Calls for Avaulta Recall Due to Vaginal Mesh Side Effects
Avaulta Recall Requests
Since the FDA warning for Avaulta and other transvaginal mesh systems, the public has been petitioning that an Avaulta recall be issued. Doctors, patients and vaginal mesh lawyers alike are beginning to believe that the Bard Avaulta mesh is defective, and that defect may be causing many of the Avaulta side effects being reported by female patients. However, even though transvaginal mesh systems have been associated with serious side effects, including mesh infections, an Avaulta recall has not been issued.
If you have suffered from Avaulta mesh problems following vaginal prolapse surgery, you do not have to wait for an Avaulta recall to find out if you can make a claim for financial compensation. Fill out our free case evaluation form today to find out if you can recover compensation for medical bills and other damages resulting from your Avaulta mesh problems.
Avaulta Mesh Defect
An Avaulta mesh recall has been requested due to reports that women who have undergone mesh surgery have suffered from serious complications. Although the exact cause of the Avaulta mesh problems is still unknown, some believe that the design of the vaginal mesh prevents the surrounding tissue from receiving nutrients and oxygen, preventing proper healing. As a result, the pubovaginal sling may cause serious Avaulta transvaginal mesh complications, such as mesh erosion or infection. These Avaulta mesh side effects may require further surgery, possibly to remove the vaginal mesh.
Causes of Avaulta Mesh Side Effects
A vaginal mesh infection is a serious complication which can cause problems for women who have been implanted with a Bard Avaulta mesh. Infections due to the placement of a transvaginal mesh can occur in one of two ways. First, a vaginal mesh infection may develop during pelvic prolapse repair surgery due to bladder, bowel or blood vessel perforation. Second, an Avaulta vaginal mesh infection may develop due to the reported mesh design defect which prohibits the surrounding tissue from receiving proper nutrients and oxygen.
Have you developed a mesh infection or other Avaulta side effect? Our Avaulta recall lawyers would like to hear from you.
Avaulta Recall Attorneys
Although the public has requested an Avaulta recall since the FDA’s vaginal mesh warning in 2008, Avaulta has not been withdrawn from the market. Still, women who have experienced Avaulta mesh side effects do not have to wait for a vaginal mesh recall to learn about their legal options. If you have been implanted with an Avaulta sling and are experiencing complications, contact our Avaulta recall lawyers today for a free legal consultation.