FDA Communications on Urogynecologic Mesh

This article will address the communications from the FDA regarding Urogynecologic mesh when used transvaginally in the correction of pelvic organ prolapse. The FDA issued the first Public Health Notification regarding this device in 2008, then in 2011 issued an update on the safety and effectiveness of transvaginal mesh used in repair of pelvic organ prolapse.
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An Overview of the FDA Warnings on Urogynecologic Mesh

This article describes the FDA warnings associated with urogynecologic mesh as used in pelvic organ prolapse transvaginal surgical applications, as based on a recently published Current Urology Reports study,
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