May 3, 2013~ “My name is Cherie Storozinski. I am 50 years old and live in Dauphin, Manitoba, Canada. I am a victim of transvagnial mesh.” That’s how Cherie started her email to MDND. Cherie, 50, had a wonderful life in rural Manitoba, Canada. She and her husband, Curt, live on 20 acres and run
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April 9, 2013 ~ Dr. Robert Bendavid is a well-known hernia surgeon who in this editorial for the Africa Middle East Hernia Society discusses surgical mesh. Past president and a founding father of the American Hernia Society, Dr. Bendavid has performed thousands of procedures and is presently associated with the Shouldice Hospital in Toronto where the natural tissue, mesh-free,
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April 3, 2013 ~ Dr. Anthony Visco is Chief of Urogynecology at Duke Univ. Medical Center and President of AUGS. The American Urogynecologic Society (AUGS) was founded in 1979 and is a professional organization of 1,400 physicians and allied health professionals who care for women with pelvic floor disorders, specifically pelvic organ prolapse (POP) and
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March 29, 2013 ~ In September 2011, the U.S. Food and Drug Administration convened a panel of experts to try and get a handle on the concerning number of complications the agency was receiving about surgical mesh used to treat pelvic organ prolapse (POP) and stress urinary incontinence (SUI). The experts suggested that because of the
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Safety of Trans Vaginal Mesh procedure: retrospective study of 684 patients. This is the study by the French researchers known as the TVM group who were perfecting the Prolift technique, learning to develop tools or trocars to implant the mesh in a woman’s pelvic area. Find it here. The study had an average follow-up rate
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December 31, 2012 ~ “I had originally had my surgery scheduled December 2010. I cancelled it because on the internet I saw 1,900 mesh complication complaints.” Hope Pagano, 49, got scared when she saw those reports. The Long Island mortgage broker with a thick New York accent was not going to have her incontinence treated
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October 17, 2012 ~ Court cases filed around the country naming six mesh makers currently number 10,000 and are growing, some at a rate of 100 new cases filed a week. MDND has added up the number of lawsuits pending in federal court consolidated in multidistrict litigation (MDL) as well as those cases filed
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by Deb Contestabile, October 2012 I was reading the FDA alert from July 2011, (yeah, I have strange hobbies lately) and this part gets me. It says: “from Jan. 01, 2008 through Dec. 31, 2010, the FDA received 2,874 additional reports of complications associated with surgical mesh devices used to repair POP(Pelvic Organ Prolapse) and
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September 19, 2012 ~ Last January, after a five-fold increase in complications was noted by the U.S. Food and Drug Administration (FDA) concerning synthetic mesh used in women to treat pelvic organ prolapse (POP) and stress urinary incontinence (SUI), the FDA ordered mesh makers to find out why. At the time, the unprecedented request was
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July 26, 2012 ~ A panel of federal judges will meet on Thursday, July 26, to decide whether or not to expand vaginal mesh litigation to include a sixth multidistrict litigation. Currently there are four MDLs consolidated in Charleston, West Virginia before the Honorable Judge Joseph R. Goodwin. The other MDL is in federal court
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