Events

Recall of SERVER SOFTWARE

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by SIEMENS CANADA LIMITED - HEALTHCARE.

What is this?

A correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health.

Learn more about the data here
  • Type of Event
    Recall
  • Event ID
    132600
  • Event Risk Class
    III
  • Event Initiated Date
    2010-07-28
  • Event Country
    Canada
  • Event Source
    HC
  • Notes / Alerts
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • Extra notes in the data
  • Reason
    For customers that are using the ihe displayable report profile signing off (depending on your configuration) a report will result in an automatic upload of that report to your information system. however if you create an addendum to a report that has been previously uploaded the addendum must be uploaded manually using the #send to#.# feature in the syngo dynamics reporting system. if the addendum is not sent manually the older report in your information system will not match the more recent report in your syngo dynamics system.

Device

SERVER SOFTWARE

Manufacturer

SIEMENS CANADA LIMITED - HEALTHCARE
  • Manufacturer Address
    MISSISSAUGA
  • Manufacturer Parent Company (2017)
    Siemens Ag
  • Source
    HC