A number of patients have reported experiencing transvaginal mesh side effects. Most women, however, don’t experience serious or long-term side effects after the procedure. However, transvaginal mesh does come with a risk of infection, which can be severe. Women should consult a doctor for information about transvaginal mesh before having it implanted. The FDA’s statement on transvaginal mesh side effects lists the most common complications. Click here – https://www.classactionlawyertn.com/avaulta-mesh.html
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In 2011, the Food and Drug Administration (FDA) first issued a warning about the safety of transvaginal mesh products. The agency updated its warning in 2012 to reflect more common risks. This resulted in the FDA reclassifying transvaginal mesh products from Class II to Class III. As a result, transvaginal mesh is still associated with risks and requires premarket approval applications from manufacturers.
In addition to physical pain, women who have experienced a mesh implant have experienced emotional distress as a result of the procedure. Because of these side effects, many women have sought legal redress against the manufacturers. More than 55,000 vaginal mesh lawsuits have been filed against several companies. Seven of the companies are now part of a multidistrict litigation (MDL) aimed at streamlining the growing number of similar cases and making the legal process more efficient.
The most common transvaginal mesh side effect is erosive damage. The synthetic material that surrounds the mesh can cause infection and perforation of internal organs. This could lead to serious complications and require multiple surgeries. Unfortunately, this is not uncommon and sadly, many women have suffered needlessly due to the complications associated with transvaginal mesh. Many doctors have begun to turn to non-mesh procedures for these patients.