Events

Recall of PRESTILIX 1600X REMOTE CONTROLLED R&F/RAD/TOMO SYSTEM

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
    26867
  • Event Risk Class
    II
  • Event Initiated Date
    2016-11-22
  • 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
    Ge healthcare has recently become aware of a potential safety issue due to a distar crt monitor that has fallen off the monitor suspension related to product aging. a fall of a crt monitor could result in a serious injury to a patient or operator.

Device

PRESTILIX 1600X REMOTE CONTROLLED R&F/RAD/TOMO SYSTEM
  • Model / Serial
    Model Catalog: S13001AX (Lot serial: > 10 contact manufacturer); Model Catalog: S0910JB/JD/JF/JH (Lot serial: > 10 contact manufacturer)
  • Product Description
    PRESTILIX 1600X REMOTE CONTROLLEDR&F/RAD/TOMO SYSTEM;ADVANTX LEGACY/LEGACY D R/F SYSTEM
  • Manufacturer
    GENERAL ELECTRIC CANADA (OPERATING AS GE HEALTHCARE)

Manufacturer

GENERAL ELECTRIC CANADA (OPERATING AS GE HEALTHCARE)