Have you received a knee replacement manufactured by DePuy Synthes? Are you experiencing problems with it or have you been told you need revision surgery? The FDA has received adverse event reports regarding the Attune knee replacement. Often times, the implant failure is due to loosening along the cement border, at the tibial baseplate.
If such a failure occurs, it is likely the person would need a revision surgery to remove the device, and probably to replace it as well. Symptoms leading up to catastrophic failure may include:
- Bone damage
- Tissue damage
At Long & Long, our attorneys are currently reviewing claims related to DePuy knee replacements. If you have experienced complications or necessary revision surgery, you may have a claim against the manufacturer. Contact Long & Long today at 251-432-2277 or fill out our free case evaluation form.