Events

Sapphire Multi Therapy Pump with software Rev09Ver07 (Infusion Pump) 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-01041-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2013-10-10
  • 사례 국가
    Australia
  • 사례 출처
    DHTGA
  • 사례 출처 URL
    https://apps.tga.gov.au/Prod/sara/arn-detail.aspx?k=RC-2013-RN-01041-1
  • 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 manufacturer, q core, has received three similar reports from a customer, who experienced deviations from the duration of treatment, as programmed. the incidents occurred while using the multi step mode. while no patient injuries or deaths have been reported, the issue may result in incorrect therapy. specifically, the issue only occurs when the following conditions are met simultaneously:- multi-step mode is used, and- the pump is not plugged into an ac power outlet and is operating on battery power only, and- the pump backlight is turned off.The factory default for the backlight configuration in the sapphire multi therapy pump is on; therefore unless the pump backlight is turned off, the issue will not occur.
  • 조치
    Q Core has developed a software solution (Rev09Ver08) to address the issue. Until the Sapphire Multi Therapy pumps have been updated with the new software, users are required to: (i)Use the Sapphire Multi Therapy pump plugged into an AC power outlet; and/or (ii)Use the Sapphire Multi Therapy pump with the backlight configuration set to ON or PARTIAL. It is recommended to check all pumps that are in current operation in order to ensure correct setting of the backlight. Please note that in pumps configured with backlight OFF the screen will darken completely after 1 minute of screen inactivity. The pumps configured to have the backlight OFF require reconfiguration of the backlight setting to ON.

Device

Sapphire Multi Therapy Pump with software Rev09Ver07 (Infusion Pump)
  • 모델명 / 제조번호(시리얼번호)
    Sapphire Multi Therapy Pump with software Rev09Ver07 (Infusion Pump)Hospira List Number: 163113601ARTG Number: 201499
  • Manufacturer
    Hospira Pty Limited

Manufacturer

Hospira Pty Limited
  • 제조사 모회사 (2017)
    Pfizer
  • Source
    DHTGA