Carey & Danis Pradaxa lawyers are currently following the Pradaxa multi-district litigation (MDL) in Illinois. The Pradaxa MDL is In re: Pradaxa (Dabigatran Etexilate) Products Liability Litigation MDL no. 2385.…
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In early November, the U.S. Food and Drug Administration (FDA) released a statement about its recent research into the incidence of excessive bleeding and Pradaxa use in patients with atrial…
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Though the drug manufacturer denies Pradaxa as a defective drug, the surmounting Pradaxa bleeding deaths, injuries, and lawsuits prove otherwise. Pradaxa was introduced onto the U.S. drug market in October…
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On December 19, the U.S. Food and Drug Administration (FDA) released a safety announcement regarding the anticoagulant medicine known as Pradaxa. Pradaxa, known generically as dabigatran etexilate mesylate, is manufactured…
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Transvaginal mesh is used to treat patients with pelvic organ prolapse (POP) and stress urinary incontinence (SUI). As a national law firm representing individuals who believe their injuries (stem) from…
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In a letter from the U.S. Food and Drug Administration (FDA) dated September 19, 2012, Zimmer Holdings Inc. was issued a warning regarding their hip replacement device known as the…
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A Colorado woman's transvaginal mesh lawsuit was set to go to trial in New Jersey when C. R. Bard, the defendant in the case, decided to settle the case. Filed…
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Lawsuits involving transvaginal mesh and other surgical implants used to treat stress urinary incontinence (SUI) or pelvic organ prolapse (POP) have been consolidated into five individual Multi-District Litigation (MDL) cases…
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Transvaginal mesh lawsuits have been consolidated into five multi-district litigation (MDL) cases in the U.S. District Court for the Southern District of West Virginia. U.S. District Judge Joseph R. Goodwin…
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Endo announced a day after the U.S. Food and Administration (FDA) proposed an order to classify transvaginal mesh as a high-risk device that they had reached a settlement agreement of…
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