BlueSkyGreenEarth AntiBioBotanical & Ly)mex [Australia]

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:

Hilde Hemmes’ Herbals Wormwood Herb Recall [Australia]

Click to enlarge

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:

Gloria Herbs Liver Detox Recall [Australia]

Click to enlarge

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:

Sundial Herbal Dietary Supplement Recall [US]

Click to enlarge

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:

Active Male Dietary Supplement Recall [US]

Click to enlarge

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:

Up2 Dietary & Bow and Arrow Supplement Recall [US]

Click to enlarge

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:

Silver Bullet Male Enhancement Supplement Recall [US]

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:

Up2 All Natural Libido Dietary Supplement Recall [US]

Click to enlarge image

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:

Green Lumber Dietary Supplement Recall [US]

Click to enlarge

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:

Balquis Yemeni Spice Recall [US]

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:

Stiff Boy branded Beast Supplement Recall [US]

Click to enlarge image

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:

Life Rising Dietary Supplement Recall [US]

  Click to enlarge image

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:

Leopard Miracle Honey Dietary Supplement Recall [US]

Click to expand image

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:

Sunstone Organics Kratom Supplement Recall [US]

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:

Rhino 5k Dietary Supplement Recall [US]

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: