Recall of BRILLIANCE CT BIG BORE SYSTEM - MAIN UNIT

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by PHILIPS ELECTRONICS LTD..

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
    55529
  • Event Risk Class
    II
  • Event Initiated Date
    2012-10-24
  • 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
    The tumorloc application has the capability to generate intensity projection datasets from respiratory gated data. philips healthcare has become aware of a circumstance where these generated datasets are flipped and incorrectly labeled left to right when they are saved to disk.

Device

  • Model / Serial
    Model Catalog: 4535 670 88051 (Lot serial: >10 NUMBERS CONTACT MFG); Model Catalog: 4550 110 02031 (Lot serial: 11365); Model Catalog: 4598 001 18551 (Lot serial: 7103); Model Catalog: 4550 110 02031 (Lot serial: 11704); Model Catalog: 4550 110 02031 (Lot serial: 9127)
  • Product Description
    BRILLIANCE CT BIG BORE SYSTEM - MAIN UNIT
  • Manufacturer

Manufacturer

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