Pangea, USS II Polyaxial, Matrix Deformity, Matrix Degenerative and Pangea Degenerative Systems, Pedicle Awl 4.0mm with Canevasit and Silicone Handle (internal fixation system) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes 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-00977-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2015-10-09
  • 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
    The surgical technique guides and product labelling for the affected systems currently describe the pedicle awls as 4.0mm for use with screws (4.0mm – 7.0mm). these awls should be used with 5.0mm – 7.0mm screws. in the event that a ø4mm awl is used for a ø4mm screw, there is a risk that perforation of the cortex will be too wide and may result in screw pull-out or loosening. in the event that the cortex is perforated wider than needed for insertion of a ø4mm screw, the failure would not typically be recognised. cases may occur, however, where a surgeon’s perception of torque to insert the screw does not have the desired level of fixation. in this case, the issue may be recognised. there have not been any reports of patient injuries as a result of the current labelling, and there have been no changes to the design or manufacture of the pedicle awls.
  • 조치
    Johnson & Johnson Medical are providing a web link for users to obtain copies of the revised technique guides and labelling. This action has been closed-out on 29/08/2016.

Device

  • 모델명 / 제조번호(시리얼번호)
    Pangea, USS II Polyaxial, Matrix Deformity, Matrix Degenerative and Pangea Degenerative Systems, Pedicle Awl 4.0mm with Canevasit and Silicone Handle (internal fixation system)Multiple Technique Guides AffectedLabelling:Pedicle Awl 4.0mm with Canevasit HandleProduct Code: 388.550Pedicle Awl 4.0mm with Silicone HandleProduct Code: 388.656ARTG Number: 155807
  • Manufacturer

Manufacturer