BrightView SPECT, BrightView X and BrightView XCT (SPECT/CT diagnostic imaging system) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Philips Electronics Australia 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-00035-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2014-01-20
  • 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
    Several software issues were identified which will be corrected with the release of a new software version. 1. when positioning for a relative 180 degree non-circular acquisition, if the second (bottom) detector is not positioned correctly, it may result in an inappropriate rotation orbit calculation for the patient being imaged. this may result in the detectors coming in contact with the patient.2. as the gantry system moves to a relative 90 degree scan position of the detectors, a patient/operator may move their hands or arms into the path of the detectors, resulting in contact with the patient/operator. 3. when a user manually positions the patient for an exam and is translating the pallet into the gantry bore, the pallet catcher that supports the imaging table was higher than the imaging pallet which may result in a pinch point or table tilt if not engaged with the catcher. this problem can only occur on the brightview x or the brightview xct system.
  • 조치
    Philips Healthcare is advising users to always follow the Instruction For Use (IFU), and is providing additional instructions to prevent the issues from occurring. A software upgrade will be installed on all affected systems as a permanent correction for the issues.

Device

  • 모델명 / 제조번호(시리얼번호)
    BrightView SPECT, BrightView X and BrightView XCT (SPECT/CT diagnostic imaging system)BrightView SPECTProduct Code: 882480BrightView XProduct Code: 882478BrightView XCTProduct Code: 882482ARTG Numbers: 117642 and 117440
  • Manufacturer

Manufacturer

  • 제조사 모회사 (2017)
  • Source
    DHTGA