Mitragyna Speciosa Leaf Powder-Thai Maeng Da, sold under the brand name Herbal-Salvation.com. The powder is packaged in kraft paper, foi...
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (Salmonella contamination). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1478-2018.
Mitragyna Speciosa Leaf Powder Thai Maeng Da Kratom product is being recalled because they have the potential to be contaminated with Salmonella
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1478-2018.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Viable Solutions, Llc or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1478-2018.
Viable Solutions, LLC
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
Visit FDA.gov →📣 Report a food, supplement, or cosmetic problem to the FDA
If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
Viable Solutions, Llc Recall FAQ
Viable Solutions, Llc is the subject of a food safety report: Mitragyna Speciosa Leaf Powder-Thai Maeng Da, sold under the brand name Herbal-Salvation.com. The powder is packaged in kraft paper, foi.... The notice was published on April 18, 2018 by the U.S. Food and Drug Administration (FDA). Approximately 510 units are potentially affected.