Posted on March 30, 2021 by Recalls Direct™
Australia/Canberra:
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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Filed under: ACCC, Artemisia, Australia Therapeutic Goods Administration ("TGA"), Dietary Supplements, Drugs, Genotoxic hazard, Labeling or regulatory issues, Medical / Veterinary, mutagenic, TGA | Tagged: ACCC, ACCC PRA number: 2021/18924, Artemisia, Australian Competition & Consumer Commission, BlueSkyGreenEarth Herbs Pty, child, developmental delay hazard, dietary supplement, drug, fetus, genotoxicity hazard, medication, nutritional supplement, pregnant, Recalls Direct RIN: 14262-2021, Reproductive Damage hazard, TGA, Therapeutic Goods Administration | Leave a comment »
Posted on March 16, 2021 by Recalls Direct™
![Hilde Hemmes' Herbals Wormwood Herb Recall [Australia]](https://livingsafelyrecalls.files.wordpress.com/2021/03/14207-hildehemmesherbalswormwoodherb.jpg?w=90&h=107)
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Australia/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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Filed under: ACCC, Artemisia, Australia Therapeutic Goods Administration ("TGA"), Dietary Supplements, Drugs, Genotoxic hazard, Labeling or regulatory issues, Medical / Veterinary, mutagenic, TGA | Tagged: ACCC, ACCC PRA number: 2021/18849, Artemisia, Australian Competition & Consumer Commission, child, developmental delay hazard, dietary supplement, drug, fetus, genotoxicity hazard, Hilde Hemmes' Herbals, Hilde Hemmes' Herbals Wormwood Herb medications, medication, nutritional supplement, pregnant, Recalls Direct RIN: 14207-2021, Reproductive Damage hazard, TGA, Therapeutic Goods Administration | Leave a comment »
Posted on February 23, 2021 by Recalls Direct™
![Gloria Herbs Liver Detox Recall [Australia]](https://livingsafelyrecalls.files.wordpress.com/2021/02/14129-gloriaherbsliverdetox.jpg?w=105&h=113)
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Australia/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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Filed under: ACCC, Artemisia, Australia Therapeutic Goods Administration ("TGA"), Dietary Supplements, Drugs, Genotoxic hazard, Labeling or regulatory issues, Medical / Veterinary, mutagenic, TGA | Tagged: ACCC, ACCC PRA number: 2021/18859, Asteraceae, Australian Competition & Consumer Commission, child, developmental delay hazard, dietary supplement, Dr. Benny Fan, drug, fetus, genotoxicity hazard, Gloria Herbs, Gloria Herbs Liver Detox, medication, nutritional supplement, pregnant, Recalls Direct RIN: 14129-2021, Reproductive Damage hazard, TGA, Therapeutic Goods Administration | Leave a comment »
Posted on July 10, 2020 by Recalls Direct™
![Sundial Herbal Dietary Supplement Recall [US]](https://livingsafelyrecalls.files.wordpress.com/2020/07/13236-sundialwoodrootsupplement.jpg?w=105&h=140)
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US/Silver Spring: Sundial Herbal Products, a Bronx, New York establishment, recalls all Sundial branded Dietary and Nutritional Supplement products, marketed, sold and delivered from January 1, 2014 to the date of this notification that have labeling that contains and/or make drug claims stating the product(s) can diagnose, cure, mitigate, treat or prevent any disease or condition.
FDA: http://ht.ly/gPQa30qXznA
Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sundial-herbal-products-recalling-products-attached-because-these-products-were-misbranded-products
Additional information:
The US Food and Drug Administration (“FDA”) reports the following Dietary Supplements are subject to this recall:
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Filed under: Dietary Supplements, Drugs, Food & Drink, Labeling or regulatory issues, US FDA | Tagged: dietary supplement, FDA, increased risk of Heart Attack, nutritional supplement, Sundial Herbal Products, Supplements, unapproved drug hazard, US Food and Drug Administration | Leave a comment »
Posted on March 22, 2020 by Recalls Direct™
![Active Male Dietary Supplement Recall [US]](https://livingsafelyrecalls.files.wordpress.com/2020/03/12831-activemaledietarysupplements.jpg?w=105&h=145)
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US/Silver Spring: Natural Remedy Store, a San Antonio, Texas establishment, recalls all current batch/lots of Active Male Dietary Supplement Capsules due to suspected undeclared Tadalafil, an existing FDA approved drug for certain medical conditions and legally available only under prescription from a licensed physician. The undeclared presence of this medication can pose a serious health and safety hazard for some people.
