Medrad MRXperion MR Injection System 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Imaxeon 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-2016-RN-00828-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2016-06-21
  • 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 manufacturer, bayer, has identified that a 4205 error message may occur when mrxperion is installed in a magnetic resonance imaging suite which houses a 3t mr scanner. the occurrence of a 4205 error message is the result of electromagnetic interference when the mrxperion is exposed to radio frequency (rf) energy during certain pulse sequences on 3t scanners. this error message indicates an internal communication error within the device and may require a re-boot of the injection system. if the 4205 error message occurs during a contrast-enhanced mr procedure, users of affected systems may experience the need to repeat the injection and imaging procedure. also, an alternative diagnostic imaging procedure may be required. there have been no patient or user injuries reported as a result of this situation.
  • 조치
    Imaxeon is advising users if they encounter a 4205 error message to take the following steps: - With the patient on the table, assess whether to re-boot the MRXperion and proceed with the current scan, proceed with a hand injection if procedure permits, or select an alternate field strength scanner or imaging study. - If the error occurs when the injector is powered on but not in use, then consider re-booting the MRXperion. Imaxeon will be implementing a hardware and software upgrade to permanently correct the issue. This action has been closed-out on 18/05/2017.

Device

  • 모델명 / 제조번호(시리얼번호)
    Medrad MRXperion MR Injection System Catalogue Number: MRXP 200ARTG Number: 156857
  • Manufacturer

Manufacturer

  • 제조사 모회사 (2017)
  • Source
    DHTGA