Miramar Labs Mira Dry 의 리콜

New Zealand Medicines and Medical Devices Safety Authority에 따르면, 해당 리콜 는 New Zealand 에서 Miramar Labs Inc 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
    19582
  • 사례 시작날짜
    2015-12-18
  • 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: Device Consulting (NZ) Pty, Level 4, 52 Symonds Street, Auckland 1010
  • 원인
    Manufacturer has been advised that some clinics overseas are using substances that have not been validated for use with the miradry system to lubricate the skin prior to using the miradry handpiece. this may prevent the cooling plate in the miradry handpiece from correctly contain and cooling the skin and cause minor burns and blisters., whilst there have not been any adverse events reported in australia, device consulting is conducting a product correction to update the user manual for the miradry system to include the statement:, “do not use lubricants other than the recommended lubricants k-y® jelly or k-y® liquid). use of other substances such as ultrasound gel or ipl coupling gel can reduce the effectiveness of the surface cooling, leading to blisters or burns.”.
  • 조치
    Instructions for use to be updated

Device

  • 모델명 / 제조번호(시리얼번호)
    Model: , Affected: all batches
  • Manufacturer

Manufacturer