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Home > Recalled Products > Food > Unintended Use > Uproar, Cummor, Zrect, Monkey Business and others Dietary Supplement

Recall: Uproar, Cummor, Zrect, Monkey Business and others Dietary Supplement

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On 2017-04-18, the FDA announced that Organic Herbal Supply is conducting a recall on Dietary Supplement due to a possible . The recalled products were sold under the brand name(s) Uproar, Cummor, Zrect and Monkey Business and others during an unspecified time period throughout the regions shown in the map below.

In recent months, there have been 1 food recalls due to potential unintended use. Additionally, there have been 114 food recalls due to other health hazards as well as 17 drug and medical device recalls.

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FDA Recall
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Company Contact Information:

Name: Organic Herbal Supply

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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: Dietary Supplement

Brand Name(s): Uproar, Cummor, Zrect, Monkey Business and others

Reason for Recall: Unapproved new drug

Official Recall Date: 2017-04-18


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Additional information provided by the FDA.gov:

Organic Herbal Supply, Inc. announced today that it is conducting a voluntary nationwide recall of all lots of Uproar, Cummor, Zrect, Monkey Business, Xrect, Rectalis, Tornado, Zdaily, BigNHard, Enhancerol Natural Male Enhancement capsules. FDA analysis has found the products to contain Tadalafil. Tadalafil is a FDA-approved drug used as treatment for male Erectile Dysfunction (ED), the presence of tadalafil in these male enhancement products renders it an unapproved drug for which safety and efficacy have not been established and, therefore, subject to recall. Organic Herbal Supply is also recalling Zrect for Women and LabidaMAX. FDA analysis has found these two products contain Flibanserin, an FDA-approved prescription drug for Hypoactive Sexual Desire Disorder (HSDD) in women. There have been no reports of illness to date. 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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