Bard Avaulta Mesh Product One of Several Transvaginal Mesh Products Drawing Scrutiny
Transvaginal mesh products have been growing in prevalence in recent years because of increased demand for help from the medical community to help manage and alleviate the symptoms of two common health issues with women - pelvic organ prolapse (POP) and stress urinary incontinence (SUI). Several different companies have formulated mesh products that are designed to help with the pain and discomfort that often accompanies these conditions, but recent reports have surfaced that have brought this entire product line, including Bard’s Avaulta Mesh product, under fire.
FDA Warning on Bard Avaulta Mesh
Below is a brief look at the conditions these mesh products are designed to help manage and the problems that have been encountered, prompting a public warning from the FDA.
Pelvic Organ Prolapse (POP)
Pelvic organ prolapse is the term that describes a condition whereby a pelvic organ such as a bladder drops (prolapses) from its normal spot and pushes against the walls of the vagina. This tends to occur when the muscles that hold the pelvic organs in place are weakened or stretched by childbirth or surgery. POP can lead to symptoms that include pain, discomfort, loss of bladder control and constipation.
Stress Urinary Incontinence (SUI)
Some estimates indicate that as many as 11 million women in the United States suffer from urinary incontinence, and it is generally defined as the sudden, involuntary loss of urine when a patient is laughing, sneezing, coughing or exercising. SUI is caused by anything that’s led to serious pelvic muscle strain or weakness, with one example being vaginal childbirth. It can be exacerbated by the estrogen loss that accompanies menopause.
The Problems Encountered by Transvaginal Mesh Products
While the mesh products introduced to the market were intended to help alleviate the problems caused by these conditions, reports have surfaced that have ultimately led to the FDA getting involved. Many of the reports of problems were initiated by the manufacturers of these products, and at this time that number is over 1,000 patients.
Therefore, the FDA has issued a public health alert that’s supposed to warn not only medical professionals but patients that these products which include Bard’s Avaulta Mesh product could cause significant damage to those who use them. These problems include pain, discomfort, internal tearing and bleeding and more problems with bladder control.
If injured or hurt from a Bard Avaulta Mesh Product:
If you or someone you love has suffered as a result of using these products, you could face a significant challenge in correcting the problem, including additional surgery. Therefore, you owe it to yourself to investigate your legal rights. Contact a defective medical products attorney today to schedule a free initial consultation to get this process started.
