The product liability team at Leigh Day has been instructed by a number of patients in Australia who have suffered failed knee replacement surgery and have had to undergo early revision operations as a result of a defective knee implant.

LCS Duofix

The LCS Duofix implant, manufactured by DePuy International Ltd in Leeds, was recalled in July 2009 as a result of increased revision rates.   DePuy has stated that Alumina particles detected in the joint space are a factor leading to third body wear and /or tissue staining.  Alumina is a bio-compatible material used to roughen the internal surface of the implant in the manufacturing process.

The LCS duofix implant was widely used and UK patients may have had to undergo additional surgery with its associated pain and additional recuperation time since being fitted with the device.  DePuy has agreed to pay for revisions, operations and rehabilitation in one case.  UK residents may be entitled to claim for compensation if they have been fitted with this faulty device.
The product liability team at Leigh Day & Co has considerable experience in handling claims relating to defective medical devices.  If you would like to speak to one of our lawyers please contact Bozena Michalowska or Jill Paterson on 020 7650 1311.