Mobile Detector Holder for DigitalDiagnost System (Digital diagnostic x-ray 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-2012-RN-01024-1
  • 사례 위험등급
    Class III
  • 사례 시작날짜
    2012-10-10
  • 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
    The wireless portable detector is fixed in the mobile detector holder via a lock mechanism. the 4 countersunk screws, that are used to attach the lock, mechanism, can become loose. if this happens and the mechanism fails, the detector may fall down when the holder is rotated 90 degrees clockwise.
  • 조치
    The user should control the lock mechanism of the Mobile Detector Holder. In case the lock mechanism can be moved without pressing the actuator, the holder should not be rotated Clockwise. Philips Healthcare will secure the 4 countersunk screws, which are used to attach the lock mechanism, with thread locker (e.g. LOCTITE 243).

Device

  • 모델명 / 제조번호(시리얼번호)
    Mobile Detector Holder for DigitalDiagnost System (Digital diagnostic x-ray System). Models: Single Detector, Dual Detector, Release 3System codes: 712020, 712022 & 712025ARTG Number: 117662
  • Manufacturer

Manufacturer

  • 제조사 모회사 (2017)
  • Source
    DHTGA