufacturer

Manufacturer