Monarch Premium Kratom Bali Gold powder is packaged in seal mylar pouches: Monarch Premium Kratom Bali Gold, 4oz powder
Summary
The FDA issued a Class I for Monarch Premium Kratom Bali Gold powder is packaged in seal mylar pouches: Mona by Lotus Vaping Technologies, LLC. Reason: Product has the potential to be contaminated with Salmonella.
Details
Source
Food Recall
External ID
H-0185-2026
Action Date
2025-11-19
Status
Terminated
Category
food
Product Description
Monarch Premium Kratom Bali Gold powder is packaged in seal mylar pouches: Monarch Premium Kratom Bali Gold, 4oz powder (112g), UPC 851006008428 Monarch Premium Kratom Bali Gold, 8oz powder (224g), UPC 706970483712
Lot/Code Info: 020123PA3F-T
Quantity Affected: 576/4oz Packages and 324/8oz Packages
Reason for Recall
Product has the potential to be contaminated with Salmonella
Distribution
nationwide
Type: Voluntary: Firm initiated
Recall Initiated: 2025-10-30
Company
Boise, ID
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 44 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Lotus Vaping Technologies, LLC has 4 FDA actions in our database, including 4 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Lotus Vaping Technologies, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Lotus Vaping Technologies, LLC have FDA actions?
Lotus Vaping Technologies, LLC has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0185-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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