More Safety Studies Pending for Transvaginal Mesh Products
Major manufacturers of transvaginal mesh implants, a widely distributed medical product that has affected thousands of women, have notified the U.S. government’s health care agency, the Food and Drug Administration (FDA), that they plan to review both the safety of implants and the appropriateness of current and possible labels.
Manufacturers have come under intense pressure after thousands of women experienced adverse health affects following their transvaginal mesh operation. For many of these women, the operation was intended to address their pelvic organ prolapse (POP) or stress urinary incontinence (SUI), but instead only added pain, discomfort, and embarrassment.
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