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FDA source record Class II Terminated

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., ...

Recall Date: 2025-05-23 Recalling Firm: Pepsi Beverages Company Record Ref: H-0012-2025

FINDARECALL QUICK READ

What this record tells you

This FDA record concerns 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., ... and names Pepsi Beverages Company as the recalling firm. Use the source fields below to narrow the match, then verify the exact item and current remedy on the issuing-agency page.

  • Firm: Pepsi Beverages Company
  • Classification: Class II
  • Status: Terminated
  • Recall date: 2025-05-23
Best identifiers to check for a FDA record

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Product Description & Identification

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 / Hazard Identified

Product labeled to be Zero Sugar contains full sugar product.

How to Check Whether Your Product Matches

A matching product name or photograph is not enough by itself. Compare every identifier available on your item or packaging with the official notice.

  1. Confirm the full product and brand or recalling-firm name.
  2. Compare package size, color, flavor, model, style, or configuration when listed.
  3. Check UPC, lot, batch, serial, date code, recall number, or USDA establishment number.
  4. Review the recall date and distribution information without assuming every seller is listed.
  5. Open the official FDA source below and follow its current instructions.

If a required identifier is missing, contact the recalling company or issuing agency through the official notice rather than guessing.

Consumer Action Recorded in the Source

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Distribution & Affected States

Product was shipped to the following states: FL, GA, SC

Verify With the Issuing Agency

This record was last updated in our index on 2026-08-09 21:59:13 UTC. Because recall enforcement statuses and instructions evolve, always verify details directly with the issuing government agency.

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Record Transparency

Issuing agency
FDA
Source ID
H-0012-2025
Indexed update
2026-08-09 21:59:13 UTC
Official source
Open issuing-agency record