Class IITerminatedVoluntary: Firm initiated

Buffalo Rock Company Inc: food recall H-0504-2025

Buffalo Rock Company Inc of Birmingham, AL recalled 7up Zero Sugar Tropical Soda, 12 FL OZ (355 mL) aluminum cans, packaged in 12 pack cardboard cartons labeled as 7up… Reason: Product mislabeled - cans are labeled as Zero Sugar, but contain full sugar product. The FDA listed it as Class II in its Enforcement Report dated Aug 27, 2025; distribution: Alabama, Florida, Georgia.

Record status as published: Terminated (terminated Apr 24, 2026). openFDA data last updated Oct 21, 2026.

Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.

Recall details

Product
7up Zero Sugar Tropical Soda, 12 FL OZ (355 mL) aluminum cans, packaged in 12 pack cardboard cartons labeled as 7up Tropical Flavored Soda, UPC (on can): 078000037975, UPC (on carton): 078000037982
Product quantity
1954 cases
Reason for recall
Product mislabeled - cans are labeled as Zero Sugar, but contain full sugar product
Codes, lots and dates on the package
Lot Numbers: XXXXBR062156 and XXXXBR062256 Use by Date: MAR 23 26
Distribution pattern
AL, FL, GA
Recalling firm
Buffalo Rock Company Inc, Birmingham, AL
Classification
Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Voluntary or mandated
Voluntary: Firm initiated
How the firm first notified customers
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Dates

EventDate
Recall initiated by the firmJul 31, 2025
Classified by the FDAAug 20, 2025
Published in the Enforcement ReportAug 27, 2025
TerminatedApr 24, 2026

All food recall records

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Sources

  • U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0504-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
  • Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.