On November 20, 2009, Ceatus Media Group unveiled a new website detailing the recent FDA recall for vertebrate body replacement products manufactured by Synthes. This Synthes FDA recall was a result of several reports stating that patients implanted with these devices suffered due to the device’s collapse. This failure can result in serious Synex side effects, including limited range of motion and increased lumbar pain.
The FDA is continuing to monitor the situation and will release further information when it is available.
