Class ITerminated in FDA datasetMar 9, 2018

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…

Recalling firm: Pdx Aromatics

Why it was recalled

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

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The exact 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)

Check the codes

Compare these FDA-provided codes, lot numbers or dates with the product you have.

Match the product, size and code together. A similar name alone does not identify your batch.

Original FDA code information

The lot code represents the day packaged. The first four digits are the year, followed by two digits for the month, followed by two digits for the day. LOT 20180216 LOT 20180217 LOT 20180218 LOT 20180219 LOT 20180220 LOT 20180221 LOT 20180222 LOT 20180223 LOT 20180224 LOT 20180225 LOT 20180226 LOT 20180227 LOT 20180228 LOT 20180301 LOT 20180302 LOT 20180303 LOT 20180304 LOT 20180305 LOT 20180306 LOT 20180307 LOT 20180308

Recall details

Recall number
F-1524-2018
Event ID
79480
FDA status
Terminated
Initiated
Mar 9, 2018
Reported
Mar 28, 2018
Classified
Jun 4, 2018
Terminated
Sep 13, 2018
Quantity
4,676 packages total
Location
Portland, OR, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

distributed throughout the U.S.

FDA source record · F-1524-2018

Data updated September 16, 2026. View official FDA data ↗

A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.