Trilogy dual prescription ventilators with software versions 13.2.04, 13.2.05, 14.0.00, and 14.1.01 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Philips Electronics Australia Ltd 에 의해 제조된 제품과 관련되어 있습니다.

이것은 무엇인가요?

의료기기에 문제가 생겼을 경우 제조사가 이를 바로잡거나 시장에서 회수하는 조치를 말한다. 회수(Recall)는 의료기기에 결함이 있거나, 건강에 위협이 되거나, 또는 결함도 있고 건강에도 위협이 될 경우에 발생한다.

데이터에 대해 더 자세히 알아보기 여기
  • 사례 유형
    Recall
  • 사례 ID
    RC-2016-RN-00107-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2016-01-28
  • 사례 국가
  • 사례 출처
    DHTGA
  • 사례 출처 URL
  • 비고 / 경고
    Australian data is current through July 2018. All of the data comes from the Australian Therapeutic Goods Administration, 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 recall data from the U.S. and Australia.
  • 데이터 추가 비고
  • 원인
    Philips respironics has become aware that trilogy ventilators with the affected software versions and dual therapy prescriptions are susceptible to an inadvertent change between prescriptions. this may occur under a particular set of operating conditions without requiring confirmation of the change by the user.- device connected to the ac power source- device software versions 13.2.04, 13.2.05, 14.0.0 or 14.1.01- dual prescription is on- menu access is limited- device powered on- the device is allowed to operate for 5 or more minutes without pressing the up arrow keypressing the right key selects the “switch to secondary settings” menu. pressing the right key again within the next 30 seconds, confirms the “switch to secondary settings” and the device will switch from the primary to the secondary settings. the devices continue to display the active prescription in the upper left hand corner of the display, however, the user may be unaware of this change.
  • 조치
    Philips is advising users that there is a software update available (my.respironics.com) for users to upgrade the device software to version 14.1.02. This action has been closed out 01 Feb 2017.

Device

  • 모델명 / 제조번호(시리얼번호)
    Trilogy dual prescription ventilators with software versions 13.2.04, 13.2.05, 14.0.00, and 14.1.01Model Numbers: 100 and 202ARTG Numbers: 159490 and 174169
  • Manufacturer

Manufacturer

  • 제조사 모회사 (2017)
  • Source
    DHTGA