Recalls & Warnings
ConsumerLab.com is keeping you informed with current product recalls and warnings.
Posted March 13, 2013
Recall: Male Sexual Enhancement Supplement Containing Drugs
Sildenafil is the active ingredient in an FDA approved prescription drug for the treatment of erectile dysfunction. This drug can cause symptoms like headache and flushing, and can interact with medications containing nitrates such as nitroglycerin, resulting in dangerously low blood pressure.
The recalled lot of Night Bullet is marked with the UPC 018505122233 and an expiration date of 10/2015. The product was sold nationwide between October 2012 and March 2013 to wholesalers and distributed as samples at some trade shows.
Consumers who have purchased this supplement should discontinue use and contact their healthcare provider if they have experienced any adverse side effects. Consumers and healthcare providers are also encouraged to report any adverse reactions to the FDA's MedWatch Adverse Event Reporting Program.
See ConsumerLab.com's Review of Sexual Enhancer Supplements for tests of related products.
See Related Warnings:
For more information about this recall, use the link below.