Patient Support (NC989001087431) for 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-2018-RN-00881-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2018-07-02
  • 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 footplate of the patient support for stitching can be fixed in upper position. philips has identified that when the fixing clamp (hook) is not in its correct locking position, the footplate is not securely held. if it falls down, it may hurt the operators or patient's foot or leg (e.G. when moving the stand or when the operator fails to fix it correctly upon moving the footplate up). the following factors are needed for this situation to occur:- hinges are worn differently on both sides;- hook does not hold;- the operator does not check that the hook securely holds the footplate;- the footplate falls unexpectedly when touched or during transport;- foot or leg is in the “target area”; and/or- foot is in the “hazard area”.
  • 조치
    Philips is advising that they plan make the following design changes: - Sturdier replacement hinges for floor plate; - Install modified hook for floor plate (adapted to new hinges); and - The brake cylinder below floor plate to minimise kinetic energy. A Philips service engineer will contact impacted customers as soon as the Field Action Kit is available to be implemented. In the interim, users are advised to always ensure the correct positioning of the hook and that it is locked in accordance with the Instructions for Use (press hook down until it is locked).

Device

  • 모델명 / 제조번호(시리얼번호)
    Patient Support (NC989001087431) for X-Ray SystemARTG Number: 117662(Philips Electronics Australia Ltd - X-ray system, diagnostic, general-purpose, stationary, digital)
  • Manufacturer

Manufacturer

  • 제조사 모회사 (2017)
  • Source
    DHTGA