Fluoron Gas Tamponade EasyGas SF6 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 IQ Medical 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-01327-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2014-12-18
  • 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
    Fluoron gmbh is voluntarily recalling the product due to a potential incorrect bottling of the longer acting gas c3f8 (12%) instead of sf6 (20%).
  • 조치
    IQ Medical is requesting surgeons/healthcare professionals to notify their patients who received the affected products about the resulting extended prohibition of flying, diving and anaesthesia using nitrous oxide of 60 days from treatment. IQ Medical is also recalling any remaining stock in the market. This action has been closed-out on 08/03/2016.

Device

  • 모델명 / 제조번호(시리얼번호)
    Fluoron Gas Tamponade EasyGas SF6Item Number: G-80950Lot Numbers: EG1 300614 and EG1 150714ARTG Number: 197089
  • Manufacturer

Manufacturer