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Class II: temporary or reversible health riskTerminated

Divinity Product Distribution Kratom capsules labeled in the following Recall

Kratom capsules labeled in the following ways: 1) Divinity Kratom 10 Capsule Dietary Su…

Divinity Product Distribution LLC · Grain Valley, MO

Risk level
Class II
Reported by FDA
Apr 25, 2018
Recall ID
F-1020-2018
Check your lot numberHow we source this data

Summary

Divinity Product Distribution recalled Kratom capsules labeled in the following starting Feb 9, 2018. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-1020-2018 on Apr 25, 2018. 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;. Status: Terminated.

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

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;

Lot numbers, UPCs & expiration codes

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

Where it was 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 to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-1020-2018
Classification
Class II
Status
Terminated
Recall initiated
Feb 9, 2018
FDA report date
Apr 25, 2018
Recall type
Voluntary: Firm initiated
Recalling firm
Divinity Product Distribution LLC

Original FDA data

Every field from FDA enforcement report F-1020-2018, exactly as published.

Show all FDA fields
City
Grain Valley
State
MO
Status
Terminated
Country
United States
Event ID
79212
Address
1119 Nw Valley Ridge Dr
Code information
All lot codes with expiration dates after 1/31/2018
Postal code
64029-9094
Report date
Apr 25, 2018
Product type
Food
Recall number
F-1020-2018
Classification
Class II
Recalling firm
Divinity Product Distribution LLC
Termination date
Sep 14, 2018
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;
Voluntary / mandated
Voluntary: Firm initiated
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;
Distribution pattern
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 initiation date
Feb 9, 2018
Initial firm notification
Telephone
Center classification date
Apr 13, 2018

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1020-2018, published Apr 25, 2018. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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