Class ITerminated in FDA datasetRecall initiated Oct 30, 2025

Monarch Premium Kratom Red Bali powder is packaged in seal mylar pouches: Monarch Premium…

Recalling firm: Lotus Vaping Technologies, LLC

Why it was recalled

Product has the potential to be contaminated with Salmonella

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Mar 26, 2026.

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Compare the exact product and package details with the label you have.

ProductMonarch Premium Kratom Red Bali powder is packaged in seal mylar pouches: Monarch Premium Kratom Red Bali, 4oz powder (112g), UPC 851006008442 Monarch Premium Kratom Red Bali, 8oz powder (224g), UPC 706970483859 Monarch Premium Kratom Red Bali, 2oz powder (56g), UPC 851006008435
Package size4oz
UPC706970483859, 851006008435, 851006008442

FDA code information

020123PA3F-R

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Monarch Premium Kratom Red Bali powder is packaged in seal mylar pouches: Monarch Premium Kratom Red Bali, 4oz powder (112g), UPC 851006008442 Monarch Premium Kratom Red Bali, 8oz powder (224g), UPC 706970483859 Monarch Premium Kratom Red Bali, 2oz powder (56g), UPC 851006008435

Extracted codes and context

TypeCode / valueContext
UPC706970483859112g), UPC 851006008442 Monarch Premium Kratom Red Bali, 8oz powder (224g), UPC 706970483859 Monarch Premium Kratom Red Bali, 2oz powder (56g), UPC 851006008435
UPC85100600843524g), UPC 706970483859 Monarch Premium Kratom Red Bali, 2oz powder (56g), UPC 851006008435
UPC851006008442in seal mylar pouches: Monarch Premium Kratom Red Bali, 4oz powder (112g), UPC 851006008442 Monarch Premium Kratom Red Bali, 8oz powder (224g), UPC 706970483859 Monarch Premium Kratom Red Bali, 2oz powder (56g

Original FDA recall reason

Product has the potential to be contaminated with Salmonella

Recall details

Recall number
H-0187-2026
Event ID
97902
FDA status
Terminated
Initiated
Oct 30, 2025
Reported
Nov 19, 2025
Classified
Nov 13, 2025
Terminated
Mar 26, 2026
Quantity
468/8oz. Packages, 216/4oz Packages, 216/2oz Packages
Location
Boise, ID, United States
Initiation type
Voluntary: Firm initiated
Notification
Press Release

Where it was distributed

nationwide

FDA source record · H-0187-2026

Data updated September 16, 2026. View official FDA data ↗

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