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Personal Injury Attorneys
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October 2008 - Washington, D.C.
The U.S. Food and Drug Administration
Issues a Black Box Warning on
the Use of Vaginal Mesh Used in Pelvic
Organ Prolapse and Stress
Urinary Incontinence Surgeries
The
U.S. Food and Drug Administration has issued a black box warning on the use of
vaginal mesh and synthetic
mesh used in pelvic organ prolapse and
stress urinary incontinence
(also referred to as Female
Urinary Incontinence) surgeries.
The FDA stated in the Black Box Warning; “Most frequent complications included erosion through vaginal epithelium, infection, pain, urinary problems, and recurrence of pelvic organ prolapse and/or stress urinary incontinence.”
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Personal Injury Attorneys
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