EVOTECH Endoscope Cleaner and Reprocessor (ECR) System (Endoscope disinfecting unit) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Johnson & Johnson Medical 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-2013-RN-00320-1
  • 사례 위험등급
    Class III
  • 사례 시작날짜
    2013-04-12
  • 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 manufacturer has determined that under certain circumstances the evotech endoscope cleaner and reprocessor system may not properly calculate the expiration date of the cidezyme xtra multi enzymatic detergent from the information entered by the user. in these circumstances, the expiration date displayed on the evotech ecr screen is one month after the labelled expiration date.
  • 조치
    Johnson & Johnson is providing instructions on how to identify if there is any discrepancy between the calculated expiration date and the labelled expiration date. Users are advised to adhere to the labelled expiration date.

Device

  • 모델명 / 제조번호(시리얼번호)
    EVOTECH Endoscope Cleaner and Reprocessor (ECR) System (Endoscope disinfecting unit)Product code: 50004All lot/serial numbers affected.ARTG number: 146438
  • Manufacturer

Manufacturer