BIRMINGHAM HIP Resurfacing (BHR) System BHR Resurfacing Head 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-00493-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2015-06-12
  • 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;) has conducted an analysis of recent national joint registry of england and wales data. the data indicate that the revision rates associated with the female gender, and smaller femoral head sizes regardless of gender, perform less well and exceed the current revision rate benchmark established by the uk national institute for health and care excellence .S&n; is informing customers that: - the use of bhr in female patients is to be contraindicated;- bhr femoral head components sized 46mm in diameter and smaller, and their corresponding acetabular cup sizes, are no longer to be used and are to be returned to s&n; and- patients requiring a 48mm femoral head size are at a moderately elevated risk of revision and should not be considered as candidates for bhr implantation.
  • 조치
    Surgeons are advised that 48mm heads should only be used in the specific circumstance of intra-operative downsizing from a pre-operatively templated 50mm to a measured 48mm at the time of surgery. Surgeons are recommended to maintain their routine follow-up protocol for patients who have undergone hip resurfacing arthroplasty. Patients who experience symptoms including limited mobility, 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. This action has beem closed-out on 31/08/2016.

Device

  • 모델명 / 제조번호(시리얼번호)
    BIRMINGHAM HIP Resurfacing (BHR) System BHR Resurfacing HeadCatalogue Numbers: 74121138, 74123140, 74121142, 74123144, 74121146BHR Acetabular CupCatalogue Numbers: 74120144, 74120146, 74122146, 74122148, 74120148, 74120150, 74122150, 74122152, 74120152, 74120154BHR Dysplasia CupCatalogue Numbers: 74120246, 74122248, 74120250, 74122252, 74120254ARTG numbers: 120078 & 124099
  • Manufacturer

Manufacturer