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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 79853

4 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
March 20, 2018
Product types
Food
Classifications
Class I
Statuses
Terminated
Recalling firm wording
Maya Distribution, LLC

Dossier provenance

Source snapshots represented here

  • openFDA Food Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

4 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

food · product 1 of 4

Dragon Ultra Ehanced Indo Extract 4-ct x 500 mg capsules in pouches.

F-1458-2018
Recall number
F-1458-2018
Initiated
March 20, 2018
Classification
Class I
Status
Terminated
Recalling firm
Maya Distribution, LLC
Quantity
Unknown

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
found the presence of Salmonella

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Samples collected by public health officials found the presence of Salmonella.

Code information

unknown

Distribution pattern

Recalled product was distributed to retail stores in AZ, IA, ID, IL, KS, MI, UT, and WY.

food · product 2 of 4

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.

F-1459-2018
Recall number
F-1459-2018
Initiated
March 20, 2018
Classification
Class I
Status
Terminated
Recalling firm
Maya Distribution, LLC
Quantity
unknown

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
found the presence of Salmonella

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Samples collected by public health officials found the presence of Salmonella.

Code information

unknown

Distribution pattern

Recalled product was distributed to retail stores in AZ, IA, ID, IL, KS, MI, UT, and WY.

food · product 3 of 4

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.

F-1460-2018
Recall number
F-1460-2018
Initiated
March 20, 2018
Classification
Class I
Status
Terminated
Recalling firm
Maya Distribution, LLC
Quantity
unknown

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
found the presence of Salmonella

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Samples collected by public health officials found the presence of Salmonella.

Code information

unknown

Distribution pattern

Recalled product was distributed to retail stores in AZ, IA, ID, IL, KS, MI, UT, and WY.

food · product 4 of 4

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.

F-1461-2018
Recall number
F-1461-2018
Initiated
March 20, 2018
Classification
Class I
Status
Terminated
Recalling firm
Maya Distribution, LLC
Quantity
unkown

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
found the presence of Salmonella

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Samples collected by public health officials found the presence of Salmonella.

Code information

unknown

Distribution pattern

Recalled product was distributed to retail stores in AZ, IA, ID, IL, KS, MI, UT, and WY.