On May 11, 2020, the FDA published a company announcement on behalf of MasterPharm, LLC., informing consumers of a voluntary nationwide recall of one lot of 1.25mg capsules of Finasteride Plus. Finasteride prescribed at this dosage is generally used to treat hair loss. The recall was initiated due to the presence of undeclared minoxidil, a medication used to treat high blood pressure, at levels higher than in FDA approved products. Ingestion of undeclared minoxidil could result in low blood pressure, a rapid heartbeat, and swelling, and could subsequently increase the risk of developing heart failure or other heart damage. The manufacturer has received 33 reports of adverse events and has arranged for the return and replacement of all recalled products. Consumers are advised to contact their health care providers if they are experiencing issues that could be related to taking this product.