Food FDA Class II Terminated Mislabeling
Dr. Pepper, ZERO SUGAR, 12 FL OZ (355 mL) ALUMINUM CAN packaged and sold as 12 packs and 24 packs cartons cases. PRODUCED UNDER THE AUTHORITY OF CB Manufacturing Company, Inc., 5829 Pepsi Pl., Jacksonville, Florida, United States of America, 32216 - 904-443-0763 who is licensed to manufacture Keurig
Pepsi Beverages Company Published Jun 11, 2025
Risk level
Class IIMay cause a temporary or reversible health problem; slight chance of serious harm.
Severity score 45/100
What should you do?
- Check whether you have this product, using the lot codes, UPCs, and dates listed below.
- Do not eat, serve, or sell the affected product.
- Return it to the place of purchase for a refund, or throw it away in a sealed bag so people and animals can’t get to it.
- Contact Pepsi Beverages Company or your place of purchase with questions, and see the source record below for full details.
Reason for recall
Product labeled to be Zero Sugar contains full sugar product.
Affected products (1)
Dr. Pepper, ZERO SUGAR, 12 FL OZ (355 mL) ALUMINUM CAN packaged and sold as 12 packs and 24 packs cartons cases. PRODUCED UNDER THE AUTHORITY OF CB Manufacturing Company, Inc., 5829 Pepsi Pl., Jacksonville, Florida, United States of America, 32216 - 904-443-0763 who is licensed to manufacture Keurig Dr. Pepper branded products.
19,203 x 12 & 24 pack cases
Code info: Prod Code XXXXRS05165, Best by Date Feb 16 2026
Affected areas
FloridaGeorgiaSouth Carolina
Timeline
- InitiatedMay 23, 2025
- PublishedJun 11, 2025
- TerminatedAug 7, 2025
- Recall number
- H-0012-2025
- Agency
- U.S. Food and Drug Administration
- Country
- US
FDA records come from the openFDA food enforcement-report dataset — the agency's full weekly enforcement list. Most entries are not issued as consumer press releases, so they won't appear on fda.gov/recalls or in a web search. The source record link above resolves this exact recall by its number.