Friday, December 7, 2018

How Effective Are The Mesh Lawsuit Claims?


Vaginal mesh lawsuit is not unheard of. More than 100,000 vaginal mesh lawsuit(s) have been filed over the years. Many have resulted in settlements, with some resulting in multimillion-dollar settlements, however, some vaginal mesh lawsuit(s) are still on-going.

Transvaginal mesh, also known as pelvic mesh or bladder slings, is a surgically implanted mesh device used to treat pelvic organ prolapse (POP) and stress urinary incontinence (SUI) in women. POP occurs when the muscles holding pelvic organs in place are weakened, resulting in the bladder dropping (or prolapsing) and pressing against the walls of the vagina. SUI, on the other hand, occurs when an activity such as coughing or sneezes causes urine to leak out of the urethra. 



Vaginal mesh is used to repair these issues by providing extra support to the weakened or damaged tissue. It is made from either porous synthetic material or biologic material. However, these devices often cause damage to the health and internal organs leading to legal claims for financial compensations, as per transvaginal meshlawsuit updates

Damages and injuries caused:

The sufferers allegedly undergo several injuries from mesh implants that are often severe and unbearable, though these could have been avoided if people were aware of the consequences and side effects. 

The most commonly found complications are infection and cut of the skin caused by the edges of the mesh during the implantation. The mesh sometimes punctures the bladder, bowel and uterus too. Complications include incontinence, extreme pain during intercourse, UTI, back pain, inability to walk, etc. Some of these infections can spread through the whole body and lead to death.

The lawsuit and the claim:

Studies estimate that the actual rate of injury is likely to increase significantly, which should not be surprising considering that more than 100,000 of these types of procedures are performed annually. There could be multiple numbers of injuries and deaths according to reports made to the FDA. Yet, sometimes these injuries can take years to develop after the initial surgery. Thousands of women have filed lawsuits alleging they were injured by pelvic mesh products.

Unfortunately, about 30 percent of women who underwent mesh surgery for POP will need another related surgery. Due to the high complication risk, the FDA has re-classified vaginal mesh used to treat POP as a high-risk device. The classification does not, however, apply to the vaginal mesh used to repair SUI.

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