Stiff Boy branded Beast Supplement Recall [US]

Click to enlarge image

US/Silver Spring: Stiff Boy LLC, a Westchester County, New York establishment, recalls all current batch/lots of The Beast Dietary Supplement Capsules due to suspected undeclared Sildenafil, an FDA approved drug for the treatment of Male Erectile Dysfunction in a class of drugs called Phosphodiesterase (“PDE-5”) Inhibitors and consequential risk of dangerous low blood pressure, injury and possible life-changing complications, all serious health and safety hazards.

FDA: http://ht.ly/FyMw30oHizo

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/stiff-boy-llc-issues-voluntary-nationwide-recall-beast-capsules-due-presence-undeclared-sildenafil

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

Advertisements

Leopard Miracle Honey Dietary Supplement Recall [US]

Click to expand image

US/Silver Spring: USA LESS, a Brooklyn, New York establishment, recalls certain batch/lots of Leopard Miracle Honey Dietary Supplement ptoducts due to undeclared Sildenafil. The presence of Sildenafil in the Leopard Miracle Honey Dietary Supplement products, renders it an unapproved drug for which safety and efficacy have not been established and, therefore, subject to recall.

FDA: http://ht.ly/OKBj30obFny

Direct link: https://www.fda.gov/Safety/Recalls/ucm634314.htm

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

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:

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: