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News & Perspective

February 29, 2016

Lawmakers Looking for Ways to Step in Against FDA’s Ineffective Monitoring of Dangerous Drugs and Medical Devices

Originally developed to protect consumers, the U.S. Food and Drug Administration is responsible for monitoring and investigating the safety, efficacy, and security of drugs and medical equipment used and prescribed in the United States. But patient advocates, federal auditors, and...

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December 17, 2015

FDA Orders Recall of Ultrasonic Medical Scope Cleaning Machines Due to Risk of Infection

Doctors and surgeons rely heavily on medical devices to ensure patient safety. Unfortunately, there is an alarming number of defective medical devices out there. When physicians learn the truth, they are often disturbed and upset, but it is the patients...

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March 12, 2015

FDA Refuses to Pull Endoscopy Devices Linked to CRE Superbug

In the last several months, two hospitals in California have reported outbreaks of what officials are referring to as the CRE superbug. At Ronald Reagan UCLA Medical Center in Los Angeles, two patients died after being infected and five others...

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December 8, 2014

Use of Laparoscopic Power Morcellators Puts Hundreds of Thousands of Women at Risk

A hysterectomy ranks second behind a cesarean section (“C-section”) as the most frequently performed medical procedure women undergo. In fact, the National Women’s Health Network lists statistics reporting an estimated 600,000 hysterectomies performed every year. It is common for laparoscopic...

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