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 AB SCIEX Pte. Ltd.

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 164 03 16 000
  • Event Initiated Date
    2016-03-24
  • Event Country
    Saudi Arabia
  • Event Source
    SFDA
  • Event Source URL
    https://ncmdr.sfda.gov.sa/Secure/CA/CaViewRecall.aspx?caid=4&rid=9089
  • 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
    An issue has been identified with analyst md software where under certain conditions a user can be presented with incorrect quantitative results.

Device

Analyst MD Software
  • Model / Serial
    Versions 1.6.1 and 1.6.2. Component of API 3200MD™ LC/MS/MS System, 3200MD QTRAP® LC/MS/MS System, Triple Quad™ 4500MD LC/MS/MS System, and QTRAP® 4500MD LC/MS/MS System Recall ID: 3258–0095 Instrument Part Number (REF) : 5024501, 5024500, 5031257, 5031231
  • Product Description
    Software
  • Manufacturer
    AB SCIEX Pte. Ltd

Manufacturer

AB SCIEX Pte. Ltd
  • Manufacturer Parent Company (2017)
    Danaher Corporation
  • Manufacturers representative
    Bio Standards
  • Source
    SFDA