Recall of Triathlon Tibial Alignment Ankle Camp Extramedullary (Referencing Instrument supplied with Triathlon Total Knee Arthroplasty procedure kit)

According to Department of Health, Therapeutic Goods Administration, this recall involved a device in Australia that was produced by Stryker 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-00699-1
  • Event Risk Class
    Class III
  • Event Initiated Date
    2013-07-10
  • 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
    Stryker orthopaedics has received complaints associated with cracks or fracture of the triathlon tibial alignment ankle clamp. as a result, there exists the potential for complications associated with extended surgery time greater than thirty minutes to retrieve a replacement ankle clamp.
  • Action
    Stryker is providing surgeons with work around instructions to implement if they are presented with a compromised Tibial Alignment Clamp during surgery.

Device

  • Model / Serial
    Triathlon Tibial Alignment Ankle Camp Extramedullary (Referencing Instrument supplied with Triathlon Total Knee Arthroplasty procedure kit)Catalogue Number: 65412609All lot numbersARTG No: 140892
  • Manufacturer

Manufacturer

  • Manufacturer Parent Company (2017)
  • Source
    DHTGA