Poseidon Platinum 3500 Supplement Recall [US]

Poseidon Platinum 3500 Supplement Recall [US]

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US FlagUS/Silver Spring: Yamtun7, a Delray Beach, Florida establishment, recalls all current batch/lots of Poseidon Platinum 3500 Supplements from the American marketplace due to reported undeclared Sildenafil and Tadalafil, two FDA approved drugs for the treatment of Male Erectile Dysfunction (“ED”), Benign Prostatic Hyperplasia (“BPH”) and certain other medical conditions and in a class of drugs called Phosphodiesterase (“PDE-5”) Inhibitors with consequential risks of dangerous low blood pressure, injury and possible life-changing complications, all serious health and safety hazards.

FDA: http://ht.ly/UArS30rHNC5

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/yamtun7-issues-voluntary-nationwide-recall-poseidon-platinum-3500-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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Premium OrgaZen & Ginseng Power Supplement Recall [US]

Premium OrgaZen 7000 and Ginseng Power 5000 Supplements Recall [US]

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US FlagUS/Silver Spring: NS NY Distributor Inc. recalls all current batch/lots of Premium OrgaZen 7000 and Ginseng Power 5000 Dietary Supplements from the American marketplace due to reported undeclared Sildenafil and Tadalafil, two FDA approved drugs for the treatment of Male Erectile Dysfunction (“ED”), Benign Prostatic Hyperplasia (“BPH”) and certain other medical conditions and in a class of drugs called Phosphodiesterase (“PDE-5”) Inhibitors with consequential risks of dangerous low blood pressure, injury and possible life-changing complications, all serious health and safety hazards.

FDA: http://ht.ly/tLLD30rEos8

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ns-ny-distributor-inc-issues-voluntary-nationwide-recall-premium-orgazen-7000-and-ginseng-power-5000

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

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Nuri Shogun-X 7000, 69MODE & Thumbs Up 7 Supplements

Nuri Shogun-X 7000, 69MODE Blue 69, Thumbs Up 7 Supplements [US]

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US FlagUS/Silver Spring: Nuri Trading, a Newton, New Jersey, establishment, recalls all current batch/lots of Shogun-X 7000 Supplement Capsules, 69MODE Blue 69 Supplement Capsules, Thumbs Up 7 (Black) 25K Supplement Capsules and Thumbs Up 7 (White) 11K Supplement Capsules from the American marketplace due to reported undeclared Sildenafil, Tadalafil and Vardenafil, three (3) FDA approved drugs for the treatment of Male Erectile Dysfunction (“ED”), Benign Prostatic Hyperplasia (“BPH”) and certain other medical conditions and in a class of drugs called Phosphodiesterase (“PDE-5”) Inhibitors with consequential risks of dangerous low blood pressure, injury and possible life-changing complications, all serious health and safety hazards.

FDA: http://ht.ly/4jiJ30rDJ1l

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/nuri-trading-llc-issues-voluntary-nationwide-recall-shogun-x-7000-thumbs-7-black-25k-thumbs-7-white

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

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Ummzy Krazy Night, Shogun-X & Thumbs Up Recall [US]

Ummzy Thumbs Up, Shogun-X & Krazy Night Recall [US]

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US FlagUS/Silver Spring: Ummzy LLC, a Palisades Park, New Jersey establishment, recalls all current batch/lots of Krazy Night Dietary Supplement Capsules, Shogun-X 15000 mg Dietary Supplement Capsules and Thumbs Up 7 Red 70K Dietary Supplement Capsules from the American marketplace due to reported undeclared Sildenafil, Tadalafil and Vardenafil, three (3) FDA approved drugs for the treatment of Male Erectile Dysfunction (“ED”), Benign Prostatic Hyperplasia (“BPH”) and certain other medical conditions and in a class of drugs called Phosphodiesterase (“PDE-5”) Inhibitors with consequential risks of dangerous low blood pressure, injury and possible life-changing complications, all serious health and safety hazards.

FDA: http://ht.ly/TkLw30rDCMy

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ummzy-llc-issues-voluntary-nationwide-recall-thumbs-7-red-70k-shogun-x-15000mg-and-krazy-night-due

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

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Bit & Bet Thumbs Up 7 Blue 69K Supplement Recall [US]

Bit & Bet Thumbs Up 7 Blue 69K Supplement Capsules

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US FlagUS/Silver Spring: Bit & Bet LLC, a Manassas, Virginia establishment, recalls all batch/lots of Bit & Bet Thumbs Up 7 Blue 69K Supplement Capsules from the American marketplace due to reported undeclared Sildenafil and Tadalafil, two FDA approved drugs for the treatment of Male Erectile Dysfunction (“ED”), Benign Prostatic Hyperplasia (“BPH”) and certain other medical conditions and in a class of drugs called Phosphodiesterase (“PDE-5”) Inhibitors with consequential risks of dangerous low blood pressure, injury and possible life-changing complications, all serious health and safety hazards.

