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Home > Recalled Products > Drugs > Contamination > Kraken Kratom, Phytoextractum, & Soul Speciosa White Vein Powder & Capsule Red Vein Powder Products

Recall: Kraken Kratom, Phytoextractum, & Soul Speciosa White Vein Powder & Capsule Red Vein Powder Products


On 2018-03-16, the FDA announced that PDX Aromatics is conducting a recall on White Vein Powder & Capsule Red Vein Powder Products due to possible contamination with salmonella. The recalled products were sold under the brand name(s) Kraken Kratom, Phytoextractum and & Soul Speciosa during an unspecified time period throughout the regions shown in the map below.

In recent months, there have been 5 drugs recalls due to potential contamination, including dietary supplement, dietary supplement and more. Additionally, there have been 18 drug and medical device recalls due to other health hazards as well as 86 food recalls.

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Phytoextractum Mitragyna Speciosa Kratom Horn MD Powder 28g
Note: Images may not be available for every version. Please review the detailed description below.

Company Contact Information:

Name: PDX Aromatics
Phone: 503-850-9225

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Detailed Recall Information

Regions Where Sold: Because the region was not specified, it is assumed that this product was available nationwide.

Product Description: White vein powder & capsule red vein powder products

Brand Name(s): Kraken Kratom, Phytoextractum, & Soul Speciosa

Reason for Recall: May contain Salmonella

Official Recall Date: 2018-03-16


Additional information provided by the

PDX Aromatics, DBA Kraken Kratom, Phytoextractum, and Soul Speciosa, is expanding the scope of their 3/9/2018 voluntary recall of certain kratom white vein powder and capsule products and red vein powder products because they have the potential to be contaminated with Salmonella. The expanded recall is being initiated in response to additional positive findings of Salmonella associated with Aromatics' products following the FDA initial investigation. Read More.

More information may be available at

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Sources may include Food & Drug Administration (FDA), United States Department of Agriculture (USDA), Health Canada and companies involved with this or a related recall.

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