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:

Advertisements

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:

Zero Xtreme branded Nutritional Supplement Recall [US]

US/Silver Spring: Zero Xtreme, a Marathon, Florida establishment, recalls certain batch/lots of Zero Xtreme branded Nutritional Supplement Capsules due to suspected presence of Sibutramine, a controlled substance under FDA regulation that was marketed as an appetite suppressant but withdrawn from the US market in 2010 due to suspected increased risks of Cardiovascular Events and Stroke, all serious health and safety hazards.

FDA: http://ht.ly/InAy30mgeRW

Direct link: https://www.fda.gov/Safety/Recalls/ucm623503.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following over-the-counter (“OTC”) drugs are subject to this recall:

MyNicNaxs Nutritional Supplement Recall [US]

US/Silver Spring: MyNicNaxs, LLC, a Deltona, Florida establishment, has recalled all lots of various Dietary Supplements due to suspected presence of Diclofenac, Phenolphthalein, Sibutramine and/or Sildenafil, all controlled substances and undeclared active pharmaceutical ingredients (“APIs”). The presence of Diclofenac, Phenolphthalein, Sibutramine and/or Sildenafil in the recalled Dietary Supplements renders them unapproved drugs for which safety and efficacy have not been established and, therefore, subject to recall. Due to their ingredients, these Supplements all pose serious health and safety hazards. FDA: http://ht.ly/zYCx30kVBsI

Direct link: https://www.fda.gov/Safety/Recalls/ucm613197.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following over-the-counter (“OTC”) drugs are subject to this recall (in alphabetical order):