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The FDA Had No Authority to Regulate the Pharmacy that Produced the Contaminated Steroids

| Oct 15, 2012 | Firm News

Many now know of the dangerous outbreak of fungal meningitis from contaminated steroid injections produced by the New England Compounding Center (NECC) and are asking why this happened.  The answer is not so simple.

As a compounding pharmacy, NECC mixes drugs at their location to provide specially ordered combinations of drugs.  Compounding pharmacies also can make a pill into a liquid or add flavoring to drugs for use by children.   But the drugs mixed at these facilities are not approved by the FDA and do not undergo pre-market review and the FDA is also unauthorized to monitor the volumes sold by these facilities.

A law passed by Congress in 1997 had given the FDA more power to regulate compounding pharmacies, but part of the law also limited their ability to advertise.  That limitations was struck down by the Supreme Court as a violation of their freedom of speech, so now the law is in limbo including the provisions about regulation.

Read more here: We Didn’t Have The Power to Stop Fungal Meningitis

Contact Our Experienced National Drug Recall Lawyers Today

At the Brandi Law Firm, we help people throughout the country who have been harmed because of a defective drug or medical device.  Instead of treating all victims of defective drugs and medical devices the same by throwing everyone into one class action lawsuit, we take a different, more personalized approach.  We use our team of experienced defective drug attorneys to a build solid case for each client harmed by a specific defective drug or medical device.

If you believe you have a potential claim, take action today by contacting us and scheduling a free consultation with our experienced defective steroid injection attorneys today.  Our goal is to provide you with information about your legal options and to help you pursue compensation and holding these drug companies responsible for their dangerous actions.