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RECALL RECORD — CLASS IIRecall closedF-0121-2013/FDA enforcement
Bottling LLC Dba Pepsi Beverages Company·Food·Feb 5, 2012

Diet Crush Orange Soda, 12 OZ Cans

What you need to know

Class II

  • What happened

    Dr Pepper/Seven Up, Inc. has initiated a recall of mislabeled Diet Crush Orange Soda produced under license issued by one of their licensed bottlers, Pepsi Beverages Company in…

  • 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.

Recall closed · classified by the FDADistribution not listedMore food

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameBottling LLC Dba Pepsi Beverages Company
Recalling firmBottling LLC Dba Pepsi Beverages CompanyPhoenix, AZ, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • APR1612ttttPW011012 (tttt represents military time)
Distribution area

Arizona

United States

Quantity affected1791 cases
Recall initiationFDA report date: October 24, 2012
FDA recall numberF-0121-2013

Beyond the headline

The recall, in context

Bottling LLC Dba Pepsi Beverages Company initiated this food recall on February 5, 2012. The FDA enforcement report states: Dr Pepper/Seven Up, Inc. has initiated a recall of mislabeled Diet Crush Orange Soda produced under license issued by one of their licensed bottlers, Pepsi Beverages Company in Phoenix, Arizona. The bottler used new graphics on cans of product made with the previous formulation which is in the process of being discontinued. The FDA report lists distribution as: Arizona.

The FDA enforcement report describes the reason as: Dr Pepper/Seven Up, Inc. has initiated a recall of mislabeled Diet Crush Orange Soda produced under license issued by one of their licensed bottlers, Pepsi Beverages Company in Phoenix, Arizona. The bottler used new graphics on cans of product made with the previous formulation which is in the process of being discontinued.

Diet Crush Orange Soda, 12 OZ Cans was made or distributed by Bottling LLC Dba Pepsi Beverages Company in Phoenix, AZ, United States. This page reflects FDA report F-0121-2013, dated October 24, 2012.

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 Diet Crush Orange Soda, 12 OZ Cans recall?

Bottling LLC Dba Pepsi Beverages Company recalled Diet Crush Orange Soda, 12 OZ Cans in an FDA Class II enforcement action reported as F-0121-2013. Dr Pepper/Seven Up, Inc. has initiated a recall of mislabeled Diet Crush Orange Soda produced under license issued by one of their licensed bottlers, Pepsi Beverages Company in…

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 Bottling LLC Dba Pepsi Beverages Company 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-0121-2013. 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

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