Posts Tagged ‘
not rare ’
Mar 29th, 2013 |
By Jane Akre
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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Posted in FDA |
10 comments
Tags: Adverse Event, Class II, Class III, Dr. Benson, erosion, FDA, Food and Drug Administration, High-Risk Device, Linda Gross v Ethicon, MDND, Mesh medical Device News Desk, non-mesh surgery, not rare, pelvic organ prolapse, POP, premarket review, Stress urinary incontinence, SUI, SUI mesh, SUI mesh injuries, SUI repairs
Oct 17th, 2012 |
By Jane Akre
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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Posted in Feature |
4 comments
Tags: American Medical Systems, Boston Scientific, C.R.Bard, Coloplast, Ethicon, gynecare, Johnson & Johnson, Judge Joseph Goodwin, MDL, MDND, mentor Ob, Mesh medical Device News Desk, Multidistrict Litigation, not rare, pelvic organ prolapse, polypropylene, POP, Southern District of West Virginia, Stress urinary incontinence, SUI
Oct 10th, 2012 |
By Jane Akre
February 3, 2012. That was the day that Deb Contestabile says her health took a downturn from which she has still not recovered. The 46-year-old mother of two boys led a predictable and comfortable life with her husband of almost 22 years who owns a machine shop. They have busy lives with the two boys
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Posted in Patient Profiles |
28 comments
Tags: American Medical Systems, Dr. Shlomo Raz, dysplasia, facebook, FDA, ischiopubic, Medical Mesh Legal Support, Mesh medical Device News Desk, Miklos and Moore, Monarc sling, Monarc TOT transobturator tape, not rare, obturator muscle, obturator nerve, osteotomy, pelvic organ prolapse, POP, stress incontinence, SUI, surgical mesh, TVT No, Urogynecologist
Oct 10th, 2012 |
By Jane Akre
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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Posted in Op-Ed |
12 comments
Tags: complications, Constestabile, Deb, elective surgery, FDA alert, mesh, not rare, pelvic organ prolapse, sex, Stress urinary incontinence, SUI POP, SUI repairs, traditional surgery
Sep 25th, 2012 |
By Jane Akre
Sept 25, 2012 ~ A recent news release from an ObGyn in Minneapolis shows that at least he is on the offensive when it comes to mesh injuries. The doctor doesn’t let the facts get in the way. For some reason the doctor, an Ob/Gyn at Oakdale Obstetrics & Gynecology in the Minneapolis, Minnesota area
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Posted in Legal News |
4 comments
Tags: bleeding, FDA, infection, mesh complications, neuro-muscular problems, not rare, Obgyn, pain, perforation, plaintiff lawyers, shrinkage, vaginal scarring
Jul 24th, 2012 |
By Jane Akre
July 24, 2012 ~ BREAKING NEWS! “Thank You God. We can finally get the word out to women.” Those are the words of Christine Scott, 53, a former runner who had a vaginal mesh implant to treat stress urinary incontinence in 2008. After that her health went downhill as the synthetic mesh eroded into
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Posted in Feature |
16 comments
Tags: Avaulta Plus Biosynthetic Support System, Breaking News, C.R.Bard, Christine Scott, eroded, FDA, incontinent, landmark, not rare, pelvic organ prolapse, POP, product liability, Prolapse, Stress urinary incontinence, SUI, synthetic transvaginal mesh, transvaginal mesh
May 29th, 2012 |
By Jane Akre
May 29, 2012 ~ According to an article published in The Patriot Ledger, Boston Scientific was sued in Boston federal court May 2, by Sheila Roach of Modesto, California. She blames a mid-urethral sling implanted in May 2008 on injuries that followed including debilitating pain and infections which necessitated corrective surgery in 2010. Natick-based Boston
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Posted in Media Reports |
No Comments »
Tags: American Medical Systems, Boston Scientific, C.R.Bard, Ethicon, FDA, mid-urethral sling, not rare
May 8th, 2012 |
By Jane Akre
The Toronto, Canada newspaper, The Globe and Mail, on May 7, Monday night published, “Time to discuss risks of surgical meshes.” These are embarrassing issues to discuss says newspaper columnist, Andre Picard, because they involve so-called “private parts.” Most reporters don’t usually write about organs that protrude through the vagina or urine leakage when one
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Posted in Media Reports |
No Comments »
Tags: 2011, Avis Favaro, class action, CTV, Ethicon, FDA, Globe and Mail, July 13, Kegels, not rare, pelvic organ prolapse, POP, Stress urinary incontinence, SUI
Apr 18th, 2012 |
By Jane Akre
April 17, 2012 ~ CTV National News on Tuesday, April 17, ran a taped story of two women who are involved in a multimillion dollar class action lawsuit in Canada over vaginal mesh. The women are now disabled and unable to work as a result of being implanted with synthetic surgical mesh as a treatment
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Posted in Legal News |
20 comments
Tags: Canadian Television, class action, complication rate, CTV, debilitating injuries, Ethicon, failure to warn, FDA warnings, Health Canada, Incontinence, Johnson & Johnson, not rare, pelvic organ prolapse, Stress urinary incontinence, transvaginal POP repair, vaginal mesh
Jan 12th, 2012 |
By Jane Akre
JANUARY 12, 2012 ~ A growing number of women from around the country who are plaintiffs in transvaginal mesh litigation have a court date of Wednesday, January 26 in Miami. The Judicial Panel on Multidistrict Litigation (MDL) is set to hear requests by plaintiff attorneys to have thousands of defective mesh lawsuits consolidated in the
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Posted in Legal News |
2 comments
Tags: American Medical Systems, Bard Avaulta mesh, Boston Scientific, Class II, Class III, Ethicon, FDA, Food and Drug Administration, Incontinence, infection, Johnson & Johnson, Judge Joseph R. Goodwin, Judicial Panel on Multidistrict Litigation, MDL, medical device, mesh complications, mesh erosion, mesh injuries, mesh migration, Multidistrict Litigation, not rare, pelvic organ prolapse, product liability litigation, transvaginal mesh