There are at least three Physiomesh cases already filed nationwide. Read more
Defects in Physiomesh were found only after it was put on the market. Read more
The FDA recently reclassified pelvic mesh devices such as those at issue in the suits as high-risk devices. Read more
Johnson & Johnson medical device maker Ethicon Inc. has settled a whistleblower claim that it fired an executive. Read more
A state appeals court in New Jersey has upheld an $11.1 million jury award to a woman who claims a Johnson & Johnson unit’s vaginal mesh product caused debilitating nerve pain, say... Read more
According to the complaint, Ms. Carlino had Ethicon’s transvaginal mesh device, marketed as Gynecare TVT, implanted on Aug. 18, 2005. Read more
In August 2013, an Ethicon Proximate stapler recall was announced after complaints from doctors indicated that the surgical staplers were too difficult to fire. Read more
There are currently approximately 83,000 individual transvaginal mesh (TVM) cases consolidated before Judge Joseph Goodwin in the United States District Court for the Southern District of We... Read more
Currently, litigation involving transvaginal mesh devices made by Ethicon and six other manufacturers is underway nationwide. More than 70,000 cases are currently consolidated into seven mul... Read more
Kern County Superior Court Judge Lorna H. Brumfield denied a motion for new trial filed by Johnson & Johnson’s Ethicon in Colleen Perry’s case. A $5.7 million jury verdict for the Califo... Read more
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