Class ITerminated in FDA datasetRecall initiated Oct 30, 2025

Monarch Premium Kratom Green Maeng Da 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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ProductMonarch Premium Kratom Green Maeng Da powder is packaged in seal mylar pouches: Monarch Premium Kratom Green Maeng Da, 4oz powder (112g), UPC 851006008466 Monarch Premium Kratom Green Maeng Da, 0.5oz powder (14g), UPC 851006008770 Monarch Premium Kratom Green Maeng Da, 2oz powder (56g), UPC 851006008459

Package size4oz

UPC851006008459, 851006008466, 851006008770

FDA code information

020123PA3F-G

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 Green Maeng Da powder is packaged in seal mylar pouches: Monarch Premium Kratom Green Maeng Da, 4oz powder (112g), UPC 851006008466 Monarch Premium Kratom Green Maeng Da, 0.5oz powder (14g), UPC 851006008770 Monarch Premium Kratom Green Maeng Da, 2oz powder (56g), UPC 851006008459

Extracted codes and context

Type	Code / value	Context
UPC	`851006008459`	851006008770 Monarch Premium Kratom Green Maeng Da, 2oz powder (56g), UPC 851006008459
UPC	`851006008466`	ylar pouches: Monarch Premium Kratom Green Maeng Da, 4oz powder (112g), UPC 851006008466 Monarch Premium Kratom Green Maeng Da, 0.5oz powder (14g), UPC 851006008770 Monarch Premium Kratom Green Maeng Da,
UPC	`851006008770`	C 851006008466 Monarch Premium Kratom Green Maeng Da, 0.5oz powder (14g), UPC 851006008770 Monarch Premium Kratom Green Maeng Da, 2oz powder (56g), UPC 851006008459

Original FDA recall reason

Product has the potential to be contaminated with Salmonella

Recall details

Recall number: H-0186-2026
Event ID: 97902
FDA status: Terminated
Initiated: Oct 30, 2025
Reported: Nov 19, 2025
Classified: Nov 13, 2025
Terminated: Mar 26, 2026
Quantity: 648/4oz Packages; 360/2oz. Packages; 192/0.5oz Packages
Location: Boise, ID, United States
Initiation type: Voluntary: Firm initiated
Notification: Press Release

Where it was distributed

nationwide

FDA source record · H-0186-2026

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

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