Rhino 5k Dietary Supplement Recall [US]

US/Silver Spring: Happy Together, Inc. a Boynton Beach, Florida, establishment, recalls all current batch/lots of Rhino 5k Dietary Supplement Capsules due to suspected Sildenafil and Tadalafil contamination, all serious health and safety hazards.

FDA: http://ht.ly/JBPm30nfyPo

Direct link: https://www.fda.gov/Safety/Recalls/ucm629353.htm

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

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Rhino 50K Supplement Recall [US]

US/Silver Spring: AMA Wholesale Inc., a Woodland Hills, California establishment, recalls certain batch/lots of Rhino 69 Extreme 50000 Dietary Supplement Capsules due to suspected presence of Tadalafil, a controlled substance available only under prescription, rendering this Supplement an unapproved drug due to the possibility of fatal cardiovascular events, all serious health hazards. FDA: http://ht.ly/gfKG30jyV2G

Direct link: https://www.fda.gov/Safety/Recalls/ucm604633.htm

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

AMPT Coffee Recall [US]

US/Silver Spring: The AMPT Life, LLC recalls all batch/lots of AMPT Coffee due to suspected presence of Sildenafil and Tadalafil, active ingredients in two FDA-approved prescription drugs as well as undeclared Milk, a known allergen, source of dietary intolerance and possible trigger of Anaphylaxis, a serious and potential fatal situation, requiring immediate medical intervention. FDA: http://ht.ly/SFrx30ebqMl

Direct link: https://www.fda.gov/Safety/Recalls/ucm569558.htm

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

Super Panther Supplement Recall [US]

US/Silver Spring: Ultra Shop Supplement recalls certain batch/lots of Super Panther 7K Supplements due to suspected presence of undeclared Sildenafil and undeclared Tadalafil, both active ingredients in two FDA-approved prescription drug products, also known as phosphodiesterate 5-inhibitors (PDE-5), rendering the Supplement an unapproved drug due to the possibility of fatal cardiovascular events, all serious health hazards. FDA: http://ht.ly/KyVx30dQjQy

Direct link: https://www.fda.gov/Safety/Recalls/ucm568031.htm

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

Caverflo Natural Herbal Coffee Recall [US]

US/Silver Spring: Caverflo.com recalls all batch/lots of Caverflo branded Natural Herbal Coffee due to suspected presence of Sildenafil and Tadalafil, active ingredients in two FDA-approved prescription drugs as well as undeclared Milk, a known allergen, source of dietary intolerance and possible trigger of Anaphylaxis, a serious and potential fatal situation, requiring immediate medical intervention. The company has received a report of one (1) death linked to drinking this Coffee product. FDA: http://ht.ly/zhKU30cemKo

Direct link: https://www.fda.gov/Safety/Recalls/ucm560680.htm

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

Organic Herbal Nutritional Supplement Recall [US]

US/Silver Spring: Organic Herbal Supply, Inc. recalls certain batch/lots of Uproar, Cummor, Zrect, Monkey Business, Xrect, Rectalis, Tornado, Zdaily, BigNHard, Enhancerol Natural Male Enhancement Supplement capsules due to suspected undeclared  Tadalafil, a FDA-approved drug used as treatment for male Erectile Dysfunction (“ED”). FDA: http://ht.ly/BcXS30b681F

Direct link: https://www.fda.gov/Safety/Recalls/ucm553631.htm

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

XtraHRD Male Enhancement Supplement Recall [US]

US/Silver Spring: Organic Herbal Supply, Inc. recalls certain batch/lots of XtraHRD Natural Male Enhancement Supplements due to suspected undeclared Tadalafil, an FDA-approved drug used as treatment for male Erectile Dysfunction and consequential risk of drug interaction and adverse medical events including sudden hypotensive (i.e., low blood pressure) conditions, all serious health and safety hazards. FDA: http://ht.ly/NMHj309kFVk

Direct link: https://www.fda.gov/Safety/Recalls/ucm542499.htm

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