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

Bit & Bet Thumbs Up 7 Blue 69K Supplement Capsules

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US FlagUS/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:

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

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

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US FlagUS/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:

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BlueSkyGreenEarth AntiBioBotanical & Ly)mex [Australia]

Australia FlagAustralia/Canberra: Logo - The Australian Competition & Consumer Commission ("ACCC")BlueSkyGreenEarth Herbs Pty Ltd., an Alexandria, New South Wales establishment, recalls certain batch/lots of AntiBioBotanical and Ly)mex Herb medications from the Australian marketplace due to suspected Artemisia ingredients and consequential risks of health damage to women of childbearing age and to the health and/or safety of their developing fetus, including reproductive damage, all serious health hazards.

ACCC: http://ht.ly/ewNA30rCFEO

Direct link: https://www.productsafety.gov.au/recall/blueskygreenearth-herbs-pty-ltd-antibiobotanical-and-lymex

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

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Hilde Hemmes’ Herbals Wormwood Herb Recall [Australia]

Hilde Hemmes' Herbals Wormwood Herb Recall [Australia]

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Australia FlagAustralia/Canberra: Herbal Supplies Pty Ltd, a Ridgehaven, South Australia establishment, recalls certain batch/lots of Hilde Hemmes’ Herbals Wormwood Herb medication from the Australian marketplace due to suspected Artemisia ingredients and consequential risks of health damage to women of childbearing age and to the health and/or safety of their fetus including reproductive damage, all serious health hazards.

ACCC: http://ht.ly/Hrm630rAQ4q

Direct link: https://www.productsafety.gov.au/recall/herbal-supplies-pty-ltd-hilde-hemmes-herbals-wormwood-herb-50g

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

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Adam’s Secret Extra Strength Capsule Recall [US]

Adam's Secret Extra Strength Capsule Recall [US]

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US FlagUS/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:

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Gloria Herbs Liver Detox Recall [Australia]

Gloria Herbs Liver Detox Recall [Australia]

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Australia FlagAustralia/Canberra: Gloria Herbs Pty Ltd, a Sydney, New South Wales establishment, recalls certain batch/lots of Dr. Benny Fan’s Series Gloria Herbs branded Liver Detox medication from the Australian marketplace due to suspected Artemisia ingredients and consequential risks of damage to women of childbearing age and to the health and/or safety of their fetus including reproductive damage, all serious health hazards.

ACCC: http://ht.ly/CLRt30ry0uU

Direct link: https://www.productsafety.gov.au/recall/gloria-herbs-pty-ltd-gloria-herbs-liver-detox

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

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Crafty Bubbles Wintergreen Essential Oil Recall [US]

US FlagUS/Washington: Crafty Bubbles Wintergreen Essential Oil Recall [US]Bolek’s Craft Supplys Inc., a Dover, Ohio establishment, recalls an estimated 5,600 bottles of Crafty Bubbles Wintergreen 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/UQWZ30rjMds

Direct link: https://www.cpsc.gov/Recalls/2021/Boleks-Craft-Supplys-Recalls-Wintergreen-Essential-Oil-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-Risk-of-Poisoning

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

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Rocky Mountain Wintergreen Essential Oil Recall [US]

Rocky Mountain Wintergreen Essential Oil Recall [US]

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US FlagUS/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:

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Organic Aromas Wintergreen Essential Oil Recall [US]

13631 - CPSC - Organic Aromas Wintergreen Essential Oil Recall [US]

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US FlagUS/Washington: Organic Aromas LLC, a Boise, Idaho establishment, recalls an estimated 300 Organic Aromas Wintergreen Essential Oils 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/ow1Q30rf0XR

Direct link: https://www.cpsc.gov/Recalls/2020/Organic-Aromas-Recalls-Wintergreen-Essential-Oil-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirements-Risk-of-Poisoning-Recall-Alert

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain Organic Aromas Wintergreen Essential Oil products sold and delivered in amber glass bottles with white or black caps, as follows:

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Vitamin Shoppe Vthrive Bioactive Multivitamin Recall [US]

Vitamin Shoppe Vthrive Bioactive Multivitamin Recall [US]

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US FlagUS/Washington: The Vitamin Shoppe, a Secaucus, New Jersey establishment, recalls an estimated 8,200 bottles of Vthrive Bioactive Multivitamins 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/X2WJ30rcqVr

Direct link: https://www.cpsc.gov/Recalls/2020/The-Vitamin-Shoppe-Recalls-Vthrive-Bioactive-Multivitamins-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 Multivitamins, as follows:

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Medi-First, Medique, Dover, Otis Clapp & Ecolab Med Recall

Medi-First, Medique, Dover, Otis Clapp & Ecolab Med Recall

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US FlagUS/Washington: Medique, a Fort Myers, Florida establishment, recalls an estimated 143,300 Medi-First, Medi-First Plus, Medique, Dover, Otis Clapp and Ecolab branded medications and/or health 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/aPaY30r9OOg

Direct link: https://www.cpsc.gov/Recalls/2020/Medique-Recalls-31-Different-Over-the-Counter-Drugs-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-Risk-of-Poisoning-Sold-Exclusively-on-Amazon-com-Recall-Alert

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports the recall involves 31 different over-the-counter drugs purchased on or after June 1, 2018 that are unexpired from the following brands: Medi-First, Medi-First Plus, Medique, Dover, Otis Clapp and Ecolab, as follows (in alphabetical order):

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Red-E Male Enhancement Supplement Recall [US]

Red-E Male Enhancement Supplement Recall [US]

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US FlagUS/Silver Spring: The Protein Shoppe, LLC, a Pharr, Texas establishment, recalls certain batch/lots of Red-E Male Enhancement Tablet products from the American marketplace due to suspected undeclared Sildenafil, an FDA approved drug for the treatment of Male Erectile Dysfunction in a class of drugs called Phosphodiesterase (“PDE-5”) Inhibitors and consequential risk of dangerous low blood pressure, injury and possible life-changing complications, all serious health and safety hazards.

FDA: http://ht.ly/hLfX30r80lE

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/protein-shoppe-llc-issues-voluntary-nationwide-recall-red-e-male-enhancement-tablet-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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