Gaia Kratom (mitragyna speciosa) powder, Purple 8-1, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com

Class I Terminated Reported 20180718 Gaia Ethnobotanical LLC

Gaia Ethnobotanical LLC recalled Gaia Kratom (mitragyna speciosa) powder, Purple 8-1, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com under a Class I classification, reported 20180718. Current status: Terminated.

Recall number
D-1004-2018
Recalling firm
Gaia Ethnobotanical LLC
Classification
Class I
Status
Terminated
Report date
20180718
Initiation date
20180620
Termination date
20220126

Reason for recall

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

Product description

Gaia Kratom (mitragyna speciosa) powder, Purple 8-1, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com

What Class I means

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

Current status

This recall has been terminated by the FDA, meaning the agency considers the action no longer necessary.

What to do if you have this product

If you hold this product, stop using it as directed by the recall notice and contact the pharmacy or prescriber that supplied it for a replacement or for disposal instructions. Do not rely on this page alone: confirm lot numbers against the official FDA enforcement report before taking action.

Other recalls by Gaia Ethnobotanical LLC

RecallProductClassificationStatusReported
D-1000-2018 Gaia Kratom (mitragyna speciosa) powder, Green MD, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com Class I Terminated 20180718
D-1015-2018 Gaia Kratom (mitragyna speciosa) powder, Yellow Thai, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com Class I Terminated 20180718
D-1008-2018 Gaia Kratom (mitragyna speciosa) powder, Red Horn, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com Class I Terminated 20180718
D-0997-2018 Gaia Kratom (mitragyna speciosa) powder, Green Horn, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com Class I Terminated 20180718
D-1010-2018 Gaia Kratom (mitragyna speciosa) powder, Red MD, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com Class I Terminated 20180718
D-1013-2018 Gaia Kratom (mitragyna speciosa) powder, White MD, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com Class I Terminated 20180718

Recent Class I recalls

RecallProductFirmStatusReported
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D-0850-2026 Dextrose Injection, USP, 70 %, 2000 mL bags, Rx Only, Baxter Healthcare Corporation Deerfield, IL, 60016, Made in USA, NDC 00338-0719-06 Baxter Healthcare Corporation Ongoing 20260916
D-0865-2026 Epinephrine Injection, USP, 30 mg/30 mL (1mg/mL), 30 mL-Multiple-Dose Vial, Rx Only, For Intravenous Infusion, intramuscular and Subcutaneous Use, AMERICAN REGENT INC., SHIRLEY, NY 11967. NDC 0517-3030-01 American Regent, Inc. Ongoing 20260916
D-0869-2026 0.9% Sodium Chloride Injection, USP, 100 mL Partial Fill in 150 mL PAB Container, Sterile, Rx only, B. Braun Medical Inc., Bethlehem, PA 18018 USA, NDC 0264-1800-32. B BRAUN MEDICAL INC Ongoing 20260916
D-0849-2026 0.9% Sodium Chloride Injection USP 500 mL, VIAFLEX Plastic Containers, with 24 units per case. Baxter Healthcare Corporation, Deerfield, IL, 60015, USA, Made in USA, NDC 0338-0049-03 Baxter Healthcare Corporation Ongoing 20260909
D-0851-2026 Glutathione 200 mg/mL, 30 mL sterile multidose vial, Each vial contains: Glutathione, Ascorbic Acid, Benzyl Alcohol & sterile water for injection, For IM or IV Injection Use Only, RX only, Optimal Balance Pharmacy, 2204 Cypress Creek Pkwy Suite F, Houston, TX 77090 OPTIMAL BALANCE PHARMACY Ongoing 20260909

Frequently asked questions

What product is affected by recall D-1004-2018?
Gaia Kratom (mitragyna speciosa) powder, Purple 8-1, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com The recalling firm is Gaia Ethnobotanical LLC.

How serious is a Class I recall?
Class I is the most serious FDA recall category. It means there is a reasonable probability that using the product will cause serious adverse health consequences or death.

What should I do with the recalled product?
Stop using it, check the lot number against the official notice, and return it or ask your pharmacy how to dispose of it. Speak to a healthcare professional if you have already used it and feel unwell.

Recall records are reproduced from the FDA enforcement report. Always confirm lot numbers and current guidance with the FDA or the recalling firm before acting.