ClearSight Heart Reference Sensor 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Edwards LifeSciences 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
    2017-12-14
  • 사례 출판 날짜
    2017-12-14
  • 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: edwards lifesciences clearsight heart reference sensor medical device manufacturer, edwards lifesciences, has issued a medical device safety alert concerning its clearsight heart reference sensor [model number: evhrs; all serial numbers manufactured after 31 december 2015]. the current product as well as the affiliated labeling contains an expiration date of two years. through investigation and analysis of complaint data, the manufacturer discovered that hrs units are susceptible to experiencing an “hrs out of range” error message in the ev1000 platform that is beyond six months from the date of manufacture. as a result, the manufacturer has decided to change the expiration date to six months from the date of manufacture. additionally, this change will also require replacing the operator’s manual of the ev1000 clinical platform and the instructions for use (ifu) of the heart reference sensor. according to the manufacturer, this issue poses no risk to patients as the ev1000 clinical platform will not allow the clinician to zero the device and initiate monitoring. this would create a pre-procedural delay while the troubleshooting process is completed. affected users could continue to use the product. if the user does not encounter the “hrs out of range” message on the ev1000 clinical platform, the heart reference sensor is functioning properly and can be safely used to monitor your patients. if the user encounters the “hrs out of range” message on the ev1000 clinical platform, he/she should contact the manufacturer’s technical support. product replacement is on-going. according to the local supplier, the affected products are not distributed in hong kong. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 14 december 2017.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Edwards LifeSciences ClearSight Heart Reference Sensor
  • Manufacturer

Manufacturer