Synex II Vertebral Body Replacement Recalled by FDA
The Food and Drug Administration (FDA) notified healthcare professionals of a Class I Recall of all lots of the Synthes USA, Ti Synex II Vertebral Body Replacement, a device used in the T1-L5 portion of the spine to replace a collapsed, damaged, or unstable vertebral body. Reports of moderate to severe loss of vertebral body replacement height (caused by failure of the central body component) in situ at six to fifteen months post implantation were received. Potential adverse health issues that could be associated with this issue include neural injury, increased pain, spinal kyphosis if unrecognized, failure of supplementary fixation, and/or need for reoperation/revision surgery. Surgeons and hospitals in possession of the subject devices must stop implanting them immediately. This product was manufactured from June 8, 2007 through September 9, 2009 and distributed from July 2, 2007 through September 8, 2009.
Read the complete MedWatch 2009 Safety summary, including a link to the Class 1 recall HERE.
Read the affected part numbers HERE.
If you or a loved one have received the Synex II Vertebral Body Replacement, and have required reoperation to remove and replace the device or other adverse health affects, you may be entitled to money damages. Contact one of our product liability attorneys for a free legal consultation.