Yo!man Cucumber
Reason Product contains undeclared cyclamates.
Refrigerated Cucumber X Tarragon Ginger Beer recall
Recalled by RGB Soda, LLC. · Seattle, WA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Potential contamination with Salmonella.
Pathogen: Salmonella
Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.
The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.
What was recalled
Refrigerated Cucumber X Tarragon Ginger Beer (ginger juice). Product is juice soda and distributed in 5gal. pony keg. The kegs were distributed to the firm's own stores where they were served to glasses. The kegs were labeled with the name of the product and the day it was made.
Quantity: 10/5gal. kegs; 2/64oz containers; 2/32oz containers
Food: Cucumbers Juice & beverages
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Batch numbers: 11/4/2024 and 11/25/2024 Expiry dates: 12/15/2024-1/6/2025.
Where it was sold
Washington
FDA's distribution note: Distributed in WA.
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- RGB Soda, LLC.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Nov 29, 2024
- In FDA report of
- Jun 25, 2025
- Terminated
- Jun 24, 2025
- FDA recall number
- H-0057-2025 · event 97016
- Official record
- FDA enforcement report search
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