CLASS I Food recall · Reported 20 May 2026 · FDA Enforcement Report

Organic Peppermint Leaf Powder recalled by Pure Ground Ingredients

Pure Ground Ingredients is recalling Organic Peppermint Leaf Powder, distributed in California. The recall was initiated on 8 Apr 2026 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot#: PEPO-5234171TZM-PW-858Q, Best if used by: January 2028
Quantity recalled578 lbs (-pack size: boxes 16 @35 lbs and 1@18 lbs)

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
H-0853-2026
FDA event ID
98836
Recalling firm
Pure Ground Ingredients, Minden, NV
Classification
Class I
Status
Terminated
Recall initiated
8 Apr 2026
FDA classified
27 May 2026
Reported
20 May 2026
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Salmonella
Product category
Tea

Timeline

8 Apr 2026Recall initiated by company
20 May 2026Published in enforcement report+42 days
27 May 2026Classified by FDA+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Product has the potential to be contaminated with Salmonella.

Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.

Product as listed by the FDA

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

Where it was distributed

Distributed to CA.

California

Questions about this recall

Why was it recalled?

Product has the potential to be contaminated with Salmonella.

Which lots are affected?

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

Where was it sold?

Distributed to CA.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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