Premium OrgaZen & Ginseng Power Supplement Recall [US]

Premium OrgaZen 7000 and Ginseng Power 5000 Supplements Recall [US]

Click to enlarge

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:

Continue reading

Nuri Shogun-X 7000, 69MODE & Thumbs Up 7 Supplements

Nuri Shogun-X 7000, 69MODE Blue 69, Thumbs Up 7 Supplements [US]

Click to enlarge

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:

Continue reading

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

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

Click to enlarge

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:

Continue reading

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

Bit & Bet Thumbs Up 7 Blue 69K Supplement Capsules

Click to enlarge

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:

Continue reading

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

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

Click to enlarge image

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:

Continue reading

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:

Continue reading

Hilde Hemmes’ Herbals Wormwood Herb Recall [Australia]

Hilde Hemmes' Herbals Wormwood Herb Recall [Australia]

Click to enlarge

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:

Continue reading

Bull Wipes All-Purpose Disinfectant Wipe Recall [Canada]

Canada Flag

Canada/Ottawa: Logo - WestCan Health & Safety Ltd.WestCan Health & Safety Ltd., a Coquitlam, British Columbia establishment, recalls all current batch/lots of Bull Wipes All-Purpose Disinfectant Wipes from the Canadian marketplace due to failure to gain Canadian market authorization and risk of possible ineffectiveness and/or microbial contamination, bacterial infection, severe illness and/or possible life-changing complications, all serious health hazards.

HCSC: http://ht.ly/G32r30rAcUh

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2021/75079r-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports the following All-Purpose Disinfectant Wipes are subject to this recall:

Continue reading

Riva Senna Laxative Tablet Recall [Canada]

Canada Flag

Riva Senna Laxative Tablets Recall [Canada]

Click to enlarge

Canada/Ottawa: Laboratoire Riva Inc., a Blainville, Quebec establishment, recalls an estimated two (2) batch/lots of Riva branded Senna Laxative Tablets from the Canadian marketplace due to undisclosed microbial contamination and consequential severe illness and/or possible life-changing complications, all serious health hazards.

HCSC: http://ht.ly/3Mll30rzWIw

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2021/75089a-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports the following Senna Laxative Tablets products are subject to this recall:

Continue reading

San Rafael Chemdawg Resin Cannabis Recall [Canada]

Canada Flag

San Rafael Chemdawg Resin Cannabis Recall [Canada]

Click to enlarge image

Canada/Ottawa: Aurora Cannabis Enterprises Ltd., a Cremona, Alberta establishment, recalls an estimated 19,716 units of San Rafael ’71 OG Chemdawg Live Resin Cannabis products from the Canadian marketplace due to failure to properly label the internal package with consequential risks of overdose, liver and/or kidney damage and other life-changing injuries, all serious health and safety hazards.

HCSC: http://ht.ly/Nq9c30rzF0z

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2021/75047r-eng.php

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

Continue reading

Adam’s Secret Extra Strength Capsule Recall [US]

Adam's Secret Extra Strength Capsule Recall [US]

Click to enlarge

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:

Continue reading

We Grow BC Dried Cannabis Recall [Canada]

Canada Flag

We Grow BC Dried Cannabis Recall [Canada]

Click to enlarge

Canada/Ottawa: We Grow BC Ltd., a Calgary, Alberta establishment, recalls one batch/lot (an estimated 1,980 units) of We Grow BC Ltd.’s Qwest Pineapple Cake Dried Cannabis Pre-Roll products from the Canadian marketplace due to reported incorrect packaging with an inaccurate THC value and consequential risks of THC impairment, decreased ability to operate machines, disorientation and injury, all serious health and safety hazards.

HCSC: http://ht.ly/pCeC30ry9PP

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2021/75023r-eng.php

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

Continue reading

Gloria Herbs Liver Detox Recall [Australia]

Gloria Herbs Liver Detox Recall [Australia]

Click to enlarge

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:

Continue reading

Boots Multivitamin Supplement Recall [UK]

Boots Multivitamin Supplement Recall [UK]

Click to enlarge

UK FlagUK/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:

Continue reading

Manukaguard Allercleanse Nasal Spray Recall [US]

Manukaguard Allercleanse Nasal Spray Recall [US]

Click to enlarge

US FlagUS/Silver Spring: Ndal Manufacturing Industries, Inc., a Monterey, California establishment, recalls certain batch/lots of Manukaguard Allercleanse Nasal Spray products from the American marketplace due to suspected Yeast contamination and consequential risks of infection, severe illness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/awOM30rwSR6

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ndal-mfg-inc-issues-voluntary-nationwide-recall-manukaguard-allercleanse-nasal-spray-due

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

Continue reading

<span>%d</span> bloggers like this: