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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Mountain Rose Kudzu Root Herbal Supplement Recall [US]

Organic Kudzu Root Herbal Supplement Recall [US]

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US FlagUS/Silver Spring: Mountain Rose Herbs (“MRH”), a Eugene, Oregon establishment, recalls all current batch/lots and sizes of its Organic Kudzu Root Herbal Dietary Supplements due to suspected risk of Salmonella contamination and consequential risk of Gram-negative bacterial infection, severe illness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/1Kj730qr9b6

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/mountain-rose-herbs-recalls-organic-kudzu-root-herbal-supplement-due-possible-health-risk

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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