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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Plant Guru Wintergreen & Birch Essential Oil Recall [US]

Plant Guru Essential Oil Recall [US]

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US FlagUS/Washington: Plant Guru, a Plainfield, New Jersey establishment, recalls an estimated 25,600 bottles of Wintergreen Essential Oil, Birch Essential Oil, Headache Relief Essential Oil Blend, Headache Relief Roll-On Essential Oil Blend and Deep Muscle Essential Oil Blend 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/U8mC30rLNem

Direct link: https://www.cpsc.gov/Recalls/2021/Plant-Guru-Recalls-Wintergreen-Birch-and-Blends-of-Essential-Oils-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 Plant Guru Essential Oils, as follows:

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LifeSeasons Blood Nourish-R Supplement Recall [US]

LifeSeasons Blood Nourish-R Supplement Recall [US]

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US FlagUS/Washington: LifeSeasons Inc., a Springville, Utah establishment, recalls an estimated 7,800 bottles of LifeSeasons Blood Nourish-R Supplements 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/I2l030rLH8e

Direct link: https://www.cpsc.gov/Recalls/2021/UST-Recalls-Bottles-of-LifeSeasons-Blood-Nourish-R-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-Risk-of-Poisoning

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain LifeSeasons Blood Nourish-R Supplements marketed, sold and delivered in the United States, as follows:

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Living Free Dietary Supplement Recall [US]

Living Free branded Dietary Supplement Recall [US]

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US FlagUS/Silver Spring: Bea Lydecker’s Naturals, Inc. an Oregon City, Oregon establishment, recalls certain batch/lots of six (6) Living Free branded Dietary Supplement drug products from the American marketplace due to improperly declared Soy Lecithin, 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/prKp30rLAx8

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bea-lydeckers-naturals-inc-issues-allergy-alert-undeclared-soy-lecithin-living-free-dietary

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

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SynerClear Nutritional Supplement Recall [Canada]

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SynerClear Supplement Recall [Canada]

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Canada/Ottawa: Naturo Aid Pharmaceutical Inc., a Maple Ridge, British Columbia establishment, recalls numerous batch/lots of SynerClear Nutritional Supplement products from the Canadian 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.

HCSC: http://ht.ly/qwrD30rJm9g

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2021/75711r-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports the following Nutritional 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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Sara Lee, Chef Pierre & Devonshire Pecan Pie Recall [US]

Sara Lee, Chef Pierre and Devonshire Pecan Pie Recall [US]

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US FlagUS/Silver Spring: Sara Lee Frozen Bakery, a Kings Mountain, North Carolina establishment, recalls certain batch/lots of Chef Pierre, Devonshire and Sara Lee branded Pecan Pies from the American marketplace due to undeclared Peanuts, 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/IkpR30rHz8H

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sara-lee-frozen-bakery-issues-allergy-alert-undeclared-peanuts-pecan-pies

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Pecan Pie products are subject to this recall (in alphabetical order):

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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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E-Prime Vitamin E Gel Capsule Recall [Australia]

E-Prime Vitamin E Gel Capsule Recall [Australia]

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Australia FlagAustralia/Canberra: Usana Australia Pty Ltd., a Castle Hill, New South Wales establishment, recalls certain batch/lots of E-Prime Vitamin E Gel Capsules from the Australian marketplace due to undeclared Sulphites (Sulfites), a known allergen, source of dietary intolerance and possible trigger of Anaphylaxis, a serious and potential fatal situation, requiring immediate medical intervention.

ACCC: http://ht.ly/PHHI30rGCgw

Direct link: https://www.productsafety.gov.au/recall/usana-australia-pty-ltd-e-prime-vitamin-e-gel-capsules-60

Additional information:
The Australian Competition & Consumer Commission (“ACCC”) reports the following Vitamin Capsules are subject to this recall:

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dōTERRA Deep Blue & PastTense Essential Oil Recall [US]

dōTERRA Deep Blue & PastTense Essential Oil Recall [US]

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US FlagUS/Washington: dōTERRA International LLC, a Pleasant Grove, Utah establishment, recalls an estimated 1.3 million Deep Blue, PastTense and Deep Blue Touch branded Essential Oil products 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/H6CC30rFXd8

Direct link: https://www.cpsc.gov/Recalls/2021/doTERRA-Recalls-1-3-Million-Bottles-of-Deep-Blue-PastTense-and-Deep-Blue-Touch-Essential-Oils-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 dōTERRA Deep Blue, PastTense and Deep Blue Touch Essential Oils in 10 mL glass bottles with rollerball applicator and black cap, as follows:

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

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

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US FlagUS/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:

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