CLASS II Food recall · Reported 17 Jun 2015 · FDA Enforcement Report

Enhanced Leaf Powder in Ziploc-type freezer bags recalled

Nuevotanicals is recalling Enhanced Leaf Powder in Ziploc-type freezer bags in increments, no product label, distributed in 12 states. The recall was initiated on 1 Jul 2014 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesAll products manfactured since 6/1/2011
Quantity recalled71 kg

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-2417-2015
FDA event ID
68705
Recalling firm
Nuevotanicals, Fort Worth, TX
Classification
Class II
Status
Terminated
Recall initiated
1 Jul 2014
FDA classified
8 Jun 2015
Reported
17 Jun 2015
Type
Voluntary: Firm initiated
Customers notified by
Letter
Product category
Energy Drinks

Timeline

1 Jul 2014Recall initiated by company
8 Jun 2015Classified by FDA+342 days
17 Jun 2015Published in enforcement report+9 days

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

Reason for recall

This products contain Kratom.

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

Enhanced Leaf Powder in Ziploc-type freezer bags in 500 g increments, no product label; Bulk Raw (non-extracted) Kratom Leaf Powder in Ziploc-type freezer bags in 500 g increments, no product label.

Where it was distributed

Alabama, Arizona, California, Florida, Illinois, Nevada, New York, Ohio, Oklahoma, Oregon, Texas, and Virginia.

AlabamaArizonaCaliforniaFloridaIllinoisNevadaNew YorkOhioOklahomaOregonTexasVirginia

Questions about this recall

Is Enhanced Leaf Powder in Ziploc-type freezer bags in increments, no product label recalled?

Yes. Nuevotanicals recalled Enhanced Leaf Powder in Ziploc-type freezer bags in increments, no product label on 1 Jul 2014. The recall is Class II and its status is Terminated. Recall number F-2417-2015.

Why was it recalled?

This products contain Kratom.

Which lots are affected?

All products manfactured since 6/1/2011

Where was it sold?

Alabama, Arizona, California, Florida, Illinois, Nevada, New York, Ohio, Oklahoma, Oregon, Texas, and Virginia.

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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