balanSys UNI convex polyethylene (PE) inlay x/5 (with thickness 5)(Unicondylar knee prosthesis) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Mathys Orthopaedics 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-01502-1
  • 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
    Seven reports have been received concerning in situ inlay breakage of balansys uni convex pe inlays x/5 after approximately five years. the observed occurrence rate for inlay breakage amounts to 1.4% and this higher than anticipated rate has led to the decision by mathys orthopaedics pty ltd to remove all balansys uni convex pe inlays x/5 from the market as a precautionary measure. the breakage of a balansys uni convex pe inlay x/5 happens without prodromal symptoms. it presents itself with pe inlay dislocation that requires urgent revision to regain total functionality and toprevent the surface of the metal components from any damage.Please note that all other balansys uni convex pe inlay sizes are not affected by this action.
  • 조치
    Mathys Orthopaedics is recommending that surgeons inform affected patients implanted with an x/5 inlay about the higher than anticipated occurrence rate of PE inlay breakage and the associated potential risks while maintaining their routine follow-up protocol for patients who have undergone knee arthroplasty. The need for any additional follow-up or revision surgery should be determined on a case-by-case basis following a detailed assessment of the patients’ clinical circumstances. For more information, please see https://www.tga.gov.au/alert/balansys-uni-convex-pe-inlays-x5-used-knee-replacements . This action has been closed-out on 26/05/2017.

Device

  • 모델명 / 제조번호(시리얼번호)
    balanSys UNI convex polyethylene (PE) inlay x/5 (with thickness 5)(Unicondylar knee prosthesis)balanSys UNI convex PE inlay A/5Item Number: 77.30.0211balanSys UNI convex PE inlay B/5Item Number: 77.30.0221balanSys UNI convex PE inlay C/5Item Number: 77.30.0231balanSys UNI convex PE inlay D/5Item Number: 77.30.0241balanSys UNI convex PE inlay E/5Item Number: 77.30.0251All Batch NumbersARTG Number: 212828
  • Manufacturer

Manufacturer