RecallRadar
ModerateReported November 12, 2025

Eagle Spice Ground Ginger 16 oz.

Recalled by Eagle Spice and Extract Co., Inc.

Food recall

Eagle Spice and Extract Co., 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

Eagle Spice and Extract Co., Inc. has recalled Eagle Spice Ground Ginger 16 oz., according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on November 12, 2025 and was initiated on October 7, 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 Eagle Spice Ground Ginger 16 oz., with approximately 2,476 units affected. The company behind the recall is Eagle Spice and Extract Co., Inc., based in Brooklyn, NY. The FDA describes the product as: “Eagle Spice Ground Ginger 16 oz.”

Why was Eagle Spice Ground Ginger 16 oz. recalled?

According to the FDA, the stated reason for the recall is: “Contains elevated levels of lead (Pb).” 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 Eagle Spice Ground Ginger 16 oz., compare it against the product description and identifying codes (Lot: 24907EGGG Best Used by: 01/27/2028) before using it.

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 Eagle Spice and Extract Co., 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
Terminated
Date reported
November 12, 2025
Recall started
October 7, 2025
Distributed in
NY
What was recalled
Eagle Spice Ground Ginger 16 oz.
Why it was recalled (as stated by the FDA)
Contains elevated levels of lead (Pb)
How to identify the affected product
Lot: 24907EGGG Best Used by: 01/27/2028
Amount recalled
2,476 units

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 Eagle Spice Ground Ginger 16 oz. recalled?+

According to the FDA: Contains elevated levels of lead (Pb)

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 Eagle Spice Ground Ginger 16 oz.?+

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-0154-2026. Information last synced from the FDA on July 6, 2026.