NaturesPlus Keto Living Sugar Control Supplements [US]

NaturesPlus Keto Living Sugar Control Capsule Supplements Recall [US]

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US FlagUS/Silver Spring: Natural Organics, Inc., an Amityville, New Yoek establishment, recalls certain batch/lots of NaturesPlus Keto Living Sugar Control Capsule Supplements from the American marketplace due to suspected suspected mislabeling and consequential undeclared Gluten, a known allergen, source of dietary intolerance and possible trigger of Anaphylaxis, a serious and potential fatal situation, requiring immediate medical intervention to minimize pain and suffering as well as prevent life-altering injury or death.

FDA: http://ht.ly/1bCg30sjcpO

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/natural-organics-inc-issues-nationwide-voluntary-recall-four-lots-naturesplus-keto-living-sugar

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

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Pink Pussycat 3000 Dietary Supplements [US]

Pink Pussycat 3000 Dietary Supplements [US]

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US FlagUS/Silver Spring: F&S Medical Supply, doing business as Pink Toyz, a Chatsworth, California establishment, recalls certain batch/lots of Pink Pussycat 3000 Dietary Supplements from the American marketplace due to undeclared Sildenafil, 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 requiring immediate medical intervention to minimize pain and suffering as well as prevent life-altering injury or death.

FDA: http://ht.ly/zQoh30sgI64

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/fs-medical-supply-dba-pink-toyz-issues-voluntary-nationwide-recall-pink-pussycat-capsules-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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Reckitt Airborne Fruit Flavor Supplement Gummies [US]

Reckitt Airborne Supplement Gummies

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US FlagUS/Bethesda: RB Health (US) LLC, doing business as Reckitt, a Parsippany, New Jersey establishment, recalls an estimated 3.74 million bottles of Reckitt Airborne Assorted Fruit Flavor Supplement Gummies from the American marketplace due to suspected packaging overpressure and consequential risks of eye injury and laceration upon sudden bottle decompression, all serious health and safety hazards requiring immediate medical intervention to minimize pain and suffering as well as prevent life-altering injury.

CPSC: http://ht.ly/4s2330seym2

Direct link: https://www.cpsc.gov/Recalls/2022/Reckitt-Recalls-More-than-Three-Million-Bottles-of-Airborne-Gummies-Due-to-Injury-Hazard

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain batch/lots of Airborne Supplement Gummies marketed, sold and delivered in the United States, as follows:

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Rise Up Red Edition Capsule Dietary Supplements [US]

Rise Up Red Edition Capsule Dietary Supplements [US]

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US FlagUS/Silver Spring: Positive-Health, a Wilmington, Delaware establishment, recalls certain batch/lots of Rise Up Red Edition Capsule Dietary 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/yuHA30sbffQ

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/positive-health-issues-voluntary-nationwide-recall-rise-red-edition-capsules-due-presence-undeclared

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

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Hard Dawn Rise and Shine Supplements [US]

Hard Dawn Rise and Shine Supplements [US]

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US FlagUS/Silver Spring: Esupplementsales, LLC, an Orangevale, California establishment, recalls certain batch/lots of Hard Dawn Rise and Shine Dietary 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/WZJC30s9z9x

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/esupplementsales-llc-issues-nationwide-recall-one-lot-hard-dawn-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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Moor Herbs Angel Infant Formula [US]

Moor Herbs Angel Infant Formula Recall [US]

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US FlagUS/Silver Spring: Moor Herbs, a Detroit, Michigan establishment, recalls all batch/lots of Moor Herbs Angel Infant Formula from the American marketplace due to reported meet specific nutrition and labeling requirements for infant formula. In addition, when the product was tested, the Iron, Sodium, and Potassium content were well over the maximum allowed, which could potentially lead to Iron overload and/or Electrolyte imbalances. In addition, the product did not have Vitamin D, and a Vitamin D deficiency can potentially lead to Rickets, a softening and weakening of bones, all serious health and safety hazards requiring immediate medical intervention to minimize pain and suffering as well as prevent life-altering injury or death.

FDA: http://ht.ly/xKxe30s6Pku

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/moor-herbs-recalls-angel-formula-infant-formula-because-possible-health-risk

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

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Fountain of Youth Formula Collagen Supplement Recall [US]

Fountain of Youth Formula Collagen Protein Supplement Recall [US]

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US FlagUS/Silver Spring: BUBS Naturals, an Encinitas, California establishment, recalls certain batch/lots of Fountain of Youth Formula Collagen Protein Dietary Supplement products from the American marketplace due to suspected mislabeling and consequential undeclared Milk, a known allergen, source of dietary intolerance and possible trigger of Anaphylaxis, a serious and potential fatal situation, requiring immediate medical intervention to minimize pain and suffering as well as prevent life-altering injury or death.

FDA: http://ht.ly/QbjV30s2Wka

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bubs-naturals-recalling-two-lots-fountain-youth-collagen-powder-after-firm-testing-found-milk

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

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Genius Kids & Teens Health Supplement Recall [Canada]

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Genius Kids and Teens Natural Health Dietary Supplements 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:

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Alpha Male Plus Male Enhancer Fruit Chew Recall [US]

Alpha Male Plus Male Enhancer Fruit Chew Recall [US]

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US FlagUS/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:

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BUBS Naturals MCT Oil Powder Recall [US]

BUBS Naturals MCT Oil Powder Recall [US]

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US FlagUS/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:

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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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Bloommy Biotin Collagen Keratin Supplement Recall [US]

Bloommy Biotin Collagen Keratin Supplement Capsules Recall [US]

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US FlagUS/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:

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Whole Foods 365 Everyday Value Whey Powder Recall [US]

Whole Foods 365 Everyday Value Whey Protein Powder Recall [US]

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US FlagUS/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:

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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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