The Food and Drug Administration (FDA) has issued an urgent public notice on
transvaginal mesh surgery after receiving thousands of reports about painful complications.
About 1 in 4 women suffer from pelvic organ prolapse or stress urinary incontinence, and between 11 % and 19 %
receive mesh surgery to correct it.
If you, or a loved one, are experiencing discomfort or pain after undergoing
hernia mesh surgery, it's important that you speak to a healthcare professional as soon as possible; they will be able to offer on advice on whether the mesh implant is the cause of your suffering and recommend a course of potential treatment.
While there are countless dangerous drugs on the market, our firm concentrates on helping clients who have been injured due to transvaginal
pelvic mesh surgery or by Xarelto, a blood thinner frequently prescribed to treat those who are prone to blood clots.
The Food and Drug Administration (FDA) began reviewing the safety of the transvaginal
mesh surgery in 2011.
When the FDA first noted problems with
vaginal mesh surgery procedures, these problems were described as being rare, but not anymore.
• 2.2 % suffered bleeding during surgery • 5.5 % developed vaginal and pelvic hematomas • 1.6 % sustained bladder injury during the procedure • 5 patients developed rectal damage • 1 patient suffered ureteral damage
Post-vaginal mesh surgery, complications included:
Boston Transvaginal
Mesh Surgery Lawyer:: Stress Urinary Incontinence:: Massachusetts Surgical Mesh Attorney
You may be entitled to money damages for what you have been put through or will go through in the future because of the complications from transvaginal
pelvic mesh surgery.
If you received transvaginal
mesh surgery and sustained injuries, the product manufacturer may be liable for pain and suffering, lost wages and past and future medical expenses.
Women who have experienced serious side effects after undergoing transvaginal
mesh surgery can consult our drug injury lawyers for free legal advice.
This transvaginal
mesh surgery...
If you have been injured by this transvaginal
mesh surgery, contact our Boston product liability lawyers to discuss your options for seeking compensation.
Having received over 3,800 reports of complications, the FDA urged surgeons to consider other options before performing transvaginal
mesh surgery.
It also reported it was not clear that transvaginal
mesh surgery is more effective than non-mesh repair of POP.
Between 2005 and 2010, more than 3,800 women had reported complications and injuries following transvaginal
mesh surgery, according to the FDA.
On July 13, the FDA updated a 2008 public health notification, reporting that complications from transvaginal mesh are not rare and that it is not clear that transvaginal
mesh surgery is more effective than non-mesh repair of pelvic organ prolapse (POP).
If you have been injured during transvaginal
mesh surgery, it is important to contact an experienced Boston medical device recall lawyer who can protect your interests as the FDA conducts its review.
On July 13, the FDA issued an update on a 2008 public health notification reporting complications from surgical mesh used in transvaginal
mesh surgery are not rare.
If you have been injured as a result of transvaginal
mesh surgery, it is important to contact an attorney who is experienced in handling defective medical device cases.
During transvaginal
mesh surgery, surgical mesh is permanently implanted inside a woman's body in the form of a sling.
If you have experienced injuries as a result of transvaginal
mesh surgery, it is critical to preserve your rights.
The NHS and MHRA's proposal includes a medical registry that would allow surgeons to track the outcomes of transvaginal
mesh surgeries to better understand their efficacy and the potential side effects of transvaginal mesh.
In 2008 the Food and Drug Administration warned that transvaginal
mesh surgery has a higher risk of complications compared with other forms of surgical vaginal repair.
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