Coca-Cola recalls 12-packs of Vanilla Coke (UPC 49000 03124) due to undeclared aspartame. Consumers should check labels and contact the company for details.
“Coca-Cola Vanilla 12-Pack Recall: Undeclared Aspartame.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/29691-coca-cola-vanilla-12-pack-recall-undeclared-aspartame. Based on FDA recall #F-2088-2014 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2088-2014%22&limit=1).
The Food and Drug Administration announced on May 29, 2014, that The Coca-Cola Company is recalling Coca Cola Vanilla 12-pack/12 fl oz cans due to undeclared aspartame. The agency classified the recall as Class III.
How to tell if you have it
Coca Cola Vanilla, 12 pack/12 fl oz cans
UPC: 49000 03124
Date Code: JAN192055CC
The hazard
The product contains undeclared aspartame.
Context
GovInfoNow's records show The Coca-Cola Company has had 9 other recalls on record since March 31, 2016. Other recent recalls of similar products include Coca-Cola Topo Chico Mineral Water Recall (May 28, 2025), Coca-Cola Powerade Zero Fruit Punch 20oz Bottles Recall (Feb. 27, 2024), and Coca-Cola recalls Minute Maid Berry Punch (Nov. 10, 2021). Other recent recalls of similar products include Domino Foods Sodexo Stars Saccharin Pink Packets Recall (Jan. 13, 2026), D'Dioses Vanilla Ice Pop Recall (May 4, 2026), and 7up Tropical Recall (Aug. 20, 2026).
How to tell if you have this one
Check for the UPC 49000 03124 on the 12-pack of Vanilla Coke. The product was sold with a date code starting with JAN192055CC.
Brand
Coca-Cola
Product
Coca Cola Vanilla, 12 pack/12 fl oz cans, UPC: 49000 03124, Canned under authority of the Coca Cola Company, Atlanta
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Label
Look for the UPC 49000 03124 on the 12-pack of Vanilla Coke.
Where it went and when
Where it was distributed
Distributed in 6 states.
Listed by the agency
Not listed
FDA distribution: “CO, KS, NM, SD, UT and WY.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Colorado, Kansas, New Mexico, South Dakota, Utah, Wyoming.
Recall timeline
FDA terminated this recall 22 months after the firm started it.
1Firm started the recall
2FDA classified it Class III
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #F-2088-2014 (May 29, 2014) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2088-2014 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.