RecallRadar
FDA · FoodClass I

Pure Ground Ingredients, Inc. food recall: Pure Ground Ingredients-Organic Peppermint Leaf Powder. wholesale bulk

SalmonellaMicrobial contamination

Key facts

Agency
U.S. Food and Drug Administration (FDA)
Program
Food
Classification
Class I
Status
Terminated
Event ID
98836
Recall initiated
Apr 8, 2026
Classified by FDA
May 27, 2026
Posted in Enforcement Report
May 20, 2026
Terminated
Jul 10, 2026
Recalling firm
Pure Ground Ingredients, Inc.
Firm location
Minden, NV, United States
Initiated by
Voluntary: Firm initiated
Firm notified customers by
Telephone
Products in this event
1

What to do

Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.

View the official FDA record ↗

Reason for recall

Product has the potential to be contaminated with Salmonella.

What the classification means

  • Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.

About this recall

The firm started this recall on Apr 8, 2026. FDA classified it 49 days later, on May 27, 2026. Distribution reported by FDA: Distributed to CA. Pure Ground Ingredients, Inc. has 3 recalls in our records.

Recalled products (1)

  • H-0853-2026 Class I Terminated

    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

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

    Quantity: 578 lbs (-pack size: boxes 16 @35 lbs and 1@18 lbs)

Source and freshness

Source
U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
Official notice
FDA Enforcement Report, event 98836
Raw record
openFDA API (JSON)
Dataset last updated by FDA
Nov 3, 2026
Imported by RecallRadar
Nov 4, 2026

Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.