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Transvaginal mesh products are sometimes used to repair pelvic organ prolapse (pop) or stress urinary incontinence (sui) Fda has ordered studies to evaluate safety of the devices Despite thousands of reports of serious injuries leading to lawsuits being filed, only one transvaginal mesh device has been recalled
Though, several companies have discontinued their products. Experts have called for a recall of transvaginal and bladder sling surgical mesh products due to the risk complications If you had a bladder sling implanted and suffered injury, you may be entitled to money from a bladder sling lawsuit or settlement.
A bladder sling lawsuit is complex because it combines aspects of personal injury and product liability claims
Furthermore, it is a mass tort in which many individuals are suing the producers of surgical mesh devices for compensation. Transvaginal mesh verdicts most of the bladder sling and pelvic mesh verdicts ranging from $120,000,000 to $0 involved women with multiple complex implant removal/revision surgeries resulting in lifelong injuries with juries awarding compensatory and punitive damages Note that jury verdicts may be reversed, remanded, reduced or appealed by the losing parties and settled for amounts less than. The recall applies to mesh used in transvaginal repair of pop
The fda has not recalled the mesh that is inserted through an abdominal incision (open, laparoscopic or robotic) for pop repair, nor mesh used in midurethral sling procedures for the treatment of stress urinary incontinence. Midurethral mesh slings, commonly used to treat stress urinary incontinence (sui), have come under increasing legal and medical scrutiny due to serious complications reported by thousands of patients.
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