Anapol Schwartz is a leader in national medical device litigation. Our attorneys advocate for clients all over the country who needed revision surgery to correct problems with defective Zimmer knee implants.
The FDA recalled the Zimmer
Persona Trabecular Metal Tibial Plate in March 2015. The recall came in response to a high
complaint rate for radiolucent lines — gaps between the knee and the device — and implant loosening.
The NexGen High Flex Knee was marketed as giving patients a greater range of motion, but Zimmer is facing knee implant lawsuits alleging premature loosening and pain.
Attorneys Jim Ronca and Joshua Cohan are currently investigating and accepting cases on behalf of people nationwide who suffered pain and loosening complications with their Zimmer Persona Knee implant.
The Zimmer Persona knee implant was distributed to numerous VA hospitals across the United States, so the defective knee component may potentially affect many veteran knee replacement patients.