RecallRadar
ModerateReported February 4, 2026

Goldenroot Lemon Ginger Hibiscus Ginger Beer. 12 oz. (355 ml) UPC…

Recalled by Weaver's Brew LLC

Food recall

Weaver's Brew LLC

Class II — moderate

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

Weaver's Brew LLC has recalled Goldenroot Lemon Ginger Hibiscus Ginger Beer. 12 oz. (355 ml) UPC…, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on February 4, 2026 and was initiated on December 8, 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 Goldenroot Lemon Ginger Hibiscus Ginger Beer. 12 oz. (355 ml) UPC…, with approximately 1014 cases affected. The company behind the recall is Weaver's Brew LLC, based in Denton, TX. The FDA describes the product as: “Goldenroot Lemon Ginger Hibiscus Ginger Beer. 12 oz. (355 ml) UPC 8 50052-32821 4. Keep Cold. Manufactured By Goldenroot, 3841 Market St #113, Denton, TX 76209.”

Why was Goldenroot Lemon Ginger Hibiscus Ginger Beer. 12 oz. (355 ml) UPC… recalled?

According to the FDA, the stated reason for the recall is: “Ginger Beer products might contain ginger juice that did not undergo the required pasteurization process.”

What should you do?

If you think you may have bought Goldenroot Lemon Ginger Hibiscus Ginger Beer. 12 oz. (355 ml) UPC…, compare it against the product description and identifying codes (All Use By Dates up to 6/14/26.) 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 Weaver's Brew LLC or your local health authority.

About this recall

This recall was distributed in TX. 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
February 4, 2026
Recall started
December 8, 2025
Distributed in
TX
What was recalled
Goldenroot Lemon Ginger Hibiscus Ginger Beer. 12 oz. (355 ml) UPC 8 50052-32821 4. Keep Cold. Manufactured By Goldenroot, 3841 Market St #113, Denton, TX 76209.
Why it was recalled (as stated by the FDA)
Ginger Beer products might contain ginger juice that did not undergo the required pasteurization process.
How to identify the affected product
All Use By Dates up to 6/14/26.
Amount recalled
1014 cases

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 Goldenroot Lemon Ginger Hibiscus Ginger Beer. 12 oz. (355 ml) UPC… recalled?+

According to the FDA: Ginger Beer products might contain ginger juice that did not undergo the required pasteurization…

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 Goldenroot Lemon Ginger Hibiscus Ginger Beer. 12 oz. (355 ml) UPC…?+

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-0437-2026. Information last synced from the FDA on July 5, 2026.

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