CLASS II ONGOING Food recall · Reported 26 Nov 2025 · FDA Enforcement Report

Cinnamon Powder recalled by Haitai

Haitai is recalling Cinnamon Powder, distributed nationwide in the US. The recall was initiated on 17 Oct 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesBest By: 02/09/2025
Quantity recalled69 cases

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-0203-2026
FDA event ID
97836
Recalling firm
Haitai, Cerritos, CA
Classification
Class II
Status
Ongoing
Recall initiated
17 Oct 2025
FDA classified
19 Nov 2025
Reported
26 Nov 2025
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Lead & Heavy Metals
Product category
Spices

Timeline

17 Oct 2025Recall initiated by company
19 Nov 2025Classified by FDA+33 days
26 Nov 2025Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Elevated levels of lead in Cinnamon powder.

Lead and other heavy metals accumulate in the body. Children are most at risk; even low levels can affect development.

Product as listed by the FDA

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

Where it was distributed

Product was distributed to retail locations across the country.

Nationwide

Questions about this recall

Why was it recalled?

Elevated levels of lead in Cinnamon powder.

Which lots are affected?

Best By: 02/09/2025

Where was it sold?

Product was distributed to retail locations across the country.

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 II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

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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