RecallHawk
Class II Recall

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

Haitai, Inc.

Summary

The FDA issued a Class II for Cinnamon Powder; 8oz clear plastic container. Distributed by Haitai Inc. UPC: 0 by Haitai, Inc.. Reason: Elevated levels of lead in Cinnamon powder..

Details

Source

Food Recall

External ID

H-0203-2026

Action Date

2025-11-26

Status

Ongoing

Category

food

Product Description

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

Lot/Code Info: Best By: 02/09/2025

Quantity Affected: 69 cases

Reason for Recall

Elevated levels of lead in Cinnamon powder.

Distribution

Product was distributed to retail locations across the country.

Type: Voluntary: Firm initiated

Recall Initiated: 2025-10-17

Company

Haitai, Inc.

Cerritos, CA

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 33 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Haitai, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Haitai, Inc. have FDA actions?

This is the only FDA action we have on record for Haitai, Inc. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0203-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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