Events

Recall of Tissue Liberator Blade Up (Forceps)

According to Department of Health, Therapeutic Goods Administration, this recall involved a device in Australia that was produced by Johnson & Johnson Medical Pty Ltd T/A Depuy 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-2013-RN-00349-1
  • Event Risk Class
    Class II
  • Event Initiated Date
    2013-04-19
  • Event Country
    Australia
  • Event Source
    DHTGA
  • Event Source URL
    https://apps.tga.gov.au/Prod/sara/arn-detail.aspx?k=RC-2013-RN-00349-1
  • 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 affected lot has been labelled incorrectly as a blade up configuration instead of a blade down configuration. when the product is removed from the package, the blade down configuration is clearly visible.
  • Action
    Johnson & Johnson Medical is recalling the affected product.

Device

Tissue Liberator Blade Up (Forceps)

Manufacturer

Johnson & Johnson Medical Pty Ltd T/A Depuy Australia