ATTUNE INTUITION Tibial Articulation Surface Instruments 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 DePuy Synthes 에 의해 제조된 제품과 관련되어 있습니다.

이것은 무엇인가요?

안전성 경고는 의료기기 제품과 관련된 중요한 정보와 권고사항을 담고 있습니다. 물론 안전성 경고가 배포되었다고 해서 해당 제품이 무조건 안전하지 않은 제품이라는 것은 아닙니다. 보건의료업계 종사자와 의료기기 사용자들에게 배포되는 안전성 경고에는 회수(recall)도 포함될 수 있습니다. 제조사가 안전성 경고를 작성하기도 하지만, 보건당국에서 작성하는 경우도 있습니다.

데이터에 대해 더 자세히 알아보기 여기
  • 사례 유형
    Safety alert
  • 날짜
    2015-06-19
  • 사례 출판 날짜
    2015-06-19
  • 사례 국가
  • 사례 출처
    DH
  • 사례 출처 URL
  • 비고 / 경고
    Hong Kong data is current through September 2018. All of the data comes from the Department of Health (Hong Kong), 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 data from the U.S. and Hong Kong.
  • 데이터 추가 비고
    Medical Device Safety Alert
  • 원인
    Medical device safety alert: depuy synthes attune intuition tibial articulation surface instruments medical device manufacturer, depuy synthes, has issued a medical device safety alert concerning all lots of the attune intuition tibial articulation surface instruments used in trialing with the attune knee system. according to the safety alert, the balseal, which is a small wire spring coil located on the post feature of the articulation surface instruments, has the potential to become damaged and disassociate (come off). the balseal is constructed from implant grade stainless steel. if the balseal is separated from the post, it has the potential to enter the surgical site and be left in the patient if the surgeon is unaware of the disassociation. damage to the balseal is potentially caused by: inserting the tibial trial extractor or other instrument between the articulation surface trial and shim trial, causing contact with the balseal during intraoperative trialing or back table disassembly. cleaning that deviates from the instructions for use (ifu) procedures. to reduce the possibility of leaving a disassociated balseal in a patient, the manufacturer advises users to follow the ifu, which include inspecting the attune articulation surface instruments before, during and after use, to ensure that the balseals are not damaged and that no instruments or pieces are left in the patient. balseal disassociation potentially occurs secondary to damage to the tibial articulation surface during removal of the trial from the joint space or reprocessing. according to the local supplier, the affected products are distributed in hong kong. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 19 june 2015.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: DePuy Synthes ATTUNE INTUITION Tibial Articulation Surface Instruments
  • Manufacturer

Manufacturer