Events

Molnlycke Surgical procedure 의 리콜

New Zealand Medicines and Medical Devices Safety Authority에 따르면, 해당 리콜 는 New Zealand 에서 Molnlycke Health Care AB 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
    18962
  • 사례 시작날짜
    2015-08-10
  • 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: Molnlycke Health Care Ltd, 58 Richard Pearse Drive, Airport Oaks, Mangere, Manukau 2022
  • 원인
    Following the recall notification from convatec ltd concerning the suction tube 3m double wrap sterile, convatec ref code 530.25.300 (medsafe ref#18739) molnlycke is advising health care professionals to scrap the convatec suction tube 3m double wrap sterile contained in the procedure pak® at the time of use and instead use a single packed sterile replacement of the tubing from their stock.
  • 조치
    Product to be modified

Device

Molnlycke Surgical procedure
  • 모델명 / 제조번호(시리얼번호)
    Model: SKU: 97063288-02 97063288-02 97063288-02 and 97063288-02, Affected: 15031018 15074837 15176891 and 15196034
  • Manufacturer
    Molnlycke Health Care AB

Manufacturer

Molnlycke Health Care AB