CLASS II Food recall · Reported 25 Apr 2018 · FDA Enforcement Report

Kratom capsules labeled in the following ways recalled

Divinity Product Distribution is recalling Kratom capsules labeled in the following ways: Divinity Kratom Dietary Supplement, distributed in 44 states. The recall was initiated on 9 Feb 2018 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesAll lot codes with expiration dates after 1/31/2018

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-1020-2018
FDA event ID
79212
Recalling firm
Divinity Product Distribution, Grain Valley, MO
Brand
Kratom
Classification
Class II
Status
Terminated
Recall initiated
9 Feb 2018
FDA classified
13 Apr 2018
Reported
25 Apr 2018
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Product category
Energy Drinks

Timeline

9 Feb 2018Recall initiated by company
13 Apr 2018Classified by FDA+63 days
25 Apr 2018Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

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;

Products marketed as supplements sometimes contain undeclared prescription drug ingredients such as sildenafil or sibutramine. These can interact dangerously with other medicines.

Product as listed by the FDA

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;

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

AlaskaAlabamaArkansasArizonaCaliforniaColoradoConnecticutDistrict of ColumbiaDelawareFloridaGeorgiaIdahoIllinoisIndianaKansasKentuckyLouisianaMassachusettsMarylandMaine

Stores named: Walmart

Questions about this recall

Is Kratom capsules labeled in the following ways: Divinity Kratom Dietary Supplement recalled?

Yes. Divinity Product Distribution recalled Kratom capsules labeled in the following ways: Divinity Kratom Dietary Supplement on 9 Feb 2018. The recall is Class II and its status is Terminated. Recall number F-1020-2018.

Why was it 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 such ingredient does not present a significant or unreasonable risk of illness or injury;

Which lots are affected?

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

Where was it sold?

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

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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