Recall events
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Event 82247
Event summary
Timeline bucket February 13, 2019
Product types Drug
Classifications Class I
Statuses Terminated
Recalling firm wording Todd Holiday dba Sunstone Organics
Dossier provenance
Source snapshots represented here
openFDA Drug 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
Device root-cause evidence is not applicable to this event.
No grouped product has the official product type device; this is not an unavailable-enrichment finding.
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.
drug · product 1 of 4
Maeng Da Kratom, packaged in a) 25 gram powder (UPC 00859667007118), b) 50 gram powder (UPC 00859667007125), c) 100 gram powder (UPC 00859667007132), Sunstone Organics Springfield, Oregon 97473, 541-972-3327.
D-0986-2019
Recall number D-0986-2019
Initiated February 13, 2019
Classification Class I
Status Terminated
Quantity 800 kilograms
App-derived interpretation
Microbial contamination
reason.microbial_contamination · v1.0.0
MICROBIAL CONTAMINATION
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS: Analysis of samples were positive for Salmonella.
Code information Lot #124A
Distribution pattern California, Nebraska, Oregon, Washington
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[11222]
FDA event record
· Exact recall-number query on openFDA
drug · product 2 of 4
White Vein Kratom, packaged in a) 25 gram powder (UPC 00859667007316), b) 50 gram powder (UPC 00859667007323), c) 100 gram powder (UPC 00859667007330), Sunstone Organics Springfield, Oregon 97473, 541-972-3327.
D-0987-2019
Recall number D-0987-2019
Initiated February 13, 2019
Classification Class I
Status Terminated
Quantity 250 Kilograms
App-derived interpretation
Microbial contamination
reason.microbial_contamination · v1.0.0
MICROBIAL CONTAMINATION
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS: Analysis of samples were positive for Salmonella.
Distribution pattern California, Nebraska, Oregon, Washington
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[11083]
FDA event record
· Exact recall-number query on openFDA
drug · product 3 of 4
White Vein Kratom, packaged in a) 20 count capsules (UPC 00859667007347), b) 60 count capsules (UPC 00859667007354), c) 150 count capsules (UPC 00859667007361), Sunstone Organics Springfield, Oregon 97473 541-972-3327.
D-0988-2019
Recall number D-0988-2019
Initiated February 13, 2019
Classification Class I
Status Terminated
Quantity N/A
App-derived interpretation
Microbial contamination
reason.microbial_contamination · v1.0.0
MICROBIAL CONTAMINATION
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS: Analysis of samples were positive for Salmonella.
Distribution pattern California, Nebraska, Oregon, Washington
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[11207]
FDA event record
· Exact recall-number query on openFDA
drug · product 4 of 4
Maeng Da Kratom, packaged in a) 20 count capsules (UPC 00859667007149), b) 60 count capsules (UPC 00859667007156), c) 150 count capsules (UPC 00859667007163) , Sunstone Organics Springfield, Oregon 97473, 541-972-3327.
D-0989-2019
Recall number D-0989-2019
Initiated February 13, 2019
Classification Class I
Status Terminated
Quantity N/A
App-derived interpretation
Microbial contamination
reason.microbial_contamination · v1.0.0
MICROBIAL CONTAMINATION
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS: Analysis of samples were positive for Salmonella.
Code information Lot #124A
Distribution pattern California, Nebraska, Oregon, Washington
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[10440]
FDA event record
· Exact recall-number query on openFDA
