Mitragyna Speciosa Leaf Powder Red Vein Sumatra and Mitragyna Speciosa Leaf Powder Red Vein Bali, sold under t

Recall map → All recalls → F-1476-2018

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-salvationMitragyna Speciosa Leaf Powder Red Vein SumatraOrigin: IndonesiaDisclaimer: This product is sold as a bulk botanical without directions or claims. Keep away from children2204 Cortland Place, Nampa, ID 83678WWW.HERBAL-SALVATION.COM". The product label is read in parts: "herbal-salvationMitragyna Speciosa Leaf Powder Red Vein BaliOrigin: IndonesiaDisclaimer: This product is sold as a bulk botanical without directions or claims. Keep away from children2204 Cortland Place, Nampa, ID 83678WWW.HERBAL-SALVATION.COM". Viable Solutions, LLC · reported 2018-05-09

Terminated This recall has been closed out by the agency.

Reason for recall: 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
Classification: Class I
Recall initiated: 2018-04-18
Reported by the agency: 2018-05-09
Closed out (terminated): 2018-11-16
Recalling firm: Viable Solutions, LLC
Nampa, ID
United States
This is the firm that issued the recall — commonly a distributor or processor. It is not the origin of contamination.
Distribution (the agency's own words): Nationwide through internet sales
States we parsed from that text: AK AL AR AZ CA CO CT DC DE FL GA HI IA ID IL IN KS KY LA MA MD ME MI MN MO MS MT NC ND NE NH NJ NM NV NY OH OK OR PA RI SC SD TN TX UT VA VT WA WI WV WYour expansion
The agency wrote a broader phrase; these state names are ours, not theirs. Parse method nationwide, confidence high.
Food category: uncategorised
Assigned by a reviewed keyword rulebook over the product description, not by the agency.
Recall type: Voluntary: Firm initiated
Recall number: F-1476-2018

This page reproduces a record published by the US Food and Drug Administration. It is not real-time: recalls typically appear in FDA's Enforcement Report weeks after they begin — a median of 40 days, see publication lag. For current food safety information consult FDA and USDA FSIS directly.