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RECALL RECORD — CLASS IIRecall closedF-0361-2022/FDA enforcement
Keurig Dr Pepper·Food·Dec 9, 2021

Diet Snapple Tea Peach Tea 16 OZ

What you need to know

Class II

  • What happened

    Product labeled to be Diet and Zero Sugar in the ingredient statement may contain sugar due to an production error.

  • 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 nameKeurig Dr Pepper
Recalling firmKeurig Dr PepperFrisco, TX, United States
UPC / barcodes
0 76183 00314 50 76183 00813 3
Lot / date codes
  • ALN 09H21 (Time Stamp 18:22-23:59) and ALN 10H21 (Time Stamp 00:00-00:25)
Distribution area

Distributed to 11 warehouses who then further distributed product to retailer, institutions, businesses, etc. throughout the US.

United States

Quantity affected11, 970 cases
Recall initiationFDA report date: January 12, 2022
FDA recall numberF-0361-2022

Beyond the headline

The recall, in context

Keurig Dr Pepper initiated this food recall on December 9, 2021. The FDA enforcement report states: Product labeled to be Diet and Zero Sugar in the ingredient statement may contain sugar due to an production error. The FDA report lists distribution as: Distributed to 11 warehouses who then further distributed product to retailer, institutions, businesses, etc. throughout the US.

The FDA enforcement report describes the reason as: Product labeled to be Diet and Zero Sugar in the ingredient statement may contain sugar due to an production error.

Diet Snapple Tea Peach Tea 16 OZ was made or distributed by Keurig Dr Pepper in Frisco, TX, United States. This page reflects FDA report F-0361-2022, dated January 12, 2022.

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 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

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 Snapple Tea Peach Tea 16 OZ recall?

Keurig Dr Pepper recalled Diet Snapple Tea Peach Tea 16 OZ in an FDA Class II enforcement action reported as F-0361-2022. Product labeled to be Diet and Zero Sugar in the ingredient statement may contain sugar due to an production error.

What are the symptoms of Product safety recall exposure?

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.

Who is most at risk from Product safety recall?

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

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.

How do I get a refund from Keurig Dr Pepper?

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 F-0361-2022 and keep the packaging, lot code and proof of purchase if you have them.

Is the Keurig Dr Pepper 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-0361-2022. 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.