Events

Recall of SureSafe Wraps and DrapesMultiple product and lot numbers

According to Department of Health, Therapeutic Goods Administration, this recall involved a device in Australia that was produced by General Healthcare Supplies 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-01110-1
  • Event Risk Class
    Class II
  • Event Initiated Date
    2012-10-31
  • Event Country
    Australia
  • Event Source
    DHTGA
  • Event Source URL
    https://apps.tga.gov.au/Prod/sara/arn-detail.aspx?k=RC-2012-RN-01110-1
  • 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
    It has been identified that the machinery used during the manufacturing process of these particular lot numbers may have cause metal shaving, a residue of the grinding process, to be present in the finished product.
  • Action
    Quarantine and return affected stock for replacement by Device Technologies.

Device

SureSafe Wraps and DrapesMultiple product and lot numbers

Manufacturer

General Healthcare Supplies Pty Ltd
  • Source
    DHTGA