Data Foundry

Food recalls 2018

WHITE VEIN Kratom POWDER — Class I food recall F-1524-2018

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

Recall numberF-1524-2018
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)
Quantity4,676 packages
Reason classesmicrobial contamination
Pathogenssalmonella
Lot numbers20180216, 20180217, 20180218, 20180219, 20180220, 20180221, 20180222, 20180223, 20180224, 20180225, 20180226, 20180227, 20180228, 20180301, 20180302, 20180303, 20180304, 20180305, 20180306, 20180307, 20180308

Product

WHITE 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), 112 grams (4 ounces), and 225 grams. The varieties under each brand include: Kraken Kratom Maeng Da Thai Kratom Powder (White Vein) Kraken Kratom White Vein Borneo Kratom Powder Kraken Kratom White Vein Sumatra Powder Phytoextractum White Maeng Da Powder (including 225 g) Phytoextractum White Borneo Powder (including 225 g) Phytoextractum White Vein Sumatra Powder Soul Speciosa Borneo Kratom Powder (White Vein) Soul Speciosa Sumatra Kratom Powder (White Vein)

Reason for recall

Kraken Kratom, Phytoextractum, and Soul Speciosa products containing WHITE 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-1524-2018. 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.