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Recalls & Warnings
ConsumerLab.com is keeping you informed with current product recalls and warnings.
Posted March 19, 2014
Maker of Herbal Capsules and Extracts Warned for Manufacturing Violations
These violations include failure to perform at least one appropriate test or examination to verify the identity of any component that is a dietary ingredient before use, and failure to establish product specifications for the purity, strength, and composition of finished batches of dietary supplement products.
See Related Warnings:
Maker of Menopause Blend and Other Supplement Ingredients Warned by FDA of Violations
Supplement Company Warned For Numerous Manufacturing Violations
CoQ10 and Carnitine Supplement Company Warned For Manufacturing Violations
Maker of Sexual Enhancement Supplement Warned for Manufacturing Violations
Maker of Energy, Weight Loss, Sleep and Vitamin D Supplements Warned for Manufacturing Violations
To read the FDA's warning letter, 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.
