Trinder tests on Roche Analysers – Hitachi 902, COBAS c111, COBAS c311/501/502/701/702 & COBAS INTEGRA 400 plus/800. 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-2015-RN-00398-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2015-05-13
  • 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
    New interference claims for trinder tests have been verified by roche internal studies.Trinder tests measured in samples which contain nac, napqi, and metamizole may show inaccurate results. the severity depends on the clinical situation and the therapeutic state of the patient. it is good clinical practice not to take blood from a patient immediately after administering medication, except in the case of therapeutic drug monitoring. nevertheless under certain, rare circumstances there is insufficient time between the administration of a drug and blood sampling, which may lead to accuracy issues with the trinder tests.Roche has identified:1. falsely low crea plus results for patients with a toxic level of acetaminophen under treatment with n-acetylcysteine (nac). 2. falsely low results of crea plus after intravenous injection of metamizole.The crea plus results were below the measuring range, while plausible results were obtained with the crea jaffé method.
  • 조치
    Laboratories are advised to be aware that the recovery of Trinder tests may be falsely low when the blood sample is taken while levels of NAC, NAPQI, and Metamizole are still present.

Device

  • 모델명 / 제조번호(시리얼번호)
    Trinder tests on Roche Analysers – Hitachi 902, COBAS c111, COBAS c311/501/502/701/702 & COBAS INTEGRA 400 plus/800. An in vitro diagnostic medical device (IVD) · CREA plus, · CREP2, · LACT2, · Lactate, · GLU, · TRIGL/TG, · TRIGGB, · TRIG/GB, · CHOL/CHOL2, · HDL-C plus 3rd generation/HDLC3, · LDL_C plus 2nd generation/LDL_C, UA2/UA plusARTG: 174906, 174908 & 174909
  • Manufacturer

Manufacturer