CLASS I Food recall · Reported 16 May 2018 · FDA Enforcement Report

Dragon Bali Kratom Powder recalled by Maya Distribution

Maya Distribution is recalling Dragon Bali Kratom Powder, distributed in 8 states. The recall was initiated on 20 Mar 2018 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesunknown
Quantity recalledunkown

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-1461-2018
FDA event ID
79853
Recalling firm
Maya Distribution, Salt Lake City, UT
Classification
Class I
Status
Terminated
Recall initiated
20 Mar 2018
FDA classified
15 May 2018
Reported
16 May 2018
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Salmonella
Product category
Energy Drinks

Timeline

20 Mar 2018Recall initiated by company
15 May 2018Classified by FDA+56 days
16 May 2018Published in enforcement report+1 day

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

Reason for recall

Samples collected by public health officials found the presence of Salmonella.

Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.

Product as listed by the FDA

Dragon Bali Kratom Powder: 60g Bottle. Dragon Bali Kratom Capsules in bottles:200 ct 500mg, 80 ct x 500, 40 ct x 500mg and 20 ct x 500 mg pouch.

Where it was distributed

Recalled product was distributed to retail stores in AZ, IA, ID, IL, KS, MI, UT, and WY.

ArizonaIowaIdahoIllinoisKansasMichiganUtahWyoming

Questions about this recall

Is Dragon Bali Kratom Powder recalled?

Yes. Maya Distribution recalled Dragon Bali Kratom Powder on 20 Mar 2018. The recall is Class I and its status is Terminated. Recall number F-1461-2018.

Why was it recalled?

Samples collected by public health officials found the presence of Salmonella.

Which lots are affected?

unknown

Where was it sold?

Recalled product was distributed to retail stores in AZ, IA, ID, IL, KS, MI, UT, and WY.

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 I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

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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