FDA recall, , High risk
Pure Ground Ingredients-Organic Peppermint Leaf Powder
Organic Peppermint Leaf Powder may be contaminated with Salmonella.
Recall ended Jul 10, 2026. Still check yours.
Summary by Recall Canary from the FDA notice
What happened
Pure Ground Ingredients, Inc. of Minden, Nevada, recalled Pure Ground Ingredients-Organic Peppermint Leaf Powder in wholesale bulk because the product has the potential to be contaminated with Salmonella. The recall, which the company began on April 8, 2026, was added to the FDA's Enforcement Report on May 11, 2026, and classified on May 27, 2026. The product was sold in California.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for food recalls:
- Return it to the store where you bought it, or throw it away.
- Don't give it to anyone else, such as a food bank, or to a pet.
Is your container affected?
Compare the details below with your product and check the FDA notice to confirm whether it is affected.
Product details
Pure Ground Ingredients-Organic Peppermint Leaf Powder. wholesale bulk;
tea/food manufacturers. Closed container stored in a cool settings at ambient/room temperature, free of direct sunlight. Packaging: Box with poly liner. Net wt: total produced 581 lbs. Firm Name/Address: Pure Ground Ingredients;
2535 Business Parkway, Minden NV 89423- Lot code
- PEPO-5234171TZM-PW-858Q
Recall details
- Company began the recall
- Sold in
- Company
- Pure Ground Ingredients, Inc.Minden, Nevada
- Hazard
- Salmonella
- Risk
High risk
There is a reasonable chance that eating it could cause serious health problems or death.
FDA Class I recall · How risk is rated
- Event ID
- 98836
- Recall number
- H-0853-2026
- Quantity recalled
- 581 lbs (-pack size: boxes 16 @35 lbs and 1@18 lbs)
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report
Listed on Recall Canary
In FDA's weekly enforcement report
Classified by FDA
Recall ended
Archived
