RecallRadar
FDA · FoodClass I

The Whole Herb Company, Inc. food recall: Celery Seed Whole Organic

SalmonellaMicrobial contamination

Key facts

Agency
U.S. Food and Drug Administration (FDA)
Program
Food
Classification
Class I
Status
Terminated
Event ID
96997
Recall initiated
May 27, 2025
Classified by FDA
Jul 9, 2025
Posted in Enforcement Report
Jul 16, 2025
Terminated
Jun 30, 2026
Recalling firm
The Whole Herb Company, Inc.
Firm location
Sonoma, CA, United States
Initiated by
Voluntary: Firm initiated
Firm notified customers by
E-Mail
Products in this event
1

What to do

Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.

View the official FDA record ↗

Reason for recall

Potential contamination with Salmonella.

What the classification means

  • Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.

About this recall

The firm started this recall on May 27, 2025. FDA classified it 43 days later, on Jul 9, 2025. Distribution reported by FDA: Domestic: IA. Foreign: Not Applicable. The Whole Herb Company, Inc. has 2 recalls in our records.

Recalled products (1)

  • H-0221-2025 Class I Terminated

    Celery Seed Whole Organic, labeled, "CELERY SEED WHL OG; Net Wt: 56.25 Lbs"

    Codes / lots: Whole Herb Item No: CEL10010. Whole Herb Lot No: 003150ST. Supplier Item No: CEL-15698. Supplier Lot No: 3-34086.

    Quantity: 439 bags (56.25 lbs/bag) = 24,694 lbs

Source and freshness

Source
U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
Official notice
FDA Enforcement Report, event 96997
Raw record
openFDA API (JSON)
Dataset last updated by FDA
Nov 3, 2026
Imported by RecallRadar
Nov 4, 2026

Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.

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