Events

Recall of Intelerad Inteleviewer software

According to New Zealand Medicines and Medical Devices Safety Authority, this recall involved a device in New Zealand that was produced by Intelerad Medical Systems Incorporated.

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
    16377
  • Event Initiated Date
    2014-03-13
  • Event Country
    New Zealand
  • Event Source
    NZMMDSA
  • Event Source URL
    https://medsafe.govt.nz/hot/Recalls/RecallSearch.asp
  • Notes / Alerts
    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.
  • Extra notes in the data
    Recalling Organisation: Pharmaceutical Marketing New Zealand Ltd, 162 Nile Road, Milford, Auckland 0620
  • Reason
    Intelerad recently discovered a software defect (ivwl: html sequence "<" in the report text is not displayed as '<' when "overrideclientreportcolors" is set to "true"). with this bug, if you view reports in inteleviewer, you will not see the symbol "<" if it was used in the report. if you view reports in the ris, in intelebrowser, or in inteleconnect, you will see the proper version of the report with the "<" symbol if it was used.
  • Action
    Software to be upgraded

Device

Intelerad Inteleviewer software

Manufacturer

Intelerad Medical Systems Incorporated