Events

Recall of Invacare I-Fit Shower Chair

According to Department of Health, Therapeutic Goods Administration, this recall involved a device in Australia that was produced by Invacare Australia Pty 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
    RC-2012-RN-00935-1
  • Event Risk Class
    Class II
  • Event Initiated Date
    2012-09-21
  • Event Country
    Australia
  • Event Source
    DHTGA
  • Event Source URL
    https://apps.tga.gov.au/Prod/sara/arn-detail.aspx?k=RC-2012-RN-00935-1
  • 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
    Chair seats may break through the middle, potentially causing the chair to collapse.
  • Action
    Customers are being advised to discontinue use and return the affected chairs to their distributor.

Device

Invacare I-Fit Shower Chair
  • Model / Serial
    Invacare I-Fit Shower ChairModel Numbers: 9780, 9781 & 9781-1ARTG Number: 107864
  • Manufacturer
    Invacare Australia Pty Ltd

Manufacturer

Invacare Australia Pty Ltd