CLASS II Food recall · Reported 29 Oct 2025 · FDA Enforcement Report

Coca-Cola Can - 49000012781 / JUN2926MAA Coca-Cola Can recalled

Cocacola Southwest Beverages is recalling Coca-Cola Can - 49000012781 / JUN2926MAA Coca-Cola Can - 49000058468 / JUN2926MAA, distributed in Texas. The recall was initiated on 3 Oct 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codes49000012781 / JUN2926MAA 49000058468 / JUN2926MAA
Quantity recalled2322 units

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
H-0107-2026
FDA event ID
97751
Recalling firm
Cocacola Southwest Beverages, Dallas, TX
Classification
Class II
Status
Terminated
Recall initiated
3 Oct 2025
FDA classified
20 Oct 2025
Reported
29 Oct 2025
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Foreign Material
Product category
Soda

Timeline

3 Oct 2025Recall initiated by company
20 Oct 2025Classified by FDA+17 days
29 Oct 2025Published in enforcement report+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Potential presence of foreign material (metal) in the product

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

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

Where it was distributed

Texas

Texas

Questions about this recall

Why was it recalled?

Potential presence of foreign material (metal) in the product

Which lots are affected?

49000012781 / JUN2926MAA 49000058468 / JUN2926MAA

Where was it sold?

Texas

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

2 other products · FDA event 97751

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