Events

Spaplus Weekly wash Protocol and Bottles. An in vitro diagnostic medical device (IVD) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 In Vitro Technologies 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-01502-1
  • 사례 위험등급
    Class III
  • 사례 시작날짜
    2017-12-12
  • 사례 국가
    Australia
  • 사례 출처
    DHTGA
  • 사례 출처 URL
    https://apps.tga.gov.au/Prod/sara/arn-detail.aspx?k=RC-2017-RN-01502-1
  • 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 manufacturer, the binding site, have identified that the barcode label for the affected lot is incorrect and will not be recognised by the spaplus instrument. this lot number cannot be used to complete the weekly wash. there is no clinical impact associated with this issue.
  • 조치
    In Vitro Technologies is advising users to quarantine and dispose of any remaining units of the affected product.

Device

Spaplus Weekly wash Protocol and Bottles. An in vitro diagnostic medical device (IVD)
  • 모델명 / 제조번호(시리얼번호)
    Spaplus Weekly wash Protocol and Bottles. An in vitro diagnostic medical device (IVD)Item Number: TBSIK050SLot Number: 415451ARTG Number: 201721
  • Manufacturer
    In Vitro Technologies Pty Ltd

Manufacturer

In Vitro Technologies Pty Ltd