Severity
Critical
CriticalClass ITerminated
FDA Drug recall · Reported March 13, 2019
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.
MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS: Analysis of samples were positive for Salmonella.
Todd Holiday dba Sunstone Organics recalled White Vein Kratom, packaged in a) 25 gram powder (UPC 00859667007316), b) 50 gram powder … - a critical-severity action.
White Vein Kratom, packaged in a) 25 gram powder (UPC 00859667007316), b) 50 gram powder … was recalled by Todd Holiday dba Sunstone Organics in March 13, 2019. Reason: MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS: Analysis of samples were positive for Salmonella.. Check the official notice for the remedy. Verify recall #D-0987-2019 with the FDA Drug before acting.
The recall
Todd Holiday dba Sunstone Organics issued this critical-severity FDA Drug recall-MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS: Analysis of samples were positive for Salmonella..
- Critical
- severity level
- Class I
- classification
- March 13, 2019
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-0987-2019 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-0987-2019) was formally reported on March 13, 2019, with the manufacturer initiating the action on February 13, 2019. It is classified under Critical severity (Class I), with a current status of Terminated. Todd Holiday dba Sunstone Organics is listed as the recalling firm, operating out of Springfield, OR. Federal records list the affected scope as 250 Kilograms.
The documented reason for this recall is: MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS: Analysis of samples were positive for Salmonella. Distribution data in the federal record shows the product reached: California, Nebraska, Oregon, Washington. 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, 6 from FDA Drug - 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 - 14,436 drugs & medications recalls on record
Of 88,001 recalls with an agency hazard classification, 19,020 are high severity, 64,468 moderate, and 4,513 low. A further 16,157 CPSC/NHTSA recalls have no agency class and are excluded from this split. 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
250 Kilograms
Related Recalls
6
6 from same agency
Product description
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.
Reason for recall
MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS: Analysis of samples were positive for Salmonella.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | D-0987-2019 |
| Date reported | March 13, 2019 |
| Date initiated | February 13, 2019 |
| Recalling firm | Todd Holiday dba Sunstone Organics |
| Firm location | Springfield, OR |
| Affected scope | 250 Kilograms |
| Distribution | California, Nebraska, Oregon, Washington |
Profile values are sourced directly from the official FDA Drug 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 (D-0987-2019) and product description against the item you own. Search the archive
- Confirm the current status with FDA Drug 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 Drug 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? ▼
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.. Recalled by Todd Holiday dba Sunstone Organics. Units affected: 250 Kilograms.
Why was this product recalled? ▼
MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS: Analysis of samples were positive for Salmonella.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on March 13, 2019. Severity: Critical. Recall number: D-0987-2019.
Where was the recalled product distributed? ▼
Distribution: California, Nebraska, Oregon, Washington.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-0987-2019) against your product. Visit the official FDA Drug website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
Nationwide recalls with similar severity or category timing
Two federal-filing-derived peer sets for this notice, both outside the same recalling firm and filing state so the neighborhoods are not firm or geographic containment.
Similar severity · nearest report date
Same archive severity grade (Critical), closest by report date among other firms and states.
Similar Drugs & Medications · nearest report date
Same product category, closest by report date among other firms and states (deduped against the severity set).
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Drug, reported March 13, 2019. 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 August 2026.