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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Fuel Up Dietary Supplement Recall [US]

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US/Silver Spring: 6196 - FuelUpDietarySupplementReesna Inc. recalls certain Fuel Up Dietary Supplements due to undeclared Hydroxythiohomosildenafil, an analogue of Sildenafil a controlled substance. FDA: http://ht.ly/VNZPi

Direct link: http://www.fda.gov/Safety/Recalls/ucm476978.htm

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

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Detox Transforms Dietary Supplement Recall [US]

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US/Silver Spring: Detox Transforms Dietary Supplement Recall [US]Detox Transforms Health and Nutrition recalls various Dietary Supplements due to possible undeclared drug ingredients, a serious health and safety hazard. FDA: http://ht.ly/IQ2AT

Direct link: http://www.fda.gov/Safety/Recalls/ucm433513.htm

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

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Virilis Pro, PHUK, Prolifta Nutritional Supplement Recall [US]

US FDA RecallUS/Silver Spring: FDA Logo BlueHaute Health, LLC recalls all lots of Virilis Pro, PHUK and Prolifta Nutritional Supplements due to unapproved drug hazard. FDA: http://ht.ly/poWw4

Direct link: http://www.fda.gov/Safety/Recalls/ucm370506.htm

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

  • Virilis Pro is packaged in one (1) and two (2) capsule blister packs and 10 capsule bottles;
  • PHUK is packaged in one (1) and two (2) capsule blister packs and 4, 12, 24 capsule bottles and
  • Prolifta is packaged in one (1) and two (2) capsule blister packs and 4, 12, and 24 capsule bottles.

All three products were distributed nationwide to wholesale and retail customers and via the Web.

According to the FDA, Virilis Pro, PHUK and Prolifta have been found to contain amounts of the PDE-5 Inhibitor Sildenafil, which is an active ingredient in an FDA-approved drug for erectile dysfunction (ED). Sildenafil has the potential to interact with nitrates found in some prescription drugs such as nitroglycerin and may lower blood pressure to unsafe levels. The presence of the active, yet undeclared, ingredient Sildenafil makes these Nutritional Supplements unapproved drugs.

Consumers with Diabetes, high blood pressure, high cholesterol and/or heart disease often take nitrates. Additionally, Sildenafil may cause side effects, such as headaches and flushing. To date, there have been no reported adverse events associated with the presence of Sildenafil in Virilis Pro, PHUK or Prolifta.

Want to read more about this recall? Please click on the links above to visit the originating site.

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Additional information about this recall:

Recalls Direct RIN: 2013-2567
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Visit the Living Safely site: http://www.LivingSafely.org
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72HP, Evil Root, Pro Power Max Supplement Recall [US]

US FDA RecallUS/Silver Spring: Pro Power Max Supplement Recall [US]Hardmenstore.com recalls all lots of 72HP, Evil Root and Pro Power Max Nutritional Supplements due to undeclared drug hazard. FDA: http://ht.ly/ovTuG

Direct link: http://www.fda.gov/Safety/Recalls/ucm366506.htm

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

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Vicerex, Black Ant Nutritional Supplement Recall [US]

FlagUSUS/Silver Spring: American Lifestyle recalls all lots of Vicerex [UPC: 893490820087] and Black Ant [UPC: 4026666142546] Nutritional Supplements due to undeclared Tadalafil and Sildenafil, both regulated drugs. FDA: http://ht.ly/kG4hg

Direct link: http://www.fda.gov/Safety/Recalls/ucm350574.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports laboratory analysis conducted by the FDA has determined the Vicerex product contains undeclared Tadalafil and the Black Ant product contains undeclared Sildenafil. Tadalafil and Sildenafil are FDA-Approved drugs used to treat male erectile dysfunction (ED), making the Vicerex and the Black Ant products unapproved new drugs.

According to the FDA, these undeclared active ingredients poses a threat to consumers because Tadalafil and Sildenafil may interact with Nitrates found in some prescription drugs such as Nitroglycerin and may lower blood pressure to dangerous levels. Consumers with Diabetes, high blood pressure, high cholesterol or heart disease often take nitrates.

Vicerex is sold in blister packs of ten (10) capsules and Black Ant is sold in a box of four (4) individually wrapped capsules; both products are promoted to increasing sexual desire and performance. The products are sold without medical prescription using on-line sales and retail channels.

Recalls Direct RIN: 2013-1936
About the RecallsDirect service: http://wp.me/P2bVty-2
Visit the Living Safely site: http://www.livingsafely.org/
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Rock-It Man Male Enhancement Supplement Recall [US]

US FDA RecallUS/Silver Spring: Consumer Concepts recalls some Rock-It Man Male Enhancement Capsules due to undeclared prescription drug analogue. FDA: http://ht.ly/jUwnr

Direct link: http://www.fda.gov/Safety/Recalls/ucm347026.htm

Additional information:1842 - Rock-ItManSupplement
The US Food and Drug Administration (“FDA”) reports Rock-It Man Male Enhancement Capsules sold between October 2012 and April 2013 were tested and found to contain an analogue of an ingredient in an FDA-approved drug. Further tests conducted by the FDA concluded the recalled Supplements contained hydroxythiohomosildenafil.

The chemical Hydroxythiohomosildenafil is an analogue of sildenafil and is close in structure to sildenafil and is consequently, expected to possess a similar pharmacological and adverse event profile. Sildenafil is the active pharmaceutical ingredient in an FDA approved drug that is used to treat Erectile Dysfunction (“ED”) making the recalled Rock-It Man Male Enhancement an unapproved new drug.

According to the FDA, the undeclared active ingredient poses a threat to consumers because hydroxythiohomosildenafil may interact with nitrates found in some prescription drugs (such as nitroglycerin) and lower blood pressure to dangerous levels. Consumers with diabetes, high blood pressure, high cholesterol or heart disease often take nitrates as part of their treatment plan under the supervision of a medical doctor. Additionally, hydroxythiohomosildenafil, like sildenafil, may cause side effects, such as headaches and flushing.

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Recalls Direct RIN: 2013-1842
About the Recalls Direct service: http://wp.me/P2bVty-2
Visit the Living Safely site: http://www.LivingSafely.org/
E. & O. E.

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