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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Food
Food & Beverages/Dietary Supplements

Yerba Prima Bentonite + Herbal Detox Recalled for Pseudomonas Contamination

Agency Publication Date: June 17, 2025
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Summary

Yerba Prima Inc has recalled approximately 4,985 bottles of Great Plains Bentonite + Herbal Detox capsules (60-count) due to potential contamination with the bacteria Pseudomonas aeruginosa. The product is packaged in amber plastic bottles with white caps and tamper-proof seals. No illnesses or injuries have been reported to date in connection with this recall.

Risk

The product may be contaminated with Pseudomonas aeruginosa, a bacterium that can cause serious infections. These infections are particularly dangerous for individuals with weakened immune systems or specific underlying health conditions.

What You Should Do

  1. The recalled product is Yerba Prima Great Plains Bentonite + Herbal Detox (60 capsules) sold in PETE amber bottles with white plastic caps and tamper-proof seals.
  2. Check the bottle label for lot number 05051 and an expiration date of 02/2028. The product also features retail package UPC 046352005188 and Case GTIN 10046352005185.
  3. Return the product to the place of purchase for a full refund, throw it away, or contact Yerba Prima Inc for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 if you have additional questions regarding this recall.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Return the product to the place of purchase for a full refund, or contact the manufacturer or supplier for further instructions
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: Great Plains Bentonite + Herbal Detox (60 capsules)by Yerba Prima
Variants: 60 capsules
UPC Codes:
046352005188
Lot Numbers:
05051 (Exp 02/2028)
GTIN:
10046352005185

Packaged in PETE amber bottle, white plastic cap and tamper proof seal. Lot 050 corresponds to day 50 of the year 2025.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97056
Status: Resolved
Manufacturer: Yerba Prima Inc
Sold By: Retail stores
Manufactured In: United States
Units Affected: 4985 bottles
Distributed To: Arizona, California, Colorado, Connecticut, Florida, Georgia, Iowa, Illinois, Indiana, Kentucky, Maryland, Missouri, North Carolina, New Hampshire, Nevada, New York, Ohio, Pennsylvania, Texas, Virginia, Washington

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.