PENTARAY Catheters 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
    2016-04-21
  • 사례 출판 날짜
    2016-04-21
  • 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 pentaray catheters medical device manufacturer, biosense webster, has issued a medical device safety alert concerning its pentaray catheters. this involves all lots of pentaray catheters with catalogue numbers d128201, d128202, d128203, d128204, d128205, d128206, d128207, 0128208, d128209, d128210, d128211, and d128212. pentaray catheters are indicated for multiple electrode electrophysiological mapping of cardiac structures in the heart, i.E., recording or stimulation only. this catheter is intended to obtain electrograms in the atrial and ventricular regions of the heart. the manufacturer is updating the contraindication language in the instructions for use (ifu) and product labeling for this catheter relative to patients with prosthetic valves. the current language in the ifu provides a precaution against use of the pentaray catheter in patients with prosthetic valves under the contraindication section stating: “[the] use of this catheter may not be appropriate for use in patients with prosthetic valves.” the manufacturer is updating the contraindication statement as follows: “do not use pentaray catheters in patients with prosthetic valves”. according to the manufacturer’s medical assessment, there is a high risk of catheter spline entanglement when using pentaray catheters in patients with prosthetic valves. if excessive force is applied on the entangled catheter spline, there is a potential for parts to detach and embolize inside the patient’s body, which may lead to serious complications like stroke, transient ischemic attack, myocardial infarction or pulmonary embolism. the likelihood of these serious complications remains low. the manufacturer advises users that they may continue to use pentaray catheters in accordance with the updated contraindication. 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 21 april 2016.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Biosense Webster PENTARAY Catheters
  • Manufacturer

Manufacturer