Dragon Ultra Enhanced Indo Extract Capsules Recall: Salmonella Risk
Maya Distribution recalls Dragon Ultra Enhanced Indo Extract 4-count capsules due to Salmonella contamination found in samples. Consumers should avoid using these products.
Lower-risk recall
Samples collected by public health officials found the presence of Salmonella.
Contact the company
What happened, in plain English
Maya Distribution is recalling Dragon Ultra Enhanced Indo Extract 4-count capsules because public health officials found Salmonella in samples. This poses a risk of foodborne illness from consuming the product. Read more at govinfonow.com/recall/19524-dragon-ultra-enhanced-indo-extract-capsules-recall-salmonella-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/19524-dragon-ultra-enhanced-indo-extract-capsules-recall-salmonella-risk · Updated October 7, 2026 · FDA enforcement record: FDA #F-1458-2018
Cite this page
“Dragon Ultra Enhanced Indo Extract Capsules Recall: Salmonella Risk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19524-dragon-ultra-enhanced-indo-extract-capsules-recall-salmonella-risk. Based on FDA recall #F-1458-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1458-2018%22&limit=1).
Why it’s dangerous
Salmonella bacteria can cause food poisoning, leading to symptoms like diarrhea, fever, and stomach cramps. The contamination was detected in samples collected by public health officials.
Who’s affected
Anyone who purchased Dragon Ultra Enhanced Indo Extract 4-count capsules from Maya Distribution. People who consume these capsules are at risk of foodborne illness.
How to tell if you have this one
Check for Dragon Ultra Enhanced Indo Extract 4-count capsules in pouches. The product was sold by Maya Distribution.
- Brand
Maya Distribution- Category
Food
All 4 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class I- Status
Terminated- Distribution
Recalled product was distributed to retail stores in AZ, IA, ID, IL, KS, MI, UT, and WY.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| F-1458-2018 | Dragon Ultra Ehanced Indo Extract 4-ct x 500 mg capsules in pouches.; unknown | Unknown |
| F-1459-2018 | Dragon Malaysian Kratom Powder: 150 g bottle. Dragon Malaysian Kratom: 200-, 80-, and 40-ct x 500mg capsules in bottles. Dragon Malaysian Kratom: 20-ct x 500 mg capsules in pouches.; unknown | unknown |
| F-1460-2018 | Dragon Maeng Da Kratom Powder: 60 g and 150 g bottle. Dragon Maeng Da Kratom: 200-, 80-, and 40-ct x 500mg capsules in bottles.; unknown | unknown |
| F-1461-2018 | 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.; unknown | unkown |
What to do — step by step
Stop Using It Now
Discard the recalled Dragon Ultra Enhanced Indo Extract 4-count capsules immediately.
Where it went and when
Where it was distributed
Distributed in 8 states.
FDA distribution: “Recalled product was distributed to retail stores in AZ, IA, ID, IL, KS, MI, UT, and WY.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arizona, Idaho, Illinois, Iowa, Kansas, Michigan, Utah, Wyoming.
Recall timeline
FDA terminated this recall 18 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-1458-2018 (March 20, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1458-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.