Coca-Cola cola; 12 oz. aluminum can; 12-pack fridge pack/case
Summary
The FDA issued a Class II for Coca-Cola cola; 12 oz. aluminum can; 12-pack fridge pack/case by COCA COLA Consolidated LLC. Reason: Potential presence of foreign matter in container..
Details
Source
Food Recall
External ID
F-0335-2022
Action Date
2021-12-29
Status
Terminated
Category
food
Product Description
Coca-Cola cola; 12 oz. aluminum can; 12-pack fridge pack/case
Lot/Code Info: Coca-Cola (AUG 1522 WM B 2) Coca-Cola (AUG 1522 WM C 2)
Quantity Affected: 3168 Cases (12- 12 oz. cans per case)
Reason for Recall
Potential presence of foreign matter in container.
Distribution
Product was shipped to the following states: AR, MS, and TN,
Type: Voluntary: Firm initiated
Recall Initiated: 2021-11-24
Company
Charlotte, NC
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 75 food recalls issued in the same week, part of 204 food-related FDA actions this month.
COCA COLA Consolidated LLC has 3 FDA actions in our database, including 3 recalls.
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 Consolidated 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 Consolidated LLC have FDA actions?
COCA COLA Consolidated LLC has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0335-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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