Recall of Philips- Brilliance 64 and Ingenuity CT

According to New Zealand Medicines and Medical Devices Safety Authority, this recall involved a device in New Zealand that was produced by Philips Medical Systems (USA).

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
  • Event ID
  • Event Initiated Date
  • Event Country
  • Event Source
  • Event Source URL
  • 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: Philips New Zealand Commercial Limited, Level 3, 123 Carlton Gore Road, Newmarket, AUCKLAND 1023
  • Reason
    A complaint was received indicating that the non-gated bolus tracking clinical scan failed to initialize with the system displaying the error message: a problem has occurred; please retry. if the problem persists contact service.
  • Action
    Software to be upgraded


  • Model / Serial
    Model: , Affected: Brilliance 64, Ingenuity Core, Ingenuity Core 128, Ingenuity CT, Software version: software version 4.1.6.XX030 or 4.1.6.XX032
  • Manufacturer


  • Manufacturer Parent Company (2017)
  • Source