The Food and Drug Administration (FDA) has issued a warning regarding the side effects of Gynecare Vaginal Mesh Repair system. The women affected with the problem of Pelvic organ prolapse (POP) and Stress urinary incontinence (SUI) were treated with Gynecare Vaginal mesh repair. The weakened tissues were replaced with the mesh on the vagina which provides the support to pelvic organs. This has caused many serious side effects to the women who were treated with this system. The side effects include infections which lead to death and urinary problems, pain during or after sexual intercourse. Few women have experienced perforation of organs during the surgical process. And also many women have experienced severe pain, profuse bleeding, extrusion and irritation on the vagina. So the women who have been affected with the side effects have undergone another surgery for removing the mesh and to get remedy for the complications. The affected women have approached the court for claiming compensation for their sufferings and pain due to the Gynecare Vaginal Mesh.
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