PS500 External Power Supply Unit used with Dräger V Series Ventilators 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Draeger Medical Australia Pty 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-2014-RN-00165-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2014-02-18
  • 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
    The batteries installed in the ps500 deplete much earlier than expected although the battery indicator showed a sufficiently charged battery. in some cases neither the “battery low” nor the “battery depleted” alarm was given, when the remaining battery capacity fell below 10%. available data indicates that the charged battery will last for at least 3 minutes. in case of a main power loss, this 3 minute battery back-up should typically be sufficient until the emergency main power supply is re-established.
  • 조치
    Draeger is advising users to only use the affected device for transport if absolutely necessary and users should not rely on the battery status indicator. Draeger is recommending users have a breathing bag available for manual ventilation as per the Instructions for Use (IFU). Draeger is advising that if the power fail alarm occurs during transport, provide manual ventilation and immediately connect the ventilator to wall power to resume ventilation. Draeger is advising that the batteries on all affected devices will be replaced as an interim correction, until a permanent fix can be developed.

Device

Manufacturer