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ACTIVE RECALL — CLASS IIActive recallH-0009-2027/FDA enforcement
Pepsico INC·Food·Sep 25, 2026

28 OZ

What you need to know

Class II

  • What happened

    Undeclared Yellow No. 6 and/or Yellow No. 5

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. 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.

Active recall · classified by the FDAAK, AL, AR, AZ +33 moreMore food

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Product identification

Source: FDA FOOD

Brand namePepsico INC
Recalling firmPepsico INCPurchase, NY, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Lot 091026 DL - JUN 07 27; Lot 091126 DL - JUN 08 27; Lot 072226 DT - APR 18 27; Lot 072426 TL - APR 20 27; Lot 073126 TL - APR 27 27; Lot 072926 TL - APR 25 27
  • Lot 073026 TL - APR 25 27; Lot 081026 TL - MAY 07 27; Lot 082126 OA - APR 18 27; Lot 080126 DL - APR 28 27; Lot 082026 DL - MAY 17 27; Lot 083126 DT - JUN 07 27
Distribution area
AKALARAZCACOFLGAHIIAIDILINKSKYLAMIMNMOMSNCNDNENJNMNVNYOHOKPASCSDTNTXUTWAWI

AK, AL, AR, AZ, CA, CO, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MI, MN, MO, MS, NC, ND, NE, NJ, NM, NV, NY, OH, OK, PA, SC, SD, TN, TX, UT, WA, WI

United States

Quantity affected122, 021 Cases (28 oz.)
Recall initiationFDA report date: October 14, 2026
FDA recall numberH-0009-2027

Beyond the headline

The recall, in context

Pepsico INC initiated this food recall on September 25, 2026. The FDA enforcement report states: Undeclared Yellow No. 6 and/or Yellow No. 5. The FDA report lists distribution as: AK, AL, AR, AZ, CA, CO, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MI, MN, MO, MS, NC, ND, NE, NJ, NM, NV, NY, OH, OK, PA, SC, SD, TN, TX, UT, WA, WI.

The FDA enforcement report describes the reason as: Undeclared Yellow No. 6 and/or Yellow No. 5

28 OZ was made or distributed by Pepsico INC in Purchase, NY, United States. This page reflects FDA report H-0009-2027, dated October 14, 2026.

Why this is a Class II recall

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

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 lot and date codes 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 28 OZ recall?

Pepsico INC recalled 28 OZ in an FDA Class II enforcement action reported as H-0009-2027. Undeclared Yellow No. 6 and/or Yellow No. 5

What are the symptoms of Undeclared allergen exposure?

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

How quickly can Undeclared allergen symptoms appear?

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

Who is most at risk from Undeclared allergen?

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

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.

How do I get a refund from Pepsico INC?

Contact the recalling company or the retailer where you purchased the product, quote the FDA recall number and ask about a refund or replacement. Keep the packaging, lot code and proof of purchase where possible. The FDA does not issue consumer refunds. Reference FDA recall H-0009-2027 and keep the packaging, lot code and proof of purchase if you have them.

Is the Pepsico INC recall still active?

Yes. As of the latest FDA enforcement report, this recall is listed as ongoing. Check the official source record for the most current status before making a decision.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record H-0009-2027. 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.