Allura Xper R9 and Azurion R1.1 systems with the QA Basic Measurement tool 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-2017-RN-01162-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2017-09-06
  • 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
    Philips has identified when using the downscale option, the measurements performed with the allura r9 or azurion r1.1 systems (using qa basic measurement tool) will not be correctly exported to the external dicom destination. the difference between the original & exported measurements can vary, and the distance value after export is factor 1 to 4 smaller than the original. the difference will depend on the acquired image & used archive settings. if the measurement is re-performed at the external dicom destination, the result will also be incorrect unless a recalibration of the image is executed. if these exported downscaled images are used during/in preparation of a procedure, the incorrect measurement values could result in the selection of an incorrectly sized device. the same applies if a measurement is re-performed at the external dicom destination without executing a recalibration of the image.To date philips is not aware of any injuries that may have occurred due to this issue.
  • 조치
    1. The Downscale option should be disabled in all Export protocols until Philips corrects this issue. 2. Distribute the notice to all users of the device. 3. Complete the supplied response form and return it to Philips. 4. The problem will be resolved by a software update, which is expected to be available by the end of 2017. 5. Philips representatives will notify users when the software update is available for installation. 6. In the interim, a similar notice will be provided along with newly manufactured devices shipped for use.

Device

  • 모델명 / 제조번호(시리얼번호)
    Allura Xper R9 and Azurion R1.1 systems with the QA Basic Measurement toolProduct Names: Allura Xper R9 7M20, Azurion 7M12, Azurion 7M20ARTG Number: 225815
  • Manufacturer

Manufacturer

  • 제조사 모회사 (2017)
  • Source
    DHTGA