CLASS III Food recall · Reported 31 Dec 2014 · FDA Enforcement Report

Coca Cola Zero pet recalled

Coca-Cola Company (The) is recalling Coca Cola Zero pet, distributed in Indiana, Kentucky, Ohio. The recall was initiated on 5 Nov 2014 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesDate code: DEC1514 CNB, Time Stamps: 12:19, 12:20, 12:21 and 12:22
Quantity recalled600 bottles (75 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-0754-2015
FDA event ID
69738
Recalling firm
Coca-Cola Company (The), Atlanta, GA
Classification
Class III
Status
Terminated
Recall initiated
5 Nov 2014
FDA classified
23 Dec 2014
Reported
31 Dec 2014
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Other Reasons
Product category
Soda

Timeline

5 Nov 2014Recall initiated by company
23 Dec 2014Classified by FDA+48 days
31 Dec 2014Published in enforcement report+8 days

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

Reason for recall

Equipment malfunction led to ingredients to be blended at levels that are inconsistent with approved formulations.

Product as listed by the FDA

Coca Cola Zero, 2 liter pet bottle, UPC 49000 05014, The Coca Cola Company

Where it was distributed

OH, KY and IN.

IndianaKentuckyOhio

Questions about this recall

Why was it recalled?

Equipment malfunction led to ingredients to be blended at levels that are inconsistent with approved formulations.

Which lots are affected?

Date code: DEC1514 CNB, Time Stamps: 12:19, 12:20, 12:21 and 12:22

Where was it sold?

OH, KY and IN.

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 III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

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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