Dangerous Drugs and Medical Devices

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...

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...

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....