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Lower risk Food recall · FDA · Published May 2, 2018

Badger Botanicals Recalls Green Suma Kratom for Potential Salmonella Risk

Badger Botanicals recalls Green Suma Kr: 250g bags made between Jan 2018 and Apr 2018 due to potential salmonella contamination. Consumers should check product dates and contact for details.

🇺🇸 FDA recall #F-1463-2018FoodBadger Botanicals ›
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Recalling firmBadger Botanicals LLC1086 N 450 W · Springville, UT 84663-5914
✎ GovInfoNow plain-language explainer

What happened, in plain English

Badger Botanicals is recalling Green Suma Kratom products from 2018 that may contain salmonella. This could cause food poisoning if consumed. Affected products were sold between January and April 2018. Read more at govinfonow.com/recall/19138-badger-botanicals-recalls-green-suma-kratom-for-potential-salmonella-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/19138-badger-botanicals-recalls-green-suma-kratom-for-potential-salmonella-risk · Updated October 7, 2026 · FDA enforcement record: FDA #F-1463-2018

Cite this page

“Badger Botanicals Recalls Green Suma Kratom for Potential Salmonella Risk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19138-badger-botanicals-recalls-green-suma-kratom-for-potential-salmonella-risk. Based on FDA recall #F-1463-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1463-2018%22&limit=1).

Why it’s dangerous

Salmonella is a bacteria that can cause food poisoning. If the Kratom products were contaminated during manufacturing, eating them could lead to illness.

Who’s affected

Anyone who purchased Green Suma Kratom 250g bags from Badger Botanicals between January 2018 and April 2018. People who have consumed the product may experience food poisoning symptoms.

How to tell if you have this one

Check for Green Suma Kratom 250g bags with a production date between January 1, 2018 and April 12, 2018. The product was sold by Badger Botanicals.

  • Brand
    Badger Botanicals
  • Category
    Food
FDA recall event · 4 products

All 4 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class I
  • Status
    Terminated
  • Distribution
    Nationwide
Recall numberProduct, codes & lotsQuantity
F-1462-2018Acadica Kratom: Red Suma 250g bags; Everything manufactured between 1/1/18 to 4/12/18.Unknown
F-1463-2018Acadica Kratom: Green Suma, 250g bags; Everything manufactured between 1/1/18 to 4/12/18.N/A
F-1464-2018Acadica Kratom: Red Hulu 2, 250g bags; Everything manufactured between 1/1/18 to 4/12/18.N/A
F-1465-2018Acadica Kratom: Green Hulu 2 Kratom, 250g bags; Everything manufactured between 1/1/18 to 4/12/18.N/A
Based on the official FDA remedy

What to do — step by step

  1. Check Product Date

    Look for the production date on the package, which should be between January 1, 2018 and April 12, 2018.

Where it went and when

Where it was distributed

Distributed nationwide.

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

Distributed nationwide.

Recall timeline

FDA terminated this recall 4 years after the firm started it.

1. Firm started the recall: May 2, 201812. FDA classified it Class I: May 15, 201823. Published in FDA’s Enforcement Report: May 16, 201834. FDA terminated the recall: Apr 19, 2022420182022
  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-1463-2018 (May 2, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1463-2018 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