FreeStyle Papillon Mini Blood Glucose Monitoring System 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Abbott Australasia Pty Ltd T/A Abbott Diabetes Care 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-2014-RN-00167-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2014-02-20
  • 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
    Abbott diabetes care has identified through internal testing and investigation that all non-applied voltage legacy meters have the potential to produce out of range control solution results and/or give blood glucose results which could affect clinical outcome or have significant medical risk when used in conjunction with any freestyle test strip lot within expiry.Br /br /this is an update to the recall initiated in november 2013 on certain lots of freestyle blood glucose test strips (rc-2013-rn-01228-1). the freestyle papillion mini blood glucose monitoring system has not been supplied in australia since 2009.Br /br /further inforamtion on this recall can be found at http://www.Tga.Gov.Au/safety/alerts-device-freestyle-strips-papillon-mini-140304.Htm.
  • 조치
    Abbott is providing consumers who are still the possession of of a FreeStyle Papillion Mini blood glucose meter with a replacement FreeStyle branded meter.

Device

Manufacturer

  • 제조사 모회사 (2017)
  • 제조사 의견
    “We are in constant communication with regulatory agencies and competent authorities worldwide which allows us to implement global recalls or in-country communication quickly and effectively,” Abbott, which now owns St. Jude Medical told ICIJ in a statement. In addition to sending global notices to physicians worldwide, we also make sure that product advisories are available online and classification of product recalls and product advisories are determined by global regulatory bodies which can impact the timing in any given country. MD companies follow varying regulations in different countries. In come countries software is not regulated so a recall in one country related to software would not be classified as a recall or field action in another. In addition, review cycles within the regulatory process can be different in each country which can impact communication and recall timing.
  • Source
    DHTGA