Intuitive Surgical 5mm Cannula and 5mm Flared Cannula (Reusable endotherapy cannula) 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-2013-RN-00583-2
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2013-06-13
  • 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 manufacturer has received a small number of customer complaints regarding damaged 5mm cannula which could lead to difficulty inserting or utilising 5mm surgical instruments. using a damaged or bent cannula can result in the loss of smooth instrument motion and/or particles of instrument shaft material being generated, which may drop into the patient.
  • 조치
    Device Technologies is updating the current instructions for use with a modified inspection process for the identification of damaged or bent cannula using an obturator which will be provided to users.

Device

  • 모델명 / 제조번호(시리얼번호)
    Intuitive Surgical 5mm Cannula and 5mm Flared Cannula (Reusable endotherapy cannula)5mm CannulaProduct code: INS-4200115mm Flared CannulaProduct code: INS-420262ARTG Number: 97289
  • Manufacturer

Manufacturer