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Stop using now Food recall · FDA · Published April 8, 2026

Pure Ground Ingredients Recalls Organic Peppermint Leaf Powder Due to Salmonella Risk

Pure Ground Ingredients recalls Organic Peppermint Leaf Powder due to potential Salmonella contamination. Check lot PEPO-5234171TZM-PW-858Q.

🇺🇸 FDA recall #H-0853-2026FoodPure Ground Ingredients ›
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Recalling firmPure Ground Ingredients, Inc.2535 Business Pkwy · Minden, NV 89423-8931
✎ GovInfoNow plain-language explainer

What happened, in plain English

Pure Ground Ingredients, Inc. is recalling Organic Peppermint Leaf Powder because the product has the potential to be contaminated with Salmonella. The recall affects approximately 578 pounds of product distributed to California. This is a Class I recall, indicating a serious health risk where use could cause serious adverse health consequences or death. Read more at govinfonow.com/recall/6557-pure-ground-ingredients-recalls-organic-peppermint-leaf-powder-due-to.

Source Summary by GovInfoNow · govinfonow.com/recall/6557-pure-ground-ingredients-recalls-organic-peppermint-leaf-powder-due-to · Updated October 9, 2026 · Official notice: FDA #H-0853-2026

Cite this page

“Pure Ground Ingredients Recalls Organic Peppermint Leaf Powder Due to Salmonella Risk.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/6557-pure-ground-ingredients-recalls-organic-peppermint-leaf-powder-due-to. Based on FDA recall #H-0853-2026.

Why it’s dangerous

Salmonella is a bacterium that can cause foodborne illness. Ingestion of contaminated peppermint leaf powder may lead to symptoms such as fever, diarrhea, abdominal cramps, and vomiting, which can be severe or life-threatening for vulnerable populations.

Who’s affected

Consumers and tea/food manufacturers who purchased wholesale bulk Organic Peppermint Leaf Powder in California are affected. Individuals with weakened immune systems, the elderly, infants, and pregnant women are at higher risk for serious infection from Salmonella.

How to tell if you have this one

Check if you have Pure Ground Ingredients Organic Peppermint Leaf Powder sold in wholesale bulk boxes with a poly liner. Specifically look for Lot Number PEPO-5234171TZM-PW-858Q and a 'Best if used by' date of January 2028. The product was distributed to California.

  • Brand
    Pure Ground Ingredients
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop Using the Product

    Do not consume or use the recalled Organic Peppermint Leaf Powder due to the potential Salmonella contamination.

  2. Discard or Return Product

    The record does not specify a return or refund process, so consumers should dispose of the product safely.

Where it went and when

Where it was distributed

Distributed in California.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: yesCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “Distributed to CA.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: California.

Recall timeline

FDA terminated this recall 3 months after the firm started it.

1. Firm started the recall: Apr 8, 202612. Published in FDA’s Enforcement Report: May 20, 202623. FDA classified it Class I: May 27, 202634. FDA terminated the recall: Jul 10, 202642026
  1. Firm started the recall
  2. Published in FDA’s Enforcement Report
  3. FDA classified it Class I
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #H-0853-2026 (April 8, 2026)
  • Plain-language summary written by qwen3.6:35b-a3b on October 9, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA