TruLight 3000, TruLight 5000, iLED 3, iLED 5 and TruVidia Lighting and Video Systems 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Trumpf Med Aust Pty 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-2015-RN-01250-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2015-12-24
  • 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
    Trumpf medical has received information stating the iled and trulight lighting systems have fallen from the central axis. the reported incidents occurred while the lights were being positioned for surgical procedures and have been involved in one injury to a user. the investigation of this issue has determinedthe root cause is due to the improper installation of the snap ring that can occur when a spring arm is attached to the central axis. the snap ring is located inside the interface and holds the spring arm in place. if the snap ring is installed improperly, the spring arm of the lighting system can descend over time, and eventually fall from the central axis. when the snap ring has been installed properly, the potential for the lighting system to fall does not exist.
  • 조치
    Hill-Rom is providing users with work around instructions to follow as an interim measure. Hill-Rom will be inspecting affected units and providing additional labelling as a permanent measure.

Device

  • 모델명 / 제조번호(시리얼번호)
    TruLight 3000, TruLight 5000, iLED 3, iLED 5 and TruVidia Lighting and Video SystemsMultiple products and serial numbers affectedARTG Numbers: 200921, 170219 and 170545
  • Manufacturer

Manufacturer