LIFEPAK 1000 Defibrillator 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Physio-Control 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-00774-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2014-07-14
  • 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
    Physio-control australia has become aware of incidents where customers have attempted to use their lifepak 1000 defibrillator and the device has shut down unexpectedly due to a very low battery. a defibrillator in this scenario has the potential to fail to deliver a shock and deliver therapy.The operating instructions provided with the device may be confusing to some customers, which has contributed to customers not replacing their battery when required. specifically, there has been confusion regarding the readiness of the device when the ok symbol is present with a low battery charge symbol. additionally, a software malfunction in the lifepak 1000 defibrillator that also contributes to some customers not replacing their battery when required. this results in the readiness display indicating a low battery charge when it should indicate a very low battery charge.
  • 조치
    Customers are advised that it is critically important to understand what the device and battery indicators mean on the defibrillator and what actions needs to be undertaken. At any time the battery charge can be verified by the instructions provided in the Operating Instructions. Batteries that are at both low battery charge and very low battery charge must be replaced with a fully charged battery, whether or not the OK symbol is present. Physio-Control continues to investigate this issue and will have a follow up communication with customers regarding this issue. This communication may include updates to Operating Instructions, software updates or additional maintenance instructions.

Device

Manufacturer

  • 제조사 모회사 (2017)
  • Source
    DHTGA