Recall of SYNGO DYNAMICS

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

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
    53141
  • Event Risk Class
    III
  • Event Initiated Date
    2016-02-01
  • Event Country
  • 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
    Siemens is notifying syngo dynamics customers of a potential issue when using the measurement package of the va10 version. if two measurements with the same name exist instances of measurement will populate both measurements definitions. one of the definitions can be edited while one cannot be seen or edited. both set of measurements are used in any associated calculations. therefore if you edit or delete one of the measurement instances the one that is hidden will not receive the edits and all instances edited and not edited will be averaged together.

Device

  • Model / Serial
    Model Catalog: VA10 (Lot serial: >10 NUMBERS CONTACT MFR)
  • Product Description
    SYNGO DYNAMICS VA10 VERSION
  • Manufacturer

Manufacturer

  • Manufacturer Address
    OAKVILLE
  • Manufacturer Parent Company (2017)
  • Source
    HC