Recall of Flexible Handle for Simplified Universal Nail System (SUN) and the Universal Nail System (UNI) (Re-usable surgical instrument supplied as part of internal fixation system implantation kit)

According to Department of Health, Therapeutic Goods Administration, this recall involved a device in Australia that was produced by Synthes 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-2013-RN-00338-1
  • Event Risk Class
    Class I
  • Event Initiated Date
    2013-04-23
  • Event Country
  • Event Source
    DHTGA
  • Event Source URL
  • 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 has identified that there is a potential lack of the ability to thoroughly clean the instrument.
  • Action
    The affected handle is being recalled and replaced with a new design of handle.

Device

  • Model / Serial
    Flexible Handle for Simplified Universal Nail System (SUN) and the Universal Nail System (UNI) (Re-usable surgical instrument supplied as part of internal fixation system implantation kit)Flexible Handle Part Number: 355.280 ARTG Number: 153950
  • Product Classification
  • Manufacturer

Manufacturer