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Recalls & Warnings
ConsumerLab.com is keeping you informed with current product recalls and warnings.
Posted December 26, 2023
Total Body Nutrition, TBN Labs, and Loud Muscle Science Banned from Selling Adulterated and Misbranded Dietary Supplements
The permanent injunction was filed in the U.S. District Court for the Eastern District of New York. According to a complaint filed at the request of the FDA, Islam and the companies violated the Federal Food, Drug and Cosmetic Act (FDCA) by manufacturing and distributing dietary supplements without establishing product specifications for finished batches, without testing the finished batches to verify that they met product specifications, and without testing dietary ingredients used in supplements to verify their identity. The companies were previously warned for manufacturing violations found during facility inspection in 2017, and for undeclared stimulant drugs in products in 2016 and 2019. In 2022, Loud Muscle issued a recall of its sexual enhancement products, which were found to contain undeclared prescription drugs in 2022.
“Dietary supplement manufacturers and distributors have an important responsibility to ensure product quality and safety,” Principal Deputy Assistant Attorney General Brian M. Boynton stated in a news release issued by the Federal Trade Commission (FTC) about the settlement. “The Justice Department will continue to work closely with the FDA and take action against manufacturers and distributors who fail to abide by laws designed to protect public health.”
For tests of related products, see ConsumerLab’s Reviews of Weight Loss Supplements, Fish Oil Supplements, and Sexual Enhancement Supplements.
For more information, use the link below.
District Court Enjoins New York and Delaware Companies from Manufacturing and Distributing Adulterated and Misbranded Dietary Supplements
See related recalls and warnings:
Total Body Nutrition Warned for Banned Stimulant in Supplements
FDA Warns of Stimulant Methylsynephrine In Supplements
DMHA and Phenibut Are Not Permitted in Dietary Supplements, Warns FDA
Male Enhancement Supplements Sold on Amazon Recalled
Organifi Settles Charges of Unsupported Claims
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.
Please complete the form below as accurately as possible. You may need to check the label on the drug.
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