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Recalls & Warnings
ConsumerLab.com is keeping you informed with current product recalls and warnings.
Posted August 20, 2016
Smart Lipo Weight Loss Supplement Found to Contain Undeclared Drugs
Sibutramine, the active ingredient in the obesity d rug Meridia, was removed from the U.S. market in October 2010 because it can substantially increase blood pressure and pulse rate in some individuals, and may present a significant risk for patients with a history of coronary artery disease, congestive heart failure, arrhythmias, or stroke. This drug may also interact, in life-threatening ways, with other medications a consumer may be taking.
Phenolphthalein, once an ingredient in some over-the-counter laxative products, was reclassified by the FDA in 1999 as "not generally recognized as safe and effective."
In addition, statements made about Smart Lipo on the product label, such as "Burns Fat," and "Suppresses Appetite" were found to be drug claims.
See ConsumerLab.com's Review of Weight Loss Supplements for tests of related products.
See Related Warnings:
"Super Herbs" Weight Loss Supplement Recalled
Ultimate Herbal Slimcaps Recalled
"Natureal" Weight Supplement Recalled
Weight and Enhancement Supplement Recall Expanded
Weight Supplement Found to Contain Drug
Five Weight Loss Supplements Recalled
Weight Loss Supplement Contains Hidden Drug
FDA Warns of Weight Loss Supplement Dangers
Recall of "Bee Pollen" Supplement Found to Contain Drug
FDA Warns Consumers of Weight Loss and Body Reshaping Supplements Containing Controlled Substance
For more about the recall, use the link below.
Report a Problem
If you have experienced an unexpected and adverse reaction to a dietary supplement, nutritional product, or generic drug, we would like to hear about it, as we may investigate the problem. Please select from one of these options:
Dietary Supplement or Nutritional Product Problem Report
If you believe that a dietary supplement (e.g., vitamin, mineral, or herbal supplement) or other nutritional product has caused an unexpected, adverse reaction, we would like to know about it. We are collecting and organizing this information and may publish it. We might test the product in the future. You may also want to report the problem to the U.S. FDA through their Safety Reporting Portal at https://www.safetyreporting.hhs.gov.
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Generic Drug Problem Report
If you believe that a generic drug has not acted like the original drug, we would like to know about it. We are collecting and organizing this information and may publish it. We might test the product in the future. You may also want to report the problem to the U.S. FDA through their MedWatch program at the FDA MedWatch website.
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