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Recalls & Warnings
ConsumerLab.com is keeping you informed with current product recalls and warnings.
Posted April 26, 2015
FDA Identifies More Products Listing Synthetic Amphetamine
The warnings follow a study published on April 7 2015 which reported the presence of BMPEA in eleven sports and weight loss products (including Fastin-XR, one of the products listed below).
The FDA stated in its warnings that BMPEA is not a legal dietary supplement ingredient and identified the following products as listing the ingredient on their labels:
- Fastin-XR,Fastin Rapid Release, and Lipodrene Extended Release by Hi-Tech Pharmaceuticals, Inc.
- Phoenix Extreme by Better Body Sports, LLC
- CORE BURNER Watermelon powder by Human Evolution Supplements, Inc.
- Critical FX and Sudden Impact by Train Naked Labs LLC
- Conquer (Fruit Punch Slam and Raspberry Lemonade flavors) by iForce Nutrition
For a list of other products found to contain BMPEA, plus our tests of related products, see ConsumerLab.com's Reviews of Weight Loss Supplements and Muscle Enhancers.
See Related Warnings:
Does Your Weight Loss or Sports Supplement Contain Synthetic Amphetamine?
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.
