Iowa Select Herbs Dietary Supplement Recall [US]

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US/Silver Spring: 5849 - IowaSelectHerbsDietarySupplementsIowa Select Herbs recalls for dozens of Dietary Supplements due to the production and distribution of unapproved new drugs, misbranded drugs, misbranded dietary supplements and dietary supplements not manufactured in compliance with the current Good Manufacturing Practice regulations for Dietary Supplements, and therefore adulterated, all serious health hazards. FDA: http://ht.ly/SlHLS

Direct link: http://www.fda.gov/Safety/Recalls/ucm462536.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Dietary Supplements are subject to this recall:

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Vicerex, Black Ant Nutritional Supplement Recall [US]

FlagUSUS/Silver Spring: American Lifestyle recalls all lots of Vicerex [UPC: 893490820087] and Black Ant [UPC: 4026666142546] Nutritional Supplements due to undeclared Tadalafil and Sildenafil, both regulated drugs. FDA: http://ht.ly/kG4hg

Direct link: http://www.fda.gov/Safety/Recalls/ucm350574.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports laboratory analysis conducted by the FDA has determined the Vicerex product contains undeclared Tadalafil and the Black Ant product contains undeclared Sildenafil. Tadalafil and Sildenafil are FDA-Approved drugs used to treat male erectile dysfunction (ED), making the Vicerex and the Black Ant products unapproved new drugs.

According to the FDA, these undeclared active ingredients poses a threat to consumers because Tadalafil and Sildenafil may interact with Nitrates found in some prescription drugs such as Nitroglycerin and may lower blood pressure to dangerous levels. Consumers with Diabetes, high blood pressure, high cholesterol or heart disease often take nitrates.

Vicerex is sold in blister packs of ten (10) capsules and Black Ant is sold in a box of four (4) individually wrapped capsules; both products are promoted to increasing sexual desire and performance. The products are sold without medical prescription using on-line sales and retail channels.

Recalls Direct RIN: 2013-1936
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