Drug recall
Mitragyna Speciosa Leaf Powder-GREEN Horn, sold under the brand name Herbal-Salvation.com. The powder is…
FDA recall event 79836 · Class I · Viable Solutions, LLC
Key facts
| Event ID | 79836 |
|---|---|
| Recall numbers | F-1476-2018, F-1477-2018, F-1478-2018 |
| Recalling firm | Viable Solutions, LLC |
| Product type | Food |
| Products | Mitragyna Speciosa Leaf Powder-GREEN Horn, sold under the brand name Herbal-Salvation.com. The powder is packaged in kraft paper, foil-lined heat sealed pouches and sold in 25g, 100g, 250g, and 1000g…, Mitragyna Speciosa Leaf Powder Red Vein Sumatra and Mitragyna Speciosa Leaf Powder Red Vein Bali, sold under the brand name Herbal-Salvation.com. The powder is packaged in kraft paper, foil-lined heat…, Mitragyna Speciosa Leaf Powder-Thai Maeng Da, sold under the brand name Herbal-Salvation.com. The powder is packaged in kraft paper, foil-lined heat sealed pouches and sold in 25g, 100g, 250g, and… |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Mitragyna Speciosa Leaf Powder Green Horn Kratom product is being recalled because they have the potential to be contaminated with Salmonella, Mitragyna Speciosa Leaf Powder Red Vein Sumatra and Mitragyna Speciosa Leaf Powder Red Vein Bali Kratom products are being recalled because they have the potential to be contaminated with Salmonella, Mitragyna Speciosa Leaf Powder Thai Maeng Da Kratom… |
| Initiation date | Apr 18, 2018 |
| Report date | May 9, 2018 |
| Termination date | Nov 16, 2018 |
| City | Nampa |
| State | ID |
| Country | United States |
| FEI number | 3010431241 |
At a glance
- 1–9 Products in this recall
- None 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: