WHITE VEIN Kratom POWDER, sold under brand names Kraken Kratom, Phytoextractum, and Soul Speciosa. The powder

Recall map → All recalls → F-1524-2018

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 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) Pdx Aromatics · reported 2018-03-28

Terminated This recall has been closed out by the agency.

Reason for recall: Kraken Kratom, Phytoextractum, and Soul Speciosa products containing WHITE VEIN Kratom Powder are recalled due to potential contamination with Salmonella.
Classification: Class I
Recall initiated: 2018-03-09
Reported by the agency: 2018-03-28
Closed out (terminated): 2018-09-13
Recalling firm: Pdx Aromatics
Portland, OR
United States
This is the firm that issued the recall — commonly a distributor or processor. It is not the origin of contamination.
Distribution (the agency's own words): distributed throughout the U.S.
States we parsed from that text: could not be parsed
No state list could be read from the agency's text. Absence here is not evidence the product stayed put.
Food category: uncategorised
Assigned by a reviewed keyword rulebook over the product description, not by the agency.
Recall type: Voluntary: Firm initiated
Recall number: F-1524-2018

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This page reproduces a record published by the US Food and Drug Administration. It is not real-time: recalls typically appear in FDA's Enforcement Report weeks after they begin — a median of 40 days, see publication lag. For current food safety information consult FDA and USDA FSIS directly.