SynFix-LR Surgical Implant Holder 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Synthes Australia 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-2014-RN-00445-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2014-04-28
  • 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
    Complaints have been received which describe the synfix lr implant holder breaking at the interface between the implant and holder breaking at the interface between the implant and holder. if an unretrieved device fragment remains threaded into the plate, it will not be possible to properly attach the synfix aiming device to the implant (plate). proper attachment of the aiming device to the plate is required for accurate insertion of the four synfix screws into the synfix implant (plate) and vertebral bodies. if the tip of the implant holder should break, the potential exists for an unretrieved device fragment (urdf) to be left in the synfix-lr implant.
  • 조치
    DePuy Synthes is updating the SynFix-LR Surgical Technique Guide and notifying their customers that the SynFix Set Case design has been updated to incorporate two additional wrenches to facilitate correct assembly/disassembly and an additional implant holder to facilitate continuation of surgery. Customers are also reminded that an alternative instrument to the implant holder (SQUID, 03.802.121) can be used for the insertion of the implant in suitable cases.

Device

  • 모델명 / 제조번호(시리얼번호)
    SynFix-LR Surgical Implant HolderPart Number: 036.000.915ARTG Number: 153950
  • Manufacturer

Manufacturer