Events

translation missing: ko.activerecord.attributes.event.titles.recall_field_safety_notice

Saudi Food & Drug Authority에 따르면, 해당 translation missing: ko.activerecord.attributes.event.types.recall_field_safety_notice 는 Saudi Arabia 에서 VOLCANO CORPORATION 에 의해 제조된 제품과 관련되어 있습니다.

이것은 무엇인가요?

현장 안전성 서한은 의료기기 제조사 또는 제조사 대리인이 시중에 유통되고 있는 자사 의료기기 제품에 대하여 취할 수 있는 조치를 알리는 소통방식입니다. 주요 대상층은 보건의료업계 종사자와 의료기기 사용자들입니다. 여기에는 회수(recall) 조치와 경고도 포함될 수 있습니다.

데이터에 대해 더 자세히 알아보기 여기
  • 사례 유형
    Recall / Field Safety Notice
  • 사례 ID
    mdprc 105 10 18 000
  • 사례 시작날짜
    2018-10-21
  • 사례 국가
    Saudi Arabia
  • 사례 출처
    SFDA
  • 사례 출처 URL
    https://ncmdr.sfda.gov.sa/Secure/CA/CaViewRecall.aspx?caid=4&rid=13357
  • 비고 / 경고
    Saudi data is current through January 2019. All of the data comes from the Saudi Food & Drug 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 Saudi Arabia.
  • 데이터 추가 비고
    Report Source: NCMDR
    SFDA urges all hospitals that have devices subjected to recall, to contact the company.
  • 원인
    Philips has received complaints that approximately 20% of devices in affected lots may demonstrate an inability to insert the guidewire into the catheter. this has caused no known adverse events. this issue is seen before entering the patient's body, and can lead to a delay of case while the defective product is exchanged for another device.

Device

IVUS Catheter
  • 모델명 / 제조번호(시리얼번호)
    Catalog number: 88901, 81234 - Please check attachment for batch numbers -
  • 제품 설명
    Catheter
  • Manufacturer
    VOLCANO CORPORATION

Manufacturer

VOLCANO CORPORATION
  • 제조사 모회사 (2017)
    Philips
  • 제조사 대표
    Ikar Establishment
  • Source
    SFDA