Birmingham Hip Modular Head (BHMH) (component of MoM total hip replacement systems) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Smith & Nephew Surgical 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-2015-RN-00318-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2015-04-20
  • 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
    Smith & nephew (s&n;) is issuing an update to the oct 2012 hazard alert after analysis of new information identified that patients implanted with the bhmh may be at greater risk of revision surgery. the new revision risk estimate for the bhmh is: -10.6% (95% ci: 9.55, 11.65) at six years follow-up from the national joint registry for england, wales and northern ireland (data accessed in january 2015).. - 11.7% (95% cl: 9.7, 14.0) at ten years of follow-up from aoa njrr (report published in october 2014 based on data collected to end december 2013).Also, a small clinical study undertaken in the uk with patients implanted with sleeved bhmh and uncemented synergy stems indicates that there is a potential increased risk of fretting corrosion and accelerated release of metal debris at the taper junctions of the modular taper sleeve interface with the stem and with the head.
  • 조치
    S&N; recommends that physicians maintain their routine follow-up protocol for patients who have undergone total hip arthroplasty. Patients may present with pain and limited mobility, potentially leading to a greater risk of revision surgery. Patients who experience symptoms including pain, swelling, enlarged bursae, pseudotumors, tissue masses, fluid collections, or local build-up of excessive metal particles or metal hypersensitivity, may require revision surgery, with attendant risks and the potential for impaired function. The need for any additional follow-up, including the necessity for diagnostic imaging and blood tests, should be determined on a case-by-case basis following a detailed assessment of the patients’ clinical circumstances. For more information, please see http://www.tga.gov.au/alert/birmingham-hip-modular-head-used-hip-replacements This action has been closed-out on 31/08/2016.

Device

  • 모델명 / 제조번호(시리얼번호)
    Birmingham Hip Modular Head (BHMH) (component of MoM total hip replacement systems)BHMH 38MM~62MM (Sleeved) Catalogue Numbers: 74222138 to 7422216212/14 Modular Taper Sleeve Catalogue Numbers: 74222100, 74222200, 74222300, 74222400All batches/lotsARTG Number: 124100
  • Manufacturer

Manufacturer