Dr. Pepper, ZERO SUGAR, 12 FL OZ (355 mL) ALUMINUM CAN packaged and sold as 12 packs and 24 packs cartons cases. PRODUCE
Summary
The FDA issued a Class II for Dr. Pepper, ZERO SUGAR, 12 FL OZ (355 mL) ALUMINUM CAN packaged and sold as 12 p by Pepsi Beverages Company. Reason: Product labeled to be Zero Sugar contains full sugar product..
Details
Source
Food Recall
External ID
H-0012-2025
Action Date
2025-06-11
Status
Terminated
Category
food
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.
Lot/Code Info: Prod Code XXXXRS05165, Best by Date Feb 16 2026
Quantity Affected: 19,203 x 12 & 24 pack cases
Reason for Recall
Product labeled to be Zero Sugar contains full sugar product.
Distribution
Product was shipped to the following states: FL, GA, SC
Type: Voluntary: Firm initiated
Recall Initiated: 2025-05-23
Company
Jacksonville, FL
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 123 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Pepsi Beverages Company) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Pepsi Beverages Company have FDA actions?
This is the only FDA action we have on record for Pepsi Beverages Company in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0012-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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