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Transvaginal placement of Bard Avaulta surgical mesh, which is used to treat Pelvic Organ Prolapse (POP) and Stress Urinary Incontinence (SUI), has recently been linked to several serious Bard Avaulta side effects. According to a health alert issued by the FDA, the most frequently-reported side effects associated with surgical mesh, including Bard Avaulta surgical mesh, include:
Other Bard Avaulta side effects may be caused during insertion of the
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The FDA has not yet determined whether specific characteristics put some patients at an increased risk for Bard Avaulta surgical mesh side effects. Factors contributing to Bard Avaulta side effects may include the patient’s overall health, the surgical mesh material, the size and shape of the Bard Avaulta mesh, the surgical technique used, concomitant procedures undertaken (e.g. hysterectomy), and possibly estrogen status.
In order to help the FDA learn more about possible side effects with transvaginal placement of surgical mesh, including Bard Avaulta mesh, physicians and patients are strongly encouraged to report side effects that may be associated with this medical device. Side effects related to Bard Avaulta mesh can be reported online, by mail, or by fax to the FDA’s MedWatch Adverse Event Reporting Program. The problems related to the Bard Avaulta surgical mesh, including mesh infections in particular, have led consumer advocates to call for a Bard Avaulta recall.
If you or a loved one has experienced the painful side effects associated with transvaginal placement of surgical mesh, such as Bard Avaulta mesh, you may be entitled to file a Bard Avaulta mesh lawsuit and seek compensation for your injuries. Contact our law firm today for a confidential and free case evaluation by our Bard Avaulta mesh side effects lawyers. Roopal Luhana is one of our lawyers working with Bard Avaulta victims. She can be reached privately at (877) 779-1414 (ext. 230) or by email at luhana@bernlieb.com.