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.