WHITE VEIN Kratom CAPSULES — Class I food recall F-1525-2018

Terminated recall by Pdx Aromatics, reported 2018-03-28, distributed nationwide. Kraken Kratom, Phytoextractum, and Soul Speciosa WHITE VEIN Kratom CAPSULES are recalled due to potential cont

Recall number	`F-1525-2018`
Product type	Food
Classification	Class I
Status	Terminated
Voluntary or mandated	Voluntary
Recalling firm	Pdx Aromatics, Portland, OR, United States
Recall initiated	2018-03-09
Classified	2018-06-04
Reported by FDA	2018-03-28
Terminated	2018-09-13
Distributed	Nationwide (US)
Quantity	1,097 packages
Reason classes	microbial contamination
Pathogens	salmonella
Lot numbers	`20180216`, `20180217`, `20180218`, `20180219`, `20180220`, `20180221`, `20180222`, `20180223`, `20180224`, `20180225`, `20180226`, `20180227`, `20180228`, `20180301`, `20180302`, `20180303`, `20180304`, `20180305`, `20180306`, `20180307`, `20180308`

Product

WHITE VEIN Kratom CAPSULES, sold under brand names Kraken Kratom, Phytoextractum, and Soul Speciosa. The capsules are packaged in plastic heat sealed pouches. Each package sold in 28 grams (1 ounce), 56 grams (2 ounces), 112 grams (4 ounces). The varieties under each brand include: Kraken Kratom White Vein Borneo Kratom Capsules Phytoextractum White Maeng Da Thai Capsules Soul Speciosa White Vein Borneo Kratom Capsules

Reason for recall

Kraken Kratom, Phytoextractum, and Soul Speciosa WHITE VEIN Kratom CAPSULES 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-1525-2018. 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.