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RECALL RECORD — CLASS IIIRecall closedF-1286-2023/FDA enforcement
Pepsico INC·Food·Jul 8, 2023

Lipton Diet Green Tea Citrus, 24 Pack of 16.9floz Bottles

What you need to know

Class III

  • What happened

    Undeclared aspartame and lack of Phenylketonurics warning on immediate container (16.9fl.oz. bottle)

  • Health risk

    The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. An allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

  • Action required

    Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction.

Recall closed · classified by the FDAIN, TN, OH, KYMore food

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Product identification

Source: FDA FOOD

Brand namePepsico INC
Recalling firmPepsico INCPurchase, NY, United States
UPC / barcodes
0 12000 01722 3
Lot / date codes
  • SEP172023XXXXAG06133 Best by Date SEP 17 2023
Distribution area
INTNOHKY

IN, TN, OH, KY

United States

Quantity affected300, 24 packs (retail unit)
Recall initiationFDA report date: July 26, 2023
FDA recall numberF-1286-2023

Beyond the headline

The recall, in context

Pepsico INC initiated this food recall on July 8, 2023. The FDA enforcement report states: Undeclared aspartame and lack of Phenylketonurics warning on immediate container (16.9fl.oz. bottle). The FDA report lists distribution as: IN, TN, OH, KY.

The FDA enforcement report describes the reason as: Undeclared aspartame and lack of Phenylketonurics warning on immediate container (16.9fl.oz. bottle)

Lipton Diet Green Tea Citrus, 24 Pack of 16.9floz Bottles was made or distributed by Pepsico INC in Purchase, NY, United States. This page reflects FDA report F-1286-2023, dated July 26, 2023.

Why this is a Class III recall

Class III means the product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. In this recall, an allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

FDA definition

The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Undeclared allergen

Symptoms to watch for

Hives, swelling, wheezing, coughing, vomiting, abdominal pain or a drop in blood pressure. Anaphylaxis is a medical emergency.

When symptoms may appear

Allergic reactions often begin within minutes to a few hours of eating the allergen.

Higher-risk groups

Anyone with a diagnosed food allergy, especially children, and people with a history of anaphylaxis or asthma.

What to do now

  1. 1Do not eat or serve the affected product if you or anyone in the household has a diagnosed allergy.
  2. 2If symptoms such as swelling, wheezing or breathing difficulty occur, use the person's prescribed emergency plan and call emergency services.
  3. 3Keep the packaging, contact the retailer or manufacturer for a refund, and read the official recall notice for the exact allergen.

For a severe allergic reaction, do not wait for a callback or refund process before seeking emergency care.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Lipton Diet Green Tea Citrus, 24 Pack of 16.9floz Bottles recall?

Pepsico INC recalled Lipton Diet Green Tea Citrus, 24 Pack of 16.9floz Bottles in an FDA Class III enforcement action reported as F-1286-2023. Undeclared aspartame and lack of Phenylketonurics warning on immediate container (16.9fl.oz. bottle)

What should I do if I bought this product?

Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction. Do not eat or serve the affected product if you or anyone in the household has a diagnosed allergy. If symptoms such as swelling, wheezing or breathing difficulty occur, use the person's prescribed emergency plan and call emergency services. Keep the packaging, contact the retailer or manufacturer for a refund, and read the official recall notice for the exact allergen.

Is the Pepsico INC recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-1286-2023. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.