Genius Kids & Teens Health Supplement Recall [Canada]

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Canada/Ottawa: Nutripur Inc., a Boisbriand, Quebec establishment, recalls one (1) known batch/lot of Genius Kids and Teens Natural Health Dietary Supplements from the Canadian marketplace due to suspected Staphylococcus aureus contamination and consequential risks of Gram-positive bacterial infection, severe illness and/or possible life-changing complications, all serious health and safety hazards requiring immediate medical intervention to minimize pain and suffering as well as prevent life-changing injury.

HCSC: http://ht.ly/hGDA30rWMaj

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2021/76593a-eng.php

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

Alpha Male Plus Male Enhancer Fruit Chew Recall [US]

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US/Silver Spring: Alpha Male Plus, a Tucson, Arizona establishment, recalls all current batch/lots of Alpha Male Plus Male Enhancer Fruit Chew Supplements from the American marketplace due to reported undeclared Tadalafil, an FDA approved drug 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/8Vk130rOqJz

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/alpha-male-plus-issues-voluntary-nationwide-recall-alpha-male-plus-male-enhancer-due-presence

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

BUBS Naturals MCT Oil Powder Recall [US]

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US/Silver Spring: BUBS Naturals, an Encinitas, California establishment, recalls certain batch/lots of MCT Oil Powder Supplement from the American marketplace 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.

FDA: http://ht.ly/d2kH30rI2D4

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bubs-naturals-encinitas-ca-voluntarily-recalling-certain-lots-its-mct-oil-powder-product-due

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

Poseidon Platinum 3500 Supplement Recall [US]

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US/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:

Bloommy Biotin Collagen Keratin Supplement Recall [US]

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US/Silver Spring: Bloommy, a Pawcatuck, Connecticut establishment, recalls an estimated 13,688 units of Bloommy branded Biotin Collagen Keratin Capsules for Skin, Joint, and Hair Supplements from the American marketplace due to undeclared Fish, 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/1BOh30rHFFR

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bloommy-inc-issues-allergy-alert-undeclared-fish-bloommy-biotin-collagen-keratin-capsules

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

Whole Foods 365 Everyday Value Whey Powder Recall [US]

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US/Silver Spring: Arizona Nutritional Supplements, a Chandler, Arizona establishment, recalls certain batch/lots of Whole Foods 365 Everyday Value Whey Protein Powder – Natural Vanilla Flavor from the American marketplace due to undeclared Soy, 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/3fIY30rHhnm

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/arizona-nutritional-supplements-issues-allergy-alert-undeclared-soy-allergen-365-everyday-value-whey

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

Premium OrgaZen & Ginseng Power Supplement Recall [US]

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US/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:

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

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US/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:

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

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US/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:

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

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US/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:

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

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US/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:

Adam’s Secret Extra Strength Capsule Recall [US]

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US/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:

Boots Multivitamin Supplement Recall [UK]

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UK/London: Boots, a Nottingham, England establishment, recalls certain batch/lots of Boots Multivitamin Supplements from the British marketplace due to suspected mislabeling/mispackaging and consequential risks of dietary Iron overdose and Vitamin K deficiency, both serious health hazards.

FSA: http://ht.ly/emIC30rxdqV

Direct link: https://www.food.gov.uk/news-alerts/alert/fsa-prin-07-2021

Additional information:
The UK Food Standards Agency (“FSA”) reports the following Multivitamin Supplements are subject to recall:

Rocky Mountain Wintergreen Essential Oil Recall [US]

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US/Washington: Rocky Mountain Oils, an Orem, Utah establishment, recalls an estimated 33,000 bottles of Wintergreen Essential Oils and Oil Blends from the American marketplace due to suspected failure to meet US child resistant closure requirements under the US Poison Prevention Packaging Act and consequential risks of child poisoning, ingestion and GI tract laceration damage, all serious health and safety hazards.

CPSC: http://ht.ly/DEor30ricUa

Direct link: https://www.cpsc.gov/Recalls/2021/Rocky-Mountain-Oils-Recalls-Wintergreen-Essential-Oil-and-Oil-Blends-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-Risk-of-Poisoning-Recall-Alert

Additional information:
US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain bottles of  Wintergreen Essential Oils, as follows:

Potter’s Herbals Malt Extract with Cod Liver Oil Recall [UK]

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UK/London: Soho Florids UK Ltd, a Wigan, Lancashire establishment, recalls certain batch/lots of Potter’s Herbals branded Malt Extract with Cod Liver Oil from the British marketplace due to suspected Mould contamination and consequential risks of infection, severe illness and/or possible life-changing complications, all serious health hazards.

FSA: http://ht.ly/gE1S30ri4Zq

Direct link: https://www.food.gov.uk/news-alerts/alert/fsa-prin-51-2020

Additional information:
The UK Food Standards Agency (“FSA”) reports the following Malt Extract products are subject to recall: