RECALL RECORD — CLASS IIRecall closedF-0197-2014/FDA enforcement

Guzzler Citrus Punch, 20 FL

What you need to know

Class II
  • What happened

    There is a possibility that a part of the nozzle cap of the bottle can become dislodged through abuse (i.e. excessive chewing) then possibly ingested, and posing a potential…

  • 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 FDANationwide (US)More food

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Product identification

Source: FDA FOOD

Brand nameAmerican Beverage Corp
Recalling firmAmerican Beverage CorpVerona, PA, United States
UPC / barcodes
0 18397 00013 8
Lot / date codes
  • The following product bearing a "best buy" or "expiration date" earlier than 09/24/12 ONLY: Flavor and UPC code: Citrus Punch, 018397000138
Distribution area
Nationwide

Nationwide.

United States

Quantity affected250, 000 cases-total for all products
Recall initiationFDA report date: November 27, 2013
FDA recall numberF-0197-2014

Beyond the headline

The recall, in context

American Beverage Corp initiated this food recall on May 15, 2012. The FDA enforcement report states: There is a possibility that a part of the nozzle cap of the bottle can become dislodged through abuse (i.e. excessive chewing) then possibly ingested, and posing a potential health/safety hazard. The cap in question is no longer used by ABC and was last produced in September of 2011. Firm does not anticipate finding any impacted product in the market. The FDA report lists distribution as: Nationwide.

The FDA enforcement report describes the reason as: There is a possibility that a part of the nozzle cap of the bottle can become dislodged through abuse (i.e. excessive chewing) then possibly ingested, and posing a potential health/safety hazard. The cap in question is no longer used by ABC and was last produced in September of 2011. Firm does not anticipate finding any impacted product in the market.

Guzzler Citrus Punch, 20 FL was made or distributed by American Beverage Corp in Verona, PA, United States. This page reflects FDA report F-0197-2014, dated November 27, 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 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 Guzzler Citrus Punch, 20 FL recall?

American Beverage Corp recalled Guzzler Citrus Punch, 20 FL in an FDA Class II enforcement action reported as F-0197-2014. There is a possibility that a part of the nozzle cap of the bottle can become dislodged through abuse (i.e. excessive chewing) then possibly ingested, and posing a potential…

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 American Beverage Corp?

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-0197-2014 and keep the packaging, lot code and proof of purchase if you have them.

Is the American Beverage Corp 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-0197-2014. 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.