CLASS I Drug recall · Reported 18 Jul 2018 · FDA Enforcement Report

Gaia Kratom (mitragyna speciosa) powder recalled by Gaia Ethnobotanical

Gaia Ethnobotanical is recalling Gaia Kratom (mitragyna speciosa) powder, Yellow Vietnam packages, Gaia Ethnobotanical.com, distributed nationwide in the US. The recall was initiated on 20 Jun 2018 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot # 0102031800
Quantity recalledunknown

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-1016-2018
FDA event ID
80343
Recalling firm
Gaia Ethnobotanical, Henderson, NV
Classification
Class I
Status
Terminated
Recall initiated
20 Jun 2018
FDA classified
26 Jul 2018
Reported
18 Jul 2018
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Salmonella

Timeline

20 Jun 2018Recall initiated by company
18 Jul 2018Published in enforcement report+28 days
26 Jul 2018Classified by FDA+8 days

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

Reason for recall

Microbal Contamination of Non-Sterile Product; FDA analysis found salmonella contamination

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

Gaia Kratom (mitragyna speciosa) powder, Yellow Vietnam, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com

Where it was distributed

Nationwide.

Nationwide

Questions about this recall

Is Gaia Kratom (mitragyna speciosa) powder, Yellow Vietnam packages, Gaia Ethnobotanical.com recalled?

Yes. Gaia Ethnobotanical recalled Gaia Kratom (mitragyna speciosa) powder, Yellow Vietnam packages, Gaia Ethnobotanical.com on 20 Jun 2018. The recall is Class I and its status is Terminated. Recall number D-1016-2018.

Why was it recalled?

Microbal Contamination of Non-Sterile Product; FDA analysis found salmonella contamination

Which lots are affected?

Lot # 0102031800

Where was it sold?

Nationwide.

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

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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