Posts Tagged ‘ defective product ’

Day 13: Linda Gross v. Ethicon How is She Coping Psychologically?

Jan 30th, 2013 | By
Day 13: Linda Gross v. Ethicon  How is She Coping Psychologically?

January 30, 2013 ~ On this half day of trial in the  Linda Gross v. Ethicon case being heard in an Atlantic City courtroom, psychiatrist Dr. Ronni Seltzer was on the stand. She conducted two evaluations of Linda Gross and determined the focus of her life, along with her husband Jeff, is pain that permeates
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Day Three: Linda Gross v. Ethicon: Her Injuries From Mesh

Jan 14th, 2013 | By
Day Three: Linda Gross v. Ethicon: Her Injuries From Mesh

January 14, 2013 ~ During day three of the trial that’s put the spotlight on Johnson & Johnson (J&J) and its transvaginal mesh, Prolift, the primary care doctor for patient Linda Gross  outlined the countless procedures she has faced to remove synthetic mesh that continues to cause crippling pain. MDND thanks Courtroom View Network for
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Mississippi Court Upholds Ethicon Win in Mesh Warning Lawsuit

Aug 9th, 2012 | By
Mississippi Court Upholds Ethicon Win in Mesh Warning Lawsuit

August 8, 2012 ~ An appeals court ruling in Mississippi has upheld a lower court dismissal of a $10 million vaginal mesh case against Johnson & Johnson’s Ethicon division. The United States Court of Appeals Fifth Circuit filed the decision August 2, 2012 in the case against Ethicon by Deborah and Michael Smith. Deborah Smith
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What is a Statute of Limitations?

Jun 14th, 2012 | By
What is a Statute of Limitations?

If you are considering filing a legal action, you’ve probably heard the term “Statute of Limitations.” A “statute” is the common law that sets the time frame within which you have to file a lawsuit. A filing outside of that time frame may mean it is too late to prosecute the person or company responsible
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American Medical Systems Files its Position Statement Laying Out its Strategy in Court in Defective Mesh Lawsuits

Apr 9th, 2012 | By
American Medical Systems Files its Position Statement Laying Out its Strategy in Court in Defective Mesh Lawsuits

April 9, 2012 ~ On Friday, April 6, American Medical Systems Inc. (AMS) of Minnetonka, Minnesota filed its Position Statement with federal court in the Southern District of West Virginia laying out its strategy in its defense of its synthetic surgical mesh used to treat female conditions of pelvic organ prolapse (POP) and stress urinary
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Breaking News ~ J & J Sold Vaginal Mesh Implant Without FDA Approval

Mar 21st, 2012 | By
Breaking News ~ J & J Sold Vaginal Mesh Implant Without FDA Approval

March 21 ~ Bloomberg is reporting (here) that major medical device maker Johnson & Johnson (J&J) sold the Gynecare Prolift surgical mesh for three years before it was approved by the U.S. Food and Drug Administration (FDA). The mesh is now the subject of more than 550 lawsuits, reports Bloomberg. Prolift is a pre-cut mesh
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We hope you find this a helpful resource. National News Editor, Jane Akre, began MDND with the hope of providing the latest news, information and perspective from the regulatory, industry and patient point of view, something that goes under-reported in much of the coverage of medical devices. The public is just now becoming aware that many devices do not undergo the same scrutiny as prescription drugs and are instead grandfathered in under an FDA loophole that has gone largely unchanged since the 1970s. As a result, patients become the post-market clinical trial subjects, and many suffer devastating and permanent injuries.