Recall of ALLURA XPER FD10/10 - 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
    132523
  • Event Risk Class
    II
  • Event Initiated Date
    2017-03-30
  • 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
    Due to a leak in the detector cooling system cooling liquid may leak outside the drip tray of the chiller. if this occurs the liquid may drip onto electrical components in the r-cabinet located in the technical room which could lead to damage to the system and potentially cause thermal events such as a burning odor smoke or fire.

Device

  • Model / Serial
    Model Catalog: ALLURA XPER FD10/10 (Lot serial: ALL); Model Catalog: 722026 (Lot serial: ALL); Model Catalog: 001459 (Lot serial: ALL); Model Catalog: 722038 (Lot serial: ALL); Model Catalog: ALLURA XPER FD20 (Lot serial: ALL); Model Catalog: ALLURA XPER FD10 (Lot serial: ALL); Model Catalog: ALLURA XPER FD20/10 (Lot serial: ALL)
  • Product Description
    ALLURA XPER FD10/10-MAIN UNIT
  • Manufacturer

Manufacturer

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