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How Many Manufacturers Are Responsible for TVM Complications?

April 16, 2012

For many women, transvaginal mesh (TVM) is a painful reality in more ways than one. Physically, what started as a pelvic organ prolapse (POP) or stress urinary incontinence (SUI) has ultimately become out-of-control complications that may include infection, pain, bowel and bladder perforation, discomfort, and dyspareunia.


Unfortunately, these patients’ experience with the law governing transvaginal mesh complications may be just as unexpectedly frustrating. The Food and Drug Administration (FDA) has reported that at least nine medical device manufacturers may be responsible for the TVM product that caused their pain and discomfort and their family’s suffering. Why is this important? To advance a patients’ legal rights, a successful attorney must not only be able to point to the injury their child sustained, but also the party responsible. Connecting cause and effect can be challenging.


Fortunately, the attorneys at Fears Nachawati are skilled at making this important legal and factual connection. With years of experience and dedicated expertise, we know how to fight for our clients and to help them protect their legal interests. Talk to our attorneys today for a free consultation. Just call us at 1.866.545.8364 or email


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