JCM Compact Base for Neptune and Triton wheelchairs 의 리콜

New Zealand Medicines and Medical Devices Safety Authority에 따르면, 해당 리콜 는 New Zealand 에서 JCM Seating Solutions 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
    19125
  • 사례 시작날짜
    2015-09-15
  • 사례 국가
  • 사례 출처
    NZMMDSA
  • 사례 출처 URL
  • 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: Medifab Medical Fabrication, 32 Detroit Drive, Izone Business Hub, Rolleston 7675
  • 원인
    Jcm has received reports of isolated incidents involving the instability of the compact base when used in certain conditions. whilst the compact base design in itself is structurally sound and has no mechanical issue, the following guidelines have been revised for safe use:, * the compact base should be used with the neptune size 1 and triton size 0 chairs only, * maximum user weight to compact base should not exceed 40kg., * any seating system larger than the neptune size 1 and triton size 0 should be used with a multi height & tilt base or other approved jcm base/wheelchair base to ensure complete stability.
  • 조치
    Instructions for use to be updated

Device

Manufacturer