Rhino 50K Supplement Recall [US]

US FlagUS/Silver Spring: Rhino 50K Supplement Recall [US]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:

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Super Panther Supplement Recall [US]

US FlagUS/Silver Spring: Super Panther Supplement Recall [US]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:

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XtraHRD Male Enhancement Supplement Recall [US]

US FlagUS/Silver Spring: XtraHRD Male Enhancement Supplement Recall [US]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:

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