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Recalls & Warnings
ConsumerLab.com is keeping you informed with current product recalls and warnings.
Posted January 03, 2022
Seller of Wormwood, Aloe Supplement Warned by FDA
On December 7, 2021, the FDA issued a warning letter for Western Herb Products, Inc. following an inspection of the company's manufacturing facility in Washington, which found the company's products to be adulterated because they were prepared, packed, or held in conditions that do not meet Current Good Manufacturing Practice (cGMP) for dietary supplements.
In addition, the company's Wormwood/Aloes dietary supplement was misbranded because the label of this product fails to identify the appropriate part of the plants from which the botanical dietary ingredient in the product is derived. The label also fails to declare the net quantity of contents on the principal display panel. According to the warning the product is adulterated because the company did not have written specifications to ensure purity, strength, and composition of the dietary supplement.
The company has 15 days to respond to the FDA in writing to explain the specific steps taken to address any violations.
Learn more about aloe juices, gels, and supplements in ConsumerLab's Aloe Juices, Gels, and Supplements Review.
For more information, use the link below.
Warning Letter: Western Herb Products, Inc.
See related recalls and warnings:
Seller of Prostate, Immune Supplements & More Warned for Manufacturing Violations
Seller of Aloe Products Warned for Claiming to Treat Joint Stiffness
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.
