PlainRecalls
FDA Food Critical Class I Terminated

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

Reported: March 28, 2018 Initiated: March 9, 2018 #F-1525-2018

Product Description

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.

Details

Recalling Firm
Pdx Aromatics
Units Affected
1097 packages total
Distribution
distributed throughout the U.S.
Location
Portland, OR

Frequently Asked Questions

What product was recalled? ▼
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. Recalled by Pdx Aromatics. Units affected: 1097 packages total.
Why was this product recalled? ▼
Kraken Kratom, Phytoextractum, and Soul Speciosa WHITE VEIN Kratom CAPSULES are recalled due to potential contamination with Salmonella.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on March 28, 2018. Severity: Critical. Recall number: F-1525-2018.

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