Recall record at a glance
| Official record | F-1527-2018 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Pdx Aromatics |
| Report date | Mar 28, 2018 |
| Recall initiation date | Mar 9, 2018 |
| Quantity | 20,546 pkgs. |
| Location | Portland, OR, United States |
Official product description
GREEN Kratom POWDER, sold under brand names Kraken Kratom, Phytoextractum, and Soul Speciosa. The powder 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 OG Bali Powder Kraken Kratom Super Green Malaysian Kratom Powder Phytoextractum OG Bali Powder Phytoextractum Green Vein Thai Kratom Powder Phytoextractum Super Green Malaysian Kratom Powder Soul Speciosa OG Bali Powder Soul Speciosa Thai Kratom Powder (Green Vein) Soul Speciosa Super Green Malaysian Kratom Powder
Why the product was recalled
Kraken Kratom, Phytoextractum, and Soul Speciosa GREEN VEIN Kratom POWDER are recalled due to potential contamination with Salmonella.
Distribution information
distributed throughout the U.S.
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.