FDA: http://ht.ly/GcCM30rDtk4

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bit-bet-llc-issues-voluntary-nationwide-recall-thumbs-7-blue-69k-due-presence-undeclared-sildenafil

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

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Antoto-K Thumbs Up 7 Red 70K Supplement Recall [US]

Antoto-K Thumbs Up 7 Red 70K Supplement Recall [US]

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US FlagUS/Silver Spring: Antoto-K, a Manassas, Virginia establishment, recalls all batch/lots of Thumbs Up 7 Red 70K Capsules from the American marketplace due to suspected undeclared Sildenafil and Tadalafil, two FDA approved drugs for the treatment of Male Erectile Dysfunction (“ED”), Benign Prostatic Hyperplasia (“BPH”) and certain other medical conditions and in a class of drugs called Phosphodiesterase (“PDE-5”) Inhibitors with consequential risks of dangerous low blood pressure, injury and possible life-changing complications, all serious health and safety hazards.

FDA: http://ht.ly/S1MB30rDgNO

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/antoto-k-issues-voluntary-nationwide-recall-thumbs-7-red-70k-due-presence-undeclared-sildenafil-and

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

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Adam’s Secret Extra Strength Capsule Recall [US]

Adam's Secret Extra Strength Capsule Recall [US]

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US FlagUS/Silver Spring: Adamssecret.co, a Fairview, New Jersey establishment, recalls all batch/lots of Adam’s Secret branded Extra Strength 1500 and 3000 Capsules  from the American marketplace due to suspected undeclared Sildenafil and Tadalafil, two FDA approved drugs for the treatment of Male Erectile Dysfunction (“ED”), Benign Prostatic Hyperplasia (“BPH”) and certain other medical conditions and in a class of drugs called Phosphodiesterase (“PDE-5”) Inhibitors with consequential risks of dangerous low blood pressure, injury and possible life-changing complications, all serious health and safety hazards.

FDA: http://ht.ly/cUYB30ryp01

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/adamssecretco-issues-voluntary-nationwide-recall-adams-secret-extra-strength-1500-and-3000-capsules

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

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Man of Steel brand Supplement Recall [US]

US FlagUS/Silver Spring: Man of Steel brand Supplement Recall [US]Man of Steel recalls certain batch/lots of Man of Steel 1 and Man of Steel 2 Supplements due to suspected presence of Sildenafil, an active ingredient in FDA-approved prescription drug products, also known as phosphodiesterate 5-inhibitors (PDE-5), rendering the Supplements unapproved Drugs due to the possibility of serious complications and fatal cardiovascular events, all serious health hazards. FDA: http://ht.ly/j6jW30e3ymH

Direct link: https://www.fda.gov/Safety/Recalls/ucm569173.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Dietary 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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Maxagra Dietary Supplement Recall [Australia]

Australia ACCC RecallAustralia/Canberra: 6752 - MaxagraDietarySupplementsCleanicall recalls all current batch/lots of Maxagra Capsule Dietary Supplements due to undeclared Sildenafil and oxytetracycline, both available by prescription only in Australia due to possible dangerous side effects and/or potential for antibiotic resistance. ACCC: http://ht.ly/101qcz

Direct link: http://www.recalls.gov.au/content/index.phtml/itemId/1083657

Additional information:
The Australian Competition & Consumer Commission (“ACCC”) reports the following Dietary Supplements are subject to this recall:

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R Thomas Marketing Dietary Supplement Recall [US]

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US/Silver Spring: FDA Logo BlueR Thomas Marketing LLC in conjunction with Just Enhance LLC recalls various Dietary Supplements due to undeclared Sildenafil, a prescription drug, this making these Supplements untested and unapproved new drugs, a serious health hazard. FDA: http://ht.ly/WRRE4

Direct link: http://www.fda.gov/Safety/Recalls/ucm481054.htm

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

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APEXXX & OPAL Dietary Supplement Recall [US]

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US/Silver Spring: FDA Logo BlueNuway Distributors LLC recalls APEXXX Dietary Supplements due to undeclared Sildenafil, a PDE-5 Inhibitor, the active ingredient in an FDA-approved drug for Erectile Dysfunction (“ED”) making this product an unapproved drug and serious health hazard. FDA: http://ht.ly/WkG9S

Direct link: http://www.fda.gov/Safety/Recalls/ucm478919.htm

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

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