Recall: VitaliKOR Dietary Supplement for Sexual Enhancement
On 2013-11-14, the FDA announced that Vitality Research Labs is conducting a recall on Dietary Supplement for Sexual Enhancement due to a possible lack of fda approval. The recalled products were sold under the brand name(s) VitaliKOR during an unspecified time period throughout the regions shown in the map below.
In recent months, there have been 3 drugs recalls due to potential lack of fda approval, including dietary supplement for erectile dysfunction, dietary supplement for sexual enhancement and more. Additionally, there have been 26 drug and medical device recalls due to other health hazards as well as 94 food recalls.
Company Contact Information:
Name: Vitality Research Labs
Phone: (855) 424-1954
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Detailed Recall Information
Regions Where Sold: Nationwide
Product Description: Dietary Supplement
Brand Name(s): VitaliKOR
Reason for Recall: Unapproved new drug
Official Recall Date: 2013-11-13
Note: Although this recall announcement is dated 11/13/2013, it was not published by the FDA until 11/14/2013.
Additional information provided by the FDA.gov:
November 13, 2013 – Vitality Research Labs, LLC, the repackager of the VitaliKOR Products, is voluntarily recalling lots K58Q and F50Q of VitaliKOR Fast Acting to the consumer level. FDA laboratory analysis on VitaliKOR has determined that this product contains undeclared Vardenafil and Tadalafil. Vardenafil and Tadalafil are active ingredients of FDA-approved drugs used to treat erectile dysfunction (ED), making VitaliKOR Fast Acting an unapproved drug. Read More.
More information may be available at FDA.gov
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Sources may include Food & Drug Administration (FDA), United States Department of Agriculture (USDA), Health Canada and companies involved with this or a related recall.