RecallHawk
Class I Recall

Pure Ground Ingredients-Organic Peppermint Leaf Powder. wholesale bulk; tea/food manufacturers. Closed container stored

Pure Ground Ingredients, Inc.

Summary

The FDA issued a Class I for Pure Ground Ingredients-Organic Peppermint Leaf Powder. wholesale bulk; tea/food by Pure Ground Ingredients, Inc.. Reason: Product has the potential to be contaminated with Salmonella..

Details

Source

Food Recall

External ID

H-0853-2026

Action Date

2026-05-20

Status

Completed

Category

food

Product Description

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 Info: Lot#: PEPO-5234171TZM-PW-858Q, Best if used by: January 2028

Quantity Affected: 581 lbs (-pack size: boxes 16 @35 lbs and 1@18 lbs)

Reason for Recall

Product has the potential to be contaminated with Salmonella.

Distribution

Distributed to CA.

Type: Voluntary: Firm initiated

Recall Initiated: 2026-04-08

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 97 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

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 (Pure Ground Ingredients, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Pure Ground Ingredients, Inc. have FDA actions?

This is the only FDA action we have on record for Pure Ground Ingredients, Inc. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0853-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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