The Whole Herb Company, INC. Recall History
The Whole Herb Company, INC. has had 1 FDA-tracked food recall since 2025, including 1 Class I recall (most serious). 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
- 1
- Years in FDA Data
- Since 2025
- Class I (Most Serious)
- 1
- Most Common Reason
- Salmonella contamination (1)
- Latest Recall
- Nov 21, 2025
- First Recorded Recall
- Nov 21, 2025
- States Affected
- CA, NJ
- Currently Active
- 1
- Data Source
- FDA openFDA + USDA FSIS
Complete Recall List (1 Records)
Every The Whole Herb Company, INC. 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 |
|---|---|---|---|
| Nov 21, 2025 | SENNA LEAVES F/C OG Item No: SEN15001 Net Wt: 44.75 Lbs D... | Class I | 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, The Whole Herb Company, INC. has 1 FDA food recall on record, including 1 Class I (dangerous) recall. There is currently 1 active recall.
The Whole Herb Company, INC. currently has 1 active recall. Check the recall details above to see if your specific product is affected. If you have a recalled product, do not consume it.
The Whole Herb Company, INC.'s 1 recall break down by severity: 1 Class I (may cause serious health issues), 0 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.
The Whole Herb Company, INC. recalls have affected CA, NJ. 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).
For this entity, the underlying data on this page comes from the FDA openFDA enforcement-report API. The breakdown above is the federal record; the paragraphs below add the per-entity context that makes the headline numbers usable for a real decision rather than just a data lookup.
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.