VITROS 5,1 FS Chemistry Systems using Software Version 2.8 & Below. An in vitro diagnostic medical device (IVD). 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Ortho-Clinical Diagnostics 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-2015-RN-00214-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2015-03-13
  • 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
    Ortho-clinical diagnostics, inc. (ocd) has confirmed two instances where a vitros microslide cartridge was misidentified. both instances occurred when an operator accessed slide supply 1 (ss1) before the green indicator light was illuminated and subsequently proceeded to load a slide cartridge into slide supply 2. in each occurrence, the loaded cartridge in slide supply 2 was misidentified.
  • 조치
    If an operator inadvertently accesses a Slide Supply load door before the green indicator light is illuminated and the system generates a TAS-70E or TAS-20E condition code the operator must open and close both Slide Supply doors (Slide Supply #1 & 2), not remove or add any cartridges, and initialise the system. This will cause the system software to scan all slots of both Slide Supplies in order to properly identify the contents. Discuss any concerns regarding previously reported results with your Laboratory Medical Director to determine the appropriate course of action. The resolution to this issue will be contained in the next version of software currently under development. This action has been closed-out on 31/05/2016.

Device

  • 모델명 / 제조번호(시리얼번호)
    VITROS 5,1 FS Chemistry Systems using Software Version 2.8 & Below. An in vitro diagnostic medical device (IVD). Product Codes: 6801375 & 6801890ARTG Number: 180199
  • Manufacturer

Manufacturer