STERIS Quick Connects (used with the Steris System 1 Express and System 1 Plus sterilisers) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Device Technologies 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-2016-RN-00251-1
  • 사례 위험등급
    Class III
  • 사례 시작날짜
    2016-03-04
  • 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
    Quick connects provide directed flow of sterilant use dilution and rinse water into the internal lumens of specifically identified endoscopes to achieve liquid chemical sterilisation.Steris has learned that one of the hysteroscope models (karl storz 11264bbu1) listed for processing in stqkc1736int and st-qkc-1737int has one inlet port rather than two inlet ports as indicated in the quick connect processing instructions. a user who connects the karl storz 11264bbu1 hysteroscope according to the processing instructions will observe an unused quick connect port adapter. steris performed testing on the karl storz 11264bbu1 hysteroscope which confirmed that despite this unused port adapter, the flow provided to the lumen is more than adequate. therefore, the efficacy of the liquid chemical sterilisation process is not affected. however, there is potential for user confusion due to the unused quick connect port adaptor if used for this hysteroscope.
  • 조치
    Device Technologies is advising users that updated labelling kits and instructions for use will be provided. The impacted hysteroscope can be processed using the ST-QKC-1705INT processing manual. This action has been closed-out on 30/01/2017.

Device

  • 모델명 / 제조번호(시리얼번호)
    STERIS Quick Connects (used with the Steris System 1 Express and System 1 Plus sterilisers)Product Codes: ST-QKC1736INT and ST-QKC-1737INTARTG Number: 113489
  • Manufacturer

Manufacturer