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Outpatient Surgery E-Weekly

Contact Congress Over Drug Shortage Issues

A Kentucky congressman is urging surgical facilities to contact their members of Congress and request that they sign his letter demanding changes to...

N.J. Posts ASC Inspection Reports Online

State and federal inspection reports of New Jersey's ASCs are now available online, giving patients an opportunity to make more informed choices abo...

Are Opioids Necessary?

While it's not always practical, or even possible, to eliminate opioids from your post-op pain management regiment, reducing their use in favor of n...

Home > News > October, 2008

FDA Issues Surgical Mesh Warning

Agency has received reports of complications following two commonly performed GYN procedures.

Published: October 24, 2008
Categories: GYN/Urology, News

Surgical mesh used to treat pelvic organ prolapse and stress urinary incontinence can cause severe complications when placed through incisions in the vagina, according to a warning issued by the Food and Drug Administration. Potential complications include erosion of the vagina’s wall, infection, pain, urinary problems and recurrence of the prolapse or incontinence.

The FDA has also received reports of mesh erosion causing scarring of the vagina, which led to discomfort and pain during sexual intercourse and required additional surgery to remove mesh that had eroded into the vagina.

Daniel Cook

© Copyright Herrin Publishing Partners LP 2011. REPRODUCTION OF THIS COPYRIGHTED CONTENT IS STRICTLY PROHIBITED. We encourage LINKING to this content; view our linking policy here.


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© Copyright Herrin Publishing Partners LP 2011. REPRODUCTION OF THIS COPYRIGHTED CONTENT IS STRICTLY PROHIBITED. We encourage LINKING to this content; view our linking policy here.

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