DePuy Synthes ATTUNE Intuition Distal Femoral Jig 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Johnson & Johnson Medical Pty Ltd T/A Depuy Australia 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-2014-RN-01190-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2014-11-18
  • 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
    Johnson & johnson medical pty ltd (jjm) has identified that the metal pin bushing was incorrectly assembled during the manufacturing process in some instruments. jjm has also determined that if the metal pin bushing is overloaded by over tightening, there is the potential for partial or full displacement of the metal pin bushing along with fracture of the plastic around the metal pin bushing. if the plastic around the metal pin bushing fractures, there is the potential for fragments of the fractured plastic to be left in the patient. this displacement is potentially caused by excessive loading applied during pinning of the jig to the distal femoral condyles. the use of the pins in the distal resection plate is optional and the complaint rate of the bushings partially or fully displacing is 0.018%.
  • 조치
    JJM staff will contact hospitals to assist with the inspection and swap of potentially affected units and informing the surgeons that jigs may continue to be used at the discretion of the medical professional following the instructions provided in the letter. JJM is also providing surgeons with a Safety Alert notification to ensure the correct load is applied during pinning of the jig to the distal femoral condyles. This action has been closed-out on 14/07/2016.

Device

Manufacturer