Affirm Lateral Arm Upright Biopsy Accessory(accessory to the Affirm Breast Biopsy Guidance System for Selenia Dimensions) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Hologic 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-00988-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2017-08-30
  • 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
    Hologic has received four complaints at the time of device installation that it was not possible to properly align small-diameter spring loaded core biopsy needles with the blue needle guide.The blue needle guide is used when a lateral left side approach is chosen for biopsy. investigation revealed a component issue that could impact needle alignment for all left approach lateral biopsy procedures. the impact on the position of the needle within the breast, and thus on the aspiration of the intended tissue, is case-dependent and can be observed in the post-fire, post-biopsy, and specimen images when those are used during a procedure.The right side approach is not affected by the reported problem. to date, no patient injury has been reported.
  • 조치
    1. A replacement part (blue needle guide) is available and Hologic will schedule an appointment for a field service engineer to install the new blue needle guide. 2. Complete, sign and return the supplied customer response form. Should you have any additional questions please contact Hologic. 3. Pass this letter on to all those who need to be aware within your organisation or to any facility where the potentially affected devices have been transferred.

Device

  • 모델명 / 제조번호(시리얼번호)
    Affirm Lateral Arm Upright Biopsy Accessory(accessory to the Affirm Breast Biopsy Guidance System for Selenia Dimensions)Catalogue Number: ASY-09880ARTG Number: 281546
  • Manufacturer

Manufacturer