FDA: http://ht.ly/W7RA30qrMHX
Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/natural-remedy-store-issues-voluntary-worldwide-recall-active-male-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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Filed under: Dietary Supplements, Drugs, Food & Drink, Labeling or regulatory issues, Tadalafil, US FDA | Tagged: Active Male, dietary supplement, FDA, increased risk of Heart Attack, Natural Remedy Store, nutritional supplement, Recalls Direct RIN: 12831-2020, suspected-presence-of-Tadalafil, unapproved drug hazard, US Food and Drug Administration | Leave a comment »
Posted on February 24, 2020 by Recalls Direct™
![Up2 Dietary & Bow and Arrow Supplement Recall [US]](https://livingsafelyrecalls.files.wordpress.com/2020/02/12713-upnutritionalsupplements.jpg?w=105&h=122)
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US/Silver Spring: Med Man Distribution, a Sault Sainte Marie, Ontario establishment, recalls certain batch/lots of Up2 Dietary Supplement and Bow and Arrow Dietary Supplement products 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/uwGo30qkrwi
Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/med-man-expands-voluntary-nationwide-recall-up2-and-bow-arrow-due-presence-undeclared-sildenafil
Additional information:
The US Food and Drug Administration (“FDA”) reports the following Dietary Supplement Capsules are subject to this recall:
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Filed under: Dietary Supplements, Drugs, Food & Drink, Labeling or regulatory issues, Sildenafil, US FDA | Tagged: Bow and Arrow, dietary supplement, FDA, increased risk of Heart Attack, Med Man Distribution, nutritional supplement, Recalls Direct RIN: 12713-2020, suspected-presence-of-Sildenafil, unapproved drug hazard, UP2, US Food and Drug Administration | Leave a comment »
Posted on November 15, 2019 by Recalls Direct™
US/Silver Spring:
Spring: Nature’s Rx, a Claremont, California establishment, recalls batch/lots of Nature’s Rx Silver Bullet Male Enhancement Capsules 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/67hD30pTxfA
Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/natures-rx-issues-voluntary-nationwide-recall-silver-bullet-10-male-enhancement-capsules-due
Additional information:
The US Food and Drug Administration (“FDA”) reports the following Dietary Supplement Capsules are subject to this recall:
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Filed under: Dietary Supplements, Drugs, Food & Drink, Labeling or regulatory issues, Sildenafil, US FDA | Tagged: dietary supplement, FDA, increased risk of Heart Attack, Nature's Rx, Nature's Rx Silver Bullet Male Enhancement Capsules, nutritional supplement, Recalls Direct RIN: 12287-2019, Silver Bullet, Silver Bullet Male Enhancement Capsules, suspected-presence-of-Sildenafil, unapproved drug hazard, US Food and Drug Administration | Leave a comment »
Posted on November 12, 2019 by Recalls Direct™
![Up2 All Natural Libido Dietary Supplement Recall [US]](https://livingsafelyrecalls.files.wordpress.com/2019/11/12275-up2allnaturallibidodietarysupplement.jpg?w=150&h=136)
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US/Silver Spring: Med Man Distribution, a Sault Ste. Marie, Ontario establishment, recalls certain batch/lots of Up2 There Is No Other All Natural Libido for Men & Women Dietary Supplements 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/8Bao30pSpI4
Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/med-man-issues-voluntary-nationwide-recall-up2-due-presence-undeclared-sildenafil
Additional information:
The US Food and Drug Administration (“FDA”) reports the following Dietary Supplement Capsules are subject to this recall:
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Filed under: Dietary Supplements, Drugs, Food & Drink, Labeling or regulatory issues, Sildenafil, US FDA | Tagged: dietary supplement, FDA, increased risk of Heart Attack, Med Man, nutritional supplement, Recalls Direct RIN: 12275-2019, suspected-presence-of-Sildenafil, unapproved drug hazard, Up2 There Is No Other All Natural Libido for Men & Women Dietary Supplements, US Food and Drug Administration | Leave a comment »
Posted on October 23, 2019 by Recalls Direct™
![Green Lumber Dietary Supplement Recall [US]](https://livingsafelyrecalls.files.wordpress.com/2019/10/12200-greenlumbersupplement.jpg?w=101&h=125)
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US/Silver Spring: GL Holdings, a Newport Beach, California establishment, recalls numerous batch/lots of Green Lumber Dietary Supplement Capsules due to suspected undeclared Tadalafil, an existing FDA approved drug for certain medical conditions. The undeclared presence of this medication can pose a serious health and safety hazard for some people.
