Severity
Moderate
ModerateClass IITerminated
FDA Food recall · Reported June 11, 2025
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 labeled to be Zero Sugar contains full sugar product.
Pepsi Beverages Company recalled Dr. Pepper, ZERO SUGAR, 12 FL OZ (355 mL) ALUMINUM CAN packaged and sold as 12 packs and … - a moderate-severity action.
Dr. Pepper, ZERO SUGAR, 12 FL OZ (355 mL) ALUMINUM CAN packaged and sold as 12 packs and … was recalled by Pepsi Beverages Company in June 11, 2025. Reason: Product labeled to be Zero Sugar contains full sugar product.. Check the official notice for the remedy. Verify recall #H-0012-2025 with the FDA Food before acting.
The recall
Pepsi Beverages Company issued this moderate-severity FDA Food recall-Product labeled to be Zero Sugar contains full sugar product..
- Moderate
- severity level
- Class II
- classification
- June 11, 2025
- reported
Sourced from official FDA Food enforcement records. Verify recall #H-0012-2025 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #H-0012-2025) was formally reported on June 11, 2025, with the manufacturer initiating the action on May 23, 2025. It is classified under Moderate severity (Class II), with a current status of Terminated. Pepsi Beverages Company is listed as the recalling firm, operating out of Jacksonville, FL. Federal records list the affected scope as 19,203 x 12 & 24 pack cases.
The documented reason for this recall is: Product labeled to be Zero Sugar contains full sugar product. Distribution data in the federal record shows the product reached: Product was shipped to the following states: FL, GA, SC. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 2 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Food recalls over time
Where this recall sits in its category - 25,126 food recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
19,203 x 12 & 24 pack cases
Related Recalls
6
2 from same agency
Product description
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 for recall
Product labeled to be Zero Sugar contains full sugar product.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | H-0012-2025 |
| Date reported | June 11, 2025 |
| Date initiated | May 23, 2025 |
| Recalling firm | Pepsi Beverages Company |
| Firm location | Jacksonville, FL |
| Affected scope | 19,203 x 12 & 24 pack cases |
| Distribution | Product was shipped to the following states: FL, GA, SC |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (H-0012-2025) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by Pepsi Beverages Company. Units affected: 19,203 x 12 & 24 pack cases.
Why was this product recalled? ▼
Product labeled to be Zero Sugar contains full sugar product.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on June 11, 2025. Severity: Moderate. Recall number: H-0012-2025.
Where was the recalled product distributed? ▼
Distribution: Product was shipped to the following states: FL, GA, SC.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (H-0012-2025) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Compare this recall with Conair Recalls Over One Million Cuisinart Grill Brushes Due… →
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported June 11, 2025. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.