The dietary supplement Ginko biloba, which some believe helps improve memory (although studies have shown it is ineffective), has been linked to cancer in ratrs and mice. The new study, conducted by scientists at the National Toxicology Program (NTP), found that animals who received the supplement were more likely to develop tumors in the liver and thyroid than animals who were not given the extract. In the study, scientists gave 50 male and female rats corn oil solutions with 100, 300, or 1,000 milligrams of Gingko biloba extract per kilogram of body weight five times a week for two years. Another group received 200, 600, or 2000 mg/kg every day. Those concentrations fall within the range of what is on the market. The supplier of the extract does supply material to companies in the … [Read more...]
Despite FDA Warning About DMAA, One Company Continues Its Use
At least 86 incidents of illness or death associated with diet supplements containing the stimulant dimethylamylamine (DMAA) have been reported to the Food and Drug Administration (FDA). The illnesses reported include: heart problems, nervous system problems, and psychiatric disorders, according to the agency. Most of these reports have been voluntary from consumers and their health care providers, which does not necessarily establish a cause and effect relationship, the agency says. DMAA is most commonly used in supplements that promise weight loss, muscle building and performance enhancement. It can elevate blood pressure, leading to cardiovascular problems, such as shortness of breath, tightening in the chest or heart attack. DMAA is particularly dangerous when used with … [Read more...]
Consumer Concepts Recalls Dietary Supplement
Consumer Concepts is recalling ROCK-It Male Enhancement Capsules because they contain an analogue of an ingredient in an FDA-approved drug, making these products unapproved new drugs. Tests found that the products contain hydroxythiohomosildenafil, an analogue of sildenafil. All codes of the supplement are included in the recall. The products are blue capsules individually packaged on a cardboard blister card. They were sold nationwide in the U.S. to distributors who further distributed it through internet sales and at retail. There have not been any reports of adverse events related to this recall to date. If you purchased this product, return it to the place of purchase for a refund. For questions and more information, call 310-228-8965 Monday through Friday from 9:00 am to 4:00 pm … [Read more...]
New Chapter Probiotic Elderberry Recalled for Undeclared Soy
New Chapter, Inc. is recalling its Probiotic Elderberry dietary supplement because it may contain soy, one of the major food allergens. There have been no illnesses reported to date in connection with the consumption of this product. The product is Probiotic Elderberry in a 90 count amber glass jar with an outer cardboard carton. The carton is marked with Lot number 01230049332, expiration date 01/31/15, and UPC number 7-27783-00123-8. No other New Chapter products are affected by this recall. The product was distributed nationwide through retail stores, mail order, and direct delivery. If you purchased this product and are allergic to soy, return it to the place of purchase for a full refund. For questions and more information, call the company at 1-800-543-7279. … [Read more...]
Night Bullet Dietary Supplement Recalled for Hazardous Ingredient
Green Plant, Inc. is recalling a product sold over the counter as a dietary supplement under the brand name "Night Bullet" because it contains trace amounts of an FDA-approved drug. The finished product contained trace amounts of Sulfohydroxyhomosildenafil and Aminotadalafil, which are analogues of sildenafil. Sildenafil is an FDA-approved active pharmaceutical ingredient used to treat erectile dysfunction (ED), which makes this product an unapproved drug. The batch lot number of the recalled product is B43N032, the UPC number is 018505122233, and expiration date is 10/2015. It was sold nationwide between October 2012 and March 2013 to wholesalers and samples provided at trade shows. If you purchased this product, immediately discontinue use. Contact your doctor if you experience any … [Read more...]
Maxiloss Weight Advanced Softgels Recalled for Sibutramine
Olaax Corp. is recalling the company's dietary supplement sold under the brand name Maxiloss Weight Advanced Softgels because they contain undeclared Sibutramine. FDA testing found the drug in the supplement. Sibutramine was a previously approved controlled substance that was removed from the market in October 2010 because it can substantially increase blood pressure and/or pulse rate in some patients. This may be a significant health risk to anyone with a history of coronary artery disease, congestive heart failure, arrhythmias, or stroke. No illnesses or injuries have been reported to date. The recall includes all lot numbers and known to be counterfeit lot numbers of authentic lots. Any packaging types different from those listed are counterfeit. Any lot numbers not listed are … [Read more...]
