7up Zero Sugar Tropical Soda, 12 FL OZ (355 mL) aluminum cans, packaged in 12 pack cardboard cartons labeled as 7up Trop
Summary
The FDA issued a Class II for 7up Zero Sugar Tropical Soda, 12 FL OZ (355 mL) aluminum cans, packaged in 12 pa by Buffalo Rock Company Inc. Reason: Product mislabeled - cans are labeled as Zero Sugar, but contain full sugar product.
Details
Source
Food Recall
External ID
H-0504-2025
Action Date
2025-08-27
Status
Terminated
Category
food
Product Description
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
Lot/Code Info: Lot Numbers: XXXXBR062156 and XXXXBR062256 Use by Date: MAR 23 26
Quantity Affected: 1954 cases
Reason for Recall
Product mislabeled - cans are labeled as Zero Sugar, but contain full sugar product
Distribution
AL, FL, GA
Type: Voluntary: Firm initiated
Recall Initiated: 2025-07-31
Company
Birmingham, AL
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 90 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Buffalo Rock Company Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Buffalo Rock Company Inc have FDA actions?
This is the only FDA action we have on record for Buffalo Rock Company Inc in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0504-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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