Kratom capsules labeled in the following ways: 1) Divinity Kratom 10… — Class II food recall F-1020-2018
Terminated recall by Divinity Product Distribution LLC, reported 2018-04-25, distributed in AK, AL, AR, AZ, CA, CO, CT, DC…. The firm's dietary supplement products contain kratom (Mitragyna speciosa), a new dietary ingredient for which
| Recall number | F-1020-2018 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Divinity Product Distribution LLC, Grain Valley, MO, United States |
| Recall initiated | 2018-02-09 |
| Classified | 2018-04-13 |
| Reported by FDA | 2018-04-25 |
| Terminated | 2018-09-14 |
| Distributed | AK, AL, AR, AZ, CA, 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, UT, VA, WA, WI, WV |
| Countries outside the US | AT, CA, GB |
Product
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;
Reason for recall
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;
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-1020-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.