Coca-Cola 12oz Can - 24 pack 49000012781 / JUN2926MAA Coca-Cola 12o…
Recalled by COCACOLA SOUTHWEST BEVERAGES LLC
Food recall
COCACOLA SOUTHWEST BEVERAGES LLC
Class II — moderate
Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
COCACOLA SOUTHWEST BEVERAGES LLC has recalled Coca-Cola 12oz Can - 24 pack 49000012781 / JUN2926MAA Coca-Cola 12o…, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on October 29, 2025 and was initiated on October 3, 2025. It is classified as a Class II recall, which means using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.
What was recalled?
This recall covers Coca-Cola 12oz Can - 24 pack 49000012781 / JUN2926MAA Coca-Cola 12o…, with approximately 2322 units affected. The company behind the recall is COCACOLA SOUTHWEST BEVERAGES LLC, based in Dallas, TX. The FDA describes the product as: “Coca-Cola 12oz Can - 24 pack 49000012781 / JUN2926MAA Coca-Cola 12oz Can - 35 pack 49000058468 / JUN2926MAA”
Why was Coca-Cola 12oz Can - 24 pack 49000012781 / JUN2926MAA Coca-Cola 12o… recalled?
According to the FDA, the stated reason for the recall is: “Potential presence of foreign material (metal) in the product.” In plain terms, this recall relates to foreign material.
A foreign material recall means that pieces of something which should not be in food — such as metal, plastic, or glass — may be present. These can pose a choking hazard or cause injury. Recalls like these are issued to remove the affected product before anyone is hurt.
What should you do?
If you think you may have bought Coca-Cola 12oz Can - 24 pack 49000012781 / JUN2926MAA Coca-Cola 12o…, compare it against the product description and identifying codes (49000012781 / JUN2926MAA 49000058468 / JUN2926MAA) before using it.
The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact COCACOLA SOUTHWEST BEVERAGES LLC or your local health authority.
About this recall
This recall was distributed in TX. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.
Full recall details
- Status
- Terminated
- Date reported
- October 29, 2025
- Recall started
- October 3, 2025
- Distributed in
- TX
What you can do
Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.
Quick answers
Why was Coca-Cola 12oz Can - 24 pack 49000012781 / JUN2926MAA Coca-Cola 12o… recalled?+
According to the FDA: Potential presence of foreign material (metal) in the product
How serious is this recall?+
Class II — moderate. Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
What should I do if I have Coca-Cola 12oz Can - 24 pack 49000012781 / JUN2926MAA Coca-Cola 12o…?+
Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.
Opens the U.S. Food and Drug Administration (FDA) data for this recall.
Recall number: H-0107-2026. Information last synced from the FDA on July 6, 2026.