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RECALL RECORD — CLASS IIRecall closedF-1906-2018/FDA enforcement
The Coca-cola Company·Food·Aug 3, 2018

Consumer Packaging (Pet Bottle): Minute Maid Tropical Blend Flavored Juice Beverage 12 FL Oz…

What you need to know

Class II

  • What happened

    Foreign matter believed to be glass observed in retain samples of product.

  • 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 FDAVAMore food

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameThe Coca-cola Company
Recalling firmThe Coca-cola CompanyAtlanta, GA, United States
UPC / barcodes
0 25000 06229 200 025000 06241 4
Lot / date codes
  • Production Date: July 9, 2018 Best By Date: January 7, 2018 (JAN0719/NPA) UPC Bottles: 0 25000 06229 2 Master Case: GTIN number 00025000062414 (no UPC)
Distribution area
VA

Retail product distributed to VA. Identity of distributor(s) of the 432 bottles was not provided and is not available at this time. RES currently shows 1 distributor and will be updated with any new information that is received. Update (08/24/18): Product was distributed to 4 distributors - 2 of these distributors distributed the 432 bottles (18 cases); see uploaded e-mails beginning with "8-22-18" and "8-24-18".

United States

Quantity affected432 bottles (18 cases packed 24/12 fluid oz. bottles)
Recall initiationFDA report date: September 5, 2018
FDA recall numberF-1906-2018

Beyond the headline

The recall, in context

The Coca-cola Company initiated this food recall on August 3, 2018. The FDA enforcement report states: Foreign matter believed to be glass observed in retain samples of product. The FDA report lists distribution as: Retail product distributed to VA. Identity of distributor(s) of the 432 bottles was not provided and is not available at this time. RES currently shows 1 distributor and will be updated with any new information that is received. Update (08/24/18): Product was distributed to 4 distributors - 2 of these distributors distributed the 432 bottles (18 cases); see uploaded e-mails beginning with "8-22-18" and "8-24-18".

The FDA enforcement report describes the reason as: Foreign matter believed to be glass observed in retain samples of product.

Consumer Packaging (Pet Bottle): Minute Maid Tropical Blend Flavored Juice Beverage 12 FL Oz… was made or distributed by The Coca-cola Company in Atlanta, GA, United States. This page reflects FDA report F-1906-2018, dated September 5, 2018.

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 Consumer Packaging (Pet Bottle): Minute Maid Tropical Blend Flavored Juice Beverage 12 FL Oz… recall?

The Coca-cola Company recalled Consumer Packaging (Pet Bottle): Minute Maid Tropical Blend Flavored Juice Beverage 12 FL Oz… in an FDA Class II enforcement action reported as F-1906-2018. Foreign matter believed to be glass observed in retain samples of product.

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 The Coca-cola 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-1906-2018. 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.