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:

Organic Aromas Wintergreen Essential Oil Recall [US]

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US/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:

Vitamin Shoppe Vthrive Bioactive Multivitamin Recall [US]

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US/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:

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

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US/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):

Simplers Botanicals Wintergreen Essential Oil Recall [US]

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US/Washington: Nutraceutical Corporation, a Park City, Utah establishment, recalls an estimated 14,000 bottles of Simplers Botanicals branded Organic Wintergreen (Gaultheria Fragrantissiam) 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/Go2i30r4Rjh

Direct link: https://www.cpsc.gov/Recalls/2020/Nutraceutical-Recalls-Simplers-Botanicals-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 Organic Wintergreen Essential Oils, as follows:

Nature’s Oil Wintergreen & Birch Essential Oil Recall [US]

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US/Washington: Bulk Apothecary, an Aurora, Ohio establishment, recalls an estimated 20,240 bottles of Nature’s Oil Wintergreen and Birch 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/i2xU30r3gRL

Direct link: https://www.cpsc.gov/Recalls/2020/Bulk-Apothecary-Recalls-Natures-Oil-Wintergreen-and-Birch-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 Nature’s Oil Wintergreen and Birch Essential Oils, as follows:

Pranarom Wintergreen Essential Oil Recall [US]

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US/Washington: Pranarom, a Minneapolis, Minnesota establishment, recalls an estimated 960 bottles of Pranarom branded 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/cHWX30qYq0I

Direct link: https://www.cpsc.gov/Recalls/2020/Pranarom-Recalls-Wintergreen-Essential-Oils-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirements-Risk-of-Poisoning

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