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RECALL RECORD — CLASS IIIRecall closedF-0500-2018/FDA enforcement
The Hain Celestial Group, INC. - Worldwide Hq·Food·Dec 7, 2017

Blueprint Organic Beet Blast Vegetable & Fruit Drink 16 Fl.oz.(473ml) USDA Organic

What you need to know

Class III

  • What happened

    The label on the back of the bottle may be for the incorrect product.

  • Health risk

    The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. 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 FDACA, CO, CT, FL +9 moreMore food

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Product identification

Source: FDA FOOD

Brand nameThe Hain Celestial Group, INC. - Worldwide Hq
Recalling firmThe Hain Celestial Group, INC. - Worldwide HqNew Hyde Park, NY, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • 09JAN18 and 16JAN18
Distribution area
CACOCTFLIAILNHNJNYPATXWAWI

CA, CO, CT, FL, IA, IL, NH, NJ, NY, PA, TX, WA, WI

United States

Quantity affected1, 949 cases
Recall initiationFDA report date: December 27, 2017
FDA recall numberF-0500-2018

Beyond the headline

The recall, in context

The Hain Celestial Group, INC. - Worldwide Hq initiated this food recall on December 7, 2017. The FDA enforcement report states: The label on the back of the bottle may be for the incorrect product. The FDA report lists distribution as: CA, CO, CT, FL, IA, IL, NH, NJ, NY, PA, TX, WA, WI.

The FDA enforcement report describes the reason as: The label on the back of the bottle may be for the incorrect product.

Blueprint Organic Beet Blast Vegetable & Fruit Drink 16 Fl.oz.(473ml) USDA Organic was made or distributed by The Hain Celestial Group, INC. - Worldwide Hq in New Hyde Park, NY, United States. This page reflects FDA report F-0500-2018, dated December 27, 2017.

Why this is a Class III recall

Class III means the product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations.

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

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 Blueprint Organic Beet Blast Vegetable & Fruit Drink 16 Fl.oz.(473ml) USDA Organic recall?

The Hain Celestial Group, INC. - Worldwide Hq recalled Blueprint Organic Beet Blast Vegetable & Fruit Drink 16 Fl.oz.(473ml) USDA Organic in an FDA Class III enforcement action reported as F-0500-2018. The label on the back of the bottle may be for the incorrect 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 Hain Celestial Group, INC. - Worldwide Hq 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-0500-2018. 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.