Events

Liko Viking Mobile Lifts 의 리콜

New Zealand Medicines and Medical Devices Safety Authority에 따르면, 해당 리콜 는 New Zealand 에서 Liko AB 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
    19158
  • 사례 시작날짜
    2015-10-19
  • 사례 국가
    New Zealand
  • 사례 출처
    NZMMDSA
  • 사례 출처 URL
    https://medsafe.govt.nz/hot/Recalls/RecallSearch.asp
  • 비고 / 경고
    Data from New Zealand is current through July 2018. All of the data comes from the New Zealand Medicines and Medical Devices Safety Authority, 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 New Zealand.
  • 데이터 추가 비고
    Recalling Organisation: Universal Specialities Ltd trading as USL Medical, 494 Rosebank Road, Avondale, AUCKLAND 1026
  • 원인
    The manufacturer has received 9 complaints where the lift arm drifted down suddenly on certain viking mobile lifts. these reports have been connected to users who raise the lift arm assembly manually., the lift arm assembly is intended to only be raised by the actuator (lift motor). if the lift arm assembly is manually raised, the actuator can become damaged and get stuck in the highest position. when the actuator is stuck, the lift cannot be raised or lowered by the lift motor.
  • 조치
    Product to be modified

Device

Liko Viking Mobile Lifts
  • 모델명 / 제조번호(시리얼번호)
    Model: Viking M (2040035, 2040015, 2040005), Viking L (2040004), Viking XL or 300 (2040003), Affected: Multiple serial number ranges
  • Manufacturer
    Liko AB

Manufacturer

Liko AB