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Mylan today issued a statement announcing that it is taking immediate action to increase access to EpiPen® Auto-Injectors by expanding already existing programs in recognition of those patients who are facing the burden of higher out-of-pocket costs, reducing direct patient costs and increasing eligibility for patient assistance programs for uninsured and under-insured patients.
Continue reading »In an August 22, 2016, New York Times article, Tara Parker-Pope and Rachel Rabkin Peachman reported on the steep increase in the price of the EpiPen, a lifesaving injection device for people with severe allergies, and the outrage these price increases have caused with consumers and lawmakers.
Continue reading »How do we stay safe and keep our families safe when products we use are recalled for safety reasons? Safety recalls are very important for all of us. Rarely a week, or sometimes even a day, passes without news of some type of consumer product, medical product, medicine, automotive, or food recall.
Continue reading »Last week, the U.S. Food and Drug Administration (FDA) issued a Safety Communication advising that there are serious side effects associated with fluoroquinolone antibacterial drugs.
Continue reading »Essure is a permanent, implantable, birth control device for women, and was given approval back in 2002. Since that time, thousands of complaints have been submitted to the FDA. In September of 2015, the FDA held a hearing allowing stakeholders and other interested parties to testify before the September Advisory Committee. The FDA decided to take the following actions ...
Continue reading »On December 12, 2014, the United States Judicial Panel on Multidistrict issued a transfer order pertaining to Xarelto lawsuits pending throughout the country.
Continue reading »Power morcellators are used by gynecologists to perform hysterectomy and myomectomy procedures.
Continue reading »On October 7, 2014, Teleflex Medical recalled their Hudson RCI pediatric breathing circuits because the ends of the devices may crack or…
Continue reading »The law firm of Zoll, Kranz & Borgess, LLC, recently filed suit on behalf of fourteen plaintiffs against Howmedica Osteonics Corp. d/b/a Stryker Spine alleging injuries caused by the trial device, CerviCore.
Continue reading »As reported by Reuters, New York Federal Prosecutors are investigating whether GM – the nation’s largest automaker – may be criminally responsible for failing to disclose model defects prior to the recall initiated last month.
Continue reading »Free, confidential case review with a board-certified Texas trial lawyer. No fee unless we win.
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