Since 2008, the Food and Drug Administration (FDA) has warned consumers and patients that a widely used medical device known as transvaginal mesh has had a dangerously high malfunction rate, causing painful, potentially serious side effects. These side effects most notably include mesh erosion and mesh contraction and can be debilitating and require multiple surgeries for some female patients.
Victims of transvaginal mesh erosions and contractions routinely ask, “What should I do?” The first step is simple: record as much detail as possible about the adverse events you’re experiencing as a result of your transvaginal mesh. Your record should include the manufacturer’s name, the brand name of the product, relevant dates, the reasons for implantation, and the symptoms you’re experiencing. Next, you should contact the professionals at Fears Nachawati. With years of experience in complex class actions and victims’ rights claims, we have the ability to protect your legal and financial interests. For your free consultation, call us at 1.866.545.8364 or email mn@fnlawfirm.com.