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…
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…
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…