Recall: Silver Bullet Male Enhancement Nutritional Supplement
On 2019-01-29, the FDA announced that Nature's Rx is conducting a recall on Male Enhancement Nutritional Supplement due to possible undeclared sildenafil, tadalafil. The recalled products were sold under the brand name(s) Silver Bullet 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 undeclared ingredients, including amlodipine valsartan tablets usp, valsartan hctz tablets usp, valsartan tablets usp, losartan potassium tablets, usp and more. Additionally, there have been 17 drug and medical device recalls due to other health hazards as well as 77 food recalls.
Company Contact Information:
Name: Nature's Rx
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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: Male enhancement Nutritional Supplement
Brand Name(s): Silver Bullet
Reason for Recall: Undeclared Sildenafil and Tadalafil
Official Recall Date: 2019-01-29
Additional information provided by the FDA.gov:
Nature's Rx is voluntarily recalling quantity lots of Silver Bullet 10x, description of dosage form to the hospital, retail or consumer level. This recall has been initiated because the product was found to contain undeclared sildenafil and tadalafil, the active ingredient in Viagra and Cialis respectively, which are PDE-5 inhibitors. The undeclared PDE-5 inhibitors in the product may pose serious health risks because consumers with underlying medical issues may take the products without knowing that they can cause serious harm or interact in dangerous ways with other drugs they may be taking. For example, PDE-5 inhibitors may interact with nitrates found in some prescription drugs (such as nitroglycerin) and thus can lower blood pressure to dangerous levels. Consumers with diabetes, high blood pressure, or heart disease often take nitrates. 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.