FDA: http://ht.ly/dBa430pLE8Y
Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/gl-holdings-issues-voluntary-worldwide-recall-green-lumber-products-due-presence-undeclared
Additional information:
The US Food and Drug Administration (“FDA”) reports the following Dietary Supplement products are subject to this recall:
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Filed under: Dietary Supplements, Drugs, Food & Drink, Labeling or regulatory issues, Tadalafil, US FDA | Tagged: dietary supplement, FDA, GL Holdings, Green Lumber, increased risk of Heart Attack, nutritional supplement, Recalls Direct RIN: 12200-2019, suspected-presence-of-Tadalafil, unapproved drug hazard, US Food and Drug Administration | Leave a comment »
Posted on August 29, 2019 by Recalls Direct™
US/Silver Spring:
Makzemo LLC, a Brooklyn, New York establishment, recalls certain batch/lots of Balquis Yemeni Spice products due to suspected risk of Lead contamination, severe illness and/or possible life-changing complications, all serious health hazards.
FDA: http://ht.ly/uhbO30prmri
Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/makzemo-llc-recalls-balquis-yemeni-spice-because-possible-health-risk
Additional information:
The US Food and Drug Administration (“FDA”) reports the following Spice products are subject to this recall:
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Filed under: Food & Drink, Ingestion hazard, Labeling or regulatory issues, Lead or cadmium hazard, US FDA | Tagged: Balquis Yemeni Spice, FDA, Makzemo LLC, nutritional supplement, Recalls Direct RIN: 11976-2019, US Food and Drug Administration | Leave a comment »
Posted on May 10, 2019 by Recalls Direct™
![Stiff Boy branded Beast Supplement Recall [US]](https://livingsafelyrecalls.files.wordpress.com/2019/05/11456-stiffboybeastsupplements.jpg?w=145&h=155)
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US/Silver Spring: Stiff Boy LLC, a Westchester County, New York establishment, recalls all current batch/lots of The Beast Dietary Supplement Capsules 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/FyMw30oHizo
Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/stiff-boy-llc-issues-voluntary-nationwide-recall-beast-capsules-due-presence-undeclared-sildenafil
Additional information:
The US Food and Drug Administration (“FDA”) reports the following Dietary Supplement Capsules are subject to this recall:
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Filed under: Dietary Supplements, Drugs, Food & Drink, Labeling or regulatory issues, Sildenafil, US FDA | Tagged: dietary supplement, FDA, increased risk of Heart Attack, nutritional supplement, Recalls Direct RIN: 11456-2019, Stiff Boy, suspected-presence-of-Sildenafil, unapproved drug hazard, US Food and Drug Administration | Leave a comment »
Posted on May 3, 2019 by Recalls Direct™
![Life Rising Dietary Supplement Recall [US]](https://livingsafelyrecalls.files.wordpress.com/2019/05/11425-liferisingdietarysupplements.jpg?w=160&h=89)
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US/Silver Spring: Life Rising Corporation, a Willowbrook, Illinois establishment, recalls all current Life Rising Holder-W Holder Warmer Capsules, Life Rising Neck-ND Neck Clear Capsules and HoliCare Metabolism Cleansing (MET-CLS) Tablets due to suspected risk of Lead contamination in excess of that allowed by federal regulation and consequential risk of a wide variety of symptoms, severe illness and/or possible life-changing complications, all serious health hazards.
