Alert
Product Recall: Slim Xtreme Herbal Slimming Capsule for Undeclared Drug Ingredient
This is a reprint of the FDA Safety Alert. All lots of Slim Xtreme Herbal Slimming Capsule, 30 Capsules/Bottle, are being recalled. The products were sold and distributed nationwide via the internet and at the company’s headquarters in Hollywood, Florida. The Food and Drug Administration (FDA) is advising consumers not to purchase or use “Slim…
[...]FDA: Don’t buy drugs marketed as antimicrobial dietary supplements
This is a reprint of the FDA alert. Fast Facts The FDA is warning consumers not to use products marketed as dietary supplements that also claim to be antimicrobial (antibiotic, antifungal or antiviral) drugs. These illegal products are falsely promoted with claims to treat illnesses such as upper respiratory infections, sinusitis, pneumonia, bronchitis and the common…
[...]FDA warns about counterfeit ExtenZe dietary supplements
This is a reprint of the FDA alert. The U.S. Food and Drug Administration is warning consumers about a potentially harmful product represented as “ExtenZe,” a dietary supplement for male sexual enhancement. The counterfeit product looks similar to the actual product, but contains hidden ingredients that can cause serious harm to consumers. The counterfeit product…
[...]FDA, FTC act to remove fraudulent STD products from the market
This is a reprint of the FDA alert. The U.S. Food and Drug Administration (FDA) and the Federal Trade Commission (FTC) today announced a joint effort to remove products from the market that make unproven claims to treat, cure, and prevent sexually transmitted diseases (STDs). Among the products targeted in today’s action are Medavir, Herpaflor,…
[...]Texas Children Given Fake Antibiotics
Texas officials are investigating several over-the-counterfeit medications falsely advertised as antibiotics and warning people to avoid these fakes.
Doctors in an Austin hospital reported that several children were given these products by their parents, prompting the Texas Department of State Health Services (DSHS) to issue a warning and open an investigation.
[...]“U-Prosta”: herbal prostate product recalled as it may pose serious health risks
This is a reprint of the Health Canada alert. Advisory2011-54April 7, 2011For immediate release The issue: "U-Prosta Natural support for prostate health" is being voluntarily recalled in Canada by Sunnylife International Inc. after the U.S. Food and Drug Administration (FDA) found the product contains undeclared terazosin hydrochloride, which is a prescription drug used to treat…
[...]THE BEST Enhancer Supplement: Recall – Undeclared Drug Ingredient
RECALLED: THE BEST Enhancement SupplementPicture by USFDA via Flickr. This is a reprint of the FDA alert. March 28, 2011 – AVNS Inc announced today it is voluntarily recalling THE BEST Enhancer Supplement. AVNS Inc is conducting a voluntary recall after being informed by their manufacturer, Drive Total Energy, that the Food and Drug Administration…
[...]X-Hero and Male Enhancer: Recall – Undeclared Drug Ingredient
This is a reprint of the FDA alert. ISSUE: FDA lab analysis of X-Hero found the product contains sulfosildenafil, the analogue of the active ingredient of an FDA-approved drug used to treat erectile dysfunction (ED), making X-Hero an unapproved drug. In addition, FDA analysis of Male Enhancer sample found the product contains tadalafil, the active…
[...]Watch Out for Fake Radiation Preventatives Warns FDA
Due to public concern related to the nuclear incident in Japan, the FDA is warning consumers to be wary of drugs falsely touting radiation exposure treatment.
Potassium iodide (KI) has been approved by the FDA to prevent thyroid cancer in people internally contaminated with radioactive iodine, however the U.S. government is not recommending that residents take KI, even as a preventative. The Nuclear Regulatory Commission indicates that no part of the U.S. is expected to experience any harmful levels of radioactivity.
The FDA is warning consumers to be wary of internet sites and retail outlets promoting products that make claims to prevent or treat radiation, these claims may be false and the products may not be FDA approved.
[...]Discovery of Counterfeit Nutritional Supplements with Dangerous Ingredients Spurs Company Recall
This is a reprint of the FDA alert. February 22, 2011 -Biotab Nutraceuticals, Inc. (“Biotab”) is conducting a voluntary recall of two lots of EXTENZE nutritional supplement tablets. Some packages bearing lot numbers 0709241 and 0509075 are counterfeit products containing undeclared drug ingredients that can pose a serious risk to health. Biotab learned about the…
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