Baxter implemented labeling changes on CE-marked Peri-Guard Repair Patch and Supple Peri-Guard Repair Patch products including removal of the indications for abdominal wall defect and hernia (diaphragmatic, femoral, incisional, inguinal, lumbar, paracolostomy, scrotal and umbilical) repair from the Instruction For Use (IFU). Recall Start Date: April 16, 2024
RecallTracker