LOW RISK
Terminated
F-0995-2018
diet Pepsi, 12 FL OZ, in aluminum cans packaged in 12 pk paper cartons
Recalled by Pepsi Beverage Co
Classification
Class III — Products that are unlikely to cause any adverse health reaction, but that violate FDA labeling or manufacturing laws.
Reason for Recall
Diet Pepsi product is labeled to contain the artificial sweetener Sucralose, but actually contains Aspartame
Product Details
Product Quantity
1,972 cases
Product Type
Food
Code Info
xxxxKS03078 Use by Date Jun 18 18
Voluntary/Mandated
Voluntary: Firm initiated
Distribution & Geography
Distribution Pattern
Distributed for sale in hotels in CO, LA, MN, and TX
Company Location
Wichita, KS, 67217-4937
Timeline
Report Date
04/11/2018
Recall Initiated
03/21/2018
Classification Date
04/04/2018
Termination Date
07/20/2018
Source: U.S. Food & Drug Administration (FDA) — FDA Recalls
Last updated: July 14, 2026
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