Data Foundry

Food recalls 2018

RED Vein Kratom POWDER — Class I food recall F-1523-2018

Terminated recall by Pdx Aromatics, reported 2018-03-28, distributed nationwide. Kraken Kratom, Phytoextractum, and Soul Speciosa products containing Red Vein Kratom Powder are recalled due t

Recall numberF-1523-2018
Product typeFood
ClassificationClass I
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmPdx Aromatics, Portland, OR, United States
Recall initiated2018-03-09
Classified2018-06-04
Reported by FDA2018-03-28
Terminated2018-09-13
DistributedNationwide (US)
Quantity18,572 packages
Reason classesmicrobial contamination
Pathogenssalmonella
Lot numbers20171201, 20171202, 20171203, 20171204, 20171205, 20171206, 20171207, 20171208, 20171209, 20171210, 20171211, 20171212, 20171213, 20171214, 20171215, 20171216, 20171217, 20171218, 20171219, 20171220, 20171221, 20171222, 20171223, 20171224, 20171225, 20171226, 20171227, 20171228, 20171229, 20171230, 20171231, 20180101, 20180102, 20180103, 20180104, 20180105, 20180106, 20180107, 20180108, 20180109 and 58 more

Product

RED Vein Kratom POWDER, sold under brand names Kraken Kratom, Phytoextractum, and Soul Speciosa. The powder is packaged in plastic heat sealed pouches. Each package sold in 28 grams (1 ounce), 56 grams (2 ounces), and 112 grams (4 ounces). The varieties under each brand include: -Maeng Da Thai Kratom Powder (Horn Red) -Red Dragon Kratom Powder -Red Vein Borneo Kratom Powder -Red Vein Sumatra Kratom Powder -Red Vein Thai Kratom Powder -Super Indo Kratom Powder

Reason for recall

Kraken Kratom, Phytoextractum, and Soul Speciosa products containing Red Vein Kratom Powder are recalled due to potential contamination with Salmonella.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-1523-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.