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Digitek®, a Factory Built Prescription Error

08/1/2008
Product Defect
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Most of us have seen and heard news about prescription errors that have caused over 7,000 deaths, annually. However on April 25, 2008 Actavis Totowa, LLC, subsidiary of Iceland’s Actavis Group finally identified a very unusual problem. Actavis initiated a class I US Nationwide recall of its digoxin based cardiac […]

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Bayer Withheld Important Safety Information from the FDA about Trasylol® And an Estimated 1000 Lives A Month were Lost Over 22 Months Until the FDA Finally Took Action

07/29/2008
Product Defect
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Trasylol® (Aprotinin injection) is an amino acid that Bayer manufacturers, deriving it from the lung tissue of cows. In many instances doctors inject Trasylol to reduce blood loss and to lessen the need for blood transfusions during coronary artery bypass graft surgery (CABG). Over the years, Trasylol® has garnered much […]

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The Ortho Evra Label Changes:

07/14/2008
Product Defect
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Are They Timely Ortho-FDA Collaborative Warnings, Or Are They FDA Sanctioned Excuses for the Manufacturer The FDA has been in the news quite often, recently. Lately, consumers have seen news about caustic and blinding eye care solutions (Bausch & Lomb’ ReNu MoistureLoc and AMO’s Complete MoisturePlus), E. coli in spinach, […]

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