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Category: News

Roundup Cancer Litigation Update

April 9, 2018

MDL Judge Weighing Expert Testimony on Potential Link Between Roundup Weedkiller and Cancer

As product liability claims involving Roundup weed killer and non-Hodgkin’s lymphoma continue to be investigated by attorneys across the country, the federal judge presiding over all federal Roundup lawsuits will consider expert testimony presented by both sides…

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$55 Million Talc Powder Verdict

May 3, 2016

J&J Ordered to Pay $55 Million in Talcum Powder Cancer Lawsuit

In the second major talcum powder trial loss for Johnson & Johnson this year, the pharmaceutical company was ordered by a St. Louis jury earlier this week to pay $55 million to a 62-year-old South Dakota woman who blamed…

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Pinnacle Hip Implant Award

March 18, 2016

$498 Million Verdict Delivered in Second Pinnacle Hip Implant Bellwether Trial

Johnson & Johnson has been hit with a $498 million verdict in the second bellwether trial in the multidistrict litigation involving allegedly defective Pinnacle hip implants manufactured by the company’s DePuy Orthopaedics subsidiary. The product liability lawsuit was made…

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Essure Black Box Warning

March 2, 2016

FDA Requires New Black Box Warning on Essure Contraceptive Label

After more than 5,000 women have filed adverse event reports with the U.S. Food and Drug Administration (FDA) alleging devastating complications from Essure, the FDA is finally requiring a new “black box” warning for the permanent contraceptive device to “call…

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Multi-Million Dollar Award for Talcum Powder Cancer Death

February 24, 2016

$72 Million Awarded to Family of Alabama Woman Over Ovarian Cancer Death Allegedly Caused by Talc Powder

Johnson & Johnson has been ordered to pay the family of an Alabama woman $72 million in damages in a product liability lawsuit alleging that the pharmaceutical giant’s talcum powder products caused her…

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Vaginal Mesh a High-Risk Device

January 5, 2016

FDA Issues High-Risk Warning for Transvaginal Mesh Devices

The U.S. Food and Drug Administration (FDA) has finally responded to calls for stronger warnings on the use of transvaginal mesh, reclassifying mesh devices marketed for the transvaginal repair of pelvic organ prolapse (POP) as class III high-risk devices. According to its…

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