Endo Wrist One Vessel Sealer (INS-410322) for the da Vinci Si (IS3000) Surgical System(Single use active endotherapy device used in endoscopic procedures for cutting and or coagulating tissue) 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-2014-RN-01174-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2014-11-04
  • 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
    - during a surgical procedure, if the blade does not return to its original position within a specified timeframe, the system determines the instrument has an “exposed blade”. the da vinci si system is designed to display a recoverable fault when an “exposed blade” error occurs. a recoverable fault means that you may continue using the system after addressing the error. activating and firing the knife blade while the jaws are more than 4 mm open increases the likelihood of an exposed blade error. currently, the vessel sealer applies bipolar energy between the electrode surfaces on the interior surface of the instrument jaws in order to coagulate vessels up to 7 mm in size. users are then instructed to keep the master grips fully closed during the sealing cycle. opening the grip on the masters reduces the pressure applied to the vessel during sealing, which may result in insufficient sealing performance.
  • 조치
    Device Technologies Australia is informing their customers of the changes to the user manual to reduce the potential for exposed blade errors and providing a software upgrade to reduce the potential for insufficient sealing. Device Technologies Australia is informing the customers to continue using the Endo Wrist One Vessel Sealer. A Device Technologies Australia product specialist / technician will contact the customer and provide the updated User Manual and schedule the software upgrade which will be available in December 2014. This action has been closed-out on 18/07/2016.

Device

  • 모델명 / 제조번호(시리얼번호)
    Endo Wrist One Vessel Sealer (INS-410322) for the da Vinci Si (IS3000) Surgical System(Single use active endotherapy device used in endoscopic procedures for cutting and or coagulating tissue)Model Number: 410322 ARTG Number 132453
  • 의료기기 분류등급
  • Manufacturer

Manufacturer