Kratom capsules labeled in the following ways: 1) Divinity Kratom 10 Capsule Dietary…
Recalling firm: Divinity Product Distribution LLC
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…
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Sep 14, 2018.
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FDA code information
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Full FDA record and distribution details
Original product description
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;
Original FDA recall reason
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;
Recall details
- Recall number
- F-1020-2018
- Event ID
- 79212
- FDA status
- Terminated
- Initiated
- Feb 9, 2018
- Reported
- Apr 25, 2018
- Classified
- Apr 13, 2018
- Terminated
- Sep 14, 2018
- Quantity
- Not provided
- Location
- Grain Valley, MO, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Telephone
Where it was distributed
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
Data updated September 16, 2026. View official FDA data ↗
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