Over 25 Weight Loss, Sex Enhancement Supplements Withdrawn

Over 25 Weight Loss, Sex Enhancement Supplements Withdrawn
Over 25 Weight Loss, Sex Enhancement Supplements Withdrawn

The One Minute Miracle, Inc. announced a voluntary recall of all lots of Miracle Diet 30 and Miracle Rock 48 capsules. The recall is following a Food and Drug Administration (FDA) analysis that revealed undeclared drug ingredients present in the capsules.

Miracle Diet 30 capsules were found to contain undeclared phenolphthalein, an ingredient used in over-the-counter laxatives. Phenolphthalein was withdrawn from the market due to concerns of carcinogenicity. Long-term use could lead to serious gastrointestinal effects, irregular heartbeat, and cancer.

Miracle Rock 48 capsules were found to contain undeclared thiosildenafil, an analog of sildenafil. Sildenafil is an FDA-approved drug used for male sexual enhancement. Thiosildenafil is likely to have a similar pharmacological effect as sildenafil and concomitant use with nitrates could lead to a sudden and large drop in blood pressure.

RELATED: FDA Finds Undeclared Salicylic Acid in Weight Loss Caps

Miracle Diet 30 was marketed to support appetite control and weight loss. Affected products have expiration dates through 4/15/2018 and are packaged in 30-count bottles. Miracle Rock 48 is marketed for male sexual enhancement. Affected products have expiration dates through 6/1/2018 and are packaged in two blister packs containing two or four capsules.

The Company has also voluntarily withdrawn all lots and sizes of the following products: Miracle Cholesterol, Miracle Night Time, Miracle Joint-Flex, Miracle Stud 72, Miracle Magic Man, Male Mint Gum, Miracle 48 Hrs, Miracle Magic Woman, Miracle Cougar, Miracle Cougar Gum, Miracle Cougar G-Spot, Miracle G-Spot, Vagina Rejuvenation, Miracle Anti-Wrinkle, Miracle Stud Delay, Miracle Male Stud Spray, Miracle Male Stud Coffee, Miracle Male Coffee, Male 10, Miracle Male Stud Sublingual, Male 72 Hr, Miracle Tongue Sublingual, Miracle Tongue and Master Blaster.

For more information call (305) 947-6244 or or visit FDA.gov.

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