Advantx Legacy/Legacy-D Radiographic and Fluoroscopic System 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-2017-RN-00198-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2017-02-08
  • 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
    There have been reported incidents of a patient step detaching from the table. a fall from a patient step detaching while in use could result in an injury to a patient or operator. there have been no injuries reported as a result of this issue.
  • 조치
    GE Healthcare will correct all affected products and a GE Healthcare representative will contact affected customers to arrange for the correction. In the interim, customers are advised to check the table tub bottom pan and patient step hardware for any looseness. Discontinue use of the patient step in case of any looseness and immediately contact the GE service representative. This action has been closed-out on 1/03/2018.

Device

  • 모델명 / 제조번호(시리얼번호)
    Advantx Legacy/Legacy-D Radiographic and Fluoroscopic SystemARTG Number: 99423
  • Manufacturer

Manufacturer