MatrixORTHOGNATHIC Screws; MatrixMANDIBLE Screws; MatrixMIDFACE; MatrixNEURO Screws (Non-sterile and sterile screws supplied as part of a craniofacial fixation plate kit) 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-2013-RN-00341-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2013-04-19
  • 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 affected screws are packaged in a "clip" that has a laser etch corresponding to the length of the screw. it has been reported that the etch on the clip does not correspond to the length of the screw. there have been instances in which the screw was longer than the specified etch, as well as the screw being shorter than the specified etch.
  • 조치
    Synthes is asking users to return affected products. If the screws must be used before replacements arrive, Synthes is asking users to measure them prior to use.

Device

  • 모델명 / 제조번호(시리얼번호)
    MatrixORTHOGNATHIC Screws; MatrixMANDIBLE Screws; MatrixMIDFACE; MatrixNEURO Screws (Non-sterile and sterile screws supplied as part of a craniofacial fixation plate kit)Multiple affected lot numbers and part numbersARTG Number: 157706
  • Manufacturer

Manufacturer