GE Healthcare MRI systems with superconducting magnets 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 GE Healthcare 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-2015-RN-00103-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2015-02-06
  • 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 mru (magnet rundown unit) is a critical safety component of the mr system that quenches the magnet (i.E., makes it non-magnetic) in emergency situations, such as those that can occur when a ferrous (metal) object is brought into the magnetic field.At certain sites, the mru may not be connected to the magnet. if the mru is disconnected, the mru will not function as expected and will not quench the magnet when the button is pressed. in emergency situations, a disconnected mru could delay removal of a ferrous object from the magnet, potentially resulting in life-threatening injuries. the mru must be connected to the magnet at all times. further, there is potential for a patient to sustain injury while trapped against the mr scanner.
  • 조치
    GE Healthcare has provided instructions to assist end users to determine if the MRU is properly connected. If the MRU is not connected it is recommended that the MRI is not used and GE Healthcare is contacted immediately. GE Healthcare will inspect all affected systems and ensure the MRU is properly connected to the magnet. This will be performed by GE Healthcare service representative who will contact affected customers to arrange for this inspection and correction if needed. This action has been closed-out on 1/06/2016.

Device

Manufacturer