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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