(HealthDay) -- "Surgeon-tailored" polypropylene mesh (STPM) repair using a transobturator midurethral sling procedure alone or in combination with pelvic organ prolapse repair is an effective ...

In a Health Notification issued in October 2008 and updated in July 2011, the U.S. Food and Drug Administration (FDA) warned of serious complications associated with transvaginal placement of surgical ...

The Food and Drug Administration has issued a new warning about a medical device many say never should have been implanted in millions of women. In January, the FDA re-classified transvaginal mesh, a ...

The Food and Drug Administration on Tuesday ordered the two remaining medical device companies selling surgical mesh for the repair of pelvic organ prolapse to stop all sales and distribution in the ...

CHICAGO — The ban on further sales of transvaginal mesh for pelvic organ prolapse (POP) imposed by the US Food and Drug Administration (FDA) last month has some people cheering, some saying that an ...

There are many questions about the optimal way to evaluate and manage the outlet in clinically continent women with high-grade pelvic organ prolapse (POP). Women with POP are thought to be at high ...

The U.S.Food and Drug Administration has moved to strengthen regulations on vaginal mesh, a controversial medical device used to treat pelvic organ prolapse, a condition that can occur after ...

New York, June 22, 2021 (GLOBE NEWSWIRE) -- Reportlinker.com announces the release of the report "Urinary Incontinence & Pelvic Organ Prolapse Devices And Equipment Global Market Report 2021: COVID-19 ...

New evidence published today highlights benefits and harms of using artificial mesh when compared with tissue repair in the surgical treatment of vaginal prolapse. Slightly better repair with mesh ...

Christopher Maher is Chair of the Urogynaecological Society of Australasia . A common surgery to treat vaginal prolapse using an artificially grafted mesh has more problems than benefits, our Cochrane ...