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…
Recalling firm: Pdx Aromatics
Why it was recalled
Kraken Kratom, Phytoextractum, and Soul Speciosa WHITE VEIN Kratom CAPSULES are recalled due to potential contamination with Salmonella.
The exact 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
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-1525-2018
- Event ID
- 79480
- FDA status
- Terminated
- Initiated
- Mar 9, 2018
- Reported
- Mar 28, 2018
- Classified
- Jun 4, 2018
- Terminated
- Sep 13, 2018
- Quantity
- 1097 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.
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.