LOW RISK
Terminated
F-1344-2017
Dr. Pepper, 2 Liters (2.1 qt) plastic bottles, Bottled under the authority of Dr. Pepper Company, 5301 Legacy Drive, Plano, TX 75024.
Recalled by Coca-Cola Consolidated
Classification
Class III — Products that are unlikely to cause any adverse health reaction, but that violate FDA labeling or manufacturing laws.
Reason for Recall
Product labeled Dr. Pepper may instead contain Diet Dr. Pepper (containing undeclared Aspartame as a sweetener).
Product Details
Product Quantity
297 cases (8 bottles/case)
Product Type
Food
Code Info
Date Code MAR2717syf
Voluntary/Mandated
Voluntary: Firm initiated
Distribution & Geography
Distribution Pattern
NC
Company Location
Charlotte, NC, 28216-2905
Timeline
Report Date
02/01/2017
Recall Initiated
01/05/2017
Classification Date
01/25/2017
Termination Date
01/30/2017
Source: U.S. Food & Drug Administration (FDA) — FDA Recalls
Last updated: August 28, 2026
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