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Class II: temporary or reversible health riskOngoing

Haitai Cinnamon Powder Recall

Cinnamon Powder

Haitai, Inc. · Cerritos, CA

Risk level
Class II
Reported by FDA
Nov 26, 2025
Recall ID
H-0203-2026
Check your lot numberHow we source this data

Summary

Haitai recalled Cinnamon Powder starting Oct 17, 2025. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report H-0203-2026 on Nov 26, 2025. Reason: Elevated levels of lead in Cinnamon powder. Status: Ongoing.

Why it was recalled

Elevated levels of lead in Cinnamon powder.

Product description

Cinnamon Powder; 8oz clear plastic container. Distributed by Haitai Inc. UPC: 0 20914 81415 9

Lot numbers, UPCs & expiration codes

Best By: 02/09/2025

Where it was sold

Product was distributed to retail locations across the country.

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-0203-2026
Classification
Class II
Status
Ongoing
Recall initiated
Oct 17, 2025
FDA report date
Nov 26, 2025
Quantity
69 cases
Recall type
Voluntary: Firm initiated
Recalling firm
Haitai, Inc.

Original FDA data

Every field from FDA enforcement report H-0203-2026, exactly as published.

Show all FDA fields
City
Cerritos
State
CA
Status
Ongoing
Country
United States
Event ID
97836
Address
13151 Midway Pl
Code information
Best By: 02/09/2025
Postal code
90703-2232
Report date
Nov 26, 2025
Product type
Food
Recall number
H-0203-2026
Classification
Class II
Recalling firm
Haitai, Inc.
Product quantity
69 cases
Reason for recall
Elevated levels of lead in Cinnamon powder.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Cinnamon Powder; 8oz clear plastic container. Distributed by Haitai Inc. UPC: 0 20914 81415 9
Distribution pattern
Product was distributed to retail locations across the country.
Recall initiation date
Oct 17, 2025
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Nov 19, 2025

How we source this data

Source: U.S. Food and Drug Administration enforcement report H-0203-2026, published Nov 26, 2025. View the source record (openFDA) · FDA enforcement reports

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

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