F-1344-2017 Class III Terminated

Recalled by Coca-Cola Consolidated — Charlotte, NC

FDA food recall F-1344-2017 was initiated by Coca-Cola Consolidated on Jan 5, 2017 and is designated Class III. Reason for recall: Product labeled Dr. Pepper may instead contain Diet Dr. Pepper (containing undeclared Aspartame as a sweetener). The recall status is terminated (terminated Jan 30, 2017). Affected quantity: 297 cases (8 bottles/case).

Recall details

Product Type
Food
Report Date
Feb 1, 2017
Initiation Date
Jan 5, 2017
Termination Date
Jan 30, 2017
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
297 cases (8 bottles/case)

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.

Reason for recall

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

Distribution pattern

NC

Code information

Date Code MAR2717syf

Source

Dataset
openFDA food recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for F-1344-2017
openFDA file date
Nov 3, 2026
Loaded by RegDataLab
Nov 8, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.

Source: openFDA record for F-1344-2017. Report a data issue: hello@regdatalab.com.