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According to the West Virginia Record, a woman has filed a lawsuit against drug manufacturer Pfizer after she said the cholesterol drug Lipitor led to her getting Type 2 diabetes. The woman, Charlotte T. Kearnes, of
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A jury in West Virginia recently awarded a woman $3.27 million for injuries resulting from a Johnson & Johnson (Ethicon Inc) transvaginal mesh device. According to Reuters, the trial lasted for about two weeks, with jurors finding Ethicon
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According to the Cleveland Plain Dealer, the US Food and Drug Administration (FDA) announced last week that the dietary supplement OxyElite Pro, distributed by USPlabs LLC of Dallas and sold nationwide, has been recalled. The recall
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The law firm of Zoll & Kranz, LLC has filed another lawsuit on behalf of two more people alleged to be wrongly diagnosed with Alzheimer’s disease and depressive pseudodementia. Today, September 12, 2016, the Complaint
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Earlier this month, the U.S. Food and Drug Administration (FDA) announced it was beginning to investigate how hundreds of intravenous saline solution bags designed for training healthcare workers ended up being used on patients. According
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Earlier this month, a jury decided that Takeda Pharmaceutical Co. was not responsible for the bladder cancer death of an Illinois man who took its diabetes drug, Actos. According to Bloomberg News, the trial was the first
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The law firm of Zoll & Kranz, LLC filed a motion seeking to amend the original complaint on behalf of 34 new Plaintiffs alleging they were wrongly diagnosed with Alzheimer’s disease or another form of
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As we have reported several times in our blog, Pradaxa (dabigatran) has been linked to a 33 percent higher risk for fatal health problems when compared to individuals using the blood thinner Warfarin. Reported complications linked to
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Earlier this month, the Washington Post reported that nearly 80% of doctors have no idea how much a hip replacement costs. According to the Post, a survey of orthopedic surgeons showed that they knew very little about the costs
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Vascular Solutions is conducting a Class 1 nationwide recall of its Langston dual lumen catheters, due to serious reports that the inner catheter of some Langston V2 Dual Lumen Catheters have separated from the device
