Events

Kerr Herculite Ultra Composite Restoratives 의 리콜

New Zealand Medicines and Medical Devices Safety Authority에 따르면, 해당 리콜 는 New Zealand 에서 Kerr Corporation 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
    17206
  • 사례 시작날짜
    2014-08-28
  • 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: Henry Schein New Zealand, 23 William Pickering Drive, Albany, North Shore City, Auckland
  • 원인
    The manufacturer has received complaints that the herculite ultra product may be difficult to extrude or may not perform as intended. investigation of the retained and returned product confirmed that the composite does not extrude easily. additionally, any composite extruded was determined to exhibit signs of dryness and was not workable upon manipulation.
  • 조치
    Product to be returned to supplier

Device

Kerr Herculite Ultra Composite Restoratives
  • 모델명 / 제조번호(시리얼번호)
    Model: Part Numbers: 35166, 34348, 34448, 34338, Affected: Specific lots
  • Manufacturer
    Kerr Corporation

Manufacturer

Kerr Corporation