FDA recall record
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 s...
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of September 13, 2018. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
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
Kraken Kratom, Phytoextractum, and Soul Speciosa WHITE VEIN Kratom CAPSULES are recalled due to potential contamination with Salmonella.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
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
Code information listed by FDA
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
Distribution and firm information
Recalling firm listed by FDA: Pdx Aromatics
Firm location listed by FDA: Portland, OR, United States
Distribution reported by FDA: distributed throughout the U.S.
Product quantity listed by FDA: 1097 packages total
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.