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