Severity
Critical
CriticalClass ITerminated
FDA Food recall · Reported May 16, 2018
Dragon Bali Kratom Powder: 60g Bottle. Dragon Bali Kratom Capsules in bottles:200 ct 500mg, 80 ct x 500, 40 ct x 500mg and 20 ct x 500 mg pouch.
Samples collected by public health officials found the presence of Salmonella.
Maya Distribution, LLC recalled Dragon Bali Kratom Powder: 60g Bottle. Dragon Bali Kratom Capsules in bottles:200 ct 500m… — a critical-severity action.
Dragon Bali Kratom Powder: 60g Bottle. Dragon Bali Kratom Capsules in bottles:200 ct 500m… was recalled by Maya Distribution, LLC in May 16, 2018. Reason: Samples collected by public health officials found the presence of Salmonella.. Check the official notice for the remedy. Verify recall #F-1461-2018 with the FDA Food before acting.
The recall
Maya Distribution, LLC issued this critical-severity FDA Food recall — Samples collected by public health officials found the presence of Salmonella..
- Critical
- severity level
- Class I
- classification
- May 16, 2018
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-1461-2018 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-1461-2018) was formally reported on May 16, 2018, with the manufacturer initiating the action on March 20, 2018. It is classified under Critical severity (Class I), with a current status of Terminated. Maya Distribution, LLC is listed as the recalling firm, operating out of Salt Lake City, UT. Federal records list the affected scope as unkown.
The documented reason for this recall is: Samples collected by public health officials found the presence of Salmonella. Distribution data in the federal record shows the product reached: Recalled product was distributed to retail stores in AZ, IA, ID, IL, KS, MI, UT, and WY.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 1 from FDA Food — clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Drugs & Medications recalls over time
Where this recall sits in its category — 14,048 drugs & medications recalls on record
Where this recall sits in the database
Of 100,165 recalls in the database, 23,668 are high severity, 72,097 moderate, and 4,400 low. This recall is classified high severity.
Counts reflect market size and reporting activity, not inherent danger — we do not rank products by risk from raw recall volume.
Affected scope
unkown
Related Recalls
6
1 from same agency
Product description
Dragon Bali Kratom Powder: 60g Bottle. Dragon Bali Kratom Capsules in bottles:200 ct 500mg, 80 ct x 500, 40 ct x 500mg and 20 ct x 500 mg pouch.
Reason for recall
Samples collected by public health officials found the presence of Salmonella.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | F-1461-2018 |
| Date reported | May 16, 2018 |
| Date initiated | March 20, 2018 |
| Recalling firm | Maya Distribution, LLC |
| Firm location | Salt Lake City, UT |
| Affected scope | unkown |
| Distribution | Recalled product was distributed to retail stores in AZ, IA, ID, IL, KS, MI, UT, and WY. |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-1461-2018) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting — recall details can be updated.
- This is a Class I (high-risk) recall — stop using the product immediately and follow the disposal or return instructions. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Dragon Bali Kratom Powder: 60g Bottle. Dragon Bali Kratom Capsules in bottles:200 ct 500mg, 80 ct x 500, 40 ct x 500mg and 20 ct x 500 mg pouch.. Recalled by Maya Distribution, LLC. Units affected: unkown.
Why was this product recalled? ▼
Samples collected by public health officials found the presence of Salmonella.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on May 16, 2018. Severity: Critical. Recall number: F-1461-2018.
Where was the recalled product distributed? ▼
Distribution: Recalled product was distributed to retail stores in AZ, IA, ID, IL, KS, MI, UT, and WY..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-1461-2018) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
Continue exploring
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What to do next
A step-by-step guide to refunds, repairs, and returns after a recall.
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Data Sources
Source: FDA, CPSC, and NHTSA federal recall databases. This recall: FDA Food, reported May 16, 2018.
- Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
- Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
- Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records — no number is typed in by an editor. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of June 2026.