Drug recall
GREEN Kratom CAPSULES, sold under brand names Kraken Kratom, Phytoextractum, and Soul Speciosa. The capsules…
FDA recall event 79480 · Class I · Pdx Aromatics
Key facts
| Event ID | 79480 |
|---|---|
| Recall numbers | F-1523-2018, F-1524-2018, F-1525-2018, F-1526-2018, F-1527-2018, F-1528-2018 |
| Recalling firm | Pdx Aromatics |
| Product type | Food |
| Products | GREEN 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…, 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…, RED 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…, RED 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…, 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)… and 1 more |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Kraken Kratom, Phytoextractum, and Soul Speciosa GREEN VEIN Kratom CAPSULES are recalled due to potential contamination with Salmonella., Kraken Kratom, Phytoextractum, and Soul Speciosa GREEN VEIN Kratom POWDER are recalled due to potential contamination with Salmonella., Kraken Kratom, Phytoextractum, and Soul Speciosa products containing Red Vein Kratom Powder are recalled due to potential… |
| Initiation date | Mar 9, 2018 |
| Report date | Mar 28, 2018 |
| Termination date | Sep 13, 2018 |
| City | Portland |
| State | OR |
| Country | United States |
| FEI number | 3011935954 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: