CLASS I ONGOING Food recall · Reported 24 Dec 2025 · FDA Enforcement Report
Senna Leaves F/c Og recalled by The Whole Herb Company
The Whole Herb Company is recalling Senna Leaves F/c Og, distributed in California, New Jersey. The recall was initiated on 21 Nov 2025 and the FDA has classified it as Class I.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- H-0325-2026
- FDA event ID
- 98043
- Recalling firm
- The Whole Herb Company, Sonoma, CA
- Brand
- Senna Leaves
- Classification
- Class I
- Status
- Ongoing
- Recall initiated
- 21 Nov 2025
- FDA classified
- 18 Dec 2025
- Reported
- 24 Dec 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Salmonella
- Product category
- Other
Timeline
| 21 Nov 2025 | Recall initiated by company | |
| 18 Dec 2025 | Classified by FDA | +27 days |
| 24 Dec 2025 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Potential contamination with Salmonella.
Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.
Product as listed by the FDA
SENNA LEAVES F/C OG Item No: SEN15001 Net Wt: 44.75 Lbs Distributed By Whole Herb Company 19800 8th Street East, Sonoma, CA 95476 UPC 10031 44312
Where it was distributed
U.S. Distribution: CA, NJ Foreign Distribution: Canada
Questions about this recall
Why was it recalled?
Potential contamination with Salmonella.
Which lots are affected?
Lot No: 003279ST
Where was it sold?
U.S. Distribution: CA, NJ Foreign Distribution: Canada
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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