Events

Recall of MSK EXTREME

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by GENERAL ELECTRIC CANADA (OPERATING AS GE HEALTHCARE).

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
    93611
  • Event Risk Class
    III
  • Event Initiated Date
    2015-02-25
  • Event Country
    Canada
  • 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 latest on-site software version may not have been reinstalled at some sites after service activities were performed that required software to be reloaded. the most recently deployed on-site software version may include safety updates.

Device

MSK EXTREME

Manufacturer

GENERAL ELECTRIC CANADA (OPERATING AS GE HEALTHCARE)