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RECALL RECORD — CLASS IIRecall closedF-0923-2013/FDA enforcement
Pepsi Cola North America·Food·Dec 20, 2012

Diet Wild Cherry Pepsi Two Liter Plastic Bottles

What you need to know

Class II

  • What happened

    The labels on two-liter batches of Regular and Diet Wild Cherry Pepsi were mistakenly swapped during production. This is potential safety issue for individuals who are sensitive…

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice.

Recall closed · classified by the FDADistribution not listedMore food

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Product identification

Source: FDA FOOD

Brand namePepsi Cola North America
Recalling firmPepsi Cola North AmericaValhalla, NY, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Best Before Date of Feb2513 and a Manufacturing Code of PF11282
Distribution area

Massachusetts, Connecticut, Maine, New Hampshire and Vermont

United States

Quantity affected1476 - 8 pack cases
Recall initiationFDA report date: January 30, 2013
FDA recall numberF-0923-2013

Beyond the headline

The recall, in context

Pepsi Cola North America initiated this food recall on December 20, 2012. The FDA enforcement report states: The labels on two-liter batches of Regular and Diet Wild Cherry Pepsi were mistakenly swapped during production. This is potential safety issue for individuals who are sensitive to phenylalanine (i.e., phenylketonuric) or who are diabetic. The FDA report lists distribution as: Massachusetts, Connecticut, Maine, New Hampshire and Vermont.

The FDA enforcement report describes the reason as: The labels on two-liter batches of Regular and Diet Wild Cherry Pepsi were mistakenly swapped during production. This is potential safety issue for individuals who are sensitive to phenylalanine (i.e., phenylketonuric) or who are diabetic.

Diet Wild Cherry Pepsi Two Liter Plastic Bottles was made or distributed by Pepsi Cola North America in Valhalla, NY, United States. This page reflects FDA report F-0923-2013, dated January 30, 2013.

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, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

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

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

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 Diet Wild Cherry Pepsi Two Liter Plastic Bottles recall?

Pepsi Cola North America recalled Diet Wild Cherry Pepsi Two Liter Plastic Bottles in an FDA Class II enforcement action reported as F-0923-2013. The labels on two-liter batches of Regular and Diet Wild Cherry Pepsi were mistakenly swapped during production. This is potential safety issue for individuals who are sensitive…

What should I do if I bought this product?

Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Is the Pepsi Cola North America 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-0923-2013. 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

More recalls by Pepsi Cola North America

View brand
Class III·

Pepsi Cola North America

Regular Wild Cherry Pepsi Two Liter Plastic Bottles

The labels on two-liter batches of Regular and Diet Wild Cherry Pepsi were mistakenly swapped during production. This is potential safety issue for individuals who are sensitive…

Distribution not listedFood

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