Labrada Lean Pro 8 branded Protein Supplement Recall [US]

US FlagUS/Silver Spring: Labrada Leanpro8 branded Whey Protein Powder Recall [US]Labrada Nutrition of Houston, Texas, establishment, recalls certain batch/lots of numerous Lean Pro 8 branded Whey Protein Powder Supplements due to undeclared Egg, 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/blqc30jFYkO

Direct link: https://www.fda.gov/Safety/Recalls/ucm605564.htm

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

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Rhino 50K Supplement Recall [US]

US FlagUS/Silver Spring: Rhino 50K Supplement Recall [US]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:

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Bella branded Diet Capsule Recall [US]

US FlagUS/Silver Spring: Bella branded Diet Capsule Recall [US]Bella all Natural, a Los Angeles, California establishment, recalls certain batch/lots of Bella branded Diet Capsules due to suspected presence of N-Desmethyl Sibutramine, an active metabolite of Sibutramine, a controlled substance under FDA regulation that was marketed as an appetite suppressant but withdrawn from the US market in 2010 due to suspected increased risks of Cardiovascular Events and Stroke, all serious health and safety hazards. FDA: http://ht.ly/lVq130iG43F

Direct link: https://www.fda.gov/Safety/Recalls/ucm598087.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following over-the-counter (“OTC”) drugs are subject to this recall:

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Vegetable Vigra Nutritional Supplement Recall [US]

US FlagUS/Silver Spring: Vegetable Vigra brand Nutritional Supplement Recall [US]Natures Supplement, Inc. recalls an estimated 260 bottles of Vegetable Vigra brand Nutritional Supplements due to suspected undeclared Sildenafil an FDA approved drug for the treatment of Erectile Dysfunction, all serious health and safety hazards. FDA: http://ht.ly/N6YG30fnc98

Direct link: https://www.fda.gov/Safety/Recalls/ucm576834.htm

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

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Fluffy Unicorn Supplement Recall [Canada]

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Canada/Ottawa: Fluffy Unicorn Supplement Recall [Canada]Health Canada recalls all batch/lots of Fluffy Unicorn Workout Supplements due suspected undeclared Synephrine and higher levels of Caffeine than declared on the label and consequential health hazards. HCSC: http://ht.ly/VtEu30ekMSk

Direct link: http://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2017/64192r-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports the following Supplements are subject to this recall:

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AMPT Coffee Recall [US]

US FlagUS/Silver Spring: US Food and Drug AdministrationThe 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:

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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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LaBri’s Atomic & Xplode Supplement Recall [US]

US FlagUS/Silver Spring: LaBri's Body Health brand Atomic and Xplode Dietary SupplementsEZ Weight Loss TX LLC recalls all current batch/lots of LaBri’s Body Health brand Atomic and Xplode Dietary Supplements due to the suspected presence of Sibutramine, an appetite suppressant that was withdrawn from the US market in October 2010 for safety reasons. Due to the suspected inclusion of Sibutramine, both of the above Supplements are classed by the US Food and Drug Administration as new drugs for which safety and efficacy have not been established and, therefore subject to recall due to serious health and safety hazards. FDA: http://ht.ly/dfZx30dU5ww

Direct link: https://www.fda.gov/Safety/Recalls/ucm568364.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following 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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New Kopi Jantan Natural Herb Coffee Recall [US]

US FlagUS/Silver Spring: New Kopi Jantan Natural Herb Coffee Recall [US]Bestherbs Coffee LLC recalls certain batch/lots of New Kopi Jantan Tradisional Natural Herbs Coffee due to suspected presence of an undeclared active pharmaceutical ingredient, specifically Desmethyl carbodenafil, 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/BD6J30dNbXV

Direct link: https://www.fda.gov/Safety/Recalls/ucm567266.htm

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

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M1 Alpha & Sten Z Supplement Recall [US]

US FlagUS/Silver Spring: Andropharm M1 Alpha & Sten Z Supplement Recall [US]Andropharm recalls certain batch/lots of M1 Alpha and Sten Z Supplements due to suspected presence of Anabolic Steroids and consequential risk of a wide range of life-affecting injuries and/or conditions, all serious health hazards. FDA: http://ht.ly/mj1b30dyBbI

Direct link: https://www.fda.gov/Safety/Recalls/ucm566553.htm

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

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Ultra-Sten and D-Zine Supplement Recall [US]

US FlagUS/Silver Spring: Ultra-Sten and D-Zine Supplement Recall [US]Hardcore Formulations recalls all current batch/lots of Ultra-Sten and D-Zine Dietary Supplements due to suspected presence of Anabolic Steroids and consequential risk of a wide range of life-affecting injuries and/or conditions, all serious health hazards. FDA: http://ht.ly/g4Ee30dtRDE

Direct link: https://www.fda.gov/Safety/Recalls/ucm565827.htm

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

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Caverflo Natural Herbal Coffee Recall [US]

US FlagUS/Silver Spring: Caverflo Natural Herbal Coffee Recall [US]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:

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Tri-Ton Dietary Supplement Recall [US]

US FlagUS/Silver Spring: FDA LogoDynamic Technical Formulations, LLC recalls all current batch/lots of Tri-Ton Dietary Supplements due to suspected presence of Andarine and Ostarine both Selective Androgen Receptor Modulators (“SARMs”), substances that are considered by the FDA as unapproved drugs and Anabolic Steroid-like substances, a serious health hazard. FDA: http://ht.ly/OeRI30c9YLx

Direct link: https://www.fda.gov/Safety/Recalls/ucm559700.htm

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

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GEC Laxoplex Dietary Supplement Recall [US]

US FlagUS/Silver Spring: GEC Laxoplex Dietary Supplement Recall [US]Genetic Edge Compounds recalls all current batch/lots of GEC Laxoplex Dietary Supplement Capsules due to suspected presence of Anabolic Steroids, a serious health hazard. FDA: http://ht.ly/xRCy30bxAGM

Direct link: https://www.fda.gov/Safety/Recalls/ucm557125.htm

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

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