Philips Dameca Siesta i TS with an EGM software version lower than 4.0.8 / 7.0.8 (Anaesthesia system) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Proact Medical Systems (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-2015-RN-00365-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2015-04-24
  • 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
    It has been discovered that the touch screen on dameca siesta i ts machine may malfunction, resulting in the screen freezing or in some cases turning black during usage. this results in the user not being able to operate the machine using the touch screen, current information is not displayed and settings cannot be modified. the machine will stop automatic ventilation and an alarm will sound and the user needs to initiate manual ventilation by activating the emergency fresh-gas flow function (emergency o2) on the siesta i ts and maintaining ventilation by means of the ventilation bag (manual ventilation).The highest concern is the potential loss of ventilation and fresh gas flow. if losing ventilation and fresh gas flow, this will result in the need of manual ventilation with external fresh gas flow and emergency equipment.
  • 조치
    Users are advised that in cases where automatic ventilation stops, the machine should be restarted (while manually ventilating the patient) and then taken back into normal usage again (return to automatic ventilation and fresh-gas delivery by the electronic gas mixer) after the machine has restarted. Users are also advised to check their existing machine’s version. If EGM software version is lower than 4.0.8/7.0.8 and the problem arises a technician visit will be arranged to upgrade the software. This action has been closed-out on 15/02/2017.

Device

  • 모델명 / 제조번호(시리얼번호)
    Philips Dameca Siesta i TS with an EGM software version lower than 4.0.8 / 7.0.8 (Anaesthesia system)ARTG number: 176848
  • Manufacturer