Severity
Moderate
ModerateClass IITerminated
FDA Food recall · Reported June 25, 2025
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
Potential contamination with Pseudomonas aeruginosa.
Yerba Prima Inc recalled Great Plains Bentonite + Herbal Detox Capsules 60 capsules, packaged in PETE amber bottle… - a moderate-severity action.
Great Plains Bentonite + Herbal Detox Capsules 60 capsules, packaged in PETE amber bottle… was recalled by Yerba Prima Inc in June 25, 2025. Reason: Potential contamination with Pseudomonas aeruginosa.. Check the official notice for the remedy. Verify recall #H-0050-2025 with the FDA Food before acting.
The recall
Yerba Prima Inc issued this moderate-severity FDA Food recall-Potential contamination with Pseudomonas aeruginosa..
- Moderate
- severity level
- Class II
- classification
- June 25, 2025
- reported
Sourced from official FDA Food enforcement records. Verify recall #H-0050-2025 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #H-0050-2025) was formally reported on June 25, 2025, with the manufacturer initiating the action on June 10, 2025. It is classified under Moderate severity (Class II), with a current status of Terminated. Yerba Prima Inc is listed as the recalling firm, operating out of Ashland, OR. Federal records list the affected scope as 4985 bottles.
The documented reason for this recall is: Potential contamination with Pseudomonas aeruginosa. Distribution data in the federal record shows the product reached: Distributed in AZ, CA, CO, CT, FL, GA, IA, IL, IN, KY, MD, MO, NC, NH, NV, NY, OH, PA, TX, VA, and WA.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Children & Baby Products recalls over time
Where this recall sits in its category - 3,731 children & baby products recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
4985 bottles
Related Recalls
6
0 from same agency
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
Reason for recall
Potential contamination with Pseudomonas aeruginosa.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | H-0050-2025 |
| Date reported | June 25, 2025 |
| Date initiated | June 10, 2025 |
| Recalling firm | Yerba Prima Inc |
| Firm location | Ashland, OR |
| Affected scope | 4985 bottles |
| 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. |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (H-0050-2025) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Yerba Prima Inc. Units affected: 4985 bottles.
Why was this product recalled? ▼
Potential contamination with Pseudomonas aeruginosa.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on June 25, 2025. Severity: Moderate. Recall number: H-0050-2025.
Where was the recalled product distributed? ▼
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..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (H-0050-2025) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
Nearby Recalls in This Category
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported June 25, 2025. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.