Lower riskFood recall · FDA · Published July 8, 2023
PepsiCo Lipton Diet Green Tea Citrus Recall: Undeclared Aspartame Risk
PepsiCo recalls 24-pack of Lipton Diet Green Tea Citrus bottles due to undeclared aspartame and missing phenylketonurics warning. Consumers should check UPC #0-12000-01722-3.
“PepsiCo Lipton Diet Green Tea Citrus Recall: Undeclared Aspartame Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/10704-pepsico-lipton-diet-green-tea-citrus-recall-undeclared-aspartame-risk. Based on FDA recall #F-1286-2023 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1286-2023%22&limit=1).
The FDA announced on July 8, 2023, that PepsiCo Inc. is recalling Lipton Diet Green Tea Citrus due to undeclared aspartame and a missing Phenylketonurics warning. The recall affects 24-packs of 16.9-ounce bottles distributed in Indiana, Tennessee, Ohio, and Kentucky.
How to tell if you have it
Lipton Diet Green Tea Citrus, 24 pack of 16.9floz bottles
UPC # 0-12000-01722-3
Best by Date SEP 17 2023
The hazard
The product lacks a Phenylketonurics warning on the immediate container and contains undeclared aspartame. The FDA classified this as a Class III recall.
Context
GovInfoNow's records show PepsiCo Inc has 13 other recalls on record since March 14, 2018. Other recent recalls of similar products include Lipton Green Tea Citrus Recall (September 17, 2025) and Pepsico Recalls Root Beer Cans Due to Sugar Labeling Error (March 22, 2024). Additional similar recalls include Schweppes Zero Sugar Ginger Ale Caffeine Free Recall (March 9, 2024), Domino Foods Sodexo Stars Saccharin Pink Packets Recall (January 13, 2026), Wawa Diet Iced Tea Lemon Pint Recall (April 2, 2026), and 7up Tropical Recall (August 20, 2026).
How to tell if you have this one
Check for the UPC code 0-12000-01722-3 on the bottle. The product is a 24-pack of 16.9 fl oz Lipton Diet Green Tea Citrus bottles with a best by date of September 17, 2023.
Brand
PepsiCo
Product
Lipton Diet Green Tea Citrus, 24 pack of 16.9floz bottles. UPC # 0-12000-01722-3
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Details
Look for the UPC code 0-12000-01722-3 on the bottle to confirm it's part of the recall.
Where it went and when
Where it was distributed
Distributed in 4 states.
Listed by the agency
Not listed
FDA distribution: “IN, TN, OH, KY” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Indiana, Kentucky, Ohio, Tennessee.
Recall timeline
FDA terminated this recall 45 days 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-1286-2023 (July 8, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1286-2023 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 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.