CLASS II Food recall · Reported 8 Jan 2014 · FDA Enforcement Report

Diet Coke recalled by Coca Cola Bottling Company

Coca Cola Bottling Company United-East is recalling Diet Coke, distributed in Louisiana, Mississippi. The recall was initiated on 27 Nov 2013 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesFEB1714GBA2 with time stamps: 1830 through 1908
Quantity recalled398 cases

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-1336-2014
FDA event ID
67015
Recalling firm
Coca Cola Bottling Company United-East, Birmingham, AL
Classification
Class II
Status
Terminated
Recall initiated
27 Nov 2013
FDA classified
30 Dec 2013
Reported
8 Jan 2014
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Other Reasons
Product category
Other

Timeline

27 Nov 2013Recall initiated by company
30 Dec 2013Classified by FDA+33 days
8 Jan 2014Published in enforcement report+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

One lot of Diet Coke, 2L, may contain regular Cherry Coke which contains sugar.

Product as listed by the FDA

Diet Coke, 2L, 67.6 FL OZ (2 QT 3.6 FL OZ), UPC 4900005011

Where it was distributed

LA and MS

LouisianaMississippi

Questions about this recall

Why was it recalled?

One lot of Diet Coke, 2L, may contain regular Cherry Coke which contains sugar.

Which lots are affected?

FEB1714GBA2 with time stamps: 1830 through 1908

Where was it sold?

LA and MS

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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