Recall record at a glance
| Official record | F-1476-2018 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Viable Solutions, LLC |
| Report date | May 9, 2018 |
| Recall initiation date | Apr 18, 2018 |
| Quantity | 350 packages of Red Vein Sumatra and 350 packages of Red Vein Bali |
| Location | Nampa, ID, United States |
Official product description
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 sealed pouches and sold in 25g, 100g, 250g, and 1000g. The product label is read in parts: "***herbal-salvation***Mitragyna Speciosa Leaf Powder Red Vein Sumatra***Origin: Indonesia***Disclaimer: This product is sold as a bulk botanical without directions or claims. Keep away from children***2204 Cortland Place, Nampa, ID 83678***WWW.HERBAL-SALVATION.COM***". The product label is read in parts: "***herbal-salvation***Mitragyna Speciosa Leaf Powder Red Vein Bali***Origin: Indonesia***Disclaimer: This product is sold as a bulk botanical without directions or claims. Keep away from children***2204 Cortland Place, Nampa, ID 83678***WWW.HERBAL-SALVATION.COM***".
Why the product was recalled
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
Distribution information
Nationwide through internet sales
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: Press Release.
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.
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