Active Knee System - Patella Insert (Used as a component in total knee replacement) ASDM 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Advanced Surgical Design & Manufacture Limited 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-2012-RN-01164-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2012-11-27
  • 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
    Advanced surgical design and manufacture has become aware of elevated failure rates of the patella component of the active knee system, specifically related to the shearing of the pegs. fourteen occurrences have been reported to date, which represents a failure rate of 0.7% of patellae implanted since july 2007. batches which have been found to be affected were manufactured between 2007 and 2011, with failures presenting between 1 to 4 years after implantation.Electron microscopy of the failed patella has shown that the patella pegs are failing due to fatigue. the initiation site for the fatigue failure appears to be a small overhang artefact, between 10 to 30 microns in depth, at the base of the patella peg. this small artefact may lead to elevated stresses at the base of the peg, and therefore increases the risk of premature product failure.
  • 조치
    Advanced Surgical Design and Manufacture is advising implanting/treating surgeons on how to manage patients implanted with the affected Active Knee System. For more details, please see http://www.tga.gov.au/safety/alerts-device-active-knee-121205.htm This action has been closed-out on 12/04/2016.

Device

  • 모델명 / 제조번호(시리얼번호)
    Active Knee System - Patella Insert (Used as a component in total knee replacement) ASDM Part Number: 10-1514-075XLots manufactured prior to June 2012ARTG Number:133900
  • Manufacturer

Manufacturer