Whats up with this? Thought we had clinical history with the NexGen. https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=128986
Class 2 Device Recall Persona Trabecular Metal Tibial Plate / Persona TM Tibia http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=133978
Click that link and read the ACTION section. It's clearly states voluntary recall. Same old BS Nothing new here