10mm Direct Drive Clip Applier (Used for ligation of tubular structures or vessels in laparoscopic and general surgical procedures) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Applied Medical 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-00387-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2016-04-05
  • 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
    Due to inconsistent clip application, the 10mm direct drive clip applier is being recalled. although malformed clips are typically readily apparent to the user, this failure mode may lead to unoccluded vessels.
  • 조치
    Applied Medical is advising users to check inventory for the affected lots and return any affected product. This action has been closed-out on 30/01/2017.

Device

  • 모델명 / 제조번호(시리얼번호)
    10mm Direct Drive Clip Applier (Used for ligation of tubular structures or vessels in laparoscopic and general surgical procedures)Product Code: CA090Affected Lot Numbers: 1190181 to 1265006Expiry date: Prior to 18 March 2019Affected Kit Product Codes: CK304, GK306, GK307, GK311, GK312, GK317, GK318, GK323, GK334, GK335, K0509 and K0592ARTG Number: 221008
  • Manufacturer

Manufacturer