CLASS II Food recall · Reported 19 Jul 2023 · FDA Enforcement Report

Coca Cola Ultimate recalled

Coca Cola Bottling Group United is recalling Coca Cola Ultimate, distributed in Georgia. The recall was initiated on 1 Jul 2023 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot No. SEP2523CPA UPC: 049000552065 Best By Sept 25 2023
Quantity recalled177 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-1237-2023
FDA event ID
92652
Recalling firm
Coca Cola Bottling Group United, College Park, GA
Classification
Class II
Status
Terminated
Recall initiated
1 Jul 2023
FDA classified
7 Jul 2023
Reported
19 Jul 2023
Type
Voluntary: Firm initiated
Customers notified by
Visit
Reason category
Undeclared Allergens
Product category
Soda

Timeline

1 Jul 2023Recall initiated by company
7 Jul 2023Classified by FDA+6 days
19 Jul 2023Published in enforcement report+12 days

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

Reason for recall

Incorrect label placed on product - Undeclared Sugar

Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.

Product as listed by the FDA

Coca Cola Ultimate; packaged in 20oz PET bottles, 24 loose bottles per case *Product incorrectly labeled as Coca Cola Ultimate Zero Sugar

Where it was distributed

Georgia

Georgia

Questions about this recall

Why was it recalled?

Incorrect label placed on product - Undeclared Sugar

Which lots are affected?

Lot No. SEP2523CPA UPC: 049000552065 Best By Sept 25 2023

Where was it sold?

Georgia

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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