HomeChoice Pro Automated Peritoneal Dialysis System 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Baxter 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
    2013-11-04
  • 사례 출판 날짜
    2013-11-04
  • 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: baxter homechoice pro automated peritoneal dialysis system the australia therapeutic goods administration (tga) has issued a medical device safety alert concerning homechoice pro automated peritoneal dialysis (apd) system manufactured by baxter healthcare. products with product code r5c8320 and the serial numbers 300905, 300882, 300928, 300889 are affected. there is a potential issue with the occluder assembly of homechoice pro devices. the blade of the occluder assembly is covered with a rubber boot. the occluder blade clamps the solution lines if a power failure occurs or when the cycler is off. this prevents uncontrolled solution delivery to the patient. an occluder failure will cause an unrecoverable slow flow/no flow alarm or an unrecoverable system error. the device will fail in a safe position and prevent solution from being delivered to the patient. baxter is informing the affected hospitals of the issue. hospitals will either notify affected patients or baxter will contact patients via homecare and arrange to swap the affected machines. baxter is also advising patients to perform manual peritoneal dialysis to continue therapy if there is an unrecoverable failure. according to the local supplier, the affected products were not distributed in hong kong. for details, please visit the following tga website: http://www.Tga.Gov.Au/sara/arn-detail.Aspx?k=rc-2013-rn-01117-1 if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 4 november 2013.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Baxter HomeChoice Pro Automated Peritoneal Dialysis System
  • Manufacturer

Manufacturer