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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Food
Food & Beverages/Packaged & Processed

Cinnamon Recalled for Elevated Levels of Lead

Agency Publication Date: January 9, 2026
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Summary

EUREKA INC is recalling 32 cases of Cinnamon sold in 100G clear plastic containers because they may contain elevated levels of lead. Consumers should check their pantry for this product, which was distributed to 11 retail stores and one wholesaler in California and Michigan. If you have this product, do not use it and return it to the store where it was purchased for a refund.

Risk

The product contains high levels of lead, which is a toxic substance that can cause serious health problems, especially in children and pregnant women, including developmental delays and neurological damage.

What You Should Do

  1. Check your pantry for Cinnamon in a 100G clear plastic container with UPC 6251136 034139.
  2. Verify the lot information on the packaging: Batch No. 06 B:02 and a Best by date of May 2026.
  3. Return the product to the place of purchase for a refund, throw it away, or contact the manufacturer for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

Your Remedy Options

You have 2 options:

💰Option 1: Full Refund
How to: Return the product to the place of purchase for a full refund, or contact the manufacturer or supplier for further instructions
🗑️Option 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: Cinnamon (100G)
Variants: Clear Plastic Container
UPC Codes:
625113603413
Lot Numbers:
Batch No.: 06 B:02 (Best by date: May 2026)

Distributed to 11 retail and 1 wholesale customers.

Product Images

“Durra Ground Cinnamon 100 gram)

“Durra Ground Cinnamon 100 gram)

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97767
Status: Active
Manufacturer: EUREKA INC
Sold By: Retail customers; Wholesale customers
Manufactured In: United States
Units Affected: 32 cases
Distributed To: California, Michigan

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · FDA Press Release · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.