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Lower risk Food recall · FDA · Published January 22, 2018

Mountain Rose Prickly Ash Bark Powder Recall: Salmonella Contamination Risk

Mountain Rose Inc recalls Prickly Ash Bark Powder herbal supplements due to potential Salmonella contamination. Consumers should check product labels for lot #23574-P and take appropriate action.

🇺🇸 FDA recall #F-0757-2018FoodMountain Rose ›
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Recalling firmMountain Rose Inc4020 Stewart Rd · Eugene, OR 97402-5408
✎ GovInfoNow plain-language explainer

What happened, in plain English

Mountain Rose Inc is recalling Prickly Ash Bark Powder herbal supplements because they may contain Salmonella bacteria. This contamination could cause foodborne illness if the product is consumed. Read more at govinfonow.com/recall/19738-mountain-rose-prickly-ash-bark-powder-recall-salmonella-contamination-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/19738-mountain-rose-prickly-ash-bark-powder-recall-salmonella-contamination-risk · Updated October 7, 2026 · FDA enforcement record: FDA #F-0757-2018

Cite this page

“Mountain Rose Prickly Ash Bark Powder Recall: Salmonella Contamination Risk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19738-mountain-rose-prickly-ash-bark-powder-recall-salmonella-contamination-risk. Based on FDA recall #F-0757-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0757-2018%22&limit=1).

Why it’s dangerous

Salmonella is a bacterium that can cause food poisoning, leading to symptoms like diarrhea, fever, and abdominal cramps. Contaminated products pose a risk if ingested, particularly for individuals with compromised immune systems.

Who’s affected

Anyone who purchased Prickly Ash Bark Powder from Mountain Rose Inc, especially those who have consumed the product. People with weakened immune systems are at higher risk of foodborne illness.

How to tell if you have this one

Check for the product label that says 'Prickly Ash Bark Powder' with the manufacturer name 'Mountain Rose Herbs' and location 'Eugene, OR 97402'. The lot number is 23574-P.

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

What to do — step by step

  1. Check Product Label

    Look for the label that states 'Prickly Ash Bark Powder' with the manufacturer name 'Mountain Rose Herbs' and location 'Eugene, OR 97402'.

Where it went and when

Where it was distributed

Distributed in 29 states.

Alaska: yesAKMaine: not listedMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: not listedRIMassachusetts: not listedMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: not listedSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: not listedCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: not listedMOKentucky: yesKYWest Virginia: not listedWVVirginia: yesVAMaryland: not listedMDDelaware: not listedDEArizona: yesAZNew Mexico: not listedNMKansas: not listedKSArkansas: yesARTennessee: not listedTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: yesGAHawaii: not listedHITexas: yesTXFlorida: yesFL

FDA distribution: “distributed in AK, AR, AZ, CA, CO , FL, GA, IA, IL, IN, KY, MI, NC, NE, NH, NJ, NS, NV, NY, OH, OR, PA, SC, TX, UT, VA, VT, WA, WI, and WY.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Alaska, Arizona, Arkansas, California, Colorado, Florida, Georgia, Illinois, Indiana, Iowa, Kentucky, Michigan, Nebraska, Nevada, New Hampshire, New Jersey, New York, North Carolina, Ohio, Oregon, Pennsylvania, South Carolina, Texas, Utah, Vermont, Virginia, Washington, Wisconsin, Wyoming.

Recall timeline

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

1. Firm started the recall: Jan 22, 201812. FDA classified it Class I: Feb 5, 201823. Published in FDA’s Enforcement Report: Feb 14, 201834. FDA terminated the recall: May 1, 201842018
  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.

✎ GovInfoNow

Questions people ask

Is this product safe to use?

The product is recalled due to potential Salmonella contamination, so it is not safe to consume. Consumers should stop using it and follow the recall instructions.

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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-0757-2018 (January 22, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0757-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on October 7, 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