RGB Soda, LLC. food recall: Refrigerated Cucumber X Tarragon Ginger Beer
Key facts
- Agency
- U.S. Food and Drug Administration (FDA)
- Program
- Food
- Classification
- Class I
- Status
- Terminated
- Event ID
- 97016
- Recall initiated
- Nov 29, 2024
- Classified by FDA
- Jun 18, 2025
- Posted in Enforcement Report
- Jun 25, 2025
- Terminated
- Jun 24, 2025
- Recalling firm
- RGB Soda, LLC.
- Firm location
- Seattle, WA, United States
- Initiated by
- Voluntary: Firm initiated
- Firm notified customers by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Products in this event
- 1
What to do
Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.
Reason for recall
Potential contamination with Salmonella.
What the classification means
- Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.
About this recall
The firm started this recall on Nov 29, 2024. FDA classified it 201 days later, on Jun 18, 2025. Distribution reported by FDA: Distributed in WA.
Recalled products (1)
H-0057-2025 Class I Terminated
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.
Codes / lots: Batch numbers: 11/4/2024 and 11/25/2024 Expiry dates: 12/15/2024-1/6/2025.
Quantity: 10/5gal. kegs; 2/64oz containers; 2/32oz containers
Source and freshness
- Source
- U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
- Official notice
- FDA Enforcement Report, event 97016
- Raw record
- openFDA API (JSON)
- Dataset last updated by FDA
- Nov 3, 2026
- Imported by RecallRadar
- Nov 4, 2026
Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.