Auriga XL 4007 Laser System 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Boston Scientific 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-01215-2
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2017-09-21
  • 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
    Boston scientific has identified certain auriga xl 4007 laser system consoles which may have an incorrectly assembled trigger wire. the trigger wire functions in the start-up of the console. an incorrectly assembled trigger wire may result in error codes or failure to start the console. should the console fail to start, the most common consequence would be a delay of the procedure while the affected console is swapped for another. if a substitute console or immediate alternative treatment is not available, this issue may result in moderate risk to the patient related to repeat anaesthesia for the re-intervention at a later date.
  • 조치
    1. Users are to stop using the affected goods and complete and return the supplied correction form to indicate receipt of the letter. 2. Boston Scientific certified engineers will begin contacting customers to schedule correction of affected consoles within two weeks of this communication.

Device

  • 모델명 / 제조번호(시리얼번호)
    Auriga XL 4007 Laser SystemMaterial Number (UPN): M0068FS4007G0 Serial Numbers: 20546219 and 20575518 ARTG Number: 287772
  • Manufacturer

Manufacturer

  • 제조사 모회사 (2017)
  • 제조사 의견
    “We take a patient-first approach to assessing the applicability of every recall and communicate to regulatory bodies in all geographies where the recalled device is sold,” Boston Scientific said in a statement to ICIJ. “We have coordinated several recalls across many countries in a timely manner,” the company said, adding that it complies with all national laws, which can often vary and require different processes for reporting information or taking action on recalls. The company said it uses a rigorous and uniform process to take action on recalls and that “when we initiate a field action (e.g. recall, safety alert), every customer who has received an affected product receives a communication that includes a letter for the physician.”
  • Source
    DHTGA