Plum 360 Infusion System 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 ICU Medical 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
    2017-06-27
  • 사례 출판 날짜
    2017-06-27
  • 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: icu medical hospira plum 360 infusion system the therapeutic goods administration (tga) of australia has posted a medical device safety alert concerning hospira plum 360 infusion system [list number: 30010; multiple serial numbers], manufactured by icu medical. the manufacturer has identified a potential for the connectivity engine (ce) module to disengage from the main chassis. in a rare situation, this could lead the plum 360 infuser to power down without an alarm notification resulting in a delay of either initiation of a therapy or interruption of an active infusion. in rare circumstances, these conditions could lead to serious adverse health consequences related to changes in a patient’s vital signs. to date, the manufacturer has not received any reports of serious injury or death associated with this issue. the manufacturer will be contacting users and arranging for inspection of all affected plum 360 infusers. the chassis will be replaced as required. in the interim, the manufacturer is advising users to inspect the affected plum 360 infusers using the instructions provided in the customer letter in order to verify that the infuser is working. if at the end of testing a loose ce module or blank display is observed, the infuser is to be removed from service, and the user is to record the s/n and contact the manufacturer’s service department. otherwise, the infuser can be returned to clinical use. if the plum 360 infuser powers down without an alarm notification during infusion, use another plum 360 infuser for infusion or consider use of alternative infusion methods based on the clinical situation. for details, please refer to the tga website: http://apps.Tga.Gov.Au/prod/sara/arn-detail.Aspx?k=rc-2017-rn-00729-1 if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 27 june 2017.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: ICU Medical Hospira Plum 360 Infusion System
  • Manufacturer

Manufacturer