Active Male Dietary Supplement Recall [US]

Active Male Dietary Supplement Recall [US]

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US FlagUS/Silver Spring: Natural Remedy Store, a San Antonio, Texas establishment, recalls all current batch/lots of Active Male Dietary Supplement Capsules due to suspected undeclared Tadalafil, an existing FDA approved drug for certain medical conditions and legally available only under prescription from a licensed physician. The undeclared presence of this medication can pose a serious health and safety hazard for some people.

FDA: http://ht.ly/W7RA30qrMHX

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/natural-remedy-store-issues-voluntary-worldwide-recall-active-male-due-presence-undeclared-tadalafil

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

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Up2 Dietary & Bow and Arrow Supplement Recall [US]

Up2 Dietary & Bow and Arrow Supplement Recall [US]

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US FlagUS/Silver Spring: Med Man Distribution, a Sault Sainte Marie, Ontario establishment, recalls certain batch/lots of Up2 Dietary Supplement and Bow and Arrow Dietary Supplement products 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/uwGo30qkrwi

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/med-man-expands-voluntary-nationwide-recall-up2-and-bow-arrow-due-presence-undeclared-sildenafil

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

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Silver Bullet Male Enhancement Supplement Recall [US]

US FlagUS/Silver Spring: Logo - Silver BulletSpring: Nature’s Rx, a Claremont, California establishment, recalls batch/lots of Nature’s Rx Silver Bullet Male Enhancement 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/67hD30pTxfA

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/natures-rx-issues-voluntary-nationwide-recall-silver-bullet-10-male-enhancement-capsules-due

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

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Up2 All Natural Libido Dietary Supplement Recall [US]

Up2 All Natural Libido Dietary Supplement Recall [US]

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US FlagUS/Silver Spring: Med Man Distribution, a Sault Ste. Marie, Ontario establishment, recalls certain batch/lots of Up2 There Is No Other All Natural Libido for Men & Women Dietary Supplements 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/8Bao30pSpI4

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/med-man-issues-voluntary-nationwide-recall-up2-due-presence-undeclared-sildenafil

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

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Green Lumber Dietary Supplement Recall [US]

Green Lumber Dietary Supplement Recall [US]

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US FlagUS/Silver Spring: GL Holdings, a Newport Beach, California establishment, recalls numerous batch/lots of Green Lumber Dietary Supplement Capsules due to suspected undeclared Tadalafil, an existing FDA approved drug for certain medical conditions. The undeclared presence of this medication can pose a serious health and safety hazard for some people.

FDA: http://ht.ly/dBa430pLE8Y

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/gl-holdings-issues-voluntary-worldwide-recall-green-lumber-products-due-presence-undeclared

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

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Stiff Boy branded Beast Supplement Recall [US]

Stiff Boy branded Beast Supplement Recall [US]

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US FlagUS/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:

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Leopard Miracle Honey Dietary Supplement Recall [US]

Leopard Miracle Honey Dietary Supplement Recall [US]

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US FlagUS/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:

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