CLASS I Food recall · Reported 19 Nov 2025 · FDA Enforcement Report

Monarch Premium Kratom Green Maeng Da powder recalled

Lotus Vaping Technologies is recalling Monarch Premium Kratom Green Maeng Da powder is, distributed nationwide in the US. The recall was initiated on 30 Oct 2025 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codes020123PA3F-G
Quantity recalled648/4oz Packages; 360/2oz. Packages; 192/0.5oz Packages

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
H-0186-2026
FDA event ID
97902
Recalling firm
Lotus Vaping Technologies, Boise, ID
Brand
Monarch
Classification
Class I
Status
Terminated
Recall initiated
30 Oct 2025
FDA classified
13 Nov 2025
Reported
19 Nov 2025
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Salmonella
Product category
Energy Drinks

Timeline

30 Oct 2025Recall initiated by company
13 Nov 2025Classified by FDA+14 days
19 Nov 2025Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Product has the potential to be contaminated with Salmonella

Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.

Product as listed by the FDA

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

Where it was distributed

nationwide

Nationwide

Questions about this recall

Why was it recalled?

Product has the potential to be contaminated with Salmonella

Which lots are affected?

020123PA3F-G

Where was it sold?

nationwide

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

3 other products · FDA event 97902

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