March 2, 2016
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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February 24, 2016
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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January 5, 2016
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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November 5, 2015
Japanese parts manufacturer Takata faces what federal regulators are calling a historic $200 million fine for problems with its airbags installed in more than 30 million vehicles in the United States, which are prone to overinflate and explode, posing a…
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October 6, 2015
The U.S. Food and Drug Administration (FDA) has announced the recall of nearly 11,000 Profemur Varus/Valgus Modular Neck hip implant components, due to an unexpectedly high rate of hip implant fractures and failures. The FDA announced the…
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September 21, 2015
General Motors has admitted that it failed to warn the public about a deadly problem with ignition switches in millions of its vehicles, as part of a $900 million settlement agreement the car maker reached with the federal government…
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July 24, 2015
A new Zofran injury lawsuit has been brought against GlaxoSmithKline, alleging that side effects of Zofran, the company’s blockbuster anti-nausea medication, caused a baby boy to be born with a serious congenital birth defect called Tetralogy of Fallot. If you…
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