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Recalls & Warnings
ConsumerLab.com is keeping you informed with current product recalls and warnings.
Posted November 21, 2013
Weight Loss Supplement Recalled
Fluoxetine is an FDA approved selective serotonin reuptake inhibitor (SSRI) drug prescribed to treat depression, anxiety, and other conditions. SSRI drugs are associated with serious side effects including suicidal thinking, abnormal bleeding, and seizures, and can interact with other common medications such as aspirin and ibuprofen, which can cause ventricular arrhythmia or sudden death.
Recalled Adipotrim XT was sold directly to customers in Deseo Rebajar offices in Fajardo, Caguas and Bayamon, Puerto Rico, and on the company's website www.deseorebajar.com. It is packaged in 30-count plastic bottles labeled with lot number #052012.
(See ConsumerLab.com's Reviews of Weight Loss Supplements and Sexual Enhancement Supplements for tests of related products.)
Consumers who have purchased this supplement 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 Related Warnings:
FDA Warns of Five More Weight Loss Supplements Containing Undeclared Drugs
Weight Loss Supplement Found to Contain Drugs
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
For more about this 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.
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.
