RECALL RECORD — CLASS IIRecall closedF-1006-2020/FDA enforcement
Coca Cola·Food·Jun 18, 2020

Dr Pepper Cherry 20 OZ

What you need to know

Class II
  • What happened

    Potential that some bottles could contain glass fragments

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. Glass fragments can cause cuts, choking or internal injury if swallowed.

  • 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 FDATXMore food

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Product identification

Source: FDA FOOD

Brand nameCoca Cola
Recalling firmCoca ColaDallas, TX, United States
UPC / barcodes
0 78000 09840 2
Lot / date codes
  • SEP2920LWB
Distribution area
TX

Corpus Christi and San Antonio, TX Metropolitan areas

United States

Quantity affected3 cases
Recall initiationFDA report date: July 8, 2020
FDA recall numberF-1006-2020

Beyond the headline

The recall, in context

Coca Cola initiated this food recall on June 18, 2020. The FDA enforcement report states: Potential that some bottles could contain glass fragments. The FDA report lists distribution as: Corpus Christi and San Antonio, TX Metropolitan areas.

The FDA enforcement report describes the reason as: Potential that some bottles could contain glass fragments

Dr Pepper Cherry 20 OZ was made or distributed by Coca Cola in Dallas, TX, United States. This page reflects FDA report F-1006-2020, dated July 8, 2020.

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, glass fragments can cause cuts, choking or internal injury if swallowed.

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

Glass contamination

Possible health effects

Glass fragments can cause cuts to the mouth, throat or digestive tract. Do not inspect or taste a suspect product.

Higher-risk groups

Children, older adults and anyone who may swallow a fragment without noticing are at greater risk of injury.

What to do now

  1. 1Stop eating or using the product and do not attempt to remove fragments by tasting it.
  2. 2Seek medical care if anyone has swallowed glass, has throat or abdominal pain, or is vomiting blood.
  3. 3Keep the packaging and contact the retailer or manufacturer about a refund; follow the recall notice for disposal.

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 Dr Pepper Cherry 20 OZ recall?

Coca Cola recalled Dr Pepper Cherry 20 OZ in an FDA Class II enforcement action reported as F-1006-2020. Potential that some bottles could contain glass fragments

What injuries or health effects are linked to glass contamination?

Glass fragments can cause cuts to the mouth, throat or digestive tract. Do not inspect or taste a suspect product.

Who is most at risk from Glass contamination?

Children, older adults and anyone who may swallow a fragment without noticing are at greater risk of injury.

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 eating or using the product and do not attempt to remove fragments by tasting it. Seek medical care if anyone has swallowed glass, has throat or abdominal pain, or is vomiting blood. Keep the packaging and contact the retailer or manufacturer about a refund; follow the recall notice for disposal.

How do I get a refund from Coca Cola?

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-1006-2020 and keep the packaging, lot code and proof of purchase if you have them.

Is the Coca Cola 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-1006-2020. 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.