Lotus Vaping Technologies, LLC Recall: Product has the potential to be contaminated with Salmonella

🇺🇸 United States

1. October 30, 2025 - Recall initiated
2. November 19, 2025 - Reported by source
3. March 26, 2026 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

H-0188-2026

Event ID

97902

Status

Terminated

Classification

Class I

Company

Lotus Vaping Technologies, LLC

Product description

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

Reason

Product has the potential to be contaminated with Salmonella

Recall initiation date

October 30, 2025

Report date

November 19, 2025

Classification date

Not published in this source record

Termination date

March 26, 2026

Distribution pattern

nationwide

UPC, lot, and code information

UPC 851006008480; 020123PA3F-W

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Press Release

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 97902 with 3 other product entries in Public Health Trace.

Responsible company: Lotus Vaping Technologies, LLC

Other recalls from Lotus Vaping Technologies, LLC

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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