Events

Laerdal Suction Unit (78xxxx) 의 리콜

New Zealand Medicines and Medical Devices Safety Authority에 따르면, 해당 리콜 는 New Zealand 에서 Laerdal Medical AS 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
    20703
  • 사례 시작날짜
    2016-10-10
  • 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: Laerdal (New Zealand) Ltd, Unit O, Cain Commerical Centre, 20 Cain Road, Penrose
  • 원인
    This is a follow-up to the initial communication, to provide information on a long-term solution, with regards to the laerdal suction unit (lsu) when used with the lsu nimh battery that has been stored or installed at low temperatures for a prolonged period.
  • 조치
    Instructions for use to be updated

Device

Laerdal Suction Unit (78xxxx)
  • 모델명 / 제조번호(시리얼번호)
    Model: , Affected: 7800033 LSU WITH RESUABLE CANISTER WITH NIMH BATTERY, 78001033 WITH ABBOT RECEPTAL CANISTER WITH NIMH BATTERY, 78002033 LSU WITH BEMIS CANISTER WITH NIMH BATTERY, 78003033 WITH SERRES SUCTION BAG CANISTER SYSTEM WITH NIMH BATTERY
  • Manufacturer
    Laerdal Medical AS

Manufacturer

Laerdal Medical AS