Events

Ossur LP rotate, sizes 25-27 cat.1-6 의 리콜

New Zealand Medicines and Medical Devices Safety Authority에 따르면, 해당 리콜 는 New Zealand 에서 Ossur HF 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
    18538
  • 사례 시작날짜
    2015-07-23
  • 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: Christchurch Artificial Limb Centre, 330 Burwood Road, Christchurch 8083
  • 원인
    Ossur is recalling this device due to the outer tube threads not being machined correctly. use of the affected product may cause the patient to fall, as the shock module can become loose from the foot blade. the failure could possibly be noticed by users as they will feel looseness on ankle foot device. if use is continued, connection of shock adapter to foot blade might break and user may fall.
  • 조치
    Product to be returned to supplier

Device

Ossur LP rotate, sizes 25-27 cat.1-6
  • 모델명 / 제조번호(시리얼번호)
    Model: Product numbers LRP062, LRF062, LRPU62, and LRFU62, Affected: Manufacturing Lot Number: HF141022
  • Manufacturer
    Ossur HF

Manufacturer

Ossur HF