FDA: http://ht.ly/fNAc30oD6Mm
Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/life-rising-corporation-recalls-chinese-herbal-supplements-because-possible-health-risk
Additional information:
The US Food and Drug Administration (“FDA”) reports the following Dietary Supplements are subject to this recall:
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Filed under: Dietary Supplements, Drugs, Food & Drink, Ingestion hazard, Labeling or regulatory issues, Lead or cadmium hazard, US FDA | Tagged: dietary supplement, FDA, HoliCare Metabolism Cleansing (MET-CLS) Tablets, Life Rising Corporation, Life Rising Holder-W Holder Warmer Capsules, Life Rising NECK-ND Neck Clear Capsules, nutritional supplement, Recalls Direct RIN: 11425-2019, US Food and Drug Administration | Leave a comment »
Posted on March 25, 2019 by Recalls Direct™
![Leopard Miracle Honey Dietary Supplement Recall [US]](https://livingsafelyrecalls.files.wordpress.com/2019/03/11275-leopardmiraclehoneydietarysupplement.jpg?w=150&h=114)
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US/Silver Spring: USA LESS, a Brooklyn, New York establishment, recalls certain batch/lots of Leopard Miracle Honey Dietary Supplement ptoducts due to undeclared Sildenafil. The presence of Sildenafil in the Leopard Miracle Honey Dietary Supplement products, renders it an unapproved drug for which safety and efficacy have not been established and, therefore, subject to recall.
FDA: http://ht.ly/OKBj30obFny
Direct link: https://www.fda.gov/Safety/Recalls/ucm634314.htm
Additional information:
The US Food and Drug Administration (“FDA”) reports the following Dietary Supplement products are subject to this recall:
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Filed under: Dietary Supplements, Drugs, Food & Drink, Labeling or regulatory issues, Sildenafil, Tadalafil, US FDA | Tagged: dietary supplement, FDA, increased risk of Heart Attack, nutritional supplement, Recalls Direct RIN: 11275-2019, suspected-presence-of-Sildenafil, unapproved drug hazard, US Food and Drug Administration, USA LESS | Leave a comment »
Posted on March 5, 2019 by Recalls Direct™
US/Silver Spring:
Sunstone Organics, an Eugene, Oregon establishment, recalls certain batch/lots of Sunstone Organics branded Maeng Da Kratom and Sunstone Organics branded White Vein Kratom Supplements due to suspected risk of Salmonella contamination and consequential risk of Gram-negative bacterial infection, severe illness and/or possible life-changing complications, all serious health hazards.
FDA: http://ht.ly/TIGE30nVXu3
Direct link: https://www.fda.gov/Safety/Recalls/ucm632554.htm
Additional information:
The US Food and Drug Administration (“FDA”) reports the following Supplement products are subject to this recall:
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Filed under: Dietary Supplements, Drugs, Food & Drink, Labeling or regulatory issues, US FDA | Tagged: dietary supplement, FDA, Kratom, nutritional supplement, Recalls Direct RIN: 11194-2019, Sunstone Organics, Sunstone Organics Maeng Da Kratom, Sunstone Organics White Vein Kratom, US Food and Drug Administration | Leave a comment »
Posted on January 9, 2019 by Recalls Direct™
US/Silver Spring:
Happy Together, Inc. a Boynton Beach, Florida, establishment, recalls all current batch/lots of Rhino 5k Dietary Supplement Capsules due to suspected Sildenafil and Tadalafil contamination, all serious health and safety hazards.
FDA: http://ht.ly/JBPm30nfyPo
Direct link: https://www.fda.gov/Safety/Recalls/ucm629353.htm
Additional information:
The US Food and Drug Administration (“FDA”) reports the following Dietary Supplement products are subject to this recall:
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Filed under: Dietary Supplements, Drugs, Food & Drink, Labeling or regulatory issues, Sildenafil, Tadalafil, US FDA | Tagged: dietary supplement, FDA, Happy Together, increased risk of Heart Attack, nutritional supplement, Recalls Direct RIN: 11020-2019, Rhino, suspected-presence-of-Sildenafil, suspected-presence-of-Tadalafil, unapproved drug hazard, US Food and Drug Administration | Leave a comment »