Food Recall Check
Class I · High risk Terminated Initiated Oct 30, 2025 (11 months ago)

Monarch Premium Kratom White Elephant powder is packaged in seal mylar pouches recall

Recalled by Lotus Vaping Technologies, LLC · Boise, ID, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Product has the potential to be contaminated with Salmonella

Pathogen: Salmonella

Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.

The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.

What was recalled

Monarch Premium Kratom White Elephant powder is packaged in seal mylar pouches: Monarch Premium Kratom, White Elephant, 4oz powder (112g), UPC 851006008480 Monarch Premium Kratom, White Elephant, 0.5oz powder (14g), UPC 851006008756 Monarch Premium Kratom, White Elephant, 8oz powder (224g), UPC 706970483644

Quantity: 612/8oz Packages, 432/4oz Packages, 960/0.5oz Packages

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

020123PA3F-W

Where it was sold

Nationwide.

FDA's distribution note: nationwide

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Lotus Vaping Technologies, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Oct 30, 2025
In FDA report of
Nov 19, 2025
Terminated
Mar 26, 2026
FDA recall number
H-0188-2026 · event 97902
Official record
FDA enforcement report search

Also recalled with it (3 more products)

FDA files each product of one recall action separately; these share the same FDA event.