Events

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

According to Saudi Food & Drug Authority, this translation missing: en.activerecord.attributes.event.types.recall_field_safety_notice involved a device in Saudi Arabia that was produced by Elekta Inc..

What is this?

Field safety notices are communications sent out by medical device manufacturers or their representatives in relation to actions that they may be taking in relation to their product that is on the market. These are mainly for health workers, but also for users. They can include recalls and alerts.

Learn more about the data here
  • Type of Event
    Recall / Field Safety Notice
  • Event ID
    mdprc 055 12 18 000
  • Event Initiated Date
    2018-12-13
  • Event Country
    Saudi Arabia
  • Event Source
    SFDA
  • Event Source URL
    https://ncmdr.sfda.gov.sa/Secure/CA/CaViewRecall.aspx?caid=4&rid=13615
  • Notes / Alerts
    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.
  • Extra notes in the data
    Report Source: NCMDR
    SFDA urges all hospitals that have devices subjected to recall, to contact the company.
  • Reason
    If there are no wedge ids included in the dicom rt plan sent from the tps, the field in mosaiq will be created with no wedge.

Device

MOSAIQ Radiation Oncology
  • Model / Serial
    MOSAIQ Radiation Oncology customers using release version 1.0 and higher and Multi-ACCESS Customers using release version 6.1 and higher.
  • Product Description
    Radiology information system
  • Manufacturer
    Elekta Inc.

Manufacturer

Elekta Inc.
  • Manufacturer Parent Company (2017)
    Elekta AB
  • Manufacturers representative
    Medical Regulations Gate
  • Source
    SFDA