Weaver's Brew Goldenroot Ginger Beer Recall: Unpasteurized Ginger Juice Risk
Weaver's Brew LLC recalls Goldenroot Lemon Ginger Jalapeno Ginger Beer due to potential unpasteurized ginger juice. Products may contain unsafe levels of bacteria. Consumers should check UPC 8 50052-32820 7 and use before June 14, 2026.
Lower-risk recall
Ginger Beer products might contain ginger juice that did not undergo the required pasteurization process.
Contact the company
What happened, in plain English
Weaver's Brew LLC is recalling Goldenroot Lemon Ginger Ginger Beer because it might not have been properly pasteurized. This could lead to bacterial contamination, making the product unsafe to drink. Consumers should stop using the product if they have it. Read more at govinfonow.com/recall/6905-weaver-s-brew-goldenroot-ginger-beer-recall-unpasteurized-ginger-juice.
Source Summary by GovInfoNow · govinfonow.com/recall/6905-weaver-s-brew-goldenroot-ginger-beer-recall-unpasteurized-ginger-juice · Updated August 18, 2026 · Official notice: FDA #H-0438-2026
Cite this page
“Weaver's Brew Goldenroot Ginger Beer Recall: Unpasteurized Ginger Juice Risk.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/6905-weaver-s-brew-goldenroot-ginger-beer-recall-unpasteurized-ginger-juice. Based on FDA recall #H-0438-2026.
Why it’s dangerous
The ginger beer might not have gone through the required pasteurization process, which normally kills harmful bacteria. This could result in bacterial contamination, especially if the product is consumed without proper refrigeration.
Who’s affected
Anyone who purchased Goldenroot Lemon Ginger Jalapeno Ginger Beer with UPC 8 50052-32820 7. People who drink unpasteurized ginger beer products are at higher risk of bacterial infection.
How to tell if you have this one
Check for the UPC code 8 50052-32820 7 on the product label. The product is a 12 oz. (355 ml) bottle with a use-by date up to June 14, 2026.
- Brand
Weaver's Brew- Product
Goldenroot Lemon Ginger Jalapeno Ginger Beer. 12 oz. (355 ml) UPC 8 50052-32820 7. Keep Cold. Manufactured By- Category
Food
All 5 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Terminated- Distribution
Texas and California
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| H-0435-2026 | Goldenroot Lemon Ginger Elderberry Ginger Beer. 12 oz. (355 ml) UPC 8 50052-32818 4. Keep Cold. Manufactured By Goldenroot, 3841 Market St #113, Denton, TX 76209.; All Use By Dates up to 6/14/26. | 1066 cases |
| H-0436-2026 | Goldenroot Lemon Double Ginger, Ginger Beer. 12 oz. (355 ml) UPC 8 50052-32819 1. Keep Cold. Manufactured By Goldenroot, 3841 Market St #113, Denton, TX 76209.; All Use By Dates up to 6/14/26. | 1070 cases |
| H-0437-2026 | 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.; All Use By Dates up to 6/14/26. | 1014 cases |
| H-0438-2026 | Goldenroot Lemon Ginger Jalapeno Ginger Beer. 12 oz. (355 ml) UPC 8 50052-32820 7. Keep Cold. Manufactured By Goldenroot, 3841 Market St #113, Denton, TX 76209.; All Use By Dates up to 6/14/26. | 421 cases |
| H-0439-2026 | Goldenroot Yuzu Ginger Lemongrass Ginger Beer. 12 oz. (355 ml) UPC 8 50052-32817 7. Keep Cold. Manufactured By Goldenroot, 3841 Market St #113, Denton, TX 76209.; All Use By Dates up to 6/14/26. | 649 cases |
What to do — step by step
Check Product Label
Look for the UPC code 8 50052-32820 7 on the 12 oz. (355 ml) bottle.
Where it went and when
Where it was distributed
Distributed in California and Texas.
FDA distribution: “Texas and California” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Texas.
Recall timeline
FDA terminated this recall 56 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- FDA terminated the recall
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #H-0438-2026 (December 8, 2025)
- Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.