Mobile Digital X-Ray GM60A 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Samsung Electronics 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-2017-RN-00391-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2017-04-20
  • 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
    Samsung has been notified of an issue of over exposed x- ray images. the investigation revealed that mas value had increased without any interaction of the user even when the correct protocol had been followed by the operator. it's been observed from log files analysis that the mas values had increased during the examination and had showed that patients received different dose values than what was stored in the pre-defined protocols. it is discovered that the touch screen is sensitive to unintended touch which may occur if any liquid/ foreign bodies are on the screen. it had also been identified that in these particular incidents, the tube cable had touched the msec up button when the tube head unit of gm60a was at the parked position. protocols were set before the device had been moved & positioned by the patient. whilst the device was moved, the cable had touched the panel and increased the exposure condition to the maximum value. this may lead to unintended exposure to the patient.
  • 조치
    Samsung has developed a software update which will be implemented by a trained service engineer who will attend the users' premises. In the interim, Samsung is recommending users ensure that the GM60A system is moved into position before parameters are set and that there are no obstructions to the touchscreen which may cause an increase in values during the examination and to always ensure that the correct exposure levels have been set before exposure to the patient.

Device

  • 모델명 / 제조번호(시리얼번호)
    Mobile Digital X-Ray GM60A Serial Numbers: 509RM9BGB00001 and 509RM9BGB00002ARTG Number: 229491
  • Manufacturer

Manufacturer