Astral 100 and 150 ventilators 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Resmed Limited 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-2017-RN-00762-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2017-07-19
  • 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
    Resmed has received a number of reports about the performance of the internal battery, where false activation of a fuse leads to shut down of the internal battery. prior to the issue occurring, one or more of the following alarms were activated: battery inoperable, power fault / no charging, device overheating. if the device is running on external power then ventilation will continue. if the device is not running on external power, or external power is removed, then ventilation will stop with activation of the total power fail alarm. reconnection to external power will enable ventilation to recommence.When ventilators use the internal battery as the sole power source, any performance issue with the battery could lead to cessation of therapy. in these cases, ventilator-dependent patients may be at risk if no urgent action is taken to restore power or switch to back-up ventilation. there have been no reports of this issue in australia to date, nor any adverse health effects.
  • 조치
    ResMed is providing a Clinical Guide addendum that is to be kept with existing Clinical Guides that includes the following warning: The internal battery is NOT intended to serve as a primary power source. It should only be used briefly when necessary; for example, when changing power sources, or when other sources are temporarily unavailable. In addition, users and carers are to continue to follow all patient and device information in the Astral User and Clinical Guides, in particular the following warnings: - For ventilator-dependent patients, always have alternate ventilation equipment available, such as a back-up ventilator, manual resuscitator or similar device. Failure to do so may result in patient injury or death. - Ventilator-dependent patients should be continuously monitored by qualified personnel or adequately trained carers. These personnel and carers must be capable of taking the necessary corrective action in the event of a ventilator alarm or malfunction.

Device

  • 모델명 / 제조번호(시리얼번호)
    Astral 100 and 150 ventilatorsAll Astral External BatteriesAll Astral Battery PacksARTG Numbers: 219429 and 158756
  • Manufacturer

Manufacturer