Events

Philips EPIQ 7 Ultrasound System 의 리콜

New Zealand Medicines and Medical Devices Safety Authority에 따르면, 해당 리콜 는 New Zealand 에서 Philips Ultrasound 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
    15551
  • 사례 시작날짜
    2013-10-22
  • 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: Philips New Zealand Commercial Limited, Level 3, 123 Carlton Gore Road, Newmarket, AUCKLAND 1023
  • 원인
    Under system settings, if the system date format is set to international, dd/mm/yyyy, the system continues to interpret the date as mm/dd/yyyy on the patient data entry (pde) screen. the anomaly exists in date fields for 'last menstrual period' (lmp), 'established due date' (edd) and 'conception date'. the lmp field is presented in four exam types: obstetric (ob,) fetal echo, gynecology (gyn), and breast and populates from one exam type to the other.
  • 조치
    Software to be upgraded

Device

Philips EPIQ 7 Ultrasound System
  • 모델명 / 제조번호(시리얼번호)
    Model: Model: EPIQ 7, Affected: Software version 1.0 and 1.0.1
  • Manufacturer
    Philips Ultrasound

Manufacturer

Philips Ultrasound
  • 제조사 모회사 (2017)
    Philips
  • Source
    NZMMDSA