Class IITerminatedVoluntary: Firm initiated
Pepsi Beverages Company: food recall H-0012-2025
Pepsi Beverages Company of Jacksonville, FL recalled Dr. Pepper, ZERO SUGAR, 12 FL OZ (355 mL) ALUMINUM CAN packaged and sold as 12 packs and 24 packs cartons cases.… Reason: Product labeled to be Zero Sugar contains full sugar product. The FDA listed it as Class II in its Enforcement Report dated Jun 11, 2025; distribution: Florida, Georgia, South Carolina.
Record status as published: Terminated (terminated Aug 7, 2025). 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
- 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.
- Product quantity
- 19,203 x 12 & 24 pack cases
- Reason for recall
- Product labeled to be Zero Sugar contains full sugar product.
- Codes, lots and dates on the package
- Prod Code XXXXRS05165, Best by Date Feb 16 2026
- Distribution pattern
- Product was shipped to the following states: FL, GA, SC
- Recalling firm
- Pepsi Beverages Company, Jacksonville, FL
- 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
- Letter
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | May 23, 2025 |
| Classified by the FDA | Jun 5, 2025 |
| Published in the Enforcement Report | Jun 11, 2025 |
| Terminated | Aug 7, 2025 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0012-2025 (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.