Coca-Cola Cherry Zero Sugar Fridge Pack, 12 - 12 FL OZ CANS (144 FL OZ) in a 12-pack fridge pack carton. UPC 0490000475
Summary
The FDA issued a Class II for Coca-Cola Cherry Zero Sugar Fridge Pack, 12 - 12 FL OZ CANS (144 FL OZ) in a 12 by Swire Coca Cola USA. Reason: Exterior packaging correctly identifies the contents as Cherry Coca-Cola Zero, the cans contained in the fridge pack are incorrectly labeled as Cherry.
Details
Source
Food Recall
External ID
F-0854-2022
Action Date
2022-03-16
Status
Terminated
Category
food
Product Description
Coca-Cola Cherry Zero Sugar Fridge Pack, 12 - 12 FL OZ CANS (144 FL OZ) in a 12-pack fridge pack carton. UPC 049000047516; UPC Cherry Coca-Cola Zero Sugar can 049000047561; Cherry Coca-Cola can 04905004. There are 2 12-packs per case.
Lot/Code Info: Cherry Coca-Cola Zero Sugar, MAY3022TOA 15:25 -16:15 (time stamps) 12 oz. can in a 12-pack fridge pack. Cherry Coca-Cola, MAY3022TOA, 12 oz. can (Single Cans Only) *If removed from the above 12 pack at the store for individual sale.
Quantity Affected: 740 cases (2 12-packs/case)
Reason for Recall
Exterior packaging correctly identifies the contents as Cherry Coca-Cola Zero, the cans contained in the fridge pack are incorrectly labeled as Cherry Coca-Cola and do not include the required notification for phenylketonurics that the beverage contains phenylalanine.
Distribution
AZ, UT, WY
Type: Voluntary: Firm initiated
Recall Initiated: 2022-02-19
Company
West Valley City, UT
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 92 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 (Swire Coca Cola USA) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Swire Coca Cola USA have FDA actions?
This is the only FDA action we have on record for Swire Coca Cola USA in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0854-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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