Coca-Cola Classic 12 FL OZ metal Can UPC 04963406 packaged in cardboard 12 pack fridge pack
Summary
The FDA issued a Class II for Coca-Cola Classic 12 FL OZ metal Can UPC 04963406 packaged in cardboard 12 pack by COCA COLA SOUTHWEST BEVERAGES LLC. Reason: The product contain foreign matter (metal particles)..
Details
Source
Food Recall
External ID
F-0001-2023
Action Date
2022-10-12
Status
Terminated
Category
food
Product Description
Coca-Cola Classic 12 FL OZ metal Can UPC 04963406 packaged in cardboard 12 pack fridge pack
Lot/Code Info: JUN1123LWG; Best By Date: June 11, 2023
Quantity Affected: 745 cases
Reason for Recall
The product contain foreign matter (metal particles).
Distribution
Texas
Type: Voluntary: Firm initiated
Recall Initiated: 2022-09-14
Company
Dallas, TX
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 57 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 SOUTHWEST BEVERAGES LLC) 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 SOUTHWEST BEVERAGES LLC have FDA actions?
This is the only FDA action we have on record for COCA COLA SOUTHWEST BEVERAGES LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0001-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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