This ingredient, used as a stimulant, and for weight loss is potentially dangerous to health.
San Diego, CA (PRWEB) August 13, 2014
AttorneyOne.com, a recognized authority on law, update the website daily regarding all the latest information from the FDA on appetite control capsules.
The FDA informed consumers on August 7 that two lots of RegeneSlim appetite control capsules, by Regeneca Worldwide a division of VivaCeuticals Inc., were recalled due to presence of DMAA.
The reason for the recall is that, according to the Agency’s analysis, the product contains DMAA (also known as 1,3-dimethylamylamine, methylhexanamine, or geranium extract.) This ingredient, used as a stimulant, and for weight loss is potentially dangerous to health; it can narrow blood vessels and arteries leading to a rise in blood pressure or other cardiovascular problems like tightening in the chest, arrhythmias, shortness of breath, and heart attack.
The affected lots are: lot # EX0616R15814 and lot #11414RE5516.
Taking into consideration the latest developments, AttorneyOne.com monitor daily and update the website providing accurate information on all relevant FDA safety alerts. Sean Burke, director of Media Relations at AttorneyOne.com, adds “we are determined to keep an eye on FDA announcements concerning appetite control capsules and inform the public. For that reason", he continues, "our focus should squarely fall on investigating these safety alerts and getting the word out.”
As the FDA recommends “Consumers who have purchased affected RegeneSlim lot numbers are advised to immediately stop using the product and return it to the place of purchase.” And the Agency adds “Consumers should contact their physician or healthcare provider if they experience any problems that may be related to taking or using RegeneSlim.”
AttorneyOne.com has further information on appetite control capsules at the website including latest major drug, medical products, and food law news.
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