Class IITerminated in FDA datasetRecall initiated Feb 9, 2018

Kratom powder labeled in the following ways 1) Enhance Your Life, Kratom Essence Maeng Da…

Recalling firm: Divinity Product Distribution LLC

Why it was recalled

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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ProductKratom 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
Package size15 g

FDA code information

All lot codes with expiration dates after 1/31/2018

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Full FDA record and distribution details

Original product description

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

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-1021-2018
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

FDA source record · F-1021-2018

Data updated September 16, 2026. View official FDA data ↗

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