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eMedAlert
Recall for Vitalikor

12/13/2013

 

Re: VitaliKOR Fast Acting Recall of Lots K58Q and F50Q

 

Dear Valued Customer,

 

Vitality Research Labs, LLC (VRL), the distributor of VitaliKOR products, recently learned two lots of our VitaliKOR Fast Acting product contained the unapproved drugs Vardenafil and Tadalafil.  The undeclared active ingredients poses a threat to consumers because Vardenafil and Tadalafil may interact with nitrates found in some prescription drugs such as nitroglycerin and may lower blood pressure to unsafe levels. Consumers with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates. Additionally, the product may cause side effects, such as headaches and flushing.  A press release can be found on our website at www.vitalityresearchlabs.com/press-release

 

VRL is working with the FDA to recall and destroy the tainted batches.  As a precautionary effort, we encourage all customers to verify the lot number of their product.  Customers can find the lot information and confirm they have the effected lots K58Q and/or F50Q in one of two places; (1) printed vertically on the black label adjacent to the supplement facts table; or (2) printed directly on the bottom of the bottle.  If you have a lot affected by the recall, discontinue use immediately and contact Vitality Research Labs directly to arrange for a refund. 

 

Please contact Vitality Research Labs with any questions or concerns.  We can be contacted in a number of ways:

Email: customercare@vitalikor.com

Phone: 1-855-424-1954

Mail: 8840 W. Russell Rd. #245

 Las Vegas, NV 89148

 

We are grateful for our customers and will continue to strive to bring to market effective and safe nutritional supplements.  Please feel free to contact our office if we can be helpful in any way.