Lemon ginger jalapeno beer recalled over possibly unpasteurized ginger juice
Weaver's Brew is recalling 421 cases of Goldenroot Lemon Ginger Jalapeno Ginger Beer because the products might contain ginger juice that did not undergo the required pasteurization process.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 3/5 (High).
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: Scored 3 under the risk-of-harm criterion: a required pasteurization step may not have been applied to juice in a ready-to-drink product, and no illnesses are reported.
Plain-English summary
Goldenroot Lemon Ginger Jalapeno Ginger Beer, 12 oz (355 ml), under UPC 8 50052-32820 7, manufactured by Goldenroot of Denton, Texas, is being recalled by Weaver's Brew LLC.
The reason given in the enforcement record is that the ginger beer products might contain ginger juice that did not undergo the required pasteurization process.
The record lists 421 cases covering all use-by dates up to 6/14/26. Distribution was to Texas and California. The FDA has classified the action as Class II.
Juice that has not been through the required pasteurization step has not had that pathogen control applied. The record reports no illnesses. Consumers who have this product should not drink it and should follow the retailer's return instructions.
The recalled product
- Product
- Medline medical procedure convenience kits labeled as: NERVE BLOCK TRAY 2, Kit SKU DYNJRA2713
- Manufacturer
- Medline Industries, LP
- Category
- Food — Beverage
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (2)
- UDI/DI 10198459565861 (EA) 40198459565862 (CS)
- Lot number 25KMD285
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 15 recalled by Medline Industries, LP under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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