DePuy Synthes Craniomaxillofacial Distraction System Recalled (Class I) Because It May Reverse Directions After Surgery

The FDA informs Orthopedics, Surgery healthcare personnel, and Risk Managers that certain lots of DePuy Synthes Craniomaxillofacial Distraction System are recalled (Class I) because the device may reverse direction after surgery. Background of DePuy Synthes Craniomaxillofacial Distraction System The DePuy Synthes Craniomaxillofacial (CMF) Distraction System is an implant used to lengthen and/or stabilize the lower […]