The U.S. Food and Drug Administration (FDA) in July 2011 issued a notification stating and warning about the problems with surgical mesh products to the doctors and patients. It said that “serious complications associated with surgical mesh for transvaginal repair of POP (pelvic organ prolapse) are not rare”.
The agency received more than a thousand reports of adverse events concerning the mesh to treat POP and stress urinary incontinence (SUI) from 2005 and 2007 but the number almost tripled in the following three years.
![]() |
Get Updates on Transvaginal Mesh Lawsuits - Vmsettlements.net |
• Dyspareunia (pain during sexual intercourse)
• Chronic infection of the vagina
• Lower back pain
• Bleeding of the vagina
• Perforation of organs
• Infection
• Death
Product Defects
Injuries arise from a defectively designed mesh and the condition is called mesh erosion. The medical device erodes into or possibly even through the walls of the rectum, small intestine, vagina, or bladder and can lead to stool leakage or infection. Organs can be exposed to severe infection, necessitating surgery when the break down is too much. Bard Avaulta Solo, Johnson & Johnson, Avaulta Biosynthetic Systems, and Avaulta Plus are some of the names that have been filed in the lawsuits.
Women who are aware of the transvaginal mesh lawsuit update normally allege the following about mesh manufacturers:
• Failed in their duty to ensure the safety and efficiency of the TVMs
• Did not conduct sufficient and well controlled studies before marketing
• Provided little warnings of potential mesh complications and patient harm
• Intentionally misled the public with wrong advertisement and branding about the safety
• Was negligent about the design and manufacturing of the mesh products
If you experienced transvaginal mesh complications, you may qualify for a lawsuit which can help you recover compensation for medical bills, lost wages (past and future), and pain and suffering. Visit http://vmsettlements.net/ to know more.
No comments:
Post a Comment