RecallHawk
Class II Recall

Coca-Cola 12oz Can - 24 pack 49000012781 / JUN2926MAA Coca-Cola 12oz Can - 35 pack 49000058468 / JUN2926MAA

COCACOLA SOUTHWEST BEVERAGES LLC

Summary

The FDA issued a Class II for Coca-Cola 12oz Can - 24 pack 49000012781 / JUN2926MAA Coca-Cola 12oz Can - 35 pa by COCACOLA SOUTHWEST BEVERAGES LLC. Reason: Potential presence of foreign material (metal) in the product.

Details

Source

Food Recall

External ID

H-0107-2026

Action Date

2025-10-29

Status

Terminated

Category

food

Product Description

Coca-Cola 12oz Can - 24 pack 49000012781 / JUN2926MAA Coca-Cola 12oz Can - 35 pack 49000058468 / JUN2926MAA

Lot/Code Info: 49000012781 / JUN2926MAA 49000058468 / JUN2926MAA

Quantity Affected: 2322 units

Reason for Recall

Potential presence of foreign material (metal) in the product

Distribution

Texas

Type: Voluntary: Firm initiated

Recall Initiated: 2025-10-03

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 91 food recalls issued in the same week, part of 204 food-related FDA actions this month.

COCACOLA SOUTHWEST BEVERAGES 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 (COCACOLA 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 COCACOLA SOUTHWEST BEVERAGES LLC have FDA actions?

COCACOLA SOUTHWEST BEVERAGES 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 "H-0107-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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