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Class II: temporary or reversible health riskOngoing

Eureka Cinnamon Recall

Cinnamon, Clear Plastic Container, 100G, UPC 6251136 034139

EUREKA INC · Pomona, CA

Risk level
Class II
Reported by FDA
Jan 21, 2026
Recall ID
H-0388-2026
Check your lot numberHow we source this data

Summary

Eureka recalled Cinnamon starting Sep 9, 2025. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report H-0388-2026 on Jan 21, 2026. Reason: Elevated levels of lead. Status: Ongoing.

Why it was recalled

Elevated levels of lead.

Product description

Cinnamon, Clear Plastic Container, 100G, UPC 6251136 034139

Lot numbers, UPCs & expiration codes

Lot code: Batch No.: 06 B:02, Best by date: May 2026.

Where it was sold

a total of 11 retail and 1 wholesale customers across two states (California and Michigan)

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
H-0388-2026
Classification
Class II
Status
Ongoing
Recall initiated
Sep 9, 2025
FDA report date
Jan 21, 2026
Quantity
32 cases
Recall type
Voluntary: Firm initiated
Recalling firm
EUREKA INC

Original FDA data

Every field from FDA enforcement report H-0388-2026, exactly as published.

Show all FDA fields
City
Pomona
State
CA
Status
Ongoing
Country
United States
Event ID
97767
Address
1373 Ridgeway St
Code information
Lot code: Batch No.: 06 B:02, Best by date: May 2026.
Postal code
91768-2701
Report date
Jan 21, 2026
Product type
Food
Recall number
H-0388-2026
Classification
Class II
Recalling firm
EUREKA INC
Product quantity
32 cases
Reason for recall
Elevated levels of lead.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Cinnamon, Clear Plastic Container, 100G, UPC 6251136 034139
Distribution pattern
a total of 11 retail and 1 wholesale customers across two states (California and Michigan)
Recall initiation date
Sep 9, 2025
Initial firm notification
E-Mail
Center classification date
Jan 9, 2026

How we source this data

Source: U.S. Food and Drug Administration enforcement report H-0388-2026, published Jan 21, 2026. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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