Dr. Pepper (Coca-Cola Consolidated) – Undeclared Sweetener (2017)
Class III: A situation in which use of, or exposure to, a violative product is not likely to cause adverse health consequences
Class III recall indicates unlikely adverse health consequences.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Dr. Pepper, 2 Liters (2.1 qt) plastic bottles, Bottled under the authority of Dr. Pepper Company, 5301 Legacy Drive, Plano, TX 75024.
Brand
Coca-Cola Consolidated
Lot Codes / Batch Numbers
Date Code MAR2717syf
Products Sold
Date Code MAR2717syf
Coca-Cola Consolidated is recalling Dr. Pepper, 2 Liters (2.1 qt) plastic bottles, Bottled under the authority of Dr. Pepper Company, 53 due to Product labeled Dr. Pepper may instead contain Diet Dr. Pepper (containing undeclared Aspartame as a sweetener).. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Product labeled Dr. Pepper may instead contain Diet Dr. Pepper (containing undeclared Aspartame as a sweetener).
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
NC
Page updated: Jan 6, 2026