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Recalls & Warnings
ConsumerLab.com is keeping you informed with current product recalls and warnings.
Posted March 14, 2017
Court Shuts Down Supplement Manufacturer
The businesses share a location and have been inspected by the FDA four times since 2012. The inspections found the companies' products to be adulterated due to numerous violations of current Good Manufacturing Practices for dietary supplements, including failure to establish specifications for dietary supplement components and failure to test or verify that components and finished products meet product specifications for identity, purity, strength or composition. Follow-up inspections found that Floren repeatedly failed to make the corrections needed to comply with current Good Manufacturing Practices. Some products were also improperly labeled or promoted with drug claims.
In 2013, EonNutra issued a recall of its Growth Factor Complex containing deer antler velvet due to potential bacterial contamination.
Before the companies can resume operations, they will be required to recall their dietary supplements, hire labeling and good manufacturing practices experts and receive written permission from the FDA to resume operations.
See Related Warnings:
U.S. Department of Justice Files Permanent Injunction Against Supplement Manufacturer
Seller of Magnesium, Calcium, Silver and More Warned for Manufacturing Violations, Drug Claims
Federal Court Orders Dietary Supplement Distributor to Stop Selling Its Products
Federal Court Shuts Down Seller of Supplement Promoted for Herpes
To read the FDA's complete news release, 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.
