All Plum A+ Family of Infusers: Plum A+Single Channel Infusion Pump, Plum A+ and A+3 Infusion Pumps with MedNet Software 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Hospira Pty Limited 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-00180-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2013-02-27
  • 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.
    ICU Medical, Inc. acquired from Pfizer in early 2017, Hospira Infusion Systems, the portion of Hospira dedicated to develop infusion pumps.
  • 데이터 추가 비고
  • 원인
    The plum a+ fluid shield diaphragm may be out of specification and cause n250 "door open while pumping" or n100 "unrecognisable cassette" alarms. hospira inc have advised that these alarms invoke audible and visual warnings to the user which may occur during setup, infusion or performance verification test and will cause the device set up to be interrupted or the infusion to stop. if these alarms occur whilst the clinician is setting up the pump or an infusion is in progress, a delay or interruption in therapy may result.
  • 조치
    If the unrecognisable cassette alarm occurs during the loading process prior to infusion starting, remove the cassette and attempt to reload the cassette again. If the alarm happens multiple times it is recommended to get a new tubing set or remove the device from service. To correct this issue, Hospira has implemented a screening process to identify fluid shields that are out of specification. Plum devices shipping from Hospira since September 2012 have diaphragms that have been screened for the undersized dimension. Hospira will be contacting customers to arrange for screening and replacement of impacted fluid shields.

Device

  • 모델명 / 제조번호(시리얼번호)
    All Plum A+ Family of Infusers: Plum A+Single Channel Infusion Pump, Plum A+ and A+3 Infusion Pumps with MedNet SoftwarePlum A+Single Channel Infusion PumpCatalogue Number: 611239101Number on Pump: 12391 & 11971Plum A+ Infusion Pump with MedNet SoftwareCatalogue Number: 612079201Number on Pump: 20792Plum A+3 Infusion Pump with MedNet SoftwareCatalogue Number: 612067801Number on Pump: 20678
  • Manufacturer

Manufacturer

  • 제조사 모회사 (2017)
  • Source
    DHTGA