For thousands of women suffering from pelvic organ prolapse (POP) or stress urinary incontinence (SUI), the discovery that their POP procedure may have included unknown risks is upsetting. Although it’s difficult to imagine how a medical device manufacturer could have released into the market a surgical mesh product prone to cause serious complications such as physical pain, infection, and bleeding as well as emotional distress, FDA reports suggest that may have been exactly what happened.
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Nachawati Law Group represents parties in mass tort litigation, businesses and governmental entities in contingent litigation, and individuals in complex personal injury litigation. For more information, visit contact or call 214-890-0711.
