RecallHawk
Class II Recall

FANTA ZERO SUGAR orange 20 FL OZ (1.25 PT) 591 mL UPC 0 49000 04143 9 THE COCA-COLA COMPANY

RQA, Inc.

Summary

The FDA issued a Class II for FANTA ZERO SUGAR orange 20 FL OZ (1.25 PT) 591 mL UPC 0 49000 04143 9 THE COCA-C by RQA, Inc.. Reason: The firm discovered that bottles labeled as Fanta Orange Zero Sugar actually contains regular Fanta Orange. The regular product contains 73g of sugar .

Details

Source

Food Recall

External ID

F-1456-2023

Action Date

2023-08-30

Status

Terminated

Category

food

Product Description

FANTA ZERO SUGAR orange 20 FL OZ (1.25 PT) 591 mL UPC 0 49000 04143 9 THE COCA-COLA COMPANY

Lot/Code Info: On lid - AUG 28 On bottle - AUG2823 SYD 2145 WV2 - 21500 WV2

Quantity Affected: 150 bottles

Reason for Recall

The firm discovered that bottles labeled as Fanta Orange Zero Sugar actually contains regular Fanta Orange. The regular product contains 73g of sugar where the Fanta Zero contains 0g of sugar.

Distribution

Product was shipped to retail facilities in NC, SC & VA.

Type: Voluntary: Firm initiated

Recall Initiated: 2023-06-28

Company

RQA, Inc.

Orland Park, IL

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 63 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 (RQA, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does RQA, Inc. have FDA actions?

This is the only FDA action we have on record for RQA, Inc. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1456-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for food

Related Actions