Events

Cobas 8000 'v2' instrument drivers for Cobas IT 3000 (Used with Cobas IT 3000 versions 2.03.08 to 2.04.00); An in vitro diagnostic medical device (IVD) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Roche Diagnostics Australia 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-2012-RN-00783-3
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2012-08-06
  • 사례 국가
    Australia
  • 사례 출처
    DHTGA
  • 사례 출처 URL
    https://apps.tga.gov.au/Prod/sara/arn-detail.aspx?k=RC-2012-RN-00783-3
  • 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
    There is a potential for incorrect handling of extra-long result messages that are sent form the cobas® 8000 data manager and received into it 3000 using a “v2” instrument driver. this is applicable for messages that are greater than 33 results in length per episode and if the configuration of the predefined buffer size is not optimal. the “v2” instrument drivers for cobas® 8000 use a buffer to ensure that extra-long result messages are processed correctly. if this buffer is not configured for the specific driver that is installed, then there can be a mismatch in the amount of data that is truncated. the effect of this being that results and flags after result #33 in the string may be delayed and in some cases may not be reported to cobas® it 3000.
  • 조치
    Roche are providing work around instructions until a software upgrade can be implemented to permanently fix the issue.

Device

Cobas 8000 'v2' instrument drivers for Cobas IT 3000 (Used with Cobas IT 3000 versions 2.03.08 to...
  • 모델명 / 제조번호(시리얼번호)
    Cobas 8000 'v2' instrument drivers for Cobas IT 3000 (Used with Cobas IT 3000 versions 2.03.08 to 2.04.00); An in vitro diagnostic medical device (IVD)
  • Manufacturer
    Roche Diagnostics Australia Pty Limited

Manufacturer

Roche Diagnostics Australia Pty Limited