Viable Solutions, LLC Recall: Mitragyna Speciosa Leaf Powder Green Horn Kratom product is being recalled because they have the potential to be contaminated with Salmonella

🇺🇸 United States

1. April 18, 2018 - Recall initiated
2. May 9, 2018 - Reported by source
3. November 16, 2018 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-1477-2018

Event ID

79836

Status

Terminated

Classification

Class I

Company

Viable Solutions, LLC

Product description

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. The product label is read in parts: "***herbal-salvation***Mitragyna Speciosa Leaf Powder Green Horn***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***".

Quantity

350 packages

Reason

Mitragyna Speciosa Leaf Powder Green Horn Kratom product is being recalled because they have the potential to be contaminated with Salmonella

Recall initiation date

April 18, 2018

Report date

May 9, 2018

Classification date

Not published in this source record

Termination date

November 16, 2018

Distribution pattern

Nationwide through internet sales

UPC, lot, and code information

Recalled product has any of the following LOT Numbers: RVS1380182301; RVB1380182201; GVH1380171512; MD13120181601.

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Press Release

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 79836 with 2 other product entries in Public Health Trace.

Responsible company: Viable Solutions, LLC

Other recalls from Viable Solutions, LLC

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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