Approximately 3397 cases have been consolidated into the Ethicon multi-district litigation (MDL) being heard in the U.S. District Court for the Southern District of West Virginia. The Ethicon MDL is…
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In June 2012, Johnson & Johnson made the decision to remove their defective transvaginal mesh (TVM) medical device from the global market. Though the medical device manufacturer cites future market…
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In the United Kingdom, the Department of Health and the Medicines and Healthcare Products Regulatory Agency (MHRA) have been collaborating on a safety review of transvaginal mesh. Their collaborative effort…
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Johnson & Johnson and Ethicon mishandled internal documents that were of great importance in the Ethicon multidistrict litigation (MDL) being heard in West Virginia. As a result, U.S. Magistrate Judge…
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Though the 510(k) approval process used by the U.S. Food & Drug Administration (FDA) to quickly and efficiently clear medical devices similar to already approved products has its benefits, the…
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Transvaginal mesh lawsuits have been consolidated into the Ethicon multidistrict litigation (MDL) in West Virginia. In a court document filed in early December 2013, plaintiffs' legal counsel argued that Johnson…
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The first trial of 1,800 regarding Johnson & Johnson's defective Gynecare Prolift vaginal mesh was heard in a New Jersey state court in Atlantic City last week. The trial, known…
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In the Ethicon transvaginal mesh multidistrict litigation (MDL) in the U.S. District Court for the Southern District of West Virginia deposition scheduling process is the topic of one of the…
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Published April 25, 2013 by PR Web St. Louis, Missouri (PRWEB) April 25, 2013 Pelvic mesh lawyers at Carey Danis & Lowe continue to follow Ethicon MDL 2327 proceedings currently taking place…
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In 2013, a jury verdict awarded the plaintiffs in a transvaginal mesh lawsuit being heard in a New Jersey court an $11 million compensatory package. The transvaginal mesh lawsuit involved…
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