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Recalls & Warnings
ConsumerLab.com is keeping you informed with current product recalls and warnings.
Posted February 28, 2014
Weight Loss Supplement Contains Undeclared Drug
Sibutramine, the active ingredient in the obesity drug 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.
LV Shou Reduces Fat is packaged in white plastic bottles containing white and green capsules. It is available for sale to U.S. consumers through major online retailers and through the company's website, www.lvshou.us/Product.
The warning also included weight loss supplements STB Summit of the Thin Body S Woman Degreasing Burning Pill and Lightning 10.0+ Reduces Weight; however, these products do not appear to be available for sale to U.S. consumers.
(See ConsumerLab.com's Review of Weight Loss Supplements for tests of related products.)
See Related Warnings:
Weight Loss Supplement Recall Expanded to Include Additional Products
Weight Loss Supplement Containing Drug Recalled
FDA Warns Consumers Of Weight Loss Supplement Containing Undeclared Drug
Weight Loss Supplement Recalled Due To Undeclared Drug
FDA Seizes Weight Loss Supplements Containing Undeclared Drug
Rx Drugs Found in Weight Loss and Enhancement Supplements
Recall of "Slimming" Supplements Spiked with Drug
To read Health Canada's warning, 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.
Please complete the form below as accurately as possible. You may need to check the label on the product.
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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.
Please complete the form below as accurately as possible. You may need to check the label on the drug.
Thank you for submitting your report.
