RecallRadar
ModerateReported December 24, 2025

BaiLiFeng Dried Cinnamon Powder

Recalled by Good Way Trading Group Inc

Food recall

Good Way Trading Group Inc

Class II — moderate

Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

See all recalls involving elevated lead levels

Good Way Trading Group Inc has recalled BaiLiFeng Dried Cinnamon Powder, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on December 24, 2025 and was initiated on October 24, 2025. It is classified as a Class II recall, which means using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.

What was recalled?

This recall covers BaiLiFeng Dried Cinnamon Powder, with approximately 150 bags affected. The company behind the recall is Good Way Trading Group Inc, based in Maspeth, NY. The FDA describes the product as: “BaiLiFeng Dried Cinnamon Powder; Net Wt 4 oz/114G; Good Way Trading Group Inc 58-51 Maspeth Avenue Maspeth NY 11378; Product of China; Ingredients: Dried Cinnamon; UPC code: 4 897055 79940 1”

Why was BaiLiFeng Dried Cinnamon Powder recalled?

According to the FDA, the stated reason for the recall is: “contains high levels of lead (10.7 mg/kg).” In plain terms, this recall relates to elevated levels of a heavy metal.

Some recalls are issued when testing finds elevated levels of a heavy metal such as lead. Long-term exposure to certain heavy metals is a recognized health concern, particularly for young children. Regulators set limits and recall products that exceed them.

What should you do?

If you think you may have bought BaiLiFeng Dried Cinnamon Powder, compare it against the product description and identifying codes (Best by date: EXP.11.12.2026 ; Item 37514) before using it. This recall is currently listed as ongoing.

The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact Good Way Trading Group Inc or your local health authority.

About this recall

This recall was distributed in NY. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.

Full recall details

Status
Ongoing
Date reported
December 24, 2025
Recall started
October 24, 2025
Distributed in
NY
What was recalled
BaiLiFeng Dried Cinnamon Powder; Net Wt 4 oz/114G; Good Way Trading Group Inc 58-51 Maspeth Avenue Maspeth NY 11378; Product of China; Ingredients: Dried Cinnamon; UPC code: 4 897055 79940 1
Why it was recalled (as stated by the FDA)
contains high levels of lead (10.7 mg/kg)
How to identify the affected product
Best by date: EXP.11.12.2026 ; Item 37514
Amount recalled
150 bags

What you can do

Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.

Quick answers

Why was BaiLiFeng Dried Cinnamon Powder recalled?+

According to the FDA: contains high levels of lead (10.7 mg/kg)

How serious is this recall?+

Class II — moderate. Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

What should I do if I have BaiLiFeng Dried Cinnamon Powder?+

Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.

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View the official FDA record

Opens the U.S. Food and Drug Administration (FDA) data for this recall.

Recall number: H-0313-2026. Information last synced from the FDA on July 6, 2026.