Monarch Premium Kratom Red Bali powder is packaged in seal mylar po…
Recalled by Lotus Vaping Technologies, LLC
Food recall
Lotus Vaping Technologies, LLC
Class I — most serious
There is a reasonable chance that using this product could cause serious health problems or death.
Lotus Vaping Technologies, LLC has recalled Monarch Premium Kratom Red Bali powder is packaged in seal mylar po…, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on November 19, 2025 and was initiated on October 30, 2025. It is classified as a Class I recall, which means there is a reasonable chance that using this product could cause serious health problems or death.
Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.
What was recalled?
This recall covers Monarch Premium Kratom Red Bali powder is packaged in seal mylar po…, with approximately 468/8oz. Packages, 216/4oz Packages, 216/2oz Packages affected. The company behind the recall is Lotus Vaping Technologies, LLC, based in Boise, ID. The FDA describes the product as: “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 (56…”
Why was Monarch Premium Kratom Red Bali powder is packaged in seal mylar po… recalled?
According to the FDA, the stated reason for the recall is: “Product has the potential to be contaminated with Salmonella.” In plain terms, this recall relates to Salmonella.
Salmonella is a group of bacteria that is one of the most common causes of foodborne illness in the United States. Public health authorities note that infections can lead to symptoms such as fever, diarrhea, and stomach cramps, and that young children, older adults, and people with weakened immune systems are at higher risk of serious illness. Because it can spread through contaminated food, regulators treat Salmonella findings seriously.
What should you do?
If you think you may have bought Monarch Premium Kratom Red Bali powder is packaged in seal mylar po…, compare it against the product description and identifying codes (020123PA3F-R) before using it.
The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact Lotus Vaping Technologies, LLC or your local health authority.
About this recall
This recall was distributed in ID. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.
Full recall details
- Status
- Terminated
- Date reported
- November 19, 2025
- Recall started
- October 30, 2025
- Distributed in
- ID
What you can do
Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.
Quick answers
Why was Monarch Premium Kratom Red Bali powder is packaged in seal mylar po… recalled?+
According to the FDA: Product has the potential to be contaminated with Salmonella
How serious is this recall?+
Class I — most serious. There is a reasonable chance that using this product could cause serious health problems or death.
What should I do if I have Monarch Premium Kratom Red Bali powder is packaged in seal mylar po…?+
Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.
Opens the U.S. Food and Drug Administration (FDA) data for this recall.
Recall number: H-0187-2026. Information last synced from the FDA on July 5, 2026.