Following the recent FDA warnings against the significantly higher risk of complications associated with using transvaginally implanted mesh, many female patients have pursued lawsuits against Johnson […]

In the past few years, hundreds of thousands of patients have been treated with transvaginal mesh, like Johnson & Johnson’s Gynecare Prosima for the conditions of […]

On 7/13/2011, the U.S. Food and Drug Administration released a warning addressed to health care professionals as well as the general public regarding the risks associated […]

After the issuance of multiple warnings by the FDA regarding the use of transvaginal mesh used for the treatment of Pelvic Organ Prolapse, many patients have […]

Mentor’s ObTape sling is a surgically inserted medical device used to treat female patients who suffer from stress urinary incontinence, or SUI. This condition, also known […]

Bladder slings are medical devices used in the treatment of pelvic organ prolapse (POP) and stress urinary incontinence (SUI). Many bladder slings have not met reasonable […]

Recently, several lawsuits have been filed against the Mentor Corporation with regards to its poorly designed and manufactured ObTape Sling device. The trans-obturator tape sling was […]

Transvaginal Mesh (Mesh Erosion) Bladder Slings (Mesh Erosion) ObTape (Mesh Erosion) Surgical Mesh FDA Warning On October 20, 2008, the U.S. Food and Drug Administration issued […]

Recently, an El Paso woman filed a transvaginal mesh lawsuit against American Medical Systems (AMS) due to issues with her vaginal mesh implant manufactured by American […]