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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Pur Naturals brand Bone Broth Protein Recall [Canada]

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Pur Naturals brand Bone Broth Protein Recall [Canada]

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Canada/Ottawa: Pur-Natural Ingredients of Canada recalls certain batch/lots of Pur Naturals brand Bone Broth Protein products due to undeclared Milk, a known allergen, source of dietary intolerance and possible trigger of Anaphylaxis, a serious and potential fatal situation, requiring immediate medical intervention.

CFIA: http://ht.ly/zvyj30o6gzR

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/inspection/2019/69346r-eng.php

Additional information:
The Canadian Food Inspection Agency (“CFIA”) reports the following Bone Broth Protein products are subject to this recall:

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Sunstone Organics Kratom Supplement Recall [US]

US FlagUS/Silver Spring: Logo - US Food and Drug AdministrationSunstone Organics, an Eugene, Oregon establishment, recalls certain batch/lots of Sunstone Organics branded Maeng Da Kratom and Sunstone Organics branded White Vein Kratom 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/TIGE30nVXu3

Direct link: https://www.fda.gov/Safety/Recalls/ucm632554.htm

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

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Rhino 5k Dietary Supplement Recall [US]

US FlagUS/Silver Spring: Rhino 5k Dietary Supplement Recall [US]Happy Together, Inc. a Boynton Beach, Florida, establishment, recalls all current batch/lots of Rhino 5k Dietary Supplement Capsules due to suspected Sildenafil and Tadalafil contamination, all serious health and safety hazards.

FDA: http://ht.ly/JBPm30nfyPo

Direct link: https://www.fda.gov/Safety/Recalls/ucm629353.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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Zero Xtreme branded Nutritional Supplement Recall [US]

US FlagUS/Silver Spring: Zero Xtreme branded Nutritional Supplement Recall [US]Zero Xtreme, a Marathon, Florida establishment, recalls certain batch/lots of Zero Xtreme branded Nutritional Supplement Capsules due to suspected presence 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/InAy30mgeRW

Direct link: https://www.fda.gov/Safety/Recalls/ucm623503.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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MyNicNaxs Nutritional Supplement Recall [US]

US FlagUS/Silver Spring: MyNicNaxs Nutritional Supplement Recall [US]MyNicNaxs, LLC, a Deltona, Florida establishment, has recalled all lots of various Dietary Supplements due to suspected presence of Diclofenac, Phenolphthalein, Sibutramine and/or Sildenafil, all controlled substances and undeclared active pharmaceutical ingredients (“APIs”). The presence of Diclofenac, Phenolphthalein, Sibutramine and/or Sildenafil in the recalled Dietary Supplements renders them unapproved drugs for which safety and efficacy have not been established and, therefore, subject to recall. Due to their ingredients, these Supplements all pose serious health and safety hazards. FDA: http://ht.ly/zYCx30kVBsI

Direct link: https://www.fda.gov/Safety/Recalls/ucm613197.htm

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

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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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