Vertebrae Replacement Implants Recall Issued Due to Failure Risk
The FDA announced a Class I recall on Thursday for all lots of the Synthes USA, Ti Synex II Vertebral Body Replacement (VBR), which are used to replace damaged vertebrae.
The FDA announced a Class I recall on Thursday for all lots of the Synthes USA, Ti Synex II Vertebral Body Replacement (VBR), which are used to replace damaged vertebrae.