FDA recall record
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 kraf...
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of November 16, 2018. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
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. 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. COM***".
Reason
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
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
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. 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. COM***".
Code information listed by FDA
Recalled product has any of the following LOT Numbers: RVS1380182301; RVB1380182201; GVH1380171512; MD13120181601.
Distribution and firm information
Recalling firm listed by FDA: Viable Solutions, LLC
Firm location listed by FDA: Nampa, ID, United States
Distribution reported by FDA: Nationwide through internet sales
Product quantity listed by FDA: 350 packages of Red Vein Sumatra and 350 packages of Red Vein Bali
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.