Maxi Air Blower Unit - Model 230V(A device designed as a stretcher that is intended for use together with a patient transfer lifting for lifting a patient who is moveable only in a horizontal lying position.) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Huntleigh Healthcare 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-00859-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2015-09-08
  • 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
    The plastic enclosure used in the maxi air supply motor for models 230v is not fire retardant. this can be seen by the "arrows" on the moulded part and was confirmed by an ad-hoc flammability test. this may increase the risk of a fire spreading.
  • 조치
    An ArjoHuntleigh representative is attending the hospital to replace the affected blower unit.

Device

  • 모델명 / 제조번호(시리얼번호)
    Maxi Air Blower Unit - Model 230V(A device designed as a stretcher that is intended for use together with a patient transfer lifting for lifting a patient who is moveable only in a horizontal lying position.)Serial Number: 1310000127ARTG Number: 215885
  • Manufacturer

Manufacturer