Events

Recall of G-scan Brio Magnetic Resonance System

According to Department of Health, Therapeutic Goods Administration, this recall involved a device in Australia that was produced by Emergo Asia Pacific Pty Ltd T/a Emergo Australia.

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
    RC-2016-RN-00499-1
  • Event Risk Class
    Class II
  • Event Initiated Date
    2016-04-26
  • Event Country
    Australia
  • Event Source
    DHTGA
  • Event Source URL
    https://apps.tga.gov.au/Prod/sara/arn-detail.aspx?k=RC-2016-RN-00499-1
  • Notes / Alerts
    Australian data is current through July 2018. All of the data comes from the Australian Therapeutic Goods Administration, 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 Australia.
  • Extra notes in the data
  • Reason
    The manufacturer is providing users with additional safety instructions for the safe use of the magnetic resonance system g-scan brio. if not addressed, the issue described could lead to an unsafe exam condition.A potential weakness in the foot rest and the left bed rail of the patient table has been identified. this weakness may lead to a fracture of the patient table within the foot rest and the left bed rail in certain conditions. in particular this may happen if a heavy patient applies a strong dynamic stress (bouncing stress) to that part of the table to access or descend from the bed. there is a chance of a patient falling, or patient injury to the head or back if this situation occurs. there have been no reports of injuries as a result of this issue.
  • Action
    Emergo is providing users with work around instructions to follow to prevent the issue from occurring. The Instructions for Use (IFU) will be updated to include the additional information. This action has been closed-out on 13/10/2016.

Device

G-scan Brio Magnetic Resonance System

Manufacturer

Emergo Asia Pacific Pty Ltd T/a Emergo Australia