Combur-Test and ChoiceLine 10 test kits (urine test strips). 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-2016-RN-01198-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2016-09-13
  • 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
    The instructions for use (ifu) contain an error regarding gram-status of bacteria for the nitrite test. in the limitations or accuracy section, gram-negative bacteria have been incorrectly referred to as gram-positive. however, the strip performance is not affected, so the product can still be used as specified. if a physician is not aware that a positive nitrite result is indicative of gram-negative bacteria, but follows the incorrect classification within the ifu, an insufficient class of antibiotic may be chosen for the initial treatment of urinary tract infection (uti). however, the “gram-classification” of bacteria should be common medical knowledge and use of recommended processes for identification of uti-causing bacteria (such as urine culture methods) will mitigate risk. nevertheless, a medical risk for patients due to an insufficient antibiotic chosen initially cannot entirely be excluded.
  • 조치
    Roche is advising users of the correct wording for the Instructions for Use (IFU). A revised IFU will be provided to users, and additional information provided with each lot of product until the IFU is corrected. This action has been closed-out on 18/05/2017.

Device

  • 모델명 / 제조번호(시리얼번호)
    Combur-Test and ChoiceLine 10 test kits (urine test strips). An in vitro diagnostic medical device (IVD) ChoiceLine 10 testMaterial Number: 03504379023Combur10 Test UXMaterial Number: 11544373049Combur10 TestMaterial Number: 04510089056 Combur9 TestMaterial Number: 04510054056All lots affectedARTG Number: 224003
  • Manufacturer

Manufacturer