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Medtronic Recalls Guidewires Because of Serious Risks to Patients

Related Links: 5 Things You Need to Know About the Medtronic Guidewire Recall What is an FDA Class I recall and why was it issued for some Medtronic guidewires? In October 2013, Medtronic Inc. allegedly began notifying its distributors, and the hospitals that use its…

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Consumer Alert FDA to Remove Unapproved Medicine from Market

March 14, 2011 – A report from the U.S. Food and Drug Administration (FDA) announces that it will soon remove a number of unapproved medicines from the market.  According to the FDA consumer update, certain drugs have not been approved, including those designed to relieve…

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MDL petition for Shoulder Pain Pump lawsuits

Shoulder pain pump lawsuits have been filed throughout the United States concerning individuals who have developed a condition known as post-arthroscopic glenohumeral chondrolysis of PAGCL. Gray and White Law has filed a petition with the Joint Panel on Multidistrict Litigation (JPML) to consolidate all cases…

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