Weaver's Brew LLC recalls Goldenroot Lemon Double Ginger ginger beer due to potential unpasteurized ginger juice. Products may contain unsafe levels of bacteria. Consumers should check UPC 8 50052-32819 and use before June 14, 2026.
Ginger Beer products might contain ginger juice that did not undergo the required pasteurization process.
Weaver's Brew LLC is recalling Goldenroot Lemon Double Ginger ginger beer because it might not have been properly pasteurized. This could lead to bacterial contamination. Consumers should check the UPC code and use the product before June 14, 2026.
The ginger beer might contain ginger juice that wasn't pasteurized, which could allow bacteria to grow. This poses a risk of foodborne illness if consumed, but the product is only for drinking and not a high-risk item.
Anyone who owns or uses Goldenroot Lemon Double Ginger ginger beer with UPC 8 50052-32819. The risk is low as the product is only for consumption and not intended for high-risk use.
Check for the UPC code 8 50052-32819 on the product label. The product is a 12 oz. (355 ml) ginger beer with a use-by date up to June 14, 2026.
Look for the UPC code 8 50052-32819 on the 12 oz. ginger beer bottle.
Consume the product before the use-by date of June 14, 2026.
The product may contain unpasteurized ginger juice, which could lead to bacterial contamination. It is recommended to check the use-by date and consume before June 14, 2026.
Check the UPC code 8 50052-32819 and use the product before June 14, 2026. There is no need to discard it if it's still within the use-by date.
The hazard is low risk as the product is only for consumption and not intended for high-risk use. There is no mention of serious injury risks in the recall notice.
We’ve drafted a message you can send Weaver's Brew LLC to request your refund or repair — edit it as you like.
Subject: Recall H-0436-2026 — Weaver's Brew LLC Weaver's Brew LLC Hello, I own a Weaver's Brew LLC that is covered by recall H-0436-2026 from Weaver's Brew LLC. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
