Alaris GP, GP Guardrails, GP Plus & GP Plus Guardrails Infusion Pumps 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 CareFusion Australia 316 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-2013-RN-00584-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2013-06-14
  • 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
    Post market surveillance has identified an increased occurrence of stepper motor stalls due to the rear bearings not performing as designed.A motor stall condition may occur during:- start up (immediately after the start key is pressed) or;- during an infusion which may result in the early termination of an infusion. early termination of an infusion could require intervention especially if critical drugs are being administered.In either case the pump is designed to fail safe giving an audible alarm, a visual alarm displayed on the infusion pump display - "drv1" or "drv2" and the red beacon light on the infusion pump will flash, prompting the infusion pump user to intervene.
  • 조치
    End users are requested to identify all affected infusion pumps and report back to their Carefusion representative. On receipt of this information Carefusion will organise for the replacement of the motor. The infusion pumps can be continued to be used in accordance with the instructions for use. In the unlikely event that end users experience a 'DRV1' or 'DRV2' error quarantine the pump and contact your Carefusion representative immediately.

Device

  • 모델명 / 제조번호(시리얼번호)
    Alaris GP, GP Guardrails, GP Plus & GP Plus Guardrails Infusion PumpsProduct reference numbers: 80263UN01, 80263UN01-G, 9002MED01, 9002MED01-GPumps manufactured between Dec 2009 and Jan 2012ARTG number: 130389
  • Manufacturer

Manufacturer