Great Plains Bentonite + Herbal Detox Capsules 60 capsules, packaged in PETE amber bottle, white plastic cap and tamper
Summary
The FDA issued a Class II for Great Plains Bentonite + Herbal Detox Capsules 60 capsules, packaged in PETE amb by Yerba Prima Inc. Reason: Potential contamination with Pseudomonas aeruginosa..
Details
Source
Food Recall
External ID
H-0050-2025
Action Date
2025-06-25
Status
Terminated
Category
food
Product Description
Great Plains Bentonite + Herbal Detox Capsules 60 capsules, packaged in PETE amber bottle, white plastic cap and tamper proof seal. Case GTIN code:100 46352 00518 5. Retail package UPC code: 0 46352 00518 8. Yerba Prima, Inc. 740 Jefferson Ave Ashland, Oregon 97520 USA
Lot/Code Info: Lot # 05051, Expiration Date 02/2028. Lot code breaks down as follows: 050 = 3 digits pertaining to the day of the year 5 = last number of the year 2025 1 = number of batch records issued of the day
Quantity Affected: 4985 bottles
Reason for Recall
Potential contamination with Pseudomonas aeruginosa.
Distribution
Distributed in AZ, CA, CO, CT, FL, GA, IA, IL, IN, KY, MD, MO, NC, NH, NV, NY, OH, PA, TX, VA, and WA.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-06-10
Company
Ashland, OR
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 56 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Yerba Prima Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Yerba Prima Inc have FDA actions?
This is the only FDA action we have on record for Yerba Prima Inc in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0050-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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