RecallHawk
Class II Recall

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

Coca Cola Bottling Group United

Summary

The FDA issued a Class II for Coca Cola Ultimate; packaged in 20oz PET bottles, 24 loose bottles per case *Pr by Coca Cola Bottling Group United. Reason: Incorrect label placed on product - Undeclared Sugar.

Details

Source

Food Recall

External ID

F-1237-2023

Action Date

2023-07-19

Status

Terminated

Category

food

Product Description

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

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

Quantity Affected: 177 cases

Reason for Recall

Incorrect label placed on product - Undeclared Sugar

Distribution

Georgia

Type: Voluntary: Firm initiated

Recall Initiated: 2023-07-01

Company

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 236 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Coca Cola Bottling Group United) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Coca Cola Bottling Group United have FDA actions?

This is the only FDA action we have on record for Coca Cola Bottling Group United in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1237-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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