Dakota Honey Company Recall History
Dakota Honey Company has had 2 FDA-tracked food recalls since 2026. The full list below — sourced from the FDA openFDA enforcement database — shows dates, products, reasons, and classifications for every recall on record.
Key Facts
- Total Recalls
- 2
- Years in FDA Data
- Since 2026
- Class I (Most Serious)
- 0
- Most Common Reason
- Foreign material (2)
- Latest Recall
- Apr 4, 2026
- First Recorded Recall
- Apr 4, 2026
- States Affected
- 54 states (nationwide)
- Currently Active
- 2
- Data Source
- FDA openFDA + USDA FSIS
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Complete Recall List (2 Records)
Every Dakota Honey Company recall in the FDA enforcement database, newest first. Each row links to the full recall notice with affected product codes, distribution, and consumer guidance.
| Date | Product | Class | Status |
|---|---|---|---|
| Apr 4, 2026 | Dakota Honey Company Spreadable Spun Honey, Salted Carame... | Class II | Active |
| Apr 4, 2026 | Dakota Honey Company Spreadable Spun Honey, Jalapeno. St... | Class II | Active |
Recall data sourced from the FDA's recalls and safety alerts database. Class I recalls indicate a reasonable probability of serious adverse health consequences. Always check the USDA FSIS recall list for meat and poultry products.
Frequently Asked Questions
Yes, Dakota Honey Company has 2 FDA food recalls on record, including 0 Class I (dangerous) recalls. There are currently 2 active recalls.
Dakota Honey Company currently has 2 active recalls. Check the recall details above to see if your specific product is affected. If you have a recalled product, do not consume it.
Dakota Honey Company's 2 recalls break down by severity: 0 Class I (may cause serious health issues), 2 Class II (may cause temporary health problems), and 0 Class III (unlikely to cause harm). See the full recall history table above for specific reasons.
Dakota Honey Company recalls have affected 54 states (nationwide distribution). Check individual recall entries for specific distribution details.
Related
Recall data is sourced from the FDA openFDA enforcement database. Classifications reflect FDA severity ratings: Class I (dangerous), Class II (may cause temporary health problems), Class III (unlikely harmful).
The this entity record above pulls directly from the FDA openFDA enforcement-report API. What follows is the per-entity context — how this entity sits in the broader U.S. FDA food, drug, and device recalls distribution and which underlying factors drive the headline numbers.
The methodology behind every numeric value on this page is publicly documented on the the FDA openFDA enforcement-report API portal and described in detail on this site’s methodology page. Refresh cadence varies by underlying series; the page surfaces the as-of date for each number so readers can trace any figure back to the source release.
Practical use of this page is in combination with the comparison and ranking pages elsewhere on the site, which surface the same data for this entity’s peers within U.S. consumer-product recalls. A single-entity reading without peer context can be misleading when an entity is an outlier on one axis but typical on another.