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Recalls & Warnings
ConsumerLab.com is keeping you informed with current product recalls and warnings.
Posted May 2, 2015
Drug Found in Two Weight Loss Supplements
Each was identified during an examination of international mail shipments:
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.
Consumers who have purchased these supplements should discontinue use immediately and contact their healthcare provider if they have experienced any adverse side effects. Consumers and healthcare providers are also encouraged to report any adverse reactions to the FDA's MedWatch Adverse Event Reporting Program.
(See ConsumerLab.com's Review of Weight Loss Supplements for tests of related products.)
See Related Warnings:
Five Weight Loss Supplements Recalled
Weight Loss Supplement Contains Hidden Drug
FDA Warns of Weight Loss Supplement Dangers
FDA Warns Consumers Not to Buy or Use Weight Loss Supplement
Weight Loss Supplements Recalled
FDA Warns Some Bee Pollen Products for Weight Loss Are Dangerous
Bee Pollen and Weight Loss Supplements Recalled
FDA Warns Consumers Not To Buy Or Use Weight Loss Supplement
Recall of "Bee Pollen" Supplement Found to Contain Drug
FDA Warns Consumers of Weight Loss and Body Reshaping Supplements Containing Controlled Substance
For more warnings and recalls, 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.
Thank you for submitting your report.
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.
