CONSERVE Shell, DYNASTY Metal Liner, RIM-LOCK Metal Liner, LINEAGE Metal Liner (components used for Metal on Metal (MoM) Total Hip Arthroplasty) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 MicroPort Orthopedics 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-00893-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2016-12-02
  • 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
    Microport orthopedics inc.’s international experience has shown an increasing overall trend in revisions from 2009 to present, and it was identified that there was a specific hazard/harm for “suspected tissue reaction to metal debris”. the potential for a patient reaction when implanted with metal on metal tha is a known risk for this product technology. the typical impairment of tissue reaction is reversed by revision surgery to remove the old device and replace it with a new device.Microport metal on metal total hip replacements have not been used in australia since 2013 and have been cancelled from the australian register of therapeutic goods (artg). in australia, published information has shown few users with low revisions. for more information, please see https://www.Tga.Gov.Au/alert/microport-orthopedics-metal-metal-hip-implant-components .
  • 조치
    MicroPort Orthopedics is contacting surgeons to make them aware of this issue. Rising levels in serial measurements of Cobalt and Chromium in blood, in conjunction with X-ray, MRI and ultrasound can be valuable in the follow-up of patients. Recipients of Total Conventional MoM implants with a large femoral head, and recipients of Total Resurfacing Implants who are female and/or have a small femoral head are at a higher risk of metal pathology related complications leading to revision. These patients should receive particularly close follow-up. The TGA has developed guidelines for the follow up of patients that have received a MoM hip replacement. These guidelines were developed in consultation with the Australian Orthopaedics Association and The Orthopaedics Sub Committee of the Advisory Committee on the Safety of Medical Devices, and can be found at: https://www.tga.gov.au/metal-metal-hip-replacement-implants .

Device

  • 모델명 / 제조번호(시리얼번호)
    CONSERVE Shell, DYNASTY Metal Liner, RIM-LOCK Metal Liner, LINEAGE Metal Liner (components used for Metal on Metal (MoM) Total Hip Arthroplasty)All implanted lots
  • Manufacturer

Manufacturer