Events

Rusch Bronchopart Tube Set Left 의 리콜

New Zealand Medicines and Medical Devices Safety Authority에 따르면, 해당 리콜 는 New Zealand 에서 Rusch 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
    17809
  • 사례 시작날짜
    2015-01-12
  • 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: Ebos Group Ltd, 14-18 Lovell Court, Rosedale, Auckland 0632
  • 원인
    Teleflex are recalling specific products following receipt of customer complaints reporting that the cobb connector detached from the main connector prior to use. this cobb connector detachment should be readily identified by the user during set-up and prior to use of the device. if during use, cobb connector separation occurs and presents as a leak in the breathing circuit and if it is unnoticed, then there is a remote probability that the patient may need to be re-intubated due to the risk of respiratory distress and hypoxia.
  • 조치
    Product to be returned to supplier

Device

Rusch Bronchopart Tube Set Left
  • 모델명 / 제조번호(시리얼번호)
    Model: Product Code: 116100-000260, Affected: 29 lots
  • Manufacturer
    Rusch Inc

Manufacturer

Rusch Inc