Allura Xper Systems with an attached 7th or 8th monitor Multiple System Codes 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Philips Electronics Australia 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-2018-RN-00071-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2018-01-19
  • 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
    Philips has been made aware of a mounting issue with the 7th or 8th monitor to the monitor ceiling suspension. the 7th or 8th monitor attached to the monitor ceiling suspension may disengage from the suspension arm and fall down.Only allura xper systems with an attached 7th or 8th monitor on the monitor ceiling suspension are affected.When a 7th or 8th monitor disengages from the suspension arm it could pose a risk for the patient, user, bystander or service engineer.
  • 조치
    Philips will be in contact with all potentially affected users and arrange for the set screws to be secured.

Device

  • 모델명 / 제조번호(시리얼번호)
    Allura Xper Systems with an attached 7th or 8th monitor Multiple System CodesARTG Number: 225815 (Philips Electronics Australia Ltd - X-ray system, diagnostic, fluoroscopic, angiographic, stationary, digital)
  • Manufacturer

Manufacturer

  • 제조사 모회사 (2017)
  • Source
    DHTGA