Class IIITerminated in FDA datasetRecall initiated Jan 5, 2017

Dr. Pepper, 2 Liters (2.1 qt) plastic bottles, Bottled under the authority of Dr. Pepper…

Recalling firm: Coca-Cola Consolidated

Why it was recalled

Product labeled Dr. Pepper may instead contain Diet Dr. Pepper (containing undeclared Aspartame as a sweetener).

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jan 30, 2017.

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ProductDr. Pepper, 2 Liters (2.1 qt) plastic bottles, Bottled under the authority of Dr. Pepper Company, 5301 Legacy Drive, Plano, TX 75024.
Package size2 Liters

FDA code information

Date Code MAR2717syf

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Full FDA record and distribution details

Original product description

Dr. Pepper, 2 Liters (2.1 qt) plastic bottles, Bottled under the authority of Dr. Pepper Company, 5301 Legacy Drive, Plano, TX 75024.

Original FDA recall reason

Product labeled Dr. Pepper may instead contain Diet Dr. Pepper (containing undeclared Aspartame as a sweetener).

Recall details

Recall number
F-1344-2017
Event ID
76271
FDA status
Terminated
Initiated
Jan 5, 2017
Reported
Feb 1, 2017
Classified
Jan 25, 2017
Terminated
Jan 30, 2017
Quantity
297 cases (8 bottles/case)
Location
Charlotte, NC, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

NC

FDA source record · F-1344-2017

Data updated September 16, 2026. View official FDA data ↗

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