Divinity Kratom Capsules Recall: Risk of Illness from Inadequate Safety Data
Divinity Product Distribution LLC recalls Kratom capsules due to insufficient safety data for kratom. Consumers should check labels for specific product names and expiration dates after January 31, 2018.
Recall notice
The firm's dietary supplement products contain kratom (Mitragyna speciosa), a new dietary ingredient for which there is inadequate information to provide reasonable assurance that such ingredient does not present a significant or unreasonable risk of illness or injury;
Contact the company
What happened, in plain English
Divinity Product Distribution LLC is recalling Kratom capsules because there isn't enough safety information to ensure they won't cause illness or injury. This recall affects products labeled with specific names and sold with expiration dates after January 31, 2018. Read more at govinfonow.com/recall/19688-divinity-kratom-capsules-recall-risk-of-illness-from-inadequate-safety.
Source Summary by GovInfoNow · govinfonow.com/recall/19688-divinity-kratom-capsules-recall-risk-of-illness-from-inadequate-safety · Updated October 7, 2026 · FDA enforcement record: FDA #F-1020-2018
Cite this page
“Divinity Kratom Capsules Recall: Risk of Illness from Inadequate Safety Data.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19688-divinity-kratom-capsules-recall-risk-of-illness-from-inadequate-safety. Based on FDA recall #F-1020-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1020-2018%22&limit=1).
Why it’s dangerous
Kratom is a plant-based substance with limited safety data. The recall states that there isn't enough information to ensure it won't cause illness or injury, meaning the product might pose health risks.
Who’s affected
People who own or use Divinity Kratom capsules labeled with the product names mentioned in the recall. Those most at risk are individuals who consume kratom supplements without knowing the safety risks.
How to tell if you have this one
Check for capsules labeled 'Divinity Kratom 10 Capsule Dietary Supplement', 'Divinity Bali Kratom', or similar names. Products with expiration dates after January 31, 2018, are included in this recall.
- Brand
Divinity- Category
Food
All 2 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 II- Status
Terminated- Distribution
Product distributed to the following US states and countries: AK, AL, AR, Austria, AZ, CA, Canada, CO, CT, DC, DE, FL, GA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, ND, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, United Kingdom, UT, VA, WA, WI, and WV
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| F-1020-2018 | Kratom capsules labeled in the following ways: 1) Divinity Kratom 10 Capsule Dietary Supplement, Divinity Product LLC, Blue Springs, MO 64015; 2) Divinity Bali Kratom, 10PK Capsules; 3) Divinity Bali Kratom, 20PK Capsules; 4) Divinity Bali Kratom, 40PK Capsules;; All lot codes with expiration dates after 1/31/2018 | — |
| F-1021-2018 | Kratom powder labeled in the following ways 1) Enhance Your Life, Kratom Essence Maeng Da Mitragyna speciosa, 150 gras; 2) Bali Kratom, 15 g Powdered; 3) Bali Kratom, 30 g Powdered; 4) Bali Kratom, 60 g Powdered; 5) Bali Kratom, 120 g Powdered; 6) Botany Bay, 1 oz; All lot codes with expiration dates after 1/31/2018 | — |
What to do — step by step
Check Product Labels
Look for specific product names and expiration dates after January 31, 2018 to determine if your capsules are affected.
How this recall unfolded
Recall timeline
FDA terminated this recall 7 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- 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-1020-2018 (February 9, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1020-2018 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.