Recall of XARIO XG - MAIN UNIT

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by TOSHIBA CANADA MEDICAL SYSTEMS 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
    84482
  • Event Risk Class
    II
  • Event Initiated Date
    2013-05-28
  • 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
    When a diagnostic ultrasound system with applicable software is used under the following specific conditions the temperature of the head of the transducer connected to the system may overheat:-the system is operating in 2d+pw or 2d+pw+cdi modes -the [iq balance bd] or [iq balance bcd] control is visible on the touch panel (pw/cw screen)-the same area is scanned continuously for 20 seconds or longer. this phenomenon will be corrected by installation of a free software modification.

Device

  • Model / Serial
    Model Catalog: SSA-680A (Lot serial: >100 NUMBERS CONTACT MFG); Model Catalog: SSA-790A (Lot serial: >100 NUMBERS CONTACT MFG)
  • Product Description
    XARIO XG - MAIN UNIT
  • Manufacturer

Manufacturer

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