New Recall on Acid Reflux Drug
A voluntary recall has been issued on three different lots of Nizatidine Capsules, made by Mylan Pharmaceuticals. The 150mg and 300mg Nizatidine capsules may have trace amounts of NDMA. NDMA, or nitrosodimethylamine is an impurity that has been linked to cancer according to the International Agency for Research on Cancer. This known carcinogen can be extremely harmful to humans, but no adverse reactions have been reported as of yet. The affected batches were distributed between June 2017 and August 2018. Click here for more information on the recalled products.
Mylan will be notifying its distributors and customers by mail and is in the process of arranging for customers to return their products. If you have one of the affected products, be sure to return it to the store you purchased it from. You’ll be able to receive a full refund from Mylan. If you have had any adverse reactions to any other issues with this product, be sure to report it to the FDA. You can do this through their MedWatch Adverse Event Reporting program online,by mail, or fax.
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At Begum Law Group Injury Lawyers, we understand how traumatic events like this can be. That’s why we are committed to helping victims recover compensation through personal injury lawsuits. If you have been injured and negligence may have caused the injury, you should promptly talk to an attorney with experience in personal injury and negligence cases. Your lawyer will know what your rights are under the law. You may be entitled to compensation. contact our firm today at (866) 523-4167 to schedule a free, initial evaluation of your case.