all allura xper, alluraclarity, allura cv, allura centron and uniq 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
    2015-11-20
  • 사례 출판 날짜
    2015-11-20
  • 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: philips healthcare all allura xper, alluraclarity, allura cv, allura centron and uniq systems medical device manufacturer, philips healthcare, has issued a medical device safety alert concerning all allura xper, alluraclarity, allura cv, allura centron and uniq systems. the affected product codes are 722001, 722002, 722003, 722005, 722006, 722008, 722010, 722011, 722012, 722013, 722015, 722019, 722020, 722022, 722023, 722025, 722026, 722027, 722028, 722029, 722031, 722033, 722034, 722035, 722038, 722039, 722058 and 722400. the safety alert informs users that the use of the above systems regarding live images and still images can lead to still images being interpreted as live images. if it were to re-occur, it could adversely affect the outcome of a clinical procedure. this can happen when: while doing fluoroscopy, the user presses the single shot exposure pedal, resulting in a single shot still image being displayed on the screen. the user does not realize that the single shot exposure pedal is still active, and that exposure therefore is still active. by design, exposure imaging takes priority over fluoroscopy imaging, so no fluoroscopy is started until the exposure pedal is released. at the same time the user does not realize that live x-ray imaging is not active, although the still image icon is displayed and all legally required live x-ray indicators (such as dose rate, x-ray active icon, fluoro timer, and audible signal —x-ray buzzer-) are inactive. while a fluoroscopy pedal is pressed and fluoroscopy is active, the user (accidently) presses a second fluoroscopy pedal and then releases the first fluoroscopy pedal. upon releasing the first fluoroscopy pedal, the system stops live imaging. the user does not realize that the first fluoroscopy pedal was still pressed when pressing the second fluoroscopy pedal. at the same time the user does not realize that live x-ray imaging is not active, although the still image icon is displayed and all legally required live x-ray indicators (such as dose rate, x-ray active icon, fluoro timer, audible signal —x-ray buzzer-) are inactive. according to the manufacturer, the system is working fully within specification and accordance with its intended use. the manufacturer will inform users via the field safety notice (fsn) about the presence of the live and still image indications on the system as mentioned in the instructions for use. users are advised to follow the recommended actions in the fsn. 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 20 november 2015.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Philips Healthcare All Allura Xper, AlluraClarity, Allura CV, Allura Centron and UNIQ systems
  • Manufacturer

Manufacturer

  • 제조사 모회사 (2017)
  • Source
    DH