FDA Proposes Transvaginal Mesh Classified to High Risk

Medical Device Ligitation, Personal Injury Law, Surgical mesh attorneys, Transvaginal mesh lawyers, transvaginal mesh litigation

It appears after six years and thousands of lawsuits for transvaginal mesh injuries, the U.S. Food and Drug Administration (FDA) is proposing to reclassify the surgical mesh for pelvic organ prolapse (POP) repair to a “high-risk device.” Med Page Today, a news service for physicians, published an article titled: “FDA Wants High-Risk Label for Transvaginal … Read More