Food recall: Dragon Ultra Ehanced Indo Extract 4-ct x 500 mg capsules in pouches.
FDA enforcement event 79853 is a food recall by Maya Distribution, LLC of Salt Lake City, UT, initiated 20 Mar 2018 and classified Class I, with 4 product records.
FDA defines Class I as a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death. 34% of the 578 food enforcement events initiated in 2018 carry the same class.
Status: Terminated, terminated 6 Sep 2019. Initiation: voluntary: firm initiated. This is the only enforcement event on this register for Maya Distribution, LLC.
Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.
Recalling firm
Maya Distribution, LLC, Salt Lake City, UT.
Reason for recall
"Samples collected by public health officials found the presence of Salmonella."
Distribution
"Recalled product was distributed to retail stores in AZ, IA, ID, IL, KS, MI, UT, and WY."
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-1458-2018 | Dragon Ultra Ehanced Indo Extract 4-ct x 500 mg capsules in pouches. | Unknown | Class I | Terminated | 16 May 2018 |
| 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 | Class I | Terminated | 16 May 2018 |
| 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 | Class I | Terminated | 16 May 2018 |
| 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. | unkown | Class I | Terminated | 16 May 2018 |
Context
Questions and answers
Why was this food recalled?
FDA's record gives the reason for recall as: "Samples collected by public health officials found the presence of Salmonella."
What does Class I mean?
FDA classifies recalls by relative degree of health hazard. Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.
Where was the product distributed?
FDA's distribution pattern field reads: "Recalled product was distributed to retail stores in AZ, IA, ID, IL, KS, MI, UT, and WY."
Is the recall still ongoing?
FDA lists the status as Terminated; the termination date is 6 Sep 2019. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.
Where does this data come from?
openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.
Provenance
Source: openFDA food enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.