Recall Ledger

Pure Ground Ingredients-Organic Peppermint Leaf Powder. wholesale bulk recall (Pure Ground Ingredients, Inc.)

FoodClass ITerminated

Summary: Pure Ground Ingredients, Inc. is recalling 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;. Reason: Product has the potential to be contaminated with Salmonella.

What is being recalled

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

Why

Product has the potential to be contaminated with Salmonella.

How serious is it

Class I is the most serious level: FDA considers there is a reasonable probability that using or being exposed to this product will cause serious health problems or death.

Where it was sold

Distributed to CA. (states named: California)

How to tell if yours is affected

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

What to do

Check the product name and the codes above against what you have. If they match, do not eat or use it. Throw it away or return it to the store where you bought it, and contact the recalling company with questions.

Recall facts

Recall numberH-0853-2026
CategoryFood
AgencyU.S. Food and Drug Administration (FDA)
SeverityClass I
StatusTerminated
Recall startedApril 8, 2026
ReportedMay 20, 2026
CompanyPure Ground Ingredients, Inc.
Company locationMinden, NV, United States
Initiated byVoluntary: Firm initiated
Quantity578 lbs (-pack size: boxes 16 @35 lbs and 1@18 lbs)

More recalls from Pure Ground Ingredients, Inc. · all food recalls · recalls from April 2026

Official FDA record