FDA recall F-1344-2017

Product

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

NC

Key facts

Status

Terminated

Initiation date

2017-01-05

Report date

2017-02-01

Termination date

2017-01-30

Voluntary/Mandated

Voluntary: Firm initiated

Location

Charlotte, NC, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=F-1344-2017