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According to LifeSiteNews.com, a former Olympic hopeful who sustained multiple blood clots and was forced out of the 2014 winter games is speaking out over the contraceptive NuvaRing. The site reported that Megan Henry, a
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According to the Madison-St. Clair Record, four men have filed $2 million lawsuits against Takeda Pharmaceuticals after they allegedly developed bladder cancer by taking Actos to treat Type 2 diabetes. The Record reported that the plaintiffs, John McLane, David Steele,
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On Friday April 11, the law firm of Zoll, Kranz & Borgess, LLC filed a lawsuit on behalf of a group of fourteen plaintiffs against Howmedica Osteonics Corp. (which does business as Stryker Spine) alleging
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According to Nephrologynews.com, the U.S. Food and Drug Administration (FDA) said last week that it has received one report of death that may be related to the use of recalled lots of Fresenius North America’s NaturaLyte liquid
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Fungal Meningitis victims are to receive $100 million upon judge approval. According to the NECC Plaintiffs Steering Committee, there were 64 deaths and over 750 injured victims in about 20 states, all involving the fungal
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Have you suffered injuries due to Benicar use? Multiple cases have been filed, including several in Ohio and New Jersey, and they all allege patients were harmed after taking the drug Benicar. On December 18,
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According to the Chicago Tribune, Baxter Healthcare Corp is recalling multiple models of infusion pumps used to deliver medicine, blood and other fluids after it received over 3,500 reports of the product malfunctioning. The U.S. Food and
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According to the Chicago Tribune, Baxter Healthcare Corp is recalling multiple models of infusion pumps used to deliver medicine, blood and other fluids after it received over 3,500 reports of the product malfunctioning. The U.S. Food and
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The Baxter Vascular Patch for peripheral vascular reconstruction is involved in a product recall. A FDA Class I recall is “a situation in which there is a reasonable probability that the use of or exposure
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A recent worldwide recall was voluntarily executed by the Baxter International Inc. for their Dextrose and Sodium Chloride injection. Particulate matter was found in one lot of 5% Dextrose injection, USP and four lots of
