Transvaginal mesh is a type of medical device that is used to treat Pelvic Organ Prolapse (POP) and Stress Urinary Incontinence (SUI), both are conditions that commonly occur after childbirth and pregnancy. The transvaginal mesh/sling device is surgically implanted to treat these conditions.
The Food and Drug Administration (FDA) reported that over 1,000 incidents of potentially fatal complications have been associated with Transvaginal Mesh patches. Due to the rise in numbers of serious health issues associated with this device, in 2008 the FDA issued a public health notification warning the medical community of the problem. The most common serious injury reported from defective Transvaginal Mesh patches is the puncture of the bladder, intestines and bowels, as well as blood vessels in and around the vaginal wall.
Shipman & Wright is currently accepting cases of those who have suffered complications resulting from transvaginal mesh/sling implants. For further information please contact us to discuss your situation regarding the defective transvaginal mesh device.
In August of 2009, Shipman & Wright attorney, Jean Martin featured this issue on her InjuryBoard blog. view blog
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