VITROS Chemistry Products PHYT Slides. An in vitro diagnostic medical device (IVD)(utilised with VITROS 250/350/5, 1 FS and 4600 Chemistry Systems and VITROS 5600 Integrated Systems) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Ortho-Clinical Diagnostics Australia Pty Ltd 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-2017-RN-00941-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2017-08-30
  • 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 (ortho) has determined that negatively biased results may occur when processing citrate plasma samples using vitros chemistry products phyt slides. as a result, citrate plasma is being removed as a recommended specimen type for vitros phyt slides. internal testing by ortho confirmed negatively biased patient results using vitros phty slides for citrate plasma samples. the majority of the bias may be attributed to the dilution effect of the liquid anticoagulant in the citrate plasma tubes with the sample. serum and/or heparin plasma samples obtained from the same patients did not exhibit biased results. the average negative bias observed using citrate plasma samples when compared to serum samples is approximately 18% across the phyt reportable measuring range of 3.00–40.00 µg/ml (11.88–158.40 µmol/l).
  • 조치
    Citrate plasma is being removed as a recommended specimen type for VITROS PHYT Slides. 1. Immediately discontinue using citrate plasma samples for VITROS PHYT Slides: 2. Retain this notification as verification of the revised instructions. 3. Notify laboratory and medical staff of this change. 4. Continue using heparin plasma or serum samples to process VITROS PHYT Slides. 5. Complete the supplied Customer Acknowledgement form of Receipt and return. 6. Post the notification by each VITROS System or with the user documentation. 7. Forward the notification if you have distributed these products outside of your facility.

Device

  • 모델명 / 제조번호(시리얼번호)
    VITROS Chemistry Products PHYT Slides. An in vitro diagnostic medical device (IVD)(utilised with VITROS 250/350/5, 1 FS and 4600 Chemistry Systems and VITROS 5600 Integrated Systems)Unique Identifier Number: 10758750004690Product Code: 8298671Affects expired, current (in date) and future products GENsARTG Number: 245278
  • Manufacturer

Manufacturer