On March 12, 2015, the FDA announced a Class 2 Recall for portions of the Zimmer Persona knee replacement system. Specifically it appears that the Trabecular Metal Tibia Plate and TM Tibia are failing and causing premature loosening and failure of Zimmer Persona knee replacements.
Approximately 11,658 of these devices were distributed.
If you or a loved one had a Zimmer knee replacement that is loosening and failing early, please contact our experienced Zimmer Persona attorneys at (888) 606-5297 for a free consultation about your potential Zimmer knee replacement lawsuit. We can help you determine what type of product was used in your knee replacement and whether you may have a lawsuit.