Used to treat conditions that frequently occur after childbirth, vaginal mesh products are made of polypropylene and are surgically implanted. The increasing number of complications reported with these products prompted the Food and Drug Administration (FDA) to require the manufacturers to investigate the causes, which resulted in the recall of many of their products from the market. And recently, the FDA has proposed orders to reclassify transvaginal mesh from a moderate risk device to a high risk device.
The number of women harmed by these implants is growing into the hundreds of thousands. If you or someone you know is suffering from the complications of transvaginal mesh, it is not too late to contact an attorney.
Prior results do not guarantee a similar outcome.