diet Pepsi recall
Recalled by Pepsi Beverage Co · Wichita, KS, United States
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it was recalled
Diet Pepsi product is labeled to contain the artificial sweetener Sucralose, but actually contains Aspartame
A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.
What was recalled
diet Pepsi, 12 FL OZ, in aluminum cans packaged in 12 pk paper cartons
Quantity: 1,972 cases
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
xxxxKS03078 Use by Date Jun 18 18
Where it was sold
Colorado Louisiana Minnesota Texas
FDA's distribution note: Distributed for sale in hotels in CO, LA, MN, and TX
Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Pepsi Beverage Co
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Mar 21, 2018
- In FDA report of
- Apr 11, 2018
- Terminated
- Jul 20, 2018
- FDA recall number
- F-0995-2018 · event 79617
- Official record
- FDA enforcement report search