FDA recall record
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.,...
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of August 7, 2025. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
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.
Reason
Product labeled to be Zero Sugar contains full sugar product.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
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.
Code information listed by FDA
Prod Code XXXXRS05165, Best by Date Feb 16 2026
Distribution and firm information
Recalling firm listed by FDA: Pepsi Beverages Company
Firm location listed by FDA: Jacksonville, FL, United States
Distribution reported by FDA: Product was shipped to the following states: FL, GA, SC
Product quantity listed by FDA: 19,203 x 12 & 24 pack cases
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.