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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El Rashidi El Mizan Pure Natural Honey Recall [Canada]

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El Rashidi El Mizan Pure Natural Honey Recall [Canada]

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Canada/Ottawa: Noble Hope Import & Export recalls certain batch/lots of El Rashidi El Mizan branded Pure Natural Honey products from the Canadian marketplace due to suspected Ciprofloxacin, Enrofloxacin, Sulfadiazine, Sulfamethazine and Sulfamethoxazole contamination and consequential risks of bacterial and/or viral resistance, drug overdose, severe illness and/or possible life-changing complications, all serious health hazards.

CFIA: http://ht.ly/qPC130rNaWZ

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/inspection/2021/75997r-eng.php

Additional information:
The Canadian Food Inspection Agency (“CFIA”) reports the following Pure Natural Honey 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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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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Protat Sea Salt Piercing Aftercare Spray Recall [Australia]

Australia FlagAustralia/Canberra: Protat Natural Sea Salt Piercing Aftercare Spray Recall [Australia]Protat Pty Ltd., a Brompton, South Australia establishment, recalls certain batch/lots of Protat Natural Sea Salt Plus Tea Tree Hygienic Body Piercing Aftercare Spray from the Australian marketplace due to suspected Pseudomonas aeruginosa contamination and consequential risks of Gram-negative bacterial infection, severe illness and/or possible life-changing complications, all serious health hazards.

ACCC: http://ht.ly/uD1430rJsr3

Direct link: https://www.productsafety.gov.au/recall/protat-pty-ltd-protat-natural-sea-salt-plus-tea-tree-hygienic-body-piercing-aftercare-spray-50ml

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

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DermOtic Oil Ear Drops Recall [Canada]

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DermOtic Oil Ear Drops Recall [Canada]

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Canada/Ottawa: Hill Dermaceuticals Inc., a Mississauga, Ontario establishment, recalls numerous batch/lots of DermOtic Oil Ear Drops from the Canadian marketplace due to suspected Glass Fragment Contamination and consequential risks of outer ear injury, tympanic membrane laceration, infection hearing damage, all serious health and safety hazards.

HCSC: http://ht.ly/WmHi30rJf7L

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2021/75709r-eng.php

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

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MSIKU White Wedding Dried Cannabis Recall [Canada]

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MSIKU White Wedding Dried Cannabis Recall [Canada]

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Canada/Ottawa: AtlantiCann Medical Inc., a Sackville, Nova Scotia establishment, recalls an estimated 4176 units of MSIKU White Wedding Dried Cannabis products from the Canadian marketplace due to suspected incorrect THC values with consequential risks of underdose, failure to relieve pain and/or nausea and possible compensatory overdose, all serious health and safety hazards.

HCSC: http://ht.ly/jQx230rILW5

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2021/75609r-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports the following Cannabis products 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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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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Welmate Lidocaine Numbing Cream Recall [US]

Welmate Lidocaine Numbing Cream Recall [US]

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US FlagUS/Washington: YYBA Corp., doing business as Wellspring, a Monsey, New York establishment, recalls an estimated 15,000 jars of Welmate Lidocaine Numbing Cream from the American marketplace due to 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/DH9A30rGou9

Direct link: https://www.cpsc.gov/Recalls/2021/YYBA-Recalls-Welmate-Lidocaine-Numbing-Cream-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-Risk-of-Poisoning-Recall-Alert

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves Welmate Lidocaine Numbing Cream marketed, sold and delivered in the United States, as follows:

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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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