COMPLICATIONS FROM GYNECARE PROLIFT AND BARD AVAULTA MESH PRODUCTS

           If you have had a Gynecare Prolift prolene mesh or Bard Avaulta mesh product placed in your body for pelvic floor repair or urinary incontinence, and have suffered complications, you may have a viable product liability claim against the manufacturers of those products.   Ethicon, which is a division of Johnson & Johnson manufacturers the Gynecare Prolift and C.R. Bard, Inc. manufactures the Bard Avaulta.  The known complications include, but are not limited to, mesh erosion, mesh shrinkage, infection, granuloma formation, dyspareunia (pain with sexual relations) and neuropathic pain.  The failure of the Gynecare Prolift and Bard Avaulta mesh products can lead to the need for multiple operations to remove the mesh, and can result in additional severe injuries such as scar tissue, neuropathic pain and urinary problems.  These problems have recently been recognized by the FDA in Public Health Notifications issued in October 2008 and February 2009, in which over 1000 reports and complaints regarding mesh products were lodged. 
            We are currently litigating against Ethicon and Johnson & Johnson, and are expanding our litigation against C.R. Bard.  If you believe that you have been seriously injured due to these products, and you are interested in learning more about how we can help, please provide the following information:

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DISCLAIMER: This does not constitute legal advice.  By providing the requested information you are not entering into an attorney-client relationship with this law firm.  Only a written retainer agreement between you and our law firm can create such a relationship.