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Home > Recalled Products > Drugs > Undeclared Ingredients > Euphoric Marketed As Dietary Supplement- Capsules

Recall: Euphoric Marketed As Dietary Supplement- Capsules

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On 2018-04-16, the FDA announced that Epic Products is conducting a recall on Marketed As Dietary Supplement- Capsules due to possible undeclared sildenafil, tadalafil. The recalled products were sold under the brand name(s) Euphoric during an unspecified time period throughout the regions shown in the map below.

In recent months, there have been 7 drugs recalls due to potential undeclared ingredients, including rhino 69 extreme 50000 capsules, muscle strength and nighttime recovery dietary supplements and more. Additionally, there have been 23 drug and medical device recalls due to other health hazards as well as 96 food recalls.

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Rx bottle w/ "unapproved" stamped over it
Note: Images may not be available for every version. Please review the detailed description below.

Company Contact Information:

Name: Epic Products
Phone: 1-800-589-1470

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Detailed Recall Information



Regions Where Sold: Because the region was not specified, it is assumed that this product was available nationwide.

Product Description: Marketed as dietary supplement- capsules

Brand Name(s): Euphoric

Reason for Recall: Undeclared Sildenafil and Tadalafil

Official Recall Date: 2018-04-16


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Additional information provided by the FDA.gov:

Overland Park, KS, Epic Products, LLC is voluntarily recalling all lots of Euphoric capsules, packaged in 1 count blister cards, 3 count bottles, and 12 count bottles to the consumer level. FDA analysis found samples of Euphoric to be tainted with undeclared sildenafil and tadalafil, active ingredients in two FDA-approved prescription drug products, also known as phosphodiesterase 5-inhibitors (PDE-5 inhibitors), used to treat male erectile dysfunction (ED). The presence of sildenafil and tadalafil in Euphoric renders it an unapproved drug for which safety and efficacy have not been established and, therefore subject to recall. 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.

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