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Lower risk Food recall · FDA · Published March 16, 2020

Mountain Rose Herbs Kudzu Root Recall: Salmonella Risk

Mountain Rose Herbs recalls kudzu root herbal supplements sold in clear plastic or poly-woven bags from 4 oz to 20 lbs due to potential Salmonella contamination.

🇺🇸 FDA recall #F-0892-2020FoodMountain Rose Herbs ›
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Recalling firmMountain Rose Inc. dba Mountain Rose Herbs4020 Stewart Rd · Eugene, OR 97402-5408
✎ GovInfoNow plain-language explainer

Mountain Rose Herbs is recalling kudzu root supplements sold in clear plastic or poly-woven bags weighing 4 ounces to 20 pounds because they may contain Salmonella. This poses a risk of foodborne illness if consumed. Read more at govinfonow.com/recall/15795-mountain-rose-herbs-kudzu-root-recall-salmonella-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/15795-mountain-rose-herbs-kudzu-root-recall-salmonella-risk · Updated October 5, 2026 · FDA enforcement record: FDA #F-0892-2020

Cite this page

“Mountain Rose Herbs Kudzu Root Recall: Salmonella Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/15795-mountain-rose-herbs-kudzu-root-recall-salmonella-risk. Based on FDA recall #F-0892-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0892-2020%22&limit=1).

The FDA announced on March 16, 2020, that Mountain Rose Inc. dba Mountain Rose Herbs is recalling Kudzu Root due to a potential Salmonella contamination. The firm initiated this voluntary Class I recall for products distributed nationwide in the U.S. and Canada.

How to tell if you have it

  • Brand: Mountain Rose Herbs
  • Product: Kudzu Root (Pueraria montana var. lobata)
  • Packaging: Clear plastic bag or poly-woven bags
  • Lot codes: 24247 and #24247-X
  • Sizes: Net weight ranges from 4 ounces to 20 pounds

The hazard

The product poses a Salmonella contamination risk. The FDA classified this as a Class I recall, indicating a reasonable probability that the food will cause serious adverse health consequences or death.

Context

GovInfoNow's records show Mountain Rose Inc. dba Mountain Rose Herbs has one other recall on record since July 18, 2019, including a Fennel Whole Seed recall for Salmonella contamination risk. Other recent recalls of similar products include Solina Garlic Herb Topping Recall (April 24, 2026), Bell Industries Zen Cleanse Blend Herbal Tea Recall (Nov. 24, 2025), and Celebration Herbals Senna Leaf Tea Recalled for Salmonella Risk (Nov. 25, 2025).

How to tell if you have this one

Check for kudzu root supplements labeled with 'Mountain Rose Herbs' in clear plastic or poly-woven bags, with net weights between 4 ounces and 20 pounds.

  • Brand
    Mountain Rose Herbs
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the product name 'Kudzu Root' and the label indicating 'Mountain Rose Herbs' in clear plastic or poly-woven bags.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “nationwide in the US and in Canada.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA terminated this recall 10 months after the firm started it.

1. Firm started the recall: Mar 16, 202012. FDA classified it Class I: Apr 10, 202023. Published in FDA’s Enforcement Report: Apr 22, 202034. FDA terminated the recall: Jan 6, 2021420202021
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report
  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 #F-0892-2020 (March 16, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0892-2020 to see it in context.
  • Plain-language summary written by qwen3:4b on October 5, 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