Medi-vac Flex Advantage Suction Liners and Canisters 의 리콜

New Zealand Medicines and Medical Devices Safety Authority에 따르면, 해당 리콜 는 New Zealand 에서 Cardinal Health 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
    13621
  • 사례 시작날짜
    2012-10-24
  • 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: Medline International New Zealand Limited, 14 George Bourke Drive, Mt Wellington, Auckland 1060
  • 원인
    Safety alert notice advising customers that some users of the product:, 1. may be testing functionality by "bumping" the medi-vac liners. as indicated in the warning section of the product's dfu, premature shut-off of the vacuum may occur if the canister is bumped., 2. may be testing vacuum/ suction by occluding the medi-vac liner's patient port with their finger. this practice may activate the mechanical shut-off and consequently turn offf the vacuum. occlusion of the patient port as a testing method is not included in the product's dfu and therefore is not a recommended test.
  • 조치
    Manufacturer to issue advice regarding use

Device

  • 모델명 / 제조번호(시리얼번호)
    Model: 65652-6ll, 65652-616, 65652-631, 65651-910C, 65651-920C and 65651-930C, Affected: All lots
  • Manufacturer

Manufacturer