OmniDiagnost-Eleva and OmniDiagnost-Classic 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-00595-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2018-05-18
  • 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 received reported instances in which the table of the omnidiagnost system (od-eleva) suddenly started to rotate from 0 to 90 degrees (table arm down) with high speed. the cause of this unexpected rotation movement is related to an issue with the fixation of the upper and lower tilt actuator. this rotating movement cannot be stopped by the user.If the system rotates uncontrolled, there is a risk of injury for the patient on the table. a rotating table also might hit a user or bystander standing near the system.
  • 조치
    Philips is advising they will be in contact with users to replace affected components on the upper and lower tilt actuator in the impacted systems. It is expected that this action will commence July 2018. In the interim, users should monitor the tables for any of the following, stop use of, and contact Philips immediately if they occur: - the table height or tilt movement is not working; - a cracking or snapping sound is heard during system operation; - a blockade is experienced in the table height or tilt movement during system movements; - the system is having an unexpected collision or the system had an unexpected collision in the past 2 months; - a CPR stand that obstructed the system when in use,; or - any (other) unusual system behaviour beyond the normal use of the system.

Device

  • 모델명 / 제조번호(시리얼번호)
    OmniDiagnost-Eleva and OmniDiagnost-Classic System Codes: 708026, 708027, 708028, 20859, 708023, 708024, 708025ARTG Number: 98560(Philips Electronics Australia Ltd - X-ray system, diagnostic, fluoroscopic, general-purpose, stationary, digital)
  • Manufacturer

Manufacturer

  • 제조사 모회사 (2017)
  • Source
    DHTGA