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Lower risk Food recall · FDA · Published March 21, 2018

Soap Kor: Herbalist Red MD Kratom Powder May Contain Salmonella

Soap Korner recalls Herbalist Red MD Kratom powder due to potential Salmonella contamination. Consumers should check lot numbers for affected products.

🇺🇸 FDA recall #F-1012-2018FoodSoap Korner ›
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Recalling firmSoap Korner3707 Parkmoor Village Dr, Suite#104 · Colorado Springs, CO 80917-6251
✎ GovInfoNow plain-language explainer

What happened, in plain English

Soap Korner is recalling Herbalist Red MD Kratom powder because it may be contaminated with Salmonella. This poses a risk of foodborne illness if consumed. Read more at govinfonow.com/recall/19523-soap-kor-herbalist-red-md-kratom-powder-may-contain-salmonella.

Source Summary by GovInfoNow · govinfonow.com/recall/19523-soap-kor-herbalist-red-md-kratom-powder-may-contain-salmonella · Updated October 7, 2026 · FDA enforcement record: FDA #F-1012-2018

Cite this page

“Soap Kor: Herbalist Red MD Kratom Powder May Contain Salmonella.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19523-soap-kor-herbalist-red-md-kratom-powder-may-contain-salmonella. Based on FDA recall #F-1012-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1012-2018%22&limit=1).

Why it’s dangerous

Salmonella is a bacteria that can cause food poisoning, leading to symptoms like diarrhea, fever, and abdominal cramps. Contaminated products may pose a risk if ingested.

Who’s affected

Anyone who purchased Soap Korner Herbalist Red MD Kratom powder from the manufacturer's website. Those with the highest risk are individuals who consume the product regularly.

How to tell if you have this one

Check for lot numbers: 1710508, N-6192017-4, or MR0120417-9 on the packaging. The product is sold online through soapkorner.com.

  • Brand
    Soap Korner
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Lot Number

    Look for lot numbers 1710508, N-6192017-4, or MR0120417-9 on the packaging.

How this recall unfolded

Recall timeline

FDA terminated this recall 7 months after the firm started it.

1. Firm started the recall: Mar 21, 201812. FDA classified it Class I: Apr 12, 201823. Published in FDA’s Enforcement Report: Apr 18, 201834. FDA terminated the recall: Oct 31, 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.

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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-1012-2018 (March 21, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1012-2018 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