AERONEB PRO-X - CONTROLLER KIT 의 리콜

Health Canada (via FOI)에 따르면, 해당 리콜 는 Canada 에서 AEROGEN 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
    25407
  • 사례 위험등급
    II
  • 사례 시작날짜
    2014-09-05
  • 사례 국가
  • 사례 출처
    HC
  • 비고 / 경고
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • 데이터 추가 비고
  • 원인
    Aerogen has received a small number of complaints in relation to the mains power adapter manufactured by friwo gmbh and used in the aeroneb solo and pro nebuliser systems. the complaints received identified that the power adapter cover had broken and dislodged from the body of the adapter prior to use. however it cannot be ruled out that the adapter may fail during use. if the failure was to occur during use then the internal electrical components of the mains power adapter would become exposed to the user. therefore there is a potential risk of electric shock if the cover falls off during use with mains power turned on and the user makes contact with specific recessed components inside the adapter housing.

Device

  • 모델명 / 제조번호(시리얼번호)
    Model Catalog: AG-PX1000-US (Lot serial: N/A); Model Catalog: AG-AP1040-US (Lot serial: N/A)
  • 제품 설명
    AERONEB PRO X CONTROLLER
  • Manufacturer

Manufacturer

  • 제조사 주소
    DANGAN
  • 제조사 모회사 (2017)
  • Source
    HC