Beater-Positioner-Aligner(Multipurpose Impactor Handle - Orthopaedic implant inserter/extractor) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Lima Orthopaedics 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-2017-RN-01331-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2017-10-17
  • 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
    A lima orthopaedics investigation detected substandard welding performed by the supplier on the beater-positioner-aligner. specifically, the absence of base material pre-fusion and under-dimensioned welding radius was identified. there is a risk of injury to the surgeon or the patient, in case the flange of the instrument breaks and detaches with high speed from the body of the instrument.
  • 조치
    Lima is advising users to quarantine affected stock from use. Lima Orthopaedics will replacing the affected stock in the consignment sets.

Device

  • 모델명 / 제조번호(시리얼번호)
    Beater-Positioner-Aligner(Multipurpose Impactor Handle - Orthopaedic implant inserter/extractor)Product Code: 9057.20.555Lot Numbers: 15AG0V0 and 16AG02JARTG Number: 176877
  • Manufacturer

Manufacturer