SERIOUS COMPLICATIONS from Vaginal Mesh Implants include:
Organ perforation
Pain during sexual intercourse
Mesh Erosion
Infection
Bleeding
Recurrent prolapse
On January 4, 2016, the U.S. Food and Drug Administration (FDA) issued an order to reclassify transvaginal mesh products to a class III device. Class III devices are generally the highest risk devices and are subject to the highest levels of regulatory control.
Along with the reclassification, the FDA is requiring transvaginal mesh manufacturers to address significant safety concerns like pelvic pain and organ perforation.
Boston Scientific and C.R. Bard have approved settlement agreements totaling hundreds of millions of dollars to compensate tens of thousands of women who were injured by their vaginal mesh products.
There is existing litigation against several other manufacturers which may increase the total settlement dollars into the billions.
We make the Vaginal Mesh claim process EASY!
You may be able to file a claim without ever having to leave your home.
There is no mandatory travel and most clients never have to go to court.
No upfront fees and no fees paid out for our services unless you are awarded a settlement
Our professional staff is here to answer your questions
