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Recalls & Warnings
ConsumerLab.com is keeping you informed with current product recalls and warnings.
Posted September 25, 2018
Seller of B Vitamins, Multis, Glucosamine & More Warned for Manufacturing Violations
These violations include to failure to establish a specification for any point, step, or stage in the manufacturing process where control is necessary to ensure the quality of the dietary supplement, and failure to prepare and follow a written master manufacturing record (MMR) for each unique formulation of dietary supplement manufactured, as required by federal regulations.
See ConsumerLab.com's Reviews of B Vitamin Supplements, Multivitamin Supplements, Milk Thistle Supplements, Joint Health Supplements, and Protein Powders, Shakes and Drinks for tests of related products.
See Related Warnings:
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Seller of Apple Cider Vinegar, Joint Supplements & More Warned for Drug Claims
FDA Warns Seller of Milk Thistle, Chromium, Joint Supplements & More for Manufacturing Violations
Seller of Male Enhancement, Prostate Supplements & More Warned for Drug Claims
To read the full